Podcasts about international pain foundation

This episode is focused on a topic that does NOT get enough attention: chronic pain. A 2022 study published in the journal Pain found that 50.2 million adults in the U.S. (that's over 20% of us) reported pain on most days or every day… that makes it one of the most common chronic health conditions in America. Let's rip the band-aid off! I'm joined by one of my favorite advocates for this important discussion… Barby Ingle from the International Pain Foundation.

Batista Gremaud is the CEO and president of Dr Fitness International, Strength Training Expert, No1 Best Selling author of Feminine Body Design, Empowering Fitness For A Pain-Free Life, co-creator of the Feminine Body Design online strength training mentoring system, co-host of the Esoteric Principles of Bodybuilding, and producer of the Dr. Fitness USA's show; Recipient of the most outstanding fitness program 2019 by The Winners Circle, Mastermind at Sea. She writes for The Heart Of Hollywood Magazine and was featured in The Los Angeles Tribune Magazine and Voyage LA. She appeared as an expert authority speaker at the International Pain Foundation and is a presenter at various health summits such as “Life Mastery”, “Girl You Are Enough” and “The Teen Suicide Prevention Show”.   I never thought lifting weights would be the key to a pain-free life. As a dancer, my body was constantly breaking down, and I tried every holistic approach out there. But it wasn't until I met Dr. Fitness USA that everything changed. He introduced me to strength training, and I was skeptical at first, but the results were undeniable. My injuries healed, and my body became stronger than ever. Now, I'm passionate about sharing this transformative experience with others, especially women balancing work and fitness. It's time to ditch the pain and embrace strength training. Are you ready to join me on this journey.   In this episode, you will be able to: Grasp the significance of strength training in promoting balance and alleviating pain. Gain insight into overcoming osteoporosis using result-driven resistance training practices. Realize the rewards of merging body, mind, and spiritual facets in your fitness journey. Appreciate the value of skilled guidance and continuous learning in achieving fitness goals. Comprehend the vital relationship between muscle mass, metabolism, and enduring health rewards.   Get in touch with Batista: https://www.drfitnessusa.com https://www.instagram.com/femininebodydesign/ https://www.facebook.com/batistagremaud https://www.linkedin.com/in/batistagremaud/ https://twitter.com/batistagremaud   Get Our Award-Winning 6-Week Fat Loss Program Completely FREE In this program, you will be able to: Figure out what works Destress your body Boost your Metabolism And lose weight with real food https://offer.drfitnessusa.com/fatloss   Get in touch with Jana and listen to more Podcasts: https://www.janashort.com/   Show Music ‘Hold On' by Amy Gerhartz https://www.amygerhartz.com/music.   Get the Best Holistic Life Magazine APP! One of the fastest-growing independent magazines centered around holistic living. https://www.bestholisticlife.com/bhl-subscription/     Grab your gift today: https://www.janashort.com/becoming-the-next-influencers-download-offer/ Connect with Jana Short: https://www.janashort.com/contact/

Are you or someone you love living with a chronic disease (1 in 3 people do)? If so, then medical bills and expenses can be a headache.  Join us as we explore different ways to manage the costs of chronic diseases, including negotiating with medical providers and insurance companies, going directly to pharmaceutical manufacturers for discounts, bargaining for services and skills, and applying for financial assistance. Learn the tips you need to help make living with chronic disease more affordable! About Our Guest Barby Ingle is a best-selling author, reality personality, and lives with multiple rare and chronic diseases. Barby is a chronic pain educator, patient advocate, and president of the International Pain Foundation. She is also a motivational speaker and best-selling author on pain topics. Her blog, reality shows, and media appearances are used as a platform to help her become an e-Patient advocate, and she presents at healthcare conferences, speaking publicly, sharing her story, and educating and advocating for patients across the globe. She has received more than 25 commendations for her advocacy efforts. She is the reigning Mrs Southwest Petite USA. Connect with Barby Twitter: barbyingle Instagram: barbyingleofficial Facebook: Barby Ingle Official Additional Resources Visit Our Website Dr. Virgie Bright Ellington Demystifies Medical Bills | Ep. 228  

Batista Gremaud is the CEO and president of Dr Fitness International, Strength Training Expert, No1 Best Selling author of Feminine Body Design, Empowering Fitness For A Pain-Free Life, co-creator of the Feminine Body Design online strength training mentoring system, co-host of the Esoteric Principles of Bodybuilding, and producer of the Dr Fitness USA's show; Recipient of the most outstanding fitness program 2019 by The Winners Circle, Mastermind at Sea. She writes for The Heart Of Hollywood Magazine, was featured in The Los Angeles Tribune Magazine and Voyage LA. She appeared as an expert authority speaker on the International Pain Foundation, and is a presenter on various health summits such as “Life Mastery”, “Girl You Are Enough”  and  “The Teen Suicide Prevention Show”.How to Be Balanced, Beautiful and Abundant?For more information go to…https://www.rebeccaelizabethwhitman.com/Https://linktr.ee/rebeccaewhitman This is The Quickest & Easiest Way To Your Own Side Hustle!Show me how----->https://balancedbeautifulabundant.com/

Connect with Batista Gremaud: Batista Gremaud is the CEO and president of Dr Fitness International, Strength Training Expert, No1 Best Selling author of Feminine Body Design, Empowering Fitness For A Pain-Free Life, co-creator of the Feminine Body Design online strength training mentoring system, co-host of the Esoteric Principles of Bodybuilding, and producer of the Dr Fitness USA's show; Recipient of the most outstanding fitness program 2019 by The Winners Circle, Mastermind at Sea. She writes for The Heart Of Hollywood Magazine, was featured in The Los Angeles Tribune Magazine and Voyage LA. She appeared as an expert authority speaker on the International Pain Foundation, and is a presenter on various health summits such as “Life Mastery”, “Girl You Are Enough”  and  “The Teen Suicide Prevention Show”. SCULPT YOUR BODY - SCULPT YOUR BRAIN Build Your Body With Neuroscience Business Name: Dr Fitness USA / Dr Fitness International Location/Address: 313 Grand Blvd #1031, Venice, CA 90291 Guest's Name & Position: Batista Gremaud: Co-Founder Cell Phone: 310.562.6047 Bus Phone: 424.245.6560 Fax: (310) 382-2459 Skype: DrFitnessUSA Email: batista@drfitnessusa.com Website: DrFitnessUSA.com – DrFitnessInt.com https://www.linkedin.com/in/batistagremaud/ https://twitter.com/batistagremaud https://www.facebook.com/drfitnessusa Connect with Host Terry Lohrbeer Facebook: https://www.facebook.com/groups/2658545911065461/ LinkedIn: https://www.linkedin.com/in/terrylohrbeer/ Instagram: kickassboomers Twitter: @kickassboomers   Connect to Premiere Podcast Pros for podcast editing: premierepodcastpros@gmail.com

Connect with Batista Gremaud: Batista Gremaud is the CEO and president of Dr Fitness International, Strength Training Expert, No1 Best Selling author of Feminine Body Design, Empowering Fitness For A Pain-Free Life, co-creator of the Feminine Body Design online strength training mentoring system, co-host of the Esoteric Principles of Bodybuilding, and producer of the Dr Fitness USA's show; Recipient of the most outstanding fitness program 2019 by The Winners Circle, Mastermind at Sea. She writes for The Heart Of Hollywood Magazine, was featured in The Los Angeles Tribune Magazine and Voyage LA. She appeared as an expert authority speaker on the International Pain Foundation, and is a presenter on various health summits such as “Life Mastery”, “Girl You Are Enough”  and  “The Teen Suicide Prevention Show”. SCULPT YOUR BODY - SCULPT YOUR BRAIN Build Your Body With Neuroscience Business Name: Dr Fitness USA / Dr Fitness International Location/Address: 313 Grand Blvd #1031, Venice, CA 90291 Guest's Name & Position: Batista Gremaud: Co-Founder Cell Phone: 310.562.6047 Bus Phone: 424.245.6560 Fax: (310) 382-2459 Skype: DrFitnessUSA Email: batista@drfitnessusa.com Website: DrFitnessUSA.com – DrFitnessInt.com https://www.linkedin.com/in/batistagremaud/ https://twitter.com/batistagremaud https://www.facebook.com/drfitnessusa Connect with Host Terry Lohrbeer Facebook: https://www.facebook.com/groups/2658545911065461/ LinkedIn: https://www.linkedin.com/in/terrylohrbeer/ Instagram: kickassboomers Twitter: @kickassboomers   Connect to Premiere Podcast Pros for podcast editing: premierepodcastpros@gmail.com

I got to speak with Barby Ingle. Barby Ingle is a best-selling author and reality personality living with multiple rare and chronic diseases. Barby is a chronic pain educator, patient advocate, and president of the International Pain Foundation. She is also a motivational speaker and best-selling author on pain topics. Her blog, reality shows, and media appearances are used as a platform to help her become a Patient advocate. She presents at healthcare conferences, speaking publicly, sharing her story, and educating and advocating for patients across the globe. She has received more than 25 awards for her advocacy efforts. Barby currently serves as the reigning Mrs. Southwest Petite USA. We spoke about: 2:45 Losing everything. 3:40 Having hope. 10:00 On earth for a purpose. 17:45 Life's challenges. 21:15 Don't be afraid to open doors in your life. This episode is sponsored by Nova Zora Digital experts in digital marketing. *Disclaimer: The views and opinions on Roman Prokopchuk's Digital Savage Experience are those of the guest's alone as their own, and the host's alone as his own. Information provided by the guest is fact checked to the best of our abilities. By providing background information to the show, the guest acknowledges that it is as accurate as possible. The show does not endorse, promote, or is in association with the guest's business interests.*

Barby was born in Bangkok, Thailand and now resides in Arizona.  She says she has been a chronic pain patient for over 20 years.  Her way through this battle involved her becoming the Chief of Staff of her own medical team.     It took her 3 years to get a diagnosis of what was going on with her, and then another 4 years to get on the right treatment.     Barby shares a lot of great resources for chronic pain conditions as well as dives into her journey in more detail.  She has written several books, mentors patients as a volunteer, and sits on the board of directors for internationalpain.org.  She's come a long way from being bedridden and in a wheelchair!   Learn more about Barby here: barbyingle.com Guest Bio: Barby Ingle is a best-selling author and reality personality living with multiple rare and chronic diseases.    Barby is a chronic pain educator, patient advocate, and president of the International Pain Foundation. She is also a motivational speaker and best-selling author on pain topics.    Her blog, reality shows, and media appearances are used as a platform to help her become a Patient advocate.    She presents at healthcare conferences, speaking publicly, sharing her story, and educating and advocating for patients across the globe. She has received more than 25 awards for her advocacy efforts.    Barby currently serves as the reigning Mrs. Southwest Petite USA.  ___________________ Subscribe to this podcast and download your favorite episodes to listen to later: Apple Spotify RSS Feed ___________________   ⚕️ Are you a woman healthcare professional who is struggling to juggle everything in your personal and professional life?  

Barby Ingle is a best-selling author and reality TV personality who lives with multiple rare and chronic diseases.Barby is a chronic pain educator, patient advocate, and president of the International Pain Foundation. She is also a motivational speaker and best-selling author on pain topics.Her blog, reality shows, and media appearances are used as a platform to help her become an e-Patient advocate. She presents at healthcare conferences, speaking publicly, sharing her story, and educating and advocating for patients across the globe.Today, Barby and I will discuss chronic disease and hope, enjoy the show.WATCH - https://vimeo.com/765847581http://barbyingle.com/www.internationalpain.orghttps://www.facebook.com/BarbyIngleOfficial@barbyingleofficial#pain #trauma #chronicpain #raredisease #rareillness #truehopecanada #empowerplus#healing #health #healthpodcast #health #energy #anxiety #podcasting #mindfulness #podcast #podcaster #podcastinglife #mentality #mentalhealth #mentalillness #mentalwellness #mentalhealthpodcast

When we're kids we believe we're going to live forever. Then when the years pile on we start to notice some changes. Our gait slows. It's harder to lose weight and the pounds add up. We have more aches and pains. Our range of motion lessens. And all that assumes we don't incur any major illnesses or diseases that impact our lives even further and diminish our joy in life. My guest, fitness and strength training expert Batista Gremaud thought she'd be fit forever as well. As a dancer she considered herself in great health. But when injuries led to unending pain she realized if she didn't change she'd turn from vibrant woman to old lady overnight. Her search for a solution led her on a journey that ended with her becoming an expert in fitness and creating and running wellness programs that result in remarkable improvements in reducing her students' pain and increasing their quality of life. She shares her tips with us on this episode and reveals:•How to deal with pain without pills•The program that leads to regaining hope and lust for life•What exercises to do—and what not to do•Why it's important to reverse muscle loss•The connection between physical and mental health•How your workout can keep you feeling young Whether you're 45 or 85, it's never too late to get yourself back into shape. Get your inspiration here on this energetic episode of Dream Power Radio. Batista Gremaud is the CEO and President of Dr Fitness International, International Body Designer, Empowerment Speaker, providing individual and corporate wellness programs worldwide. Batista's expertise in prescription strength training includes the structural realignment of the spine and injury prevention. Batista is the producer and host of “The Dr Fitness USA Show”, and the co-host of the 13-part series “The Esoteric Principles of BodyBuilding: Missing Links to Fitness Consciousness. She received the “Most Outstanding Fitness Program For 2019” by the Winners Circle, featured as an expert authority speaker on the “International Pain Foundation”, In the Limelight with Clarissa Burt, The Teen Suicide Prevention Summit”, NEXT Virtual Global Summit, KPFK “Inner Vision” with Dr. Richard Byrd, “People of Distinction” with Al Cole, “Amazing Women of Power”, “The Dr. Kevin Show”, Lou Hicks famous “Aimed2Purpose” global broadcast, “Sonia Uplugged”, “The Nikki Rich Show”, “Never Too Late For Fitness”, “Princess Power”, and many more. Batista Gremaud is the No1 Best Selling author of “Feminine Body Design, Empowering Fitness for a Pain-Free Life”, and co-creator of the Feminine Body Design online prescription strength training system. Other books by Batista available on Amazon include “Posture4Power”, How to Lose Weight and Look good with Strength Training”. She is a staff writer for the Los Angeles Tribune Magazine, and has written for “In The Limelight”, “Keys to Recovery” and “Recovery Illustrated” magazines and online health platforms and was featured on Voyage LA. Batista Gremaud's long time passion in quantum physics and metaphysical science inspires her to help people of all ages to achieve greater integration of body, mind and spirit through the practice of strengthening the body and the mind with the Dr Fitness USA's Body Design Formula prescription strength training coaching system. Celebrity students include Berny Dohrmann, Roger Wajed Salam, Simon Crane, Billy West, Sonia Ete, Joel Bauer, Fred Van Liew, Gerry Foster, Nicholas Zaldastani, Christy Elcker, Dr. Georges Borris, Tim Ray, Brian Kelly, Tyhson Banighen among others. Website: https://drfitnessusa.comGet a free consultation with Batista by going on her website https://drfitnessusa.com and mentioning "Dream Power Radio" when signing up.

Barby Ingle is a best-selling author, reality personality and lives with multiple rare and chronic diseases; reflex sympathetic dystrophy(RSD), migralepsy, PALB2-var breast cancer, valley fever, endometriosis, and other pain disorders. Barby is a chronic pain educator, patient advocate, and president of the International Pain Foundation. She is also a motivational speaker and best-selling author on pain topics. Her blog, reality shows, and media appearances are used as a platform to help her become an e-Patient advocate, and she presents at healthcare conferences, speaking publicly, sharing her story, and educating and advocating for patients across the globe. She has received more than 25 commendations for her advocacy efforts, including; 2012 WEGO Health Ms. Congeniality, 2012 NAF You Are Our Hero Award, 2013 International Inspirational Luminary, 2015 IDA Impact Award, and 2016 WEGO Health Lifetime Achievement. In 2017, Barby was named a Health Information Technology Top 100 Influencer by HealthScene and Top 20 Health Influencer by Insider Monkey Magazine. In 2018, Barby received the Reality All-Star Reunion Superstar award for her Social Media efforts and Top 50 Chronic Pain Advocates. In 2020, Barby is listed in the top 50 social media advocates for Rare Diseases and top 10 Healthcare Influencers for All Marketers to Follow, 2020 PharmaVOICE100, 2020 HITMC Patient Advocate of the Year. In 2021 Barby was awarded the 2021 Medigy HITmc Music Video of the year and 2021 Arizona Capitol Times Leader of the Year; Healthcare. In Feb. 2021 Barby was listed in the top 75 social media advocates for rare diseases. Barby currently serves as the reigning Mrs. Southwest Petite USA and will compete at the National event in Aug 2022. http://www.barbyingle.com/

Barby Ingle is a best-selling author, reality personality and lives with multiple rare and chronic diseases; reflex sympathetic dystrophy(RSD), migralepsy, PALB2-var breast cancer, valley fever, endometriosis, and other pain disorders. Barby is a chronic pain educator, patient advocate, and president of the International Pain Foundation.In this episode we learn what Barby's story is, and what lead her to be a patient advocate, which lead to her to start the president of her foundation.  To get a hold Barby www.BarbyIngle.comwww.internationalpain.org(This information on this website is only intended to be general summary information for public use. This information does not replace written law or regulations, nor does it replace professional medical advice, diagnosis, or treatment. If you have questions about a medical condition, always seek the advice of a doctor or other qualified health professional)ZBiotics Pre-Alcohol ProbioticBreaks down the byproduct of alcohol responsible for rough mornings after drinking.Brand

Season 3 Replay: Even after an accident left her in chronic pain, Barby Ingle knew that God had a plan for her life. Barby, the president of the International Pain Foundation, credits God for a new life post-accident that was even better than before. He even sent Barby her Ken! Her encouragement to others suffering from chronic pain is true to her unofficial title, the cheerleader for hope.   

We hear about people living with pain daily. When pain hits, we focus on the pain and not the cost of living in pain. She lost everything to pain, then slowly rebuilt her life and became an advocate for pain patients. Barby Ingle, the president of the International Pain Foundation.She's here to share her story and provide insight on the health and financial impact of pain. Barby Ingle is a best-selling author, reality personality, and lives with multiple rare and chronic diseases; reflex sympathetic dystrophy (RSD), migralepsy, PALB2-var breast cancer, valley fever, endometriosis and other pain disorders.  She is also a motivational speaker and best-selling author on pain topics. Her blog, reality shows and media appearances are used as a platform to help her become an e-Patient advocate, and she presents at healthcare conferences, speaking publicly, sharing her story, educating and advocating for patients across the globe. She has received more than 20 accommodations over the years for her advocacy work including; 2012 WEGO Health Ms. Congeniality, 2012 NAF You Are Our Hero Award, 2013 International Inspirational Luminary, 2015 IDA Impact Award, and 2016 WEGO Health Lifetime Achievement. In 2017, Barby was named a Health Information Technology Top 100 Influencer by HealthScene and Top 20 Health Influencer by Insider Monkey Magazine. In 2018, Barby received the Reality All Star Reunion Superstar award for her Social Media efforts and Top 50 Chronic Pain Advocates. In Feb. 2021 Barby was listed in the top 75 social media advocates for RareDiseases. In 2020, Barby is listed in the top 50 social media advocates for Rare Diseases and top 10 Healthcare Influencers for All Marketers to Follow, 2020 PharmaVOICE100, 2020 HITMC Patient Advocate of the Year. In 2021 Barby was awarded the 2021 Medigy HITmc Music Video of the year and 2021 Arizona Capitol Times Leader of the Year; Healthcare. For more great information or to contact Barby, please visit: http://barbyingle.com/Valuable Links:  Pharmacogenomics (PGX) - www.mygeneticmeds.com Viome  - usually $300-500. You can get the Viome gut health test at http://viome.com/raceto2million  on sale for $149.For more information and other valuable resources, make sure to subscribe, follow and visit our sites.Website: https://www.thevoiceofmany.com Instagram: https://www.instagram.com/theevoiceofmany/?hl=en Twitter: https://twitter.com/TheVoiceofMany3 Facebook: https://www.facebook.com/The-Voice-of-Many LinkedIn: www.linkedin.com/in/the-voice-of-many-podcast-1417a81b7 YouTube: https://www.youtube.com/channel/UCMmouE4IqrsPG2gnaERlY-ASupport the show

The International Pain Foundation  Barby Ingle pt 2 I have a very important topic for you today…and one that is very near and close to my heart…one which affects me as well as millions of people each and every day – and that is how to cope with chronic pain…be it from injury, as in my case, or from hereditary diseases or any number of a myriad of causes…one which many people have a hard time understanding – even very close family members… On the line with us today is Barby Ingle from http://www.internationalpain.org/ (the International Pain Foundation)…Barby is a former model and professional cheerleader. She seemed to have it all. And then things changed. Her life become totally focused on survival. Chronic pain ravaged her body. Doctors had no clue as to why. They stuck, prodded, probed and examined numerous times. All sorts of test (and can I relate to that). Then, one day, Barby decided enough was enough and SHE became her own “Chief of Staff” for her medical team.  And I will let her explain that as we get into the interview. Barby has been on our program a few times in the past and the information she shares blessed so many of our listeners, I'm sure it will do the same today as well.  She is also the author of several books dealing with this issue, such as https://amzn.to/3spAEiY (“From Wheels to Heals,”) which is the first one I read, getting ready for our first interview back in 2018! Praise God! This is part two of what turned out to be a great, two part interview! Your foundation helps people from all over the world find support services and resources to help their conditions. Can you go over a few of the most popular services? This next topic is a big one. What about managing pain killers? I know the laws and medical practices concerning prescription pain killers have changed since the last time we talked. Is it still a major issue? Pastor Bob shares about kicking his addiction to pain killers after talking with Barby Ingle and reading information from thehttp://www.internationalpain.org/ ( International Pain Foundation website…) This is the type of situation where your foundation could provide the resources to help someone in a situation similar to what I went through (and, I was reading articles, etc. from your website while going this ordeal myself). Barby, you've outlined a lot of this in your book, https://amzn.to/3spAEiY (“From Wheels to Heals,”) correct? Pastor Bob shares on how he continued to be the “Chief Medical Officer of his own body.” Barby, it's amazing what you can do when you make up your own mind, put your foot down and tell the doctor that “this is the way it is going to be.” Barby, if something we said sparked a word of enlightenment to one of our listeners and they had an “ah-ha” moment saying, “That's just like me!”  How can they get in touch with thehttp://www.internationalpain.org/ (International Pain Foundation?) If someone wanted to get in touch with you, maybe to ask a question or do an interview such as this, how can they do that? How can someone get in touch with you? Folks, pain is real. Pain is, well, painful. Some people do well bearing with pain. Some pain is the result of an injury and can be fixed. But there are times when pain is present and nobody knows why. We are talking about physical pain here. But that physical pain can definitely become psychological pain very quickly. You cannot deal with this yourself. http://www.internationalpain.org/ (International Pain Foundation) is here to help you. They will provide you with the resources to learn more about your conditions. They will provide you with the resources to get help. They will provide you with the resources to find  someone you can talk with. They are here for you. Barby Ingle founded this great organization because these resources were not in one centralized...

The International Pain Foundation  Barby Ingle pt 1 I have a very important topic for you today…and one that is very near and close to my heart…one which affects me as well as millions of people each and every day – and that is how to cope with chronic pain…be it from injury, as in my case, or from hereditary diseases or any number of a myriad of causes…one which many people have a hard time understanding – even very close family members… On the line with us today is Barby Ingle from http://www.internationalpain.org/ (the International Pain Foundation)…Barby is a former model and professional cheerleader. She seemed to have it all. And then things changed. Her life become totally focused on survival. Chronic pain ravaged her body. Doctors had no clue as to why. They stuck, prodded, probed and examined numerous times. All sorts of test (and can I relate to that). Then, one day, Barby decided enough was enough and SHE became her own “Chief of Staff” for her medical team.  And I will let her explain that as we get into the interview. Barby has been on our program a few times in the past and the information she shares blessed so many of our listeners, I'm sure it will do the same today as well.  She is also the author of several books dealing with this issue, such as https://amzn.to/3spAEiY (“From Wheels to Heals,”) which is the first one I read, getting ready for our first interview back in 2018! Praise God! Help we welcome back to the program, Barby Ingle! Barby, thank you for taking the time to come back on the program today!  It's been what, three or four years since your last interview? Our podcast listening audience has grown exponentially since the last time you were on. For those that may not know about you or your organization, http://www.internationalpain.org/ (The International Pain Foundation), tell us in your own words, “Who is Barby Ingle?” I want to back track to when you became the “Chief of Staff” of your own medical team. Can you share with us what this phrase means and how someone can implement it? Didn't the doctors tell you something like, “Stop reading all that other stuff and just listen to me?” For privacy reasons, you don't have to go into detail, but how are you doing? Are you still having some issues with your pain and your health? I'm sure your situation was much worse than mine.  But I said all of that, one, just to catch you up. But two, to demonstrate to our listeners that you are not in this alone. Only YOU can decide when “enough is enough.” There is a reason doctors have a “medical practice.” Barby, how should a person react when they get the “look” from a physician, like they really don't believe them concerning the pain they are experiencing? They think we are hypochondriacs or something? Tell us about the http://www.internationalpain.org/ (International Pain Foundation…) Folks, pain is real. Pain is, well, painful. Some people do well bearing with pain. Some pain is the result of an injury and can be fixed. But there are times when pain is present and nobody knows why. We are talking about physical pain here. But that physical pain can definitely become psychological pain very quickly. You cannot deal with this yourself. http://www.internationalpain.org/ (International Pain Foundation) is here to help you. They will provide you with the resources to learn more about your conditions. They will provide you with the resources to get help. They will provide you with the resources to find  someone you can talk with. They are here for you. CONTACT INFORMATION: https://amzn.to/3spAEiY ()   Email:  barby@internationalpain.org Website:  http://www.internationalpain.org/ (www.internationalpain.org) Personal Website:  http://www.barbyingle.com/ (www.barbyingle.com) Book: https://amzn.to/3spAEiY (“From Wheels...

Barby Ingle has received more than 20 accolades for her work in the chronic pain community over the years. She is a chronic pain educator, patient advocate, and President of the International Pain Foundation, as well as a motivational speaker and best selling author on pain topics. She has been a pain patient since developing endometriosis in 1997, and reflex sympathetic dystrophy in 2002. Barby wrapped up her live digital-tv webisode Season 8 of The Ken and Barby Show with her husband Ken Taylor late last year. Barby serves the Pain Community as a volunteer for the International Pain Foundation, Member 2006-2010, Executive Director 2011-2012, President 2013-current She also volunteers for Reality Rally, Global Genes, RDLA, CPATF, and other meaningful charity as she is able. http://www.barbyingle.com/ http://www.internationalpain.org/ Twitter @barbyIngle Facebook @barbyingleofficial Listen to more episodes at https://ResilientLifeHacks.com  MY BOOKS: Undefeated: From Trial to Triumph, How to Stop Fighting the Wrong Battles and Start Living Victoriously https://www.amazon.com/Undefeated-Trial-Triumph-Stand-Strong/dp/1640850872 Undaunted in Darkness: Finding Your Path From Broken to Bold, Your Daily Battle Plan for a Winning Life https://www.amazon.com/Undaunted-Darkness-Finding-Broken-Strong/dp/B09MYR8TH9/ Get my TOP 20 RESILIENT LIFE HACKS here! https://elizabeth-meyers.ck.page/1a1ef0ef89  Join our RESILIENT LIFE TRIBE: https://facebook.com/groups/resilientlifetribe

Growth and change are inevitable throughout our lives, so it's important to understand that it is normal to have a different experience processing grief within each stage of life. In this twenty first episode together, I am joined by Barby Ingle, best-selling author and reality personality. Barby lives with multiple rare and chronic diseases; reflex sympathetic dystrophy (RSD), migralepsy, PALB2-var breast cancer, valley fever, endometriosis and other pain disorders. Barby's best-selling book, From Wheels to Heals, demonstrates that it is possible to find successful treatment options for those living with chronic pain. Barby is a chronic pain educator, motivational speaker, patient advocate, and president of the International Pain Foundation. Throughout this episode, Barby and I talk about everything she has learned about grief from both loss and living with chronic pain. She explains her different grief experiences after losing her father, mother, grandmother, various boyfriends, a childhood classmate, and others. Barby opens up and shares how she has continued to choose happiness each day and the grief that comes with living with chronic pain. I hope this conversation with Barby reminds you that we all process grief differently and no one way is right or wrong. Tune in and listen to the twenty first episode of Grief and Happiness, and join me in learning Barby Ingle's inspiring story. In This Episode, You Will Learn:Barby's perspective of grief and happiness (1:16)How grief is different for children and adults (11:23)About Barby's loss of her father (14:06)How writing her book helped Barby practice peace (19:33)Barby's grief around living with chronic pain (21:54)Connect with Barby IngleBooksBlogFacebookInstagramTwitterWebsite Let's Connect:WebsiteLinkedInFacebookInstagramTwitterPinterestBook: Emily Thiroux Threatt - Loving and Living Your Way Through Grief Hosted on Acast. See acast.com/privacy for more information.

The inspiring co-founder of the International Pain Foundation, Barby Ingle, joined your host, Kara Fernstrom, for this episode to talk about pain, health, and self-advocacy. This important conversation covers about Barby's story, the International Pain Foundation, navigating the health system, and even a bit about navigating the potential minefield of other people's chronic pain conditions.For more of Barby's great stuff, you can find her at:BarbyIngle.comOr on InstaThis episode, like many, was brought to you by the After Dark BandWarning: This Podcast contains explicit language (probably), and casual conversation about what very well might be triggering topics (also probably). Listener Discretion is advised. Intro and background music mixed from public domain songs found on freemusicarchive.org

Season 3, Ep. 48: Even after an accident left her in chronic pain, Barby Ingle knew that God had a plan for her life. Barby, the president of the International Pain Foundation, credits God for a new life post-accident that was even better than before. He even set Barby her Ken! Her encouragement to others suffering from chronic pain is true to her unofficial title, the cheerleader for hope. 

Barby Ingle joins Alex Burket on the Rise to the Challenge Podcast. Barby talks about her personal challenges and how she has stayed focus and positives through each struggle. We talk about the International Pain Foundation and the impact it has had. We talk about her love for cheerleader and her favorite moments. She talks about being an author and why she wrote her books. We talk about so much more on the Rise to the Challenge Podcast. Check out the links below to learn more about Barby Ingle: - Blog - http://barbyingle.com/blog - Blog - https://internationalpain.org/pop-blog/ - Facebook - www.facebook.com/BarbyIngleOfficial - Facebook - www.facebook.com/iPainFoundation - Instagram – www.instagram.com/kenandbarbyshow - Instagram - https://www.instagram.com/internationalpainfoundation - Twitter - www.twitter.com/BarbyIngle - Twitter - www.twitter.com/PowerofPain - Website – www.barbyingle.com - Website - www.internationalpain.org - YouTube - www.youtube.com/user/barbyallyn

Barby Ingle is a best-selling author, reality personality, and lives with multiple rare and chronic diseases. She is a chronic pain educator, patient advocate, and president of the International Pain Foundation. Her blog, reality shows, and media appearances are used as a platform to help her become an e-Patient advocate, and she presents at healthcare conferences, speaking publicly, sharing her story, educating and advocating for patients across the globe. Barby has received more than 20 accommodations over the years for her advocacy work.

Time and money mean different to different people. For Barby Ingle, living with multiple rare chronic diseases has changed the way she views these things. Instead of 24-hours, she lives in each moment. She has also learned to live more consciously when it comes to saving. In this episode, she joins Penny Zenker to share her journey with us, inspiring us to make time for our health because then we can take our time back. Barby is a chronic pain educator, patient advocate and President of the International Pain Foundation. She also shares what helped her stay positive through it all, why being mindful with her medical bills helped save money, and how you can get through painful situations. Don't miss out on this inspiring conversation!Love the show? Subscribe, rate, review, and share! https://pennyzenker360.com/positive-productivity-podcast/

Barby Ingle is a best-selling author, reality personality, and lives with multiple rare and chronic diseases; reflex sympathetic dystrophy (RSD), migralepsy, PALB2-var breast cancer, valley fever, endometriosis and other pain disorders. Barby is a chronic pain educator, patient advocate, and president of the International Pain Foundation. She is also a motivational speaker and best-selling author on pain topics. Her blog, reality shows and media appearances are used as a platform to help her become an e-Patient advocate, and she presents at healthcare conferences, speaking publicly, sharing her story, educating and advocating for patients across the globe. She has received more than 20 accommodations over the years for her advocacy work including; 2012 WEGO Health Ms. Congeniality, 2012 NAF You Are Our Hero Award, 2013 International Inspirational Luminary, 2015 IDA Impact Award, and 2016 WEGO Health Lifetime Achievement. In 2017, Barby was named a Health Information Technology Top 100 Influencer by HealthScene and Top 20 Health Influencer by Insider Monkey Magazine. In 2018, Barby received the Reality All Star Reunion Superstar award for her Social Media efforts and Top 50 Chronic Pain Advocates. In Feb. 2021 Barby was listed in the top 75 social media advocates for RareDiseases. In 2020, Barby is listed in the top 50 social media advocates for Rare Diseases and top 10 Healthcare Influencers for All Marketers to Follow, 2020 PharmaVOICE100, 2020 HITMC Patient Advocate of the Year. In 2021 Barby was awarded the 2021 Medigy HITmc Music Video of the year and 2021 Arizona Capitol Times Leader of the Year; Healthcare.www.internationpain.org You can also check out her new movie at www.backhomeagainmovie.com

Barby Ingle is a best-selling author, reality personality, and lives with multiple rare and chronic diseases. Barby is a chronic pain educator, patient advocate, and president of the International Pain Foundation. She is also a motivational speaker and best-selling author on pain topics. Her blog, reality shows and media appearances are used as a platform to help her become an effective patient advocate. She presents at healthcare conferences, speaking publicly, sharing her story, educating and advocating for patients across the globe. She has received more than 25 accommodations over the years for her advocacy work                                        3 top tips for my audience: 1. Set the expectation through words and actions 2. Learn about your condition so you can ask for help and take on your responsibility 3. Don't get stuck Barby's Social Media Blog - http://barbyingle.com/blog Blog - https://internationalpain.org/pop-blog/ Facebook - www.facebook.com/BarbyIngleOfficial  Facebook - www.facebook.com/iPainFoundation Instagram – www.instagram.com/kenandbarbyshow Instagram - https://www.instagram.com/internationalpainfoundation LinkedIn - https://www.linkedin.com/in/barbyingle Twitter - www.twitter.com/BarbyIngle Twitter - www.twitter.com/PowerofPain Website – www.barbyingle.com Website - www.internationalpain.org YouTube - www.youtube.com/user/barbyallyn Wait, there is more!!! Have a look at  www.mystepstosobriety.com  to see which other books and projects I am involved in!  And follow me on Instagram, Podcast, Facebook and Linkedin! https://stephanneff.podbean.com/ https://www.facebook.com/stepstosobriety/ https://www.instagram.com/stepstosobriety/ https://www.linkedin.com/in/stephan-neff-author/

Featured in the media more than 1250 times with over 20 accolades to her name; Barby's best known as being a Cheerleader of HOPE, author, and reality television personality. Ken, her husband and Barby provide motivation, inspiration and energy penny saving tips for better daily living. As an Extreme Time Saver, Barby lives life to the fullest despite living in chronic pain. Ingle is a best-selling author, reality personality, and lives with multiple rare and chronic diseases; reflex sympathetic dystrophy (RSD), migralepsy, PALB2-var breast cancer, valley fever, endometriosis and other pain disorders. Barby is a chronic pain educator, patient advocate, and president of the International Pain Foundation. She is also a motivational speaker and best-selling author on pain topics. Her blog, reality shows and media appearances are used as a platform to help her become an e-Patient advocate, and she presents at healthcare conferences, speaking publicly, sharing her story, educating and advocating for patients across the globe. She has received more than 20 accommodations over the years for her advocacy work including; 2012 WEGO Health Ms. Congeniality, 2012 NAF You Are Our Hero Award, 2013 International Inspirational Luminary, 2015 IDA Impact Award, and 2016 WEGO Health Lifetime Achievement. In 2017, Barby was named a Health Information Technology Top 100 Influencer by HealthScene and Top 20 Health Influencer by Insider Monkey Magazine. In 2018, Barby received the Reality All Star Reunion Superstar award for her Social Media efforts and Top 50 Chronic Pain Advocates. In Feb. 2021 Barby was listed in the top 75 social media advocates for RareDiseases. In 2020, Barby is listed in the top 50 social media advocates for Rare Diseases and top 10 Healthcare Influencers for All Marketers to Follow, 2020 PharmaVOICE100, 2020 HITMC Patient Advocate of the Year. In 2021 Barby was awarded the 2021 Medigy HITmc Music Video of the year and 2021 Arizona Capitol Times Leader of the Year; Healthcare. Her books and additional info can be found on her website. http://barbyingle.com/

Featured in the media more than 1250 times with over 20 accolades to her name; Barby's best known as being a Cheerleader of HOPE, author, and reality television personality. Ken, her husband and Barby provide motivation, inspiration and energy penny saving tips for better daily living. As an Extreme Time Saver, Barby lives life to the fullest despite living in chronic pain. Ingle is a best-selling author, reality personality, and lives with multiple rare and chronic diseases; reflex sympathetic dystrophy (RSD), migralepsy, PALB2-var breast cancer, valley fever, endometriosis and other pain disorders. Barby is a chronic pain educator, patient advocate, and president of the International Pain Foundation. She is also a motivational speaker and best-selling author on pain topics. Her blog, reality shows and media appearances are used as a platform to help her become an e-Patient advocate, and she presents at healthcare conferences, speaking publicly, sharing her story, educating and advocating for patients across the globe. She has received more than 20 accommodations over the years for her advocacy work including; 2012 WEGO Health Ms. Congeniality, 2012 NAF You Are Our Hero Award, 2013 International Inspirational Luminary, 2015 IDA Impact Award, and 2016 WEGO Health Lifetime Achievement. In 2017, Barby was named a Health Information Technology Top 100 Influencer by HealthScene and Top 20 Health Influencer by Insider Monkey Magazine. In 2018, Barby received the Reality All Star Reunion Superstar award for her Social Media efforts and Top 50 Chronic Pain Advocates. In Feb. 2021 Barby was listed in the top 75 social media advocates for RareDiseases. In 2020, Barby is listed in the top 50 social media advocates for Rare Diseases and top 10 Healthcare Influencers for All Marketers to Follow, 2020 PharmaVOICE100, 2020 HITMC Patient Advocate of the Year. In 2021 Barby was awarded the 2021 Medigy HITmc Music Video of the year and 2021 Arizona Capitol Times Leader of the Year; Healthcare. Her books and additional info can be found on her website. http://barbyingle.com/

Meet Barby Ingles:I was living my dream. I trained and performed cheerleading, dance and gymnastics starting at age 4 through college. Straight out of college I started my own cheer/dance training company. A year later I was hired by Washington State University as the head spirit program coach. I have been battling chronic pain since 1997. First with Endometriosis which resulted in a full hysterectomy and left oophorectomy. Then in 2002, I developed Reflex Sympathetic Dystrophy (RSD), is a progressive neuro-autoimmune condition that affects multiple system in the body and needs to be treated early so that disability does not take over and TMJ. I lost my physical abilities was bed bound for years. Using a wheelchair to get to get out of bed. It took 3 years to get a proper diagnosis and another 4 years to get the proper treatment. I know firsthand how hard it is to continue looking for relief, perfect answers, and then coming up against healthcare professionals who blow you off or do not believe what you are saying could actually be what you're experiencing. As I search for a cure, I have become my own best advocate and work sharing the information so that others do not have the same life struggles that I have. Even after seeing over 100 healthcare professionals, having major surgeries I didn't need, complications such as internal bleeding, medication interactions, kidney stones, tumors, severe constipation and so much more – I did not give up or give in! I advocate for all of us challenged with a chronic care condition involving chronic pain as well as their family, caregivers, healthcare professionals and public. One in three people (116 million)  in the United States are affected with a condition that causes pain, so it is bound to affect you or someone you know. But until you feel the pain it is difficult to understand all of the challenges it brings on. Whether physical or mental, pain can and will consume you if you allow it to and only the patient can begin the process of healing! My hope is that my speaking engagements and books will inspire your eventual transformation filled with HOPE and motivation.About Ipain:iPain Foundations objectives are reached through important educational events, support, resources, and enhancement projects that are funded through private donations and grants. The Power of Pain Foundation (dba: International Pain Foundation) demonstrates its commitment to the chronic pain community by promoting new knowledge in the cause and treatment of chronic pain conditions. The ultimate goal is to provide tools and life skills to chronic pain patients giving them the ability to perform their regular activities in the community and to bolster society's ability to provide full opportunities and appropriate supports. Supporting education for pain patients, family members, caregivers and medical professionals, we make an important contribution to the overall knowledge and treatment of chronic pain. This allows our foundation to affect the lives of millions of people with chronic pain worldwide. Whether you have pain or are a caregiver, family member or friend of someone diagnosed, we'll help you face the challenges and life changes of chronic pain, head on.Connect With Barby : https://ipa That's why the BC Schizophrenia Society has launched a brand new podcast, called Look Again, Mental Illness Re-examined. Host Faydra Aldridge talks to doctors, families, and people with lived experience about how to recognize mental illness, and the specific treatments that can help. Check it out. They'll really challenge you to“look again” at what you think you know about mental illness. Support the show (https://www.patron.com/findyourrare)

What do you do when it seems like everything is against you and you have to change your dreams? You keep fighting! You keep going and you step into a dream more than you knew was possible. In this episode, I speak with Barby Ingle. She was living out her dreams as a head cheerleading coach when everything changed and she developed Reflex Sympathetic Dystrophy (RSD). She lost her physical abilities and was bed bound and in a wheel chair for years before she received a proper diagnosis and proper treatment. Most people would find this discouraging, but Barby was able to speak up for herself and keep fighting to save her life.  Now, Barby is a Cheerleader of Hope. She is a best-selling author, reality personality, chronic pain educator, patient advocate and president of the International Pain Foundation. Barby has such an incredible story to tell and her energy is radiant!  With this episode, you will leave feeling like there is hope to keep going. You will learn to advocate for whatever is going on in your life. You will be reminded that this is your life and you need to fight for it. Connect with Barby: Website: http://barbyingle.com/ Instagram: @kenandbarbyshow Facebook: https://www.facebook.com/BarbyIngleOfficial/ International Pain Foundation: https://internationalpain.org/ Connect with me, Ariel Bredder: Instagram: @beyoutifulchick Website: beyoutifulchick.com Email me podcast@beyoutifulchick.com with your questions, comments and feedback! --- This episode is sponsored by · Anchor: The easiest way to make a podcast. https://anchor.fm/app --- Send in a voice message: https://anchor.fm/beyoutiful/message Support this podcast: https://anchor.fm/beyoutiful/support

Barby lives in chronic pain.   When asked how she deals with it and keeps smiling.  Barby says was a cheerleader and says "She learned to deal with her pain through practice, and although she has difficult days, she said she took the guilt away from herself.  She speaks to how others can place guilt on those who use equipment such as walkers and canes.   They can perceive you as being weaker or lazy, however, those tools are there to give more life.Barby said she keeps track of her "energy pennies" and she says she has to decide how to spend those "energy pennies".    She said by doing so you can manage your social time.She said she went from "physical cheerleader" to "mental cheerleader", a cheerleader of hope.She speaks to the difficulty of being properly diagnosed as well.You can find Barby at the following websites:www.barbyingle.comwww.kenandbarby.comwww.internationalpain.orgMore about Barby:Barby Ingle is a best-selling author, reality personality, and lives with multiple rare and chronic diseases; reflex sympathetic dystrophy(RSD), migralepsy, PALB2-var, endometriosis and other pain disorders. Barby is a chronic pain educator, patient advocate, and president of the International Pain Foundation. She is also a motivational speaker and best-selling author on pain topics.From Wheels to Heals by Barby IngleFree Book with any $20+ Podcast Support Make Up Not Required - How to Brand the TRUE You by LaurieAnn & Contribution by Roy MillerBE A GUEST/FIND A GUEST Start for Free! PODMATCH is innovative, provides easy communication and dashboard scheduling! My pick of the month!Buzzsprout - Let's get your podcast launched! Start for FREEDisclaimer: This post contains affiliate links. If you make a purchase, I may receive a commission at no extra cost to you.Support the show (https://paypal.me/iamthatgal)

Barby Ingle is a best-selling author, reality personality, and lives with multiple rare and chronic diseases; reflex sympathetic dystrophy(RSD), migralepsy, PALB2-var, endometriosis, and other pain disorders. Barby is a chronic pain educator, patient advocate, and president of the International Pain Foundation.   She is an advocate for all with chronic care conditions involving chronic pain as well as their family, caregivers, healthcare professionals, and the public.   After becoming bed-bound and using a wheelchair to get out of bed. It took 3 years to get a proper diagnosis and another 4 years to get the proper treatment. Barby knows firsthand how hard it is to continue looking for relief, perfect answers, and then coming up against healthcare professionals who blow you off or do not believe what you are saying could actually be what you're experiencing.   Quote: It is health that is real wealth and not pieces of gold and silver. Mahatma Gandhi   Connect with Barby: Website – www.barbyingle.com Website - www.internationalpain.org Book: From Wheels to Heals   Show hashtag: #TrinaTalk LinkedIn: https://www.linkedin.com/in/trina-l-martin Facebook: https://www.facebook.com/TrinaTalk Instagram: @trina.l.martin  Twitter: @TrinaLMartin

Barby Ingle is a best-selling author, reality personality, and lives with multiple rare and chronic diseases; reflex sympathetic dystrophy(RSD), migralepsy, PALB2-var, endometriosis, and other pain disorders. Barby is a chronic pain educator, patient advocate, and president of the International Pain Foundation. She is also a motivational speaker and best-selling author on pain topics. Barby knows grief from the loss of loved ones in her life as well, both her parents, and her grandparents have passed on.Barby was living her dream. She trained and performed cheerleading, dance, and gymnastics starting at age 4 through college. Straight out of college. Barby started a cheer/dance training company. A year later she was hired by Washington State University as the head spirit program coach. Barby has been battling chronic pain since 1997. First with Endometriosis which resulted in a full hysterectomy and left oophorectomy. Then in 2002, she developed Reflex Sympathetic Dystrophy (RSD), a progressive neuro-autoimmune condition that affects multiple systems in the body and needs to be treated early so that disability does not take over and TMJ. Barby lost her physical abilities was bedbound for years.  Barby used a wheelchair to get out of bed. It took 3 years to get a proper diagnosis and another 4 years to get the proper treatment. As she searches for a cure, she has become her own best advocate and work sharing the information so that others do not have the same life struggles that I have. Even after seeing over 100 healthcare professionals, having major surgeries she didn't need, complications such as internal bleeding, medication interactions, kidney stones, tumors, severe constipation and so much more – Barby did not give up or give in!In this interview, Barby teaches how we can also become our own best advocates.Her blog, reality shows, and media appearances are used as a platform to help her become an e-Patient advocate, and she presents at healthcare conferences, speaking publicly, sharing her story, educating and advocating for patients across the globe.ℹ️  https://www.barbyingle.comSupport the show (https://www.patreon.com/grief2growth)

What can we learn about hope from a cheerleader living with multiple rare & chronic illnesses? A lot it would seem! In this episode Stacie and Barby, discuss how to find hope when things feel bad, and the importance of getting to know who we are. Through Barby's inspiring story of life-changing events, we'll explore how to help cultivate and hold on to hope even in our darkest moments.Barby also shares with us a practical exercise that has been a crucial tool within her journey, that will help you to appreciate all that you are - which we hope you will try.If you've ever felt hopeless, then this beautifully light hearted and uplifting chatepisode is for you…About Our GuestBarby IngleAuthor & Cheerleader of Hopewww.barbyingle.comBarby Ingle is a best-selling author, reality personality, and lives with multiple rare and chronic diseases. She is a chronic pain educator, patient advocate, and president of the International Pain Foundation. Barby started out as a Cheerleader & Dance trainer, since no longer being able to physically cheer, she now uses all the skills and spirit of her cheerleading past to inspire hope in peoples lives, when they most need it.Support the show (https://www.kindlink.com/fundraising/quiet-connections-cic/podcast)

Creativity through the lens of a best selling author and multifaceted human"To be creative is to generate something new"Barby Ingle is a best-selling author, reality personality, and lives with multiple rare and chronic diseases; reflex sympathetic dystrophy(RSD), migralepsy, PALB2-var breast cancer gene, endometriosis, arthritis and other pain disorders. Barby is a chronic pain educator, patient advocate, and president of the International Pain Foundation. She is also a motivational speaker and best-selling author on pain topics. Her blog, reality shows and media appearances are used as a platform to help her become an e-Patient advocate, and she presents at healthcare conferences, speaking publicly, sharing her story, educating and advocating for patients across the globe.Twitter: @Barby Ingle Facebook: @barbyingleofficialInstagram: @KenAndBarbyShow Website: www.barbyingle.com, www.internationalpain.org Mari's Awakening Creativity Porgram:https://courses.skillfulmeans.life/Awakening-Creativity

How To Deal With Pain In Your LIFE | Barby Ingle Barby Ingle is a best-selling author, reality personality, and lives with multiple rare and chronic diseases; reflex sympathetic dystrophy(RSD), migralepsy, PALB2-var, endometriosis and other pain disorders. Barby is a chronic pain educator, patient advocate, and president of the International Pain Foundation. She is also a motivational speaker and best-selling author on pain topics. Her blog, reality shows and media appearances are used as a platform to help her become an e-Patient advocate, and she presents at healthcare conferences, speaking publicly, sharing her story, educating and advocating for patients across the globe. She has received more than 20accommodations over the years for her advocacy work including; 2012 WEGO Health Ms. Congeniality, 2012 NAF You Are Our Hero Award, 2013 International Inspirational Luminary, 2015 IDA Impact Award, and 2016 WEGO Health Lifetime Achievement. In 2017, Barby was named a Health Information Technology Top 100Influencer by HealthScene and Top 20 Health Influencer by Insider Monkey Magazine. In 2018, Barby received the Reality All Star Reunion Superstar award for her Social Media efforts and Top 50 Chronic Pain Advocates. In Feb. 2021 Barby is listed in the top 75 social media advocates for RareDiseases. In 2020,Barby is listed in the top 50 social media advocates for Rare Diseases and top10 Healthcare Influencers for All Marketers to Follow, 2020 PharmaVOICE100, 2020 HITMC Patient Advocate of the Year. More About Barby Ingle:http://barbyingle.com/More About Rozza Mindset:Visit my website:https://www.rozzamindset.com/Follow me on Instagram:https://www.instagram.com/rozzamindset/Connect with me on LinkedIn:https://www.linkedin.com/in/richard-r...

In this episode of Theoretically Theatrical we speak to Barby Ingle about how performance and creativity can be used to promote charity and causes that you are passionate about. Barby is the president of the International Pain Foundation and has produced several songs to empower people who live with chronic pain. You can read more about ipain here: https://internationalpain.orgSupport the show (https://ko-fi.com/beech_hedge_witch)

In today's episode, Marsha speaks with one of the most resilient guests who has not only conquered battles with her health, but also with the battle for getting proper healthcare and becoming her own best health advocate. It is through her health journey that she founded The International Chronic Pain Foundation.   For years Barby struggled with chronic pain which left her not only being bed bound for years and in pain but, she was left with unanswered questions, useless and devastating health solutions from doctors.   It was from one breakthrough with a doctor who put all the pieces of the puzzle together that gave her the answer to at least the proper diagnosis! From there, it was a starting point for Barby where she can now begin to treat her issue and begin to live better with the proper treatment.    The goal of this episode is for you to take charge of your health and become your best advocate. No one knows your body better than YOU! You must be the voice for your health and foundations such as the International Chronic Pain Foundation can support you on your journey. Relevant Links: https://www.healthcoach4women.com/work-with-me https://podcasts.apple.com/ph/podcast/health-coach-4-women/id1524164980 https://open.spotify.com/show/5Q4qGtou9ReyssJNb35XJc https://www.youtube.com/channel/UC7KhEkiM0f5bb--2o_An5AQ http://barbyingle.com/ https://www.facebook.com/BarbyIngleOfficial/ https://www.instagram.com/kenandbarbyshow/ https://www.linkedin.com/in/barbyingle/ https://twitter.com/BarbyIngle Guest Bio   Barby Ingle is a best-selling author, reality personality, and lives with multiple rare and chronic diseases; reflex sympathetic dystrophy(RSD), migralepsy, PALB2-var, endometriosis and other pain disorders. Barby is a chronic pain educator, patient advocate, and president of the International Pain Foundation. She is also a motivational speaker and best-selling author on pain topics. Her blog, reality shows and media appearances are used as a platform to help her become an e-Patient advocate, and she presents at healthcare conferences, speaking publicly, sharing her story, educating and advocating for patients across the globe. She has received more than 20 accommodations over the years for her advocacy work. #healthcoach4women #marsharoopchandwalker #voiceforchange #health #selfempowerment #selflove #healthcare #mentalhealth #howtostayhealthy #healthandwellness #bestlife #womenshealth #healing #wellness #selfcare #selflove #selfawareness #newepisode #podcast #barbyingle

“They say time is money. For me, energy is money.” – Barby Ingle Today's featured award-winning bestselling author is reality show personality, chronic pain educator, patient advocate, and the International Pain Foundation president, Barby Ingle. Barby and I talk about how she remains cheerful despite living with multiple rare and chronic diseases, how to save money on your medical bills, and more!!!   Key Thing's You'll Learn: How she defines what a true cheerleader is. What helps her transmute her pain into power. How to save thousands of dollars on your medical bills. The 3 major lessons she learned from her Army mom.   Barby's Site: https://barbyingle.com/ Barby's Books: https://www.amazon.com/Barby%20Ingle/e/B002RIU4O0/ref=la_B002RIU4O0_st?rh=n%3A283155%2Cp_82%3AB002RIU4O0&qid=1512248193&sort=date-desc-rank&pldnSite=1 International Pain Foundation: https://internationalpain.org/ My Genetic Meds: https://mygeneticmeds.com/     You May Also Like…   Host 2 Host Special - "Faith, Reinvention & Biblical Character Development" with Bob Thibodeau (@bob_thibodeau): https://www.goingnorthpodcast.com/host-2-host-special-faith-reinvention-biblical-character-development-with-bob-thibodeau-bob_thibodeau/   178 - "Mindful Meals" with Kimberly Spencer (@RealKimSpencer): https://www.goingnorthpodcast.com/178-mindful-meals-with-kimberly-spencer-realkimspencer/   Ep. 372 – “The Grit Factor” with Shannon Huffman Polson (@ABorderLife): https://www.goingnorthpodcast.com/ep-372-the-grit-factor-with-shannon-huffman-polson-aborderlife/   202 - "Your Divine Human Blueprint" with Julie Renee Doering (@RevJulieRenee): https://www.goingnorthpodcast.com/202-your-divine-human-blueprint-with-julie-renee-doering-revjulierenee/   208 – “The 50 Year Secret” with Julie MacNeil (@talljewels6ft4): https://www.goingnorthpodcast.com/208-the-50-year-secret-with-julie-macneil-talljewels6ft4/   231 – “Stroke Forward” with Marcia Moran (@Stroke_Forward): https://www.goingnorthpodcast.com/231-stroke-forward-with-marcia-moran-stroke_forward/   252 – “Live Calm with Cancer… and Beyond” with David Dachinger and Tamara Green, LCSW (@LovingMeditator): https://www.goingnorthpodcast.com/252-live-calm-with-cancer-and-beyond-with-david-dachinger-and-tamara-green-lcsw-lovingmeditator/   105 - "A Short Path to Change" with Jenny Mannion (@jennymannion): https://www.goingnorthpodcast.com/105-a-short-path-to-change-with-jenny-mannion-jennymannion/   97.5 (Thanksgiving Bonus Episode) - "MindShift On Demand" with Donna Blevins (@BigGirlPoker): https://www.goingnorthpodcast.com/975-thanksgiving-bonus-episode-mindshift-on-demand-with-donna-blevins-biggirlpoker/   220 – “Medical Intuition” with Wendie Colter (@PracticalPathUS): https://www.goingnorthpodcast.com/220-medical-intuition-with-wendie-colter-practicalpathus/   290 – “The Forgiveness Solution” with Rev. Misty Tyme (@Rev_Misty_Tyme): https://www.goingnorthpodcast.com/290-the-forgiveness-solution-with-rev-misty-tyme-rev_misty_tyme-c2h/   Ep. 380 – “The Simplicity of Self-Healing” with Lisa Warner: https://www.goingnorthpodcast.com/ep-380-the-simplicity-of-self-healing-with-lisa-warner/   Ep. 341.5 – “Playful Cheeks” with Dr. Alison J. Kay (@ajkbliss): https://www.goingnorthpodcast.com/ep-3415-playful-cheeks-with-dr-alison-j-kay-ajkbliss/   201 - "Fortitude Wins the Battle" with Connie Bramer (@ConstanceBramer): https://www.goingnorthpodcast.com/201-fortitude-wins-the-battle-with-connie-bramer-constancebramer-chaostoclarity/

“They say time is money. For me, energy is money.” – Barby Ingle Today's featured award-winning bestselling author is reality show personality, chronic pain educator, patient advocate, and the International Pain Foundation president, Barby Ingle. Barby and I talk about how she remains cheerful despite living with multiple rare and chronic diseases, how to save money on your medical bills, and more!!!   Key Thing's You'll Learn: How she defines what a true cheerleader is. What helps her transmute her pain into power. How to save thousands of dollars on your medical bills. The 3 major lessons she learned from her Army mom.   Barby's Site: https://barbyingle.com/ Barby's Books: https://www.amazon.com/Barby%20Ingle/e/B002RIU4O0/ref=la_B002RIU4O0_st?rh=n%3A283155%2Cp_82%3AB002RIU4O0&qid=1512248193&sort=date-desc-rank&pldnSite=1 International Pain Foundation: https://internationalpain.org/ My Genetic Meds: https://mygeneticmeds.com/     You May Also Like…   Host 2 Host Special - "Faith, Reinvention & Biblical Character Development" with Bob Thibodeau (@bob_thibodeau): https://www.goingnorthpodcast.com/host-2-host-special-faith-reinvention-biblical-character-development-with-bob-thibodeau-bob_thibodeau/   178 - "Mindful Meals" with Kimberly Spencer (@RealKimSpencer): https://www.goingnorthpodcast.com/178-mindful-meals-with-kimberly-spencer-realkimspencer/   Ep. 372 – “The Grit Factor” with Shannon Huffman Polson (@ABorderLife): https://www.goingnorthpodcast.com/ep-372-the-grit-factor-with-shannon-huffman-polson-aborderlife/   202 - "Your Divine Human Blueprint" with Julie Renee Doering (@RevJulieRenee): https://www.goingnorthpodcast.com/202-your-divine-human-blueprint-with-julie-renee-doering-revjulierenee/   208 – “The 50 Year Secret” with Julie MacNeil (@talljewels6ft4): https://www.goingnorthpodcast.com/208-the-50-year-secret-with-julie-macneil-talljewels6ft4/   231 – “Stroke Forward” with Marcia Moran (@Stroke_Forward): https://www.goingnorthpodcast.com/231-stroke-forward-with-marcia-moran-stroke_forward/   252 – “Live Calm with Cancer… and Beyond” with David Dachinger and Tamara Green, LCSW (@LovingMeditator): https://www.goingnorthpodcast.com/252-live-calm-with-cancer-and-beyond-with-david-dachinger-and-tamara-green-lcsw-lovingmeditator/   105 - "A Short Path to Change" with Jenny Mannion (@jennymannion): https://www.goingnorthpodcast.com/105-a-short-path-to-change-with-jenny-mannion-jennymannion/   97.5 (Thanksgiving Bonus Episode) - "MindShift On Demand" with Donna Blevins (@BigGirlPoker): https://www.goingnorthpodcast.com/975-thanksgiving-bonus-episode-mindshift-on-demand-with-donna-blevins-biggirlpoker/   220 – “Medical Intuition” with Wendie Colter (@PracticalPathUS): https://www.goingnorthpodcast.com/220-medical-intuition-with-wendie-colter-practicalpathus/   290 – “The Forgiveness Solution” with Rev. Misty Tyme (@Rev_Misty_Tyme): https://www.goingnorthpodcast.com/290-the-forgiveness-solution-with-rev-misty-tyme-rev_misty_tyme-c2h/   Ep. 380 – “The Simplicity of Self-Healing” with Lisa Warner: https://www.goingnorthpodcast.com/ep-380-the-simplicity-of-self-healing-with-lisa-warner/   Ep. 341.5 – “Playful Cheeks” with Dr. Alison J. Kay (@ajkbliss): https://www.goingnorthpodcast.com/ep-3415-playful-cheeks-with-dr-alison-j-kay-ajkbliss/   201 - "Fortitude Wins the Battle" with Connie Bramer (@ConstanceBramer): https://www.goingnorthpodcast.com/201-fortitude-wins-the-battle-with-connie-bramer-constancebramer-chaostoclarity/

The Don't Quit Podcast takes a look at how professionals work and how you can learn from them. This episode features Barby Ingle, a best-selling author, reality personality, and lives with multiple rare and chronic diseases; reflex sympathetic dystrophy(RSD), migralepsy, PALB2-var, endometriosis, and other pain disorders. Barby is a chronic pain educator, patient advocate, and president of the International Pain Foundation.    Website: http://barbyingle.com/ Instagram: https://www.instagram.com/kenandbarbyshow/ Linkedin: https://www.linkedin.com/in/sharongrossman Facebook https://www.facebook.com/BarbyIngleOfficial — Support The Don't Quit Podcast by visiting TyypoPrints.com making dreamers into achieves through motivational art prints. Use promo code: podcast at the checkout to get 10% off your next print. Email the Host, Nick Mann at Nick@TyypoPrints.com Check out the official The Don't Quit Podcast Website: TDQPodcast.com Follow the show on Instagram: @TDQPodcast Follow the host on Twitter @MannDesigner If you enjoyed this episode please give a review on Apple Podcasts. Thank you for listening!

Barby Ingle was living her dream and in her words was taking life for granted.  She trained and performed cheerleading, dance, and gymnastics starting at age 4 through college. Straight out of college she started her own cheer/dance training company. A year later she was hired by Washington State University as the head spirit program coach. She's been battling chronic pain since 1997. First with Endometriosis which resulted in a full hysterectomy and left oophorectomy. Then in 2002, I developed Reflex Sympathetic Dystrophy (RSD), which is a progressive neuro-autoimmune condition that affects multiple systems in the body and needs to be treated early so that disability does not take over and TMJ.  She lost her physical abilities was bed-bound for years. Using a wheelchair to get out of bed. It took 3 years to get a proper diagnosis and another 4 years to get the proper treatment. Barby knows firsthand how hard it is to continue looking for relief, perfect answers, and then coming up against healthcare professionals who blow you off or do not believe what you are saying could actually be what you're experiencing. Barby said, "As I search for a cure,  I became my own best advocate".  Barby works sharing the information so that others do not have the same life struggles that she has. Even after seeing over 100 healthcare professionals, having major surgeries, that she didn't need, complications such as internal bleeding, medication interactions, kidney stones, tumors, severe constipation and so much more – she did not give up or give in!  Barby was tested on her limits and realized they are past the boundaries she placed on herself.  She had to become the Chief of Staff of her Own Medical Team. Barby says, "If I can do it, anyone can."  We all just need support and HOPE! Barby is a best-selling author, reality personality, and lives with multiple rare and chronic diseases; reflex sympathetic dystrophy(RSD), migralepsy, PALB2-var, endometriosis, and other pain disorders. Barby is a chronic pain educator, patient advocate, and president of the International Pain Foundation. She is also a motivational speaker and best-selling author on pain topics. Her blog, reality shows, and media appearances are used as a platform to help her become an e-Patient advocate, and she presents at healthcare conferences, speaking publicly, sharing her story, educating and advocating for patients across the globe. She has received more than 20accommodations over the years for her advocacy work including; 2012 WEGO Health Ms. Congeniality, 2012 NAF You Are Our Hero Award, 2013 International Inspirational Luminary, 2015 IDA Impact Award, and 2016 WEGO Health Lifetime Achievement. In 2017, Barby was named a Health Information Technology Top 100Influencer by HealthScene and Top 20 Health Influencer by Insider Monkey Magazine. In 2018, Barby received the Reality All-Star Reunion Superstar award for her Social Media efforts and Top 50 Chronic Pain Advocates. In Feb. 2021 Barby is listed in the top 75 social media advocates for RareDiseases. In 2020, Barby is listed in the top 50 social media advocates for Rare Diseases and top10 Healthcare Influencers for All Marketers to Follow, 2020 PharmaVOICE100, 2020 HITMC Patient Advocate of the Year.Barby IngleThe Chosen

Barby Ingle was living her dream and in her words was taking life for granted.  She trained and performed cheerleading, dance, and gymnastics starting at age 4 through college. Straight out of college she started her own cheer/dance training company. A year later she was hired by Washington State University as the head spirit program coach. She's been battling chronic pain since 1997. First with Endometriosis which resulted in a full hysterectomy and left oophorectomy. Then in 2002, I developed Reflex Sympathetic Dystrophy (RSD), which is a progressive neuro-autoimmune condition that affects multiple systems in the body and needs to be treated early so that disability does not take over and TMJ.  She lost her physical abilities was bed-bound for years. Using a wheelchair to get out of bed. It took 3 years to get a proper diagnosis and another 4 years to get the proper treatment. Barby knows firsthand how hard it is to continue looking for relief, perfect answers, and then coming up against healthcare professionals who blow you off or do not believe what you are saying could actually be what you’re experiencing. Barby said, "As I search for a cure,  I became my own best advocate".  Barby works sharing the information so that others do not have the same life struggles that she has. Even after seeing over 100 healthcare professionals, having major surgeries, that she didn’t need, complications such as internal bleeding, medication interactions, kidney stones, tumors, severe constipation and so much more – she did not give up or give in!  Barby was tested on her limits and realized they are past the boundaries she placed on herself.  She had to become the Chief of Staff of her Own Medical Team. Barby says, "If I can do it, anyone can."  We all just need support and HOPE! Barby is a best-selling author, reality personality, and lives with multiple rare and chronic diseases; reflex sympathetic dystrophy(RSD), migralepsy, PALB2-var, endometriosis, and other pain disorders. Barby is a chronic pain educator, patient advocate, and president of the International Pain Foundation. She is also a motivational speaker and best-selling author on pain topics. Her blog, reality shows, and media appearances are used as a platform to help her become an e-Patient advocate, and she presents at healthcare conferences, speaking publicly, sharing her story, educating and advocating for patients across the globe. She has received more than 20accommodations over the years for her advocacy work including; 2012 WEGO Health Ms. Congeniality, 2012 NAF You Are Our Hero Award, 2013 International Inspirational Luminary, 2015 IDA Impact Award, and 2016 WEGO Health Lifetime Achievement. In 2017, Barby was named a Health Information Technology Top 100Influencer by HealthScene and Top 20 Health Influencer by Insider Monkey Magazine. In 2018, Barby received the Reality All-Star Reunion Superstar award for her Social Media efforts and Top 50 Chronic Pain Advocates. In Feb. 2021 Barby is listed in the top 75 social media advocates for RareDiseases. In 2020, Barby is listed in the top 50 social media advocates for Rare Diseases and top10 Healthcare Influencers for All Marketers to Follow, 2020 PharmaVOICE100, 2020 HITMC Patient Advocate of the Year.Barby IngleThe Chosen

Feed Your Spirit: Join me, your host Jill Dobrowansky as I sit down with friends and nourish your spirit with stories of hope and encouragement with a whole lot of Jesus sprinkled in. At Feed Your Spirit, I like to say that we imperfectly perfect people who are uplifting others through grace-filled encouragement. I am so happy you joined me today! With the determination to consciously live in God’s word, I invite you to plug in, prepare your heart, and Feed Your Spirit.  On today's episode, I sit down and chat with the best-selling author, reality TV personality, inspirational speaker, and President of the International Pain Foundation, Barby Ingle. Barby has an incredible journey of faith, overcoming immense obstacles, and how God has a purpose for everything we face. No matter if we can see it or not, He is always with us. Connect with Barby  on her website: Barby Ingle Learn more about the International Pain Foundation: IPF   Follow Barby on Facebook: Barby Ingle  Follow Jill on her website: Jill Dobrowansky  Purchase Jill’s New Book: Faith & Fasting: Scripture & Plant-Based Recipes to Nourish Your Body & Soul  Follow Jill on Instagram:  Jill Dobrowansky Connect with Jill on Facebook: Jill Dobrowansky Say ‘Hi’ or provide show feedback: jilldobrowansky@gmail.com  Become a supporter of the podcast: Feed Your Spirit Patreon Support the podcast with some Feed Your Spirit Gear: Feed Your Spirit TeeSpring  You can also now support the show by buying me a virtual cup of coffee (YUM!): Coffee for Jill  Be sure to subscribe, rate, review,  and share the Feed Your Spirit Podcast!

In this episode of The Healers Café, Dr. Manon Bolliger, ND, chats with Batista Gremaud, CEO / President at Dr Fitness International, and best selling author. For the transcript and full story go to: https://www.drmanonbolliger.com/batista-gremaud   Highlights from today's episode include: Batista Gremaud  And what happened is when I reached my mid-40s, basically, I hit a wall. It was like my injuries were so bad, and I was losing the grip on my body. And basically, for me, it was like I was looking at losing my career really because I couldn't go on like this. And then one day I had a moment of clarity. It was in a meditation class the topic was a body-mind-spirit integration. And I woke up and I said well what do you mean body mind spirit integration? Batista Gremaud  07:17 I knew some part was missing but I didn't know what it was. I expected it to come into some type of spiritual vision. I did not expect it to come into a strength training program. Certainly not. I had no clue. Literally, I had tried just about everything. From the mindset aspect of things from the physiotherapy from...everything. And so no, I did not know what was missing. I just knew something was missing. Because, you know, body spirit and your body's falling apart. That's, not right. Batista Gremaud  12:21 Because in the system, that is the foundation of the body, because the spine is actually what is going to hold your body up. And then if it's out of alignment, or then your muscles are also tweaked and out of alignment, then you're always going to be out of alignment, it's going to do a domino effect. And this is oftentimes what is missing, we find with chiropractic treatment or other modalities that work with pain, they can be really efficient, but then if you don't rebuild the musculature around the spine, then the muscles are always going to pull you off.     About Batista Gremaud Batista Gremaud is the CEO and president of Dr Fitness International, No1 Best Selling author of Feminine Body Design, Empowering Fitness For A Pain-Free Life, co-creator of the Feminine Body Design online strength training mentoring system, co-host of the Esoteric Principles of Bodybuilding, and producer of the Dr Fitness USA's show; Recipient of the most outstanding fitness program 2019 by The Winners Circle, Mastermind at Sea. Contributor writer for the “In The Limelight” publication; featured as an expert authority speaker on the International Pain Foundation, presenter on various health summits such as “Life Mastery”, “Girl You Are Enough”  “The Teen Suicide Prevention Show” and NEXT Global Virtual Summit Core purpose/passion : I love merging universal and esoteric principles to the art of bodybuilding, according to the teachings and philosophy of International Body Designer Stephen Hercy AKA Dr Fitness USA, as an evolutionary vehicle to achieving wholeness of all elements of the Self and bringing greater understanding to the subject of body, mind spirit integration. Freebie : https://drfitnessint.com/zoomed-out-gift .   Website | Facebook | Instagram | LinkedIn | YouTube     About Dr. Manon Bolliger, ND: Dr. Manon is a Naturopathic Doctor, the Founder of Bowen College, an International Speaker, she did a TEDx talk "Your Body is Smarter Than You Think. Why Aren't You Listening?"  in Jan 2021, and is the author of Amazon best-selling books "What Patient's Don't Say if Doctors Don't Ask". & "A Healer in Every Household" For more great information to go to her weekly blog:  http://bowencollege.com/blog.    For tips on health & healing go to: https://www.drmanonbolliger.com/tips     About The Healers Café: Dr. Manon's show is the #1 show for medical practitioners and holistic healers to have heart to heart conversations about their day to day lives.   Follow Dr. Manon, ND on social media!  Facebook | Instagram |  LinkedIn  |  YouTube  |  Twitter

STEPHEN HERCY aka Dr Fitness USA is an International Body Designer, owner and founder of Dr Fitness International. No 1 Best Selling Author, Holds the prestigious title Professeur De Culture Physique Weider, certified by the IFBB International Federation of Bodybuilding. No1 Best Seller Dr Fitness USA is the creator of the Body Design Formula strength training protocol and recognized professional empowerment speaker as a pioneer for his successful work with pain management and postural realignment, which affects mood behavior and productivity. Dr Fitness USA is the leading authority in bringing his revolutionary strength training systems to the addiction and recovery community as a new tool for mood behavior stabilization, stress management, and is the first person in the world to provide strength-training programs for women suffering from endometriosis and auto-immune disorders. Dr Fitness USA received the "Most Outstanding Fitness Program For 2019" award by the Winners Circle. He regularly appears as an authority celebrity guest speaker on various platform including syndicated show Al Cole “People of Distinction”, L.J. Jackson “Amazing women of Power,” CNN show Tony O'Donnell at KCAA broadcast, Svetlana Kim “To the stars through adversity”, “The Dr. Kevin” show, Lou Hick famous Aimed 2 Purpose global broadcast, Dave Nassaney "Caregiver, avoiding burnout" broadcast and was featured as an expert authority speaker on the International Pain Foundation. Celebrity students include Roger Wajed Salam, Linda Grey, Sally Field, Wendy Mull, Simon Crane, Olivia Hussey, Chuti Tiu, Billy West, Sonia Ete, Robin Siegel, Joel Bauer, Fred Van Liew, Gerry Foster, Nicholas Zaldastani, Christy Elcker, Dr. Georges Borris, Tim Ray, Brian Kelly, Tyhson Banighen among others. Young and older people of all walks of life travel world wide to seek his unique services. Dr Fitness USA ‘s groundbreaking prescription strength training system assist men and women alike to become masters of their body independently of a personal trainer to achieve a pain free life. Welcome to the new paradigm in fitness consciousness! https://youtu.be/A1zWvNuYIQI

STEPHEN HERCY aka Dr Fitness USA is an International Body Designer, owner and founder of Dr Fitness International. No 1 Best Selling Author, Holds the prestigious title Professeur De Culture Physique Weider, certified by the IFBB International Federation of Bodybuilding. No1 Best Seller Dr Fitness USA is the creator of the Body Design Formula strength training protocol and recognized professional empowerment speaker as a pioneer for his successful work with pain management and postural realignment, which affects mood behavior and productivity. Dr Fitness USA is the leading authority in bringing his revolutionary strength training systems to the addiction and recovery community as a new tool for mood behavior stabilization, stress management, and is the first person in the world to provide strength-training programs for women suffering from endometriosis and auto-immune disorders. Dr Fitness USA received the "Most Outstanding Fitness Program For 2019" award by the Winners Circle. He regularly appears as an authority celebrity guest speaker on various platform including syndicated show Al Cole “People of Distinction”, L.J. Jackson “Amazing women of Power,” CNN show Tony O'Donnell at KCAA broadcast, Svetlana Kim “To the stars through adversity”, “The Dr. Kevin” show, Lou Hick famous Aimed 2 Purpose global broadcast, Dave Nassaney "Caregiver, avoiding burnout" broadcast and was featured as an expert authority speaker on the International Pain Foundation. Celebrity students include Roger Wajed Salam, Linda Grey, Sally Field, Wendy Mull, Simon Crane, Olivia Hussey, Chuti Tiu, Billy West, Sonia Ete, Robin Siegel, Joel Bauer, Fred Van Liew, Gerry Foster, Nicholas Zaldastani, Christy Elcker, Dr. Georges Borris, Tim Ray, Brian Kelly, Tyhson Banighen among others. Young and older people of all walks of life travel world wide to seek his unique services. Dr Fitness USA ‘s groundbreaking prescription strength training system assist men and women alike to become masters of their body independently of a personal trainer to achieve a pain free life. Welcome to the new paradigm in fitness consciousness! https://youtu.be/A1zWvNuYIQI

Batista Gremaud is the CEO and president of Dr Fitness International, No1 Best Selling author of Feminine Body Design, Empowering Fitness For A Pain-Free Life, co-creator of the Feminine Body Design online strength training mentoring system, co-host of the Esoteric Principles of Bodybuilding, and producer of the Dr Fitness USA's show; Recipient of the most outstanding fitness program 2019 by The Winners Circle, Mastermind at Sea. Contributor writer for the “In The Limelight” publication; featured as an expert authority speaker on the International Pain Foundation, presenter on various health summits such as “Life Mastery”, “Girl You Are Enough” “The Teen Suicide Prevention Show” and "NEXT Global Virtual Summit" Health is Wealth, Your Greatest Asset The anti-aging benefits of strength training for physical, emotional, and mental health. DrFitnessUSA.com DrFitnessInt.com https://boxcast.tv/view/health-is-wealth-with-bautista-gremaud-482328 

Batista Gremaud is the CEO and president of Dr Fitness International, No1 Best Selling author of Feminine Body Design, Empowering Fitness For A Pain-Free Life, co-creator of the Feminine Body Design online strength training mentoring system, co-host of the Esoteric Principles of Bodybuilding, and producer of the Dr Fitness USA's show; Recipient of the most outstanding fitness program 2019 by The Winners Circle, Mastermind at Sea. Contributor writer for the “In The Limelight” publication; featured as an expert authority speaker on the International Pain Foundation, presenter on various health summits such as “Life Mastery”, “Girl You Are Enough” “The Teen Suicide Prevention Show” and "NEXT Global Virtual Summit" Health is Wealth, Your Greatest Asset The anti-aging benefits of strength training for physical, emotional, and mental health. DrFitnessUSA.com DrFitnessInt.com https://boxcast.tv/view/health-is-wealth-with-bautista-gremaud-482328 

Tom Rhoads (00:03): Welcome to "People Always, Patients Sometimes". I'm Tom Rhodes, CEO of Spencer Health Solutions. Our podcast is focused on many of the thought leaders and executives that are calling for change and how we design and run clinical trials. We have also had patient advocates on the program like Jen Horonjeff, of the Savvy Cooperative, Pam Gavin of NORD and Barby Ingle of the International Pain Foundation. Our mission at Spencer Health Solutions is to ensure that patients are at the center of everything we do. So we are pleased to kick off a series of interviews with more patient advocates, influencers, and organizations that are focused on bringing the patient experience to the forefront of the conversation in healthcare. Kicking off our series is a conversation with Lilly Stairs and leading patient advocate advisor and founder of Patient Authentic. I know you'll find her conversation with Janet Kennedy, as interesting as I did. Janet Kennedy (01:01): "People Always, Patients Sometimes" podcast is about the change agents in healthcare who are focused on patient experience, patient engagement, or disrupting the process of clinical trials to be more patient-centric. Our guest today certainly fits that bill. Lilly Stairs is a nationally recognized patient advocate, speaker, author, and innovator. She has recently founded a new company, Patient Authentic, which I look forward to hearing more about on "People Always, Patients Sometimes." Welcome to the podcast. Lilly! Lilly Stairs (01:33): Thanks so much for having me, Janet. It's always a pleasure to connect with you. Janet Kennedy (01:38): I think entrepreneurship is a big challenge and as a patient advocate where you're already facing a series of your own personal challenges, as well as challenges in the workforce. Wow. What made you think about starting your own company? Lilly Stairs (01:55): Well, Janet, I will also say that I didn't plan to start a company the year that we ended up with a worldwide pandemic, but here we are to add that challenge to the list too. But yeah, I've always had an entrepreneurial spirit. From a very young age, I was always creative and started choreographing for a kids' theater program and took the helm there. And then in high school, I started an anti-bullying program that ended up touring around our local schools in Massachusetts. When I got to college that is when I started my patient advocacy work. And because I was diagnosed with a few different auto-immune diseases I started a campaign to raise awareness about people who were living with auto-immune diseases. There are an estimated 50 million Americans who are living with auto-immune diseases. It was called the 50 cents for 50 million. I have spent most of my career in health tech startups. It just felt right to jump in and take the plunge and make a bet on myself and start Patient Authentic. Janet Kennedy (03:17): I imagine your first 30 days you were feeling pretty euphoric and then February came and you probably started to be a little nervous. So COVID, how has that impacted your life and impacted your work? Lilly Stairs (03:31): Well, I think it's really, and I don't think this is an exaggeration, it's turned my life and everyone's lives upside down. And I, as somebody who is considered high risk because I am immunocompromised due to the medication that I am on, which depresses my immune system to treat my auto-immune diseases is certainly scary and carries a lot of weight. I am fortunate that from a work perspective, all of us in healthcare, I think have been quite busy, which is important. We've stayed busy trying to do what we can to support patients. And so from a work perspective, all has been really good. It's just that we've got a lot of COVID focused projects now. And then from a personal perspective, I think that honestly, it's been hard because it's isolating and I think a lot of people are feeling that, and there's always the fear that people are not taking it seriously enough, especially as someone who is high risk. Janet Kennedy (04:30): I understand totally what your experience is. Like my two nieces are in New York City who works at Trader Joe's and unfortunately, the misapprehensions and the willful lack of understanding is really frightening for them. One of them actually did get COVID, was fortunate that it felt like the flu, and got over it, but then found out later she had definitely had it. It has changed everything in our lives. So I'm curious as a patient advocate, and I know you are talking to patients constantly, what is the general mood among the folks that you're talking to? Are they finding that this is an incredibly scary time or are they finding that even the discussion of "at-risk" is raising awareness and making people a little more sensitive or empathetic to folks who have challenges? Lilly Stairs (05:27): Well, I have to say, I think it's a mix. And I would say generally speaking patient communities across their pubic areas have certainly been vocal about concerns that people are not taking COVID seriously enough. And I think that there are some really baseline things that everybody could be doing, like wearing a mask that would put a lot of those fears at ease. I will say warranted fears because for some contracting COVID is really a death sentence when you are somebody who's high risk. I'll be honest in saying that for me personally, I live in balance. I live in breathe and balance. That's how I operate. And for me, I've been cautiously optimistic and I'm cautious in living my life. So I don't just sit at home. I will go out, I wear a mask, but I'll go do outdoor dining in Boston. We have some awesome outdoor dining and, you know, see friends at a socially distant level because I think what we're seeing with this pandemic is a mental health pandemic kicking in because so many people are struggling with the isolation and the loneliness. So I try to weigh that out. And I think that a lot of other people in the community do that too. And it's really just about finding that mix of being safe and taking care of yourself. Janet Kennedy (06:50): I agree very wise words. Now let's back up a little bit and talk about Patient Authentic. I don't know what your company is doing. So tell me a little bit about it. Lilly Stairs (07:01): Absolutely. Well, you know, Janet, I think that I'm still learning what my company is doing and I don't know if I should be saying that, but here we are. Because I think it's evolved so much since I started in January. And a lot of that is largely because of COVID, but also because I've just ended up in places I didn't expect. And so the way that I like to talk about Patient Authentic is that it is a hybrid of healthcare marketing and patient advocacy. So all of my work is grounded in developing patient-centric deliverables alongside patients. And I'll talk to you about a few projects I'm working on just to give you a flavor of what it is that I'm doing at Patient Authentic. So I am leading patient advocacy for a health tech company and that's Clara Health, which is in the clinical trials space. Lilly Stairs (07:50): And I know that Spencer does quite a bit of work there too. I am developing and running a social media campaign with oncology patient influencers to promote a nutritional supplement, which helps to aid in the healing of mouth sores that have been developed from chemo and radiation. So out of that, we've developed the hashtag #MoreThanASore campaign, which is all about how sores are so much more than just a sore and they really impact the quality of life. And so there's the marketing in me coming out through that campaign. And then, you know, I'm working with some patient advocacy groups as well. So I'm building a masterclass to help train patients from across therapeutic areas and how they can be effective advocates on a policy level. So on Capitol Hill and at FDA advisory committees. Finally, I'm also supporting the development of a COVID-19 resource hub for the transplant patient community. My projects span across therapeutic areas and they are focused, at the heart of them, they are working with patients to create something, Janet Kennedy (08:56): Oh, that's excellent. Now, is this a single consultancy? Or do you have other patient advocates that you will bring in to support some of these projects? Lilly Stairs (09:04): Primarily it's a single consultancy, but I do often bring in patients who are paid because patients should always be paid to support the work. Janet Kennedy (09:14): I totally agree. Well, let's talk a little bit about some of the work that you've done in the past and hopefully in the future related to clinical trials, have you ever participated in a clinical trial as a patient? Lilly Stairs (09:29): I participated in a study that was through my gastroenterologist for my Crohn's disease. And it happened right when I was in the office and it was quick as could be. My gastro said, "Hey, I'm working on this study. We're trying to measure the levels in the liver because the liver is often impacted by treatments." And so I agreed to do it. And it happened all in the same office visit. It was the most convenient clinical trial experience I've ever had. Did the informed consent, all there. Probably happened in 20 minutes Janet Kennedy (10:08): Now from a standpoint of your work as a patient advocate and being around the clinical trial space and helping support companies and organizations that are involved in clinical trials. I want you to put your hat on as a patient advocate. If you were to point out one or two things that are really kind of a roadblock for patients in participating successfully in a clinical trial, regardless of whether the clinical trial is a success, what do you think are the challenges that patients face that the pharma companies, CROs and physicians that are involved in research need to be thinking more about? Lilly Stairs (10:48): I'm just going to pick two - there's a lot. And so two is tough for me to do, but I will do it. I still think that awareness and myth-busting. As much as we talk about it in our community, I think that in the professionals and the clinical trial space, we talk a lot about this, but we aren't reaching the right people. It's still a huge issue. There's still so much misunderstanding about clinical trials and risk associated with them. And am I going to get the placebo? So many questions that really plague the everyday patient when we think about clinical trials. And so I think we have a lot more work to do there. And part of the solution to me is that we need to have more people working together to raise awareness and to get into communities. And so we can't be all working in silos because we continue to work in silos. Lilly Stairs (11:45): We need to work together. That's one piece. The other big barrier that I have seen is honestly, the travel and the distance piece. There are a lot of patients who actually do want to participate in clinical trials, but they are restricted because it is too far for them to travel. And they can't either, you know, financially afford it because the trial is not going to cover the cost of travel, or it's just, it's a distance thing. And they are not well enough to travel. And I can point to through my work with all of the different companies I've worked with, I can point to so many patients from across therapeutic areas that have had this experience. Lilly Stairs (12:28): So I was recently speaking with a woman who was in a breast cancer trial. First of all, her physician didn't even bring up clinical trials to her, which is a problem in and of itself. She did the research on her own and she ended up traveling from the East coast to the West coast for a clinical trial. And she had to do a GoFundMe so that she could raise the money. And she ended up having to drop out of the trial because the GoFundMe only got her so far. So we have patients who are willing to participate in trials, but we're not making it convenient for them. I would say that we need to branch out outside of some of these research hospitals. We also need to, if we can't do that, build money into the budget to help the patients get there in a comfortable manner. Janet Kennedy (13:14): So is the challenge that a lot of the research hospitals are in major metro areas, and if you don't live in New York or Boston or Atlanta or Los Angeles, you're going to miss out on an opportunity. Lilly Stairs (13:26): Yes. Precisely. Janet Kennedy (13:29): All right. Well, what would solve some of those problems? Lilly Stairs (13:33): Again, travel, being able to provide stipends for travel and not just like a $25 Uber, if somebody lives out of state, but they're really willing to participate in the trial. What can you do to facilitate accommodations, to cover the flight, to cover the hotel room? Because I'll tell you something working in the recruitment space, you're going to spend a lot more money trying to recruit patients that are nearby. Versus if you just foot the bill for flying someone out, getting them a hotel room who's eager and willing to participate. So that's one piece. And then also, I think we need to be raising more awareness within some of these community hospitals too so that physicians within community hospitals can refer out to some of the major research institutions. Because again, this is where the awareness piece comes in. There's a lack of awareness and understanding about trials. So patients don't even know they exist in the first place. Janet Kennedy (14:31): So raising awareness is a real key. Now, how are patients finding out about things? They suddenly find out they have a disease and they're just going online and doing a search and then whatever pops up pops up. Lilly Stairs (14:44): I think that online is of course a huge space. I mean, I would guess I, I won't put a statistic because I'm sure I won't be accurate, but everyone's going to Google. Everyone goes to Doctor Google. And I think that the patient advocacy organizations play a role. But I will say that we are seeing patient influencers or individual advocates are becoming more and more prominent in being the trusted go-to resource for sort of your everyday patient. So these are the patients who are sharing their stories on Instagram and TicTok now and Twitter, and they have blogs. They're on YouTube. That's where patients are going because they're able to get that sort of one-to-one support and really hear from somebody who understands them. So I've been trying to really push companies, pharmaceutical companies, biotech companies, CROs, to engage not only with the patient advocacy organizations but also with some of these patient influencers and advocates who are out there and working to fight the good fight and raise awareness. Janet Kennedy (15:49): You know, a few years ago, patient advocates were not that seen, were not that present. And I think as social media has become really an essential part of our lives, patients are realizing that there's real power there. However, there's also the challenge of my gosh, you have a chronic illness, or you have a disease that is very debilitating and social media in many ways, demands that you're up, that you are being positive, that you're being optimistic. How would you balance being someone with a chronic illness or a disease that really makes you feel bad? And these social platforms that sort of demand a much more upbeat presentation of yourself. Lilly Stairs (16:34): That's a great question. And I think it's something that's so many advocates struggle with because when you become a patient advocate and you make the decision to share your story, you're often the type of person who wants to do better and to help others, right? You're out there because you want to support other people and help them not feel like they're alone. And that can become emotionally demanding and physically demanding. Even when, especially when you are going through it in the auto-immune space, what we would call it a flare. So when you are really not well and your disease is under control. And so it's a matter of learning to say no, and to set boundaries. And so I've seen a lot of patients artfully do this, where they say, you know what, I'm turning off the comments on my Instagram because I cannot be every single person's support system. I can put this out into the world and I can try to help them, but I can't possibly respond to every single person because it's too taxing on me. And you know, some maybe sometimes you have your comments on maybe sometimes you have it off, but it's little changes and tweaks like that to help ensure that you're taking care of yourself while you're taking care of others. Janet Kennedy (17:41): I know you mentioned earlier that you're actually doing a course for patient advocates on how to use social media. There are so many platforms now, how are you focusing their energy? When I coach about social media, my advice is you can't do it all. So pick a few and do it well. But I do see some patient advocates with a lot of social platforms going on at the same time. Lilly Stairs (18:06): Oh yeah. It's hard to do. I agree with you, Janet, that picking one or two and focusing on those and making them really great is also my piece of advice. It also feels less overwhelming. I was just giving a keynote at the One Rare young adult's virtual summit. It was their first annual one. Rarer is an amazing organization run by Jen McNary. And so I highly recommend checking them out. It's a rare disease organization for young adults, but we were talking about career planning and how you build your brand as an advocate. And again, one of my key pieces of advice was to pick one platform so that you don't get overwhelmed. And so that you are not emotionally and physically drained and also pick some platforms to have that are private, that is just for you and your friends. I'm really active on Twitter professionally, but I have my Instagram private and closed so that I can just feel comfortable sharing what I want to share there and not feel like I always have to be on. Janet Kennedy (19:05): It is a huge challenge in social media and one that demands the ongoing feeding of the beast. However, do you think you can take a break from social and come back and not lose your audience? Lilly Stairs (19:18): Oh, 100%. Absolutely. If you need to take a hiatus, you can. And I think that what's interesting is that especially in the patient community, people are very forgiving of that because they know exactly what you're going through. And so they understand that it can be really taxing to have to be on all the time and they'll miss you while you're gone, but they'll be just thrilled that you've come back, Janet Kennedy (19:41): Circling back to Patient Authentic and what you had originally intended to be before COVID came. Where did you think that the company was going to take you and what were you hoping to accomplish? Lilly Stairs (19:54): Honestly, what I wanted to do, is still there. And that is to build and work on meaningful projects that support the patient community and make you move the needle in healthcare. And so I am doing that. It's just a bit of a different one than I thought. Because of my background in marketing, I always envisioned that every single thing I worked on was going to be super campaign driven. And now I find that I'm doing a little bit of strategy here, a little bit of project management, a little bit of advocacy engagement. So if anything, it's really more fitting for me because I tend to be the type of person who loves to work on a lot of different things at once. It's very rewarding for me to be able to leverage a lot of my different skills to help better the community. The opportunity to work, not only health tech and biotech and pharma, but also to work with some of these patient advocacy organizations who are really at the ground level fighting the good fight. Janet Kennedy (20:59): Oh, well, that's a great note to end on. So Lilly, tell people how they can find you. Lilly Stairs (21:04): Yes. So you can find a, learn more about Patient Authentic at www.patientauthentic.com. You can find me on Twitter @LillyStairs. You can find Patient Authentic on Instagram @PatientAuthentic. Janet Kennedy (21:24): That's excellent. Well, I can't thank you enough for being here, Lilly and I look forward to hearing more about some of the new programs and projects you're going to be involved in, in 2021. Lilly Stairs (21:35): Thanks for having me, Janet. Janet Kennedy (21:38): Thank you for listening to our interview with Lilly Stairs, founder of Patient Authentic on the "People Always, Patients Sometimes" podcast. We look forward to hearing your thoughts about the episode. You can tweet us @spencerhealth or send me an email at jkennedy@spencerhealthsolutions.com.

If you, like so many nurses, suffer work-related pain, the information in Fitness for LNCs podcast may lead you onto a path of physical and emotional wellness. Batista Gremaud’s career as a ballerina caused significant damage to her body, which was aggravated by a series of car accidents. She didn’t find relief until she discovered a unique strength training program that restored her body to fitness and balance. In this episode of Legal Nurse Podcast, we focus on Fitness for LNCs Getting your body into good physical shape doesn’t have to be painful.Unlike aerobics, strength training boosts your metabolism to produce sustained weight loss.Because emotional and physical strength are interrelated, a program that reduces stress can help with weight loss and overall well-being.Since all physical elements of the body are connected, a program or therapy that addresses skeletal alignment needs also to address muscular atrophy.Strength training brings your overall physical, mental, and emotional selves into balance. Get all these tips and more. Click here to get the transcript for this podcast! https://youtu.be/Lsf7g-2Psck Did you Miss LNC Success Livecast/ Virtual Conference, You can still get all the Recordings and Extras! Order the VIP Plan for unlimited access to the recordings and everything else. Wow! We have a treat for you – a virtual conference for legal nurse consultants. Over 100 LNCs attended our first virtual conference in July 2020. Get updated, inspired, and motivated by your experience. Feel connected to LNCs from across the country. Barbara Levin and I put together a distinguished panel of LNCs, doctors, lawyers, and also business experts to share their knowledge to you in the comfort of your own home. Who is Barbara Levin? Barbara is my colleague, friend, also an expert witness, orthopaedic nurse clinician, and much more. No airfare, no hotel, no Uber or Lyft, also no germs and no masks! Your Presenter Batista Gremaud is an International Body Designer, No1 Best Selling author of Feminine Body Design, Empowering Fitness For A Pain-Free Life, co-creator of the Feminine Body Design online strength training mentoring system, co-host of the Esoteric Principles of Bodybuilding, and producer of the Dr Fitness USA’s show. Recipient of the most outstanding fitness program 2019 by The Winners Circle, Mastermind at Sea. Contributor writer for the “In The Limelight” publication; featured as an expert authority speaker on the International Pain Foundation, presenter on various health summits such as “Life Mastery”, “Girl You Are Enough” “Weight lo Get in touch with Batista at https://www.drfitnessint.com Listen to this Podcast on your phone. Download our mobile app BIZ.EDU

ONCE UPON A GENE - EPISODE 053 Living with Chronic Pain - International Pain Foundation President Barby Ingle Barby Ingle is a fierce advocate, the President of the International Pain Foundation, a chronic pain educator and advocate, motivational speaker, Amazon best-selling author and reality tv personality. She's received more than 20 accolades for her work in the chronic pain community. EPISODE HIGHLIGHTS Where did your journey begin? When I was coaching, I was living all of my dreams. I got endometriosis, went through the treatment process and had a full hysterectomy. Just before my 30th birthday, I was hit by a van and injured, started physical therapy and discovered I had a rare disease triggered by the accident- a rare neuro-autoimmune disease called reflex sympathetic dystrophy (RSD). At first it was regional, but several surgeries complicated the condition and I was in a wheelchair for almost seven years.  Was there ever a point in your diagnosis journey where you lost hope? Even at the lowest, there was hope. The worst moment was when I had a rib removed. The surgeon made a mistake, leaving two bone spurs going into my right lung and wrapped around a nerve bundle in my shoulder. I started having lung collapses, which was disregarded as something that sometimes happens. I didn't know he was wrong and to push further. I experienced a lung collapse that led to an emergency surgery and my dad was there giving me support and hope. What organization did your family help to launch that you're a part of now? Every year, my dad had us do a family project and we would decide at Thanksgiving what it was going to be. Sometimes it would be Christmas caroling at retirement homes or serving food to the homeless. In 2006, we lost my step-sister to the same condition I have, so when Thanksgiving came around my dad led us to start a non-profit. At that time, I was wheelchair bound, bed bound and wasn't able to do much with it, but I was the face of the campaign, The Power of Pain. After the first year, the board decided we needed to broaden the scope to work with all chronic pain diseases. In 2010 I joined the executive board and in 2012 I was elected the President of the foundation. We have expanded internationally to 14 countries with the help of people leading projects to make their communities better. What are you most excited about right now that's happening with the International Pain Foundation? November, or "Nerve-mber" is a big month for us with spotlights on conditions, sources of facts and information and the International Pain Summit, which will be held virtually this year. I'll be speaking at the summit this year with my husband on empowerment for patients and caregivers with tips and tools for everyday life. LINKS AND RESOURCES MENTIONED Teal Pumpkin project https://www.foodallergy.org/our-initiatives/awareness-campaigns/living-teal/teal-pumpkin-project International Pain Foundation https://internationalpain.org/ Register for the International Pain Summit 2020 https://internationalpain.org/ipain-summit-2020/ iPain Living Magazine https://internationalpain.org/ipain-living-magazine/ Books by Barby http://barbyingle.com/books/ TUNE INTO THE ONCE UPON A GENE PODCAST Spotify https://open.spotify.com/show/5Htr9lt5vXGG3ac6enxLQ7 Apple Podcasts https://podcasts.apple.com/us/podcast/once-upon-a-gene/id1485249347 Stitcher https://www.stitcher.com/podcast/once-upon-a-gene Overcast https://overcast.fm/itunes1485249347/once-upon-a-gene CONNECT WITH EFFIE PARKS Website https://effieparks.com/ Twitter https://twitter.com/OnceUponAGene Instagram https://www.instagram.com/onceuponagene.podcast/?hl=en Built Ford Tough Facebook Group https://www.facebook.com/groups/1877643259173346/

https://DrFitnessInt.com Show Special Master Class for $1.00 normally $97.00. Go to website to sign up. Title: International Body Designer Websites: https://www.DrFitnessInt.com / https://www.drfitnessusa.com BIO Batista Gremaud is an International Body Designer, No1 Best Selling author of Feminine Body Design, Empowering Fitness For A Pain-Free Life, co-creator of the Feminine Body Design online strength training mentoring system, co-host of the Esoteric Principles of Bodybuilding, and producer of the Dr Fitness USA's show; Recipient of the most outstanding fitness program 2019 by The Winners Circle, Mastermind at Sea. Contributor writer for the “In The Limelight” publication; featured as an expert authority speaker on the International Pain Foundation, presenter on various health summits such as “Life Mastery”, “Girl You Are Enough” “Weight loss Summit” “The Suicide Prevention Show” and "Goals To Riches" DrFitnessUSA.com - @DrFitnessUSA – 424.245.6560 – batista@DrFitnessUSA.com TOPICS: Health is Wealth: Your Greatest Asset MAIN POINTS: 3 key elements to overcoming adversity and crush it in your business 1. Mind set 2. Physical / Emotional strength 3. Education

Batista Gremaud is an International Body Designer, No1 Best Selling author of Feminine Body Design, Empowering Fitness For A Pain Free Life, co-creator of the Feminine Body Design online strength training mentoring system, co-host of the Esoteric Principles of Bodybuilding and producer of the Dr Fitness USA's show; Recipient of the most outstanding fitness program 2019 by The Winners Circle, Mastermind at Sea. Contributor writer for the “In The Limelight” publication; featured as an expert authority speaker on the International Pain Foundation, presenter on various health summits such as “Life Mastery”, “Girl You Are Enough” “Weight loss Summit” and “The Suicide Prevention Show”Learn more at www.DrFitnessUSA  TOPICS: Health is Wealth: Your Next PriorityMAIN POINTS:  3 key elements to overcoming adversity.Mind setPhysical / Emotional strengthEducation Support the Show.

Batista Gremaud is an International Body Designer, No1 Best Selling author of Feminine Body Design, Empowering Fitness For A Pain Free Life, co-creator of the Feminine Body Design online strength training mentoring system, co-host of the Esoteric Principles of Bodybuilding and producer of the Dr Fitness USA's show; Recipient of the most outstanding fitness program 2019 by The Winners Circle, Mastermind at Sea. Contributor writer for the “In The Limelight” publication; featured as an expert authority speaker on the International Pain Foundation, presenter on various health summits such as “Life Mastery”, “Girl You Are Enough” “Weight loss Summit” and “The Suicide Prevention Show” Learn more at www.DrFitnessUSA  TOPICS: Health is Wealth: Your Next Priority MAIN POINTS:  3 key elements to overcoming adversity. Mind setPhysical / Emotional strengthEducation  

Batista Gremaud is an International Body Designer, No1 Best Selling author of Feminine Body Design, Empowering Fitness For A Pain Free Life, co-creator of the Feminine Body Design online strength training mentoring system, co-host of the Esoteric Principles of Bodybuilding and producer of the Dr Fitness USA's show; Recipient of the most outstanding fitness program 2019 by The Winners Circle, Mastermind at Sea. Contributor writer for the “In The Limelight” publication; featured as an expert authority speaker on the International Pain Foundation, presenter on various health summits such as “Life Mastery”, “Girl You Are Enough” “Weight loss Summit” and “The Suicide Prevention Show” Learn more at www.DrFitnessUSA  TOPICS: Health is Wealth: Your Next Priority MAIN POINTS:  3 key elements to overcoming adversity. Mind setPhysical / Emotional strengthEducation  

Batista Gremaud is an International Body Designer, No1 Best Selling author of Feminine Body Design, Empowering Fitness For A Pain Free Life, co-creator of the Feminine Body Design online strength training mentoring system, co-host of the Esoteric Principles of Bodybuilding and producer of the Dr Fitness USA’s show; Recipient of the most outstanding fitness program 2019 by The Winners Circle, Mastermind at Sea. Contributor writer for the “In The Limelight” publication; featured as an expert authority speaker on the International Pain Foundation, presenter on various health summits such as “Life Mastery”, “Girl You Are Enough” “Weight loss Summit” and “The Suicide Prevention Show” Learn more at www.DrFitnessUSA  TOPICS: Health is Wealth: Your Next Priority MAIN POINTS:  3 key elements to overcoming adversity. Mind setPhysical / Emotional strengthEducation  

Tom Rhoads: The patient perspective is an integral part of how we at Spencer Health Solutions approach our work from UX and human factors testing and designing Spencer all the way through our customer interactions. We always look at how the patient evaluates their experience with our system. In this episode of our podcast, we asked chronic pain patient advocate Barby Ingle, founder of the International Pain Foundation, to share her perspective on improving clinical trials. I know you enjoy this episode of "People Always, Patients Sometimes". Janet Kennedy (00:37): Hi, my name's Janet Kennedy and I'm your host for "People Always, Patients Sometimes", a production of Spencer Health Solutions. I am really looking forward to my conversation today with Barby Ingle. Barby is a bestselling author, a reality live-streaming personality, she lives with reflex sympathetic dystrophy, Migralepsy, endometriosis, and other pain disorders. Not a surprise. Barby is also a chronic pain educator, a patient advocate, and president of the International Pain Foundation. I am very, very excited to have Barby here today and also because she is an avid user of social media to share her story. Barby, welcome to People Always, Patient Sometimes. Barby Ingle (01:21): Thank you so much Janet for having me. I'm so glad to be with your audience today. Janet Kennedy (01:26): You know, we talked to a lot of different people in pharma, in health care and clinical research, and I have spoken with some other patients, but I have to say in reading your bio and the things that you're dealing with, while the title of our podcast is people always patients, sometimes I have to think that sometimes it feels like a flip for you, that it's really patient. Always people sometimes. Yeah. Well, I think I'm both all the time. Is it a situation where you literally can never not think about what you're feeling? Barby Ingle (02:02): I absolutely have to pay attention. I have to plan and be prepared, and luckily before I was chronically sick, I was already organized, so I definitely used the skills that I learned in cheerleading, including organization and responsibility in dealing with the healthcare challenges that I'm faced with every day. For sure. Janet Kennedy (02:22): Now, have your challenges come as a result of your adult life, or is this something you dealt with even as a teen or preteen? Barby Ingle (02:30): I was actually pretty healthy growing up and when I was 26 I developed endometriosis. And then at 29, I developed reflex sympathetic dystrophy, RSD for short, and really endometriosis was something I got through really quickly. You know, it was like, Oh, this didn't work. These shots didn't work. What's the next thing? A laparoscopy. Okay. That made my insides very mad and the spread. And then the final thing was a hysterectomy and I was like, take it out. I'm done. I can't take this. I got past it and I thought if I could pass that I could get through anything. And then I got hit with RSD and secondary conditions after a minor car accident, which triggered it. It's actually an autoimmune disease, but it was triggered by an automobile accident and that changed my life forever. That eight seconds. Janet Kennedy (03:26): Wow. Okay. I'm going to take a moment and really think about that eight seconds. And your life has changed forever. So what does that mean day to day? How are you impacted by RSD? Barby Ingle (03:38): So prior to the impact, I was in my vehicle, a small vehicle, and I was hit by a 16 passenger van. I saw the van coming, I saw him in my rearview mirror and I twisted my body and the van impacted my car and I blacked out after that. I went to court and he testified, he said he had never, he didn't see me and he never took his foot off the gas. So after he hit me, so from that moment I started having burning fire pain. It was in my face, neck, and shoulder area. But it was so overwhelming with my thoughts, with my actions. I was, I went from being a collegiate cheer coach at a division 1A university to, I still was trying to keep coaching, but my coaching suffered, my team suffered. Barby Ingle (04:26): We were in the top five in the country rankings for cheerleading. And you know, I really was living my best life and that eight seconds that it took for this accident to happen, everything changed. And I went from well to being bed-bound for the next six months or so. I tried to continue to work and I would go to practice and I at practice would lay down on the floor and have our team doctors taking care of me. Instead of taking care of my student-athletes. I would go back to my office and lock the door and sleep because I was in so much pain, but I also was quite fatigued maybe just from having that much pain. If I turned my head to the right, I would pass out. Just literally everything in my life changed. I was married for 10 years. It's my first marriage. Barby Ingle (05:15): Did not survive the auto accident. I couldn't explain why they told me I had whiplash, but yet I had this burning fire pain. I started going from doctor to doctor to figure out what was wrong. I went to chiropractors, physical therapy, anything and everything that was suggested. I tried and then what? Oh goodness. Then I ended up over a three year period moving from Washington state down to Arizona per doctor's instructions. They said I would get better care here. I ended up seeing 43 doctors in a three year period. And finally, that 43rd doctor stopped and he had me bring in, at that time all of my medical records, which took three, three-inch binders. I'm now on binder nine of medical records. And before he even came in to meet me or see me or anything, he went through every single record from all 42 providers before him from all the different specialties. Barby Ingle (06:12): And he came in and said, I think I know what's wrong but I'm not sure and I want to run a test. And I said, well tell me about the test and I'm going to go home and study about it. And that was the first time I advocated for myself instead of just listening to and doing what the doctors told me, I stopped and said, you know, I want to go research on my own. And I and I took a week to research and talk to other patients that had had this procedure and decided to do the test and went in seven days later had the test done and I was tested positive for RSD, which is now known as central pain syndrome. Janet Kennedy (06:50): And what, is this a situation where you have to be medicated all the time? Is there a different kind of physical therapy that works for you? Barby Ingle (06:59): I'm allergic to Oxycontin so I didn't know how I would do with other opioid medications for pain. So I also didn't want to be like out of my mind so much mentally foggy cause I was already mentally foggy from the RSD symptoms. So I tried to do other treatments, but I was on pain medication for a lot of that time. Although I was on a lot lower dose and strength than many of my friends are. I supplemented it with radio frequency ablations as well as nerve box. And I even tried epidural steroid injections. I tried physical therapies. I went through a whole bunch of different, I've done three clinical trials, two medications and also a medical device and I still actually am using the medical device that I did throughout the trial and there's actually a book written and I have another family member who has the same condition as I do and he actually uses the same medical device that I used and we're both in this book that has come out about the device. Janet Kennedy (08:11): You went from literally suffering every day needing multiple physicians, changing your life totally moving to a new area. Finally got a diagnosis. You got some things maybe a little more manageable? Barby Ingle (08:24): Yes, so I was in the accident on September 26th, 2002 and I finally started doing all of these treatments and trying all of these options. I ended up in a wheelchair. I went from being face, neck, and shoulder; through surgeries, I didn't need I had a rib removed. The doctor made a mistake on that and ended up damaging my right lung and just one thing after the next went bad, I ended up in a wheelchair and bed bound to the right side of my body. My hand was curled up, my foot curled up and really just was trying to maintain being alive. In 2009 I finally went through infusion therapy in seven days in ICU infusion. I went in in a wheelchair in seven days later I walked out, I teeter-tottered out cause my legs were quite a bit atrophied and my whole body was. Barby Ingle (09:18): But I was able to walk out on my own and I was so proud of that moment. I had to come in and out of remission since December 2009 and I still have a scooter that I use when needed, but I am managing much better now that I have a good group of treatments that are working for me. Janet Kennedy (09:39): So help me understand how you made the transition from being focused on your own health to helping other patients deal with their issues. Barby Ingle (09:50): I advocate for myself first and then I joined a local support group and realized that I had a lot to offer to the group because of everything I had been through, but I didn't quite get what I needed out of it. So I reached out to a larger organization for RSD and said, you know, I'd like to be a mentor to mentor other patients. Barby Ingle (10:15): And I took on mentoring three patients, one of whom is still to this day, my best friend, and we keep in touch almost daily and it worked out. But I started by mentoring other patients and just being someone that they could talk to and someone that I could talk to and growing that into - I started to get asked to speak at events, at other people's support groups at different conferences and things that are happening in the pink community at large, not just for my disease specifically. And in sharing my story, it just really opened up a whole new Avenue of reach of people that didn't know what this is somewhat, you don't know that you need it until you're in the midst of it. And sometimes when you get into a situation where you're challenged, it's hard to see all the tools that are around you. Barby Ingle (11:09): So I kind of found them slowly moving through my own story and I said I have to help other people. No one should go through what I went through. Janet Kennedy (11:18): So I'm curious, how do we refer to chronic pain? Is it a disease? Barby Ingle (11:22): Well, chronic pain is actually now in the ICD 11 a diagnosis in and of itself. You can be diagnosed with chronic pain as an ICD code and insurance covers different treatments and things that are pertaining to that code. So it actually is a disease in itself or it can be secondary to another condition. Janet Kennedy (11:41): Well Barby, tell me about the International Pain Foundation. What is that organization? The International Pain Foundation started back in 2006 and that was just when my advocacy was starting and it was started in my honor by family members, but it soon grew to something that's much bigger, which at first it was called the power of pain foundation because I believe that pain made me a better person and more patient. Barby Ingle (12:08): And that's the message that I was spreading. My family every year would pick a charity project going into a nursing home or serving food at a homeless shelter that we could do as a family, and that year the family said, look, if Barby had this much trouble there, have to be other patients out there having trouble, so let's do something that will help them. And it's grown from just a small family organization in my honor to me actually running it and now it's an international organization with people from all over the world submitting articles, submitting quilt project pieces and crafts and education and all kinds of awareness opportunities. It really has grown from this little small family idea and project into this global network. Janet Kennedy (12:59): Oh, that's awesome. Because I think that's what patients have really demonstrated to the industry is that they will find their solutions. They will find their networks, they will join together with peer groups and solve their own problems if you won't solve them for me. Barby Ingle (13:17): Absolutely. Sometimes I wonder and now I work with pharmaceutical companies to help with clinical trials and help people become aware of those clinical trials that are going on. But before it was involved in, I didn't quite understand the clinical trial process. I would wonder why are they not listening to the patient's voice? And I think over the last few years the pharmaceutical industry has made a special effort to pay attention to what the patient voices and have patients and caregivers on their advisory boards for a clinical trial. Getting it set up and getting it organized and all the way through to the end when the results are produced or their item medication came to market or I've been involved with trials that actually didn't make it to market, but I've seen that whole entire process and been a part of it and was one of those patient voices in that process. Janet Kennedy (14:13): Tell me a little bit about your experience as a patient in a clinical trial. You don't have to name names, but I'm more curious about what did you feel was done well and what do you feel may be missed the mark as far as considering the "patient first" perspective? Barby Ingle (14:29): There's so many things. The biggest, thing is the disparity. Clinical trials should mirror the patients that will be the end-user and so many times clinical trials miss that mark and they want people in their trial who will do well on the medication, but it doesn't necessarily serve the population. For instance, we know that people that are African American or black will have sickle cell disease more often than somebody who's white, but less black people will participate in the clinical trials so when they come up with a solution that could be viable for sickle cell, it hasn't been tried on the actual population. That's the majority population for that disease or condition. So I think that's one of the things is the disparity. Also, a lot of people are limited from being a part of the clinical trials because they don't have transportation or access to the trials themselves. Barby Ingle (15:33): They're usually held in the bigger cities and that has a certain population and income level and education level. So you get less of the smaller town, rural patient population. Being a part of those clinical trials? Janet Kennedy (15:49): Well, I think from your experience too, you probably weren't solo-ambulatory, so you needed someone's help. So that's two people. Barby Ingle (15:58): Yes. And that's what I meant by transportation because I have a seizure disorder. My seizures disorder didn't start until 2014 but I had migraines right after my auto accident, but I wasn't able to drive for many years because when I twisted my head to the right, I would pass out while to change lanes, you need to be able to look and see what's next to you. So I didn't drive a lot. So I do, I rely on my caregiver and now I have a seizure disorder. Barby Ingle (16:28): So I drive even less. But if he wasn't able to take me and have a vehicle to put my scooter in or my wheelchair in, then I wouldn't be able to go. I did try to take a taxi once to a doctor's appointment and it was $126 to go less than 20 miles. Wow. And my husband now. I was able to find love in the midst of all of that pain and chaos and he's the most amazing caregiver ever. He said, you know, I will take off work for $126 like this is ridiculous. Never, ever, ever take a taxi again. We just had to find ways around it and work out a better way, but if you don't have somebody that can do that or their job doesn't let them off, then getting to the appointments can be quite a challenge to participate in the clinical trial. Janet Kennedy (17:20): Barby, you're very savvy out there in the wide world, following social media, following the innovations that are happening. Do you see any improvements for patients with all of the digital health technology that's being developed? Barby Ingle (17:34): Absolutely. I think that some of the clinical trials are coming on board and they're allowing patients to do the trials from home. They're sending them kits where they can do the monitoring from home and it can work on an app on their phone and report the results to the researchers and or their providers. If the researchers find something, they can report it back to the patient's provider to get immediate care. So we're starting to see some of those types of trials come into fruition and I think this year especially telehealth has exploded and hopefully the clinical trial process follows that same path and works in telehealth into their system so that patients that are more rural can get involved in the clinical trial so that the trials can mirror better the types of patients that are the end-user of that product. Janet Kennedy (18:32): Well, that is exactly what we hope at Spencer health solutions as well. Our Spencer device allows for medication delivery also allows for patient engagement via asking questions after someone has taken their med delivery and there's a telehealth feature and can even tie into biometric devices. So there are a lot of options there to hopefully make it easier for in-home clinical trials. Before I go, I want to know a little bit more about the Ken and Barby Show. Tell me what this is. I don't think I've ever spoken to a reality TV star. So I want to know what this program is and how it got started. Barby Ingle (19:11): Yes. So I've been on multiple television stations, like game show network and TLC and WB, CBS, ABC, NBC. But my husband, Ken and I were "Ken and Barby", and we participate in the Ken and Barby Show. It is a show that is lighthearted. It covers our adventures together and raises awareness, but not necessarily in an upfront, in your face kind of way. So we talk about different conditions and things that I'm personally going through with my health or Ken as a caregiver, some of the challenges that he's faced. But it's also, we found ourselves because of the advocacy work in quite some interesting positions and situations and have been able to meet a lot of great people who have also use their platforms to raise awareness and spread the information that they need about their condition. So we're very funny together, very interactive with our viewers. Barby Ingle (20:11): Sometimes we play games, we give out prizes. We're on season nine some of our seasons. We've had sponsors this season that we're on right now. We decided to not have a sponsor for this season. It's just Ken and Barby raw all summer long and we just want to bring positivity into everybody's life and be cheerleaders of hope - or Ken calls himself a "Care Leader of Hope". We do that in a lighthearted, fun, positive way and it gets people's minds off of the pain, but we also have people that don't have chronic pain of any kind and they're tuning in and watching and we're reaching a larger audience than just our silo of patients and their caregivers. So we're actually planting seeds and we're hoping that when that person needs the information one day that they will remember some of the topics and things that we brought up during the show. Janet Kennedy (21:07): Oh, that sounds great. Well as people know who listened to the podcast, I will have links in the show notes that will take people to not just your social media profiles, but we'll make sure that we've got a link to a couple of your cool blog posts about clinical trials and of course to the Ken and Barby Show. Barby Ingle (21:24): Thank you so much. Janet Kennedy (21:25): Oh, Barby, thank you so much for being here and I really, really enjoyed having you as a guest on "People Always, Patients Sometimes", and really look forward to meeting you in real life when we get back into face to face situations. Barby Ingle (21:41): Awesome. I can't wait to meet you as well. Thank you so much, Janet. This has been a great time. Contact Barby Ingle Website LinkedIn Twitter: International Pain Foundation Twitter: Barby Ingle

On this episode of In The Limelight, we welcome an extraordinary guest, Batista Gremaud, who is an International Body Designer, Empowerment Speaker and co-founder of the International Institute of Body Design, with Stephen Hercy aka Dr. Fitness USA. She received the "Most Outstanding Fitness Program For 2019" by the Winners Circle, featured as an expert authority speaker on the "International Pain Foundation". If you would like to know more about, or connect with Batista: Website:  DrFitnessUSA.com Social Media: Facebook: @batistagremaud Instagram:  @batistagremaud Twitter: @batistagremaud Connect with Clarissa!  Clarissa's Website: https://inthelimelightmedia.com Social Media: FollowFollowFollowFollow See all "In The Limelight" episodes

In this episode we will discuss endometriosis.  Endometriosis is a disease in which tissue similar to the lining of a woman's uterus grows in other places in the body. It is one of the most common gynecological diseases, and its primary symptoms include pain and infertility.  Our guest today is Barby Ingle, a chronic pain warrior! Barby is an author, reality personality, and lives with reflex sympathetic dystrophy (RSD), migralepsy, endometriosis and other pain disorders. Barby is a chronic pain educator, patient advocate, and president of the International Pain Foundation. She is also a motivational speaker and best-selling author on pain topics. Her blog, reality shows and media appearances are used as a platform to help her become an ePatient advocate, and she now travels the country attending healthcare conferences, speaking publicly, sharing her story, educating and advocating for patients across the globe. She has received 19 accommodations over the years for her advocacy work

Chalene sits down face to face with Canadian comedian, recording artist, choreographer, actress, dancer, singer, and YouTube personality... Nicole Arbour. Since 2015, Nicole has strategically created viral videos and entertaining content that get millions talking! Instead of backing down from the criticism, she has found freedom by focusing on her objective: using her platform as a spokesperson for the International Pain Foundation. She now helps other brands and entrepreneurs build businesses by starting with MINDSET! With more than 700 Million video views and counting (yes, you read that right), Nicole brings her expertise to BYT and will get you out of your own head… empowering you to be boldly YOU!     Find out more about Nicole's  Go Team Academy   You can check out Nicole’s Viral YouTube Videos HERE   Nicole’s Instagram   Nicole’s Facebook   Be sure you are subscribed to this podcast to automatically receive your episodes!!! Spotify   Itunes   Stitcher   Join our new awesome PodSquad on Facebook here: www.facebook.com/groups/ChalenePodSquad Here’s The System I Use Every Day to be More Organized & Crazy Productive: www.pushjournal.com Get episode show notes here: www.chalenejohnson.com/podcast   Hey! Send me a tweet & tell me what you think about the show!(Use the Hashtag) #BuildYourTribe so I know you’re a homie!XOXO Chalene   Connect with me on your fav social platform. SnapChat: ChaleneOfficial www.Facebook.com/Chalene www.Instagram.com/ChaleneJohnson    www.Twitter.com/ChaleneJohnson 

On this episode, I'm talking with Stephen Hercy AKA Dr. Fitness USA. He is an International Body Designer, owner, and founder of the International Institute of Body Design. No 1 Best Selling Author, Holds the prestigious title Professeur De Culture Physique Weider, certified by the IFBB International Federation of Bodybuilding. Dr. Fitness USA is the creator of the Body Design Formula strength training protocol and recognized professional empowerment speaker as a pioneer for his successful work with pain management and postural realignment, which affects mood, behavior, and productivity. Dr. Fitness USA is the leading authority in bringing his revolutionary strength training systems to the addiction and recovery community as a new tool for mood behavior stabilization, stress management, and is the first person in the world to provide strength-training programs for women suffering from endometriosis and auto-immune disorders. Dr. Fitness USA regularly appears as a celebrity guest empowerment speaker on radio shows including the syndicated show Al Cole “People of Distinction”, L.J. Jackson “Amazing women of Power,” CNN show Tony O'Donnell at KCAA broadcast, Svetlana Kim “To the stars through adversity”, “The Dr. Kevin” show, Lou Hick famous Aimed 2 Purpose global broadcast, Dave Nassaney "Caregiver, avoiding burnout" broadcast and was featured as an expert authority speaker on the International Pain Foundation 2017 first webinar series. Dr. Fitness USA has worked with all types of people from celebrities such as Linda Gray, Sally Fields, Simon Cranes, Billy West as well as with MD's, chiropractors, alternative health professionals, as well as students. Young and older people of all walks of life travel worldwide to seek his unique services. Dr. Fitness USA ‘s groundbreaking prescription strength training system assist's men and women alike to become masters of their body independently of a personal trainer to achieve a pain-free life. ~ Show Notes: www.thesocialchameleon.show/Stephen-Hercy ~~~ Giveaways can be found here www.thesocialchameleon.show/pickme Links & Resources www.thesocialchameleon.show Call: (480) 525-5258 Email: info@thesocialchameleon.show Connect With Us: Facebook: fb.me/SocialChameleonShow Instagram: instagram.com/socialchameleonshow Twitter: twitter.com/SocialChamShow Subscribe: YouTube: bit.ly/SCS-Subscribe Anchor: anchor.fm/social-chameleon-show Apple Podcast:apple.co/2L8hl6R Google Podcast: bit.ly/SCS-Google-Podcast Spotify: spoti.fi/2KYJ0GF Stitcher: bit.ly/SCS-Stitcher Google Music: bit.ly/SCS-Google-Music More Apps Here thesocialchameleon.show/podcast #SocialChameleonShow #StephenHercy #DrFitnessUSA --- Send in a voice message: https://anchor.fm/social-chameleon-show/message Support this podcast: https://anchor.fm/social-chameleon-show/support

Barby Ingle is a best selling author, reality personality, and lives with reflex sympathetic dystrophy (RSD), migralepsy, endometriosis and other pain disorders. Barby is a chronic pain educator, patient advocate, and president of the International Pain Foundation. She is also a motivational speaker and best-selling author on pain topics. Her blog, reality shows and media appearances are used as a platform to help her become an ePatient advocate, and she now travels the country attending healthcare conferences, speaking publicly, sharing her story, educating and advocating for patients across the globe. She has received 19 accommodations over the years for her advocacy work including; 2011 iPain Hero of Hope Award, 2012 WEGO Health Ms. Congeniality, 2012 NAF You Are Our Hero Award, 2013 International Inspirational Luminary, 2015 IDA Impact Award, and 2016 WEGO Health Lifetime Achievement. In 2017, Barby was named a Health Information Technology Top 100 Influencer by HealthScene and Top 20 Health Influencer by Insider Monkey Magazine. In 2018, Barby received the Reality All Star Reunion Superstar award for Most Social Media posts and Top 50 Chronic Pain Advocates. In Feb. 2019, Barby is listed in the top 100 social media advocates for Rare Diseases.

Barby Ingle joins me this week for a conversation about living with endomitriosis and reflex sympathy disorder, the ongoing stigma facing women with chronic pain, creating the International Pain Foundation, and preparing for the upcoming International Pain Summit. Learn more about the International Pain Foundation at internationalpain.org. Run Time - 37:15 Send your feedback to feedback@justtalkingpodcast.com.

Nicole Arbour is a comedian, entertainer, social media expert, actress, singer, dancer, choreographer, motivator, and business consultant. Her videos have been viewed more than 700 million times worldwide. She has a great story that can be inspirational to those that want to be a victor rather than a victim. After being an NBA cheerleader, choreographer, starring on the top comedy show on Much Music in Canada (Canada's MTV), helping mass brands create record breaking digital content, and working her way up to feature films and televised stand up specials, Nicole was involved in a car accident in 2008 that left her on disability and a life of medial treatments. ​Refusing to accept the lifelong disability diagnosis, Nicole utilized unconventional treatments, created the #GOTEAM movement, and very literally cheered herself and thousands of fans back to life and off of pain killers. Her hard-hitting, real, and innovative debate starting style of comedy has led her to being one of the Top-7 Youtube Channels Crushing It That You Can Learn From by Entrepreneur Magazine as well as being featured by major news outlets around the world in the last two years alone.  Nicole has been seen hosting Style New York Fashion Week at Madison Square Garden, joining the BBC Comedy Writing staff, hosting sold out events in Las Vegas and nightclubs around the world, consulting and creating content for brands that has led to tens of millions of views for her partners as well as beginning her music, beauty and book projects. ​Nicole has been humbled to receive a series of accolades in including an Honorary Hollywood  Walk of Fame star for special achievement in social media.  The Hero of Hope Award from the International Pain Foundation and was the online fan vote winner and finalist for a Shorty Award Best Comedian.

Barby Ingle President International Pain Foundation talks “How to Save Thousands on Your Medical Bills”

Barby Ingle President International Pain Foundation talks “How to Save Thousands on Your Medical Bills”

Barby Ingle President International Pain Foundation talks “How to Save Thousands on Your Medical Bills”

Batista Gremaud is the co-founder of the company Dr FitnessUSA helping busy women over 40 get 20% stronger in 20 minutes; look and feel 15 years younger and achieve a pain-free life with the Body Design Formula Prescription Strength Training System created by Dr FitnessUSA. Certified in personal training, Batista's expertise in strength training includes structural realignment of the spine and injury prevention.Batista is a No1 Best Selling author and co-creator of the Feminine Body Design prescription strength training system.She is a featured guest expert and authority speaker on the International Pain Foundation. Batista regularly writes for addiction recovery magazines and online health platforms and has appeared as a celebrity guest speaker on numerous radio shows.A visionary, also certified in hands-on healing, intuitive readings, and energy clearing. Batista Gremaud ‘s passions in quantum physique and metaphysical science inspire her to help people of all ages to achieve greater integration of body, mind, and spirit through the practice of strengthening the body and the mind with the Body Design Formula prescription strength training coaching system.During her interview, Batista shares:- Her health and fitness journey and how it has shaped how she helps her clients achieve their health and fitness results.- Why she focuses on working with women over 40 who are experiencing hormonal changes, weight gain and suffering from injuries or chronic pain.- Why her female clients seek her out and get results that they never experienced before.- Why women need strength training instead of long hours of cardio each week.- How her prescription strength training system helps women build muscle without risk of injury.- What her system gives her clients results that they can’t get from working with a personal trainer.- What you must know to make sure that you get optimal results with each piece of gym equipment.- How each program is designed to address a client’s unique health and fitness strengths and development opportunities.- Why her system produces results that are sustainable.If you would like additional information about Dr FitnessUSA or contact Batista go to:Website: drfitnessusa.com and request the Free ReportFacebook: https://www.facebook.com/drfitnessusaLinkedIn: https://www.linkedin.com/in/batistagremaud/Never Too Late for Fitness Radio with Phil Farishttp://businessinnovatorsradio.com/never-too-late-for-fitness-radio-with-phil-faris/

Barby Ingle President International Pain Foundation talks “How to Save Thousands on Your Medical Bills”PLUS 5 Minutes of Personal Finance: “Life Insurance: Term Life vs Whole Life - What's the Difference?”

Barby Ingle President International Pain Foundation talks “How to Save Thousands on Your Medical Bills”PLUS 5 Minutes of Personal Finance: “Life Insurance: Term Life vs Whole Life - What’s the Difference?”

Barby Ingle President International Pain Foundation talks “How to Save Thousands on Your Medical Bills”PLUS 5 Minutes of Personal Finance: “Life Insurance: Term Life vs Whole Life - What’s the Difference?”

Special Guest - Ken & Barby from the International Pain Foundation and the iPain Featurettes!

Special Guest - Ken & Barby from the International Pain Foundation and the iPain Featurettes!

Special Guest - Ken & Barby from the International Pain Foundation and the iPain Featurettes!

How can two twice-divorced people – who failed as a couple three decades ago – reunite after 32 years [1 billion seconds] and create a committed, lasting marriage? It happened to Poppy and Geoff Spencer, authors of 1 Billion Seconds, a fictional memoir. Poppy and Geoff are now relationship experts who will share … The Secret of the 98% Success Rate, Even for a 2nd or 3rd Marriage … Two Necessary Words for Relationships to Flourish … 5 Ways the Emotional Clock® Will Guarantee a Communication Connection. Poppy and Geoff have also created and patented a relationship tool.  www.RelationalExperts.com One in three people (116 million) in the U.S. are affected with a condition that causes pain, probably including someone you know. But until you feel the pain it is difficult to understand all of the challenges. Meet Barby Ingle, a chronic pain educator, patient advocate, and president of the International Pain Foundation.  Barby was living her dream, performing cheerleading, dance and gymnastics from age 4 through college. She then started her own cheer/dance training company and was hired by Washington State University as head spirit program coach. But that all changed. She has battled chronic pain from Reflex Sympathetic Dystrophy (RSD) and endometriosis since 1997. After consulting 100+ healthcare professionals, major surgeries she didn’t need, and more – Barby had to become the Chief of Staff of her own medical team. www.internationalpain.org

Special Guest - Barby & Ken from the International Pain Foundation and the iPain Featurettes!Do You have the Nerve to be Heard?Celebrating the month of November as #NERVEmber Ken & Barby chats with us and the iPain Featurettes Kaylee Dodrill, Jennifer Lyn Brande, Amanda Greene, and iPain Feature Kurtis VanFleet!Together bringing awareness to chronic pain and illness of all kinds including one of the most challenging conditions being NERVE pain!This is Part I of a Month long series! To learn more about the ipain Features and Featurettes click here> https://www.youtube.com/watch?v=zJvMWFhUL2E&list=PLCJSawAzRGDeZN-KQ7VsFlyIKG2UYZEb4https://powerofpain.org/https://powerofpain.org/hope-is-true/

Special Guest - Barby & Ken from the International Pain Foundation and the iPain Featurettes!Do You have the Nerve to be Heard?Celebrating the month of November as #NERVEmber Ken & Barby chats with us and the iPain Featurettes Kaylee Dodrill, Jennifer Lyn Brande, Amanda Greene, and iPain Feature Kurtis VanFleet!Together bringing awareness to chronic pain and illness of all kinds including one of the most challenging conditions being NERVE pain!This is Part I of a Month long series! To learn more about the ipain Features and Featurettes click here> https://www.youtube.com/watch?v=zJvMWFhUL2E&list=PLCJSawAzRGDeZN-KQ7VsFlyIKG2UYZEb4https://powerofpain.org/https://powerofpain.org/hope-is-true/

Special Guest - Barby & Ken from the International Pain Foundation and the iPain Featurettes! Do You have the Nerve to be Heard? Celebrating the month of November as #NERVEmber Ken & Barby chats with us and the iPain Featurettes Kaylee Dodrill, Jennifer Lyn Brande, Amanda Greene, and iPain Feature Kurtis VanFleet! Together bringing awareness to chronic pain and illness of all kinds including one of the most challenging conditions being NERVE pain! This is Part I of a Month long series! To learn more about the ipain Features and Featurettes click here> https://www.youtube.com/watch?v=zJvMWFhUL2E&list=PLCJSawAzRGDeZN-KQ7VsFlyIKG2UYZEb4 https://powerofpain.org/ https://powerofpain.org/hope-is-true/

The Arisen Strength Family Celebrates with the International Pain Foundation and the Featurettes! Debuting their NEW hit single "Hope is True" Barby Ingle, Ken Taylor and the Featurettes Alinda, Tracy and BJ of iPain take some time to Celebrate this Great accomplishment while bringing awareness to chronic pain sufferers of all kinds

The Arisen Strength Family Celebrates with the International Pain Foundation and the Featurettes!Debuting their NEW hit single "Hope is True" Barby Ingle, Ken Taylor and the Featurettes Alinda, Tracy and BJ of iPain take some time to Celebrate this Great accomplishment while bringing awareness to chronic pain sufferers of all kinds

The Arisen Strength Family Celebrates with the International Pain Foundation and the Featurettes!Debuting their NEW hit single "Hope is True" Barby Ingle, Ken Taylor and the Featurettes Alinda, Tracy and BJ of iPain take some time to Celebrate this Great accomplishment while bringing awareness to chronic pain sufferers of all kinds