Podcasts about new diagnosis

In this deeply moving episode of Warriors Unmasked, Chuck Thuss welcomes Laura DeKraker Lang-Ree, a mother, author, and fierce advocate for families navigating pediatric cancer. Laura shares her heart-wrenching yet empowering journey through her daughter Cecilia's leukemia diagnosis—a journey that sparked her mission to create resources and support for parents facing the unimaginable. Laura opens up about the shock and fear that consumed her when her three-year-old daughter was diagnosed with cancer. She recalls the early days of scouring the internet for guidance, only to find a lack of practical, emotional, and logistical resources for parents walking this difficult path. Determined to change that, Laura took her own experiences and turned them into something meaningful: her book, The Cancer Parent's Handbook: What Your Oncologist Doesn't Have Time to Tell You. Throughout this episode, Laura and Chuck discuss the emotional rollercoaster of being a cancer parent, the often-overlooked mental health challenges that come with the diagnosis, and the importance of building a strong support system. Laura's insights are both practical and heartfelt, offering listeners a candid look into what it's like to parent through a cancer diagnosis while continuing to nurture the rest of the family. Key Takeaways from Laura's Story: The Importance of Advocacy: Laura stresses how crucial it is for parents to become informed advocates for their children, even when the medical world feels overwhelming. Managing Emotions Amidst the Chaos: She shares strategies that helped her manage fear, grief, and anxiety during her daughter's treatments, including mindfulness, journaling, and leaning into her faith. The Power of a Support System: Laura talks about how she learned to accept help from others and how critical it was for her family's well-being. Turning Pain Into Purpose What started as a personal mission to survive the emotional toll of her daughter's diagnosis turned into a broader mission to help others. Laura created She Is You, an online community where parents can find support, share their stories, and access the tools they need to cope with pediatric cancer. Her book is packed with real-world advice, from handling medical jargon to advocating for your child's needs. Laura also reflects on the incredible strength she discovered within herself and within the pediatric cancer community. Her message is clear: no parent should walk this journey alone. Through her work, she hopes to ease the burden for others by providing the guidance she wished she had during those first terrifying days. Faith, Resilience, and Hope At the core of Laura's journey is her unwavering faith. She credits her relationship with God for giving her the strength to persevere through the darkest moments. Her story serves as a reminder that even in the face of unimaginable hardship, hope and healing are possible. Listen to the full episode to hear Laura's raw and inspiring story, and learn more about the resources available to parents navigating a child's cancer diagnosis. Stay Connected with Warriors Unmasked For more powerful stories of resilience and courage, visit Warriors Unmasked or book a coaching call with Chuck directly.   GUEST LINKS: cancerparentshandbook.com Instagram at @‌laura_dekraker_langree LINKS: www.thecompassionateconnection.com www.warriorsunmasked.com  Join Chuck's Text Community: 251-418-7966 Episode Minute By Minute: 00:00 Introduction and Welcome   03:12 Laura's World Shattered: Cecilia's Cancer Diagnosis   07:25 The Search for Guidance and the Lack of Resources   10:58 Becoming an “Expert” in Pediatric Cancer   15:14 The Emotional Impact of a Child's Diagnosis on the Entire Family   19:36 Strategies for Coping with Overwhelm and Fear   23:45 Creating The Cancer Parent's Handbook: A Guide for Parents   28:30 The Role of Faith and Community in Laura's Healing Journey   33:15 How to Advocate Effectively for Your Child's Medical Care   38:52 Laura's Tips for Maintaining Mental Health During Crisis   44:07 How the *She Is You* Community Offers Support to Cancer Parents   49:30 Words of Encouragement for Parents Facing a New Diagnosis   52:48 Final Thoughts: Finding Purpose Through Pain   55:11 How to Connect with Laura and Get Her Book 

Turns out his bipolar was a misdiagnosis. Hopefully this is good news for the couple. Plus, sad news for fans of 60 minutes.See omnystudio.com/listener for privacy information.

Listen in to a "throwback" episode that Mel and Tash recorded last summer, but never posted...until now! Tasha opens up about her journey toward a new diagnosis in her mental health world.

We get a lot of questions in our inbox from listeners with dietary restrictions. And sometimes, we can absolutely handle them using the expertise right in our test kitchen – no dairy? No meat? No nightshades? No problem. But not all restrictions are that simple. So we tapped registered dietician Desiree Nielsen to answer questions about cooking low-FODMAP, diabetes-friendly, and more. If you're experiencing changes in your health, make sure you contact your doctor and/or a Registered Dietician to make a plan that's right for you.Recipes featured: Super-Seedy Gluten Free Bread Blueberry Chia Seed Jam Gluten Free Carrot Cake Vegan Cacio e Pepe Black Vinegar Chicken with Radishes Kate's Feel Good Food Plan 30 Minute Green Pasta with Kale Velvety Vegan Chocolate Mousse Vegan Sausage Stuffed Acorn Squash Cashew Alfredo

This week Kevin returns to the Major Pain podcast to catch us up on his health journey. The big news is that he was recently diagnosed with Ménière's disease, adding one more diagnosis to his already long list. He was also finally approved for disability, and he discusses this process […]

I am feeling so much better. Thank you God……..I love life I truly do!

In this episode of the podcast Rob is solo as he interviews Dr. Anath Shalev, a diabetes researcher turned founder of startup Tiximed. Dr. Shalev discusses the discovery of TixnIP, a protein involved in oxidative stress in beta cells, and its potential for treating diabetes. The conversation covers the development of TIX 100, an oral medication targeting TixnIP, its implications for type 1 and type 2 diabetes, and the differences from existing diabetes treatments like SGLT2 inhibitors and GLP-1 agonists. Topics discussed: * Dr. Anas Shalev's background in diabetes research and founding of Tiximed * Discovery of TixnIP and its role in beta cell health * Potential of TIX 100 as a novel oral medication for diabetes treatment * Comparison of TIX 100 with existing diabetes treatments like SGLT2 inhibitors and GLP-1 agonists * Research process behind TixnIP inhibition and development of TIX 100 * Future of diabetes care, combination therapies, and impact on patients' lives * Information about Tiximed, clinical trials, and ways to support the research 00:18  Revolutionizing Diabetes Treatment: From Researcher to Founder 03:47  Revolutionizing Diabetes Treatment: Targeting Beta Cells and Glucagon Levels 13:47  Revolutionizing Diabetes Treatment: Targeting Beta Cells in Type 1 and Type 2 Diabetes 17:35  Revolutionizing Diabetes Treatment with Ticks 100: A Breakthrough in Addressing the Root Cause of the Disease 27:35  The Limitations and Advantages of Verapamil in Diabetes Care 29:47  Advancements in Diabetes Technology and Research: A Look into the Future 33:04  Exploring Diabetes Treatment Innovations with Dr. Shalev Topics discussed: 1. Mila's Personal Journey including leaving her job to focus on Hangry Woman full-time 2. Career Shift and Health Coaching: Transition from a marketer to a health coach 3. Bridging the gap between fear of eating and enjoying meals 4. Importance of Self-Care and Boundaries: Prioritizing self-care to avoid burnout 5. Support System in Content Creation: Managing overwhelm by acknowledging limitations 6. The role of support team members in providing feedback and managing projects 7. Navigating Changes in Diabetes Diagnosis: Transition from type 2 to type 1 diabetes diagnosis 8. Representing Diverse Voices in the Diabetes Community: Importance of diversity representation and transparency in collaborations 9. Kindness, Respect, and Accountability: Impact of chronic illness on behavior and comparison culture 10. Addressing misconceptions about online personas and supporting creators 11. Building a Supportive Diabetes App Key takeaways: * Embracing personal growth amidst challenges and life changes * Prioritizing self-care, setting boundaries, and recognizing emotional well-being * Navigating career shifts and advocating for representation in the diabetes community * Building a supportive community and offering personalized health support through technology * Upholding kindness, respect, and accountability in online interactions and content creation References: * The Hangry Woman * Glucose Guide App 00:00  Celebrating Diabetes Stories Worldwide 00:02  The Evolution of Mila Clarke: Navigating Life Changes and Diabetes Management 04:15  From Marketer to Health Coach: A Journey of Personal and Professional Growth 08:16  Learning to Set Boundaries and Prioritize Self-Care: A Journey of Self-Discovery and Growth 12:16  Navigating Burnout and Building a Support System in Content Creation 17:26  Navigating a Diabetes Diagnosis Change: Impact on Community, Relationships, and Advocacy 23:49  Navigating a New Diagnosis and its Impact on Personal Branding 28:04  Breaking Barriers and Building Bridges in the Diabetes Community 32:36  Debunking Myths and Realities of Being a Successful Black Woman Entrepreneur 42:36  Embracing Kindness and Abundance in a World of Competition 52:36  Navigating Social Media Etiquette and Misconceptions as a Creator 55:53  Navigating Online Criticism and Embracing the Journey to Success in Content Creation 01:02:49  Revolutionizing Diabetes Support with a Unique Pocket Guide App 01:06:10  Empowering Diabetes Management through Personalized Support and Community Connection 01:09:21  Building a Supportive Community Beyond Social Media Platforms 01:14:05  Empowering Health and Support Through a Unique Approach 01:17:12  The Value of Ads and Support in Providing Free Content and Services

HAVE YOU FELT LIKE GARBAGE SINCE 2019 OR BEFORE? BRAIN FOG? NERVE DAMAGE? NEW DIAGNOSIS? IT MIGHT BE SECRET WEAPONS!! HOMELAND SECURITY COMMITTEE JUST MET ON MAY 8TH TO DISCUSS SILENT WEAPONS BEING USED AGAINST US!! THE CIA, DIA AND DOD HAS STATED SILENT WEAPONS HAVE BEEN USED INS QUIET WARS. THESE SILENT WEAPONS CAN BE USED BY OTHER COUNTRIES AND HAS, AS WELL AS, ENEMY ALIEN SPECIES. LISTEN IN, YOU FUTURE AND HEALTH OF YOU AND YOUR CHILDREN DEPEND ON IT. --- Send in a voice message: https://podcasters.spotify.com/pod/show/lockdown-universe/message Support this podcast: https://podcasters.spotify.com/pod/show/lockdown-universe/support

In this episode of Diabetics Doing Things, Mila Clarke shares her personal journey of significant life changes, including career shifts, personal challenges, a re-diagnosis of LADA, and the passing of her mother due to diabetes-related complications. She discusses finding herself, managing diabetes, and embracing a new path forward. The episode also delves into the challenges of burnout, building a support system, navigating changes in diabetes diagnosis, and the importance of representation in the diabetes community. Topics discussed: 1. Mila's Personal Journey including leaving her job to focus on Hangry Woman full-time 2. Career Shift and Health Coaching: Transition from a marketer to a health coach 3. Bridging the gap between fear of eating and enjoying meals 4. Importance of Self-Care and Boundaries: Prioritizing self-care to avoid burnout 5. Support System in Content Creation: Managing overwhelm by acknowledging limitations 6. The role of support team members in providing feedback and managing projects 7. Navigating Changes in Diabetes Diagnosis: Transition from type 2 to type 1 diabetes diagnosis 8. Representing Diverse Voices in the Diabetes Community: Importance of diversity representation and transparency in collaborations 9. Kindness, Respect, and Accountability: Impact of chronic illness on behavior and comparison culture 10. Addressing misconceptions about online personas and supporting creators 11. Building a Supportive Diabetes App Key takeaways: * Embracing personal growth amidst challenges and life changes * Prioritizing self-care, setting boundaries, and recognizing emotional well-being * Navigating career shifts and advocating for representation in the diabetes community * Building a supportive community and offering personalized health support through technology * Upholding kindness, respect, and accountability in online interactions and content creation References: * The Hangry Woman * Glucose Guide App 00:00  Celebrating Diabetes Stories Worldwide 00:02  The Evolution of Mila Clarke: Navigating Life Changes and Diabetes Management 04:15  From Marketer to Health Coach: A Journey of Personal and Professional Growth 08:16  Learning to Set Boundaries and Prioritize Self-Care: A Journey of Self-Discovery and Growth 12:16  Navigating Burnout and Building a Support System in Content Creation 17:26  Navigating a Diabetes Diagnosis Change: Impact on Community, Relationships, and Advocacy 23:49  Navigating a New Diagnosis and its Impact on Personal Branding 28:04  Breaking Barriers and Building Bridges in the Diabetes Community 32:36  Debunking Myths and Realities of Being a Successful Black Woman Entrepreneur 42:36  Embracing Kindness and Abundance in a World of Competition 52:36  Navigating Social Media Etiquette and Misconceptions as a Creator 55:53  Navigating Online Criticism and Embracing the Journey to Success in Content Creation 01:02:49  Revolutionizing Diabetes Support with a Unique Pocket Guide App 01:06:10  Empowering Diabetes Management through Personalized Support and Community Connection 01:09:21  Building a Supportive Community Beyond Social Media Platforms 01:14:05  Empowering Health and Support Through a Unique Approach 01:17:12  The Value of Ads and Support in Providing Free Content and Services

This season on the podcast, co-hosts Liz and Karla will be sharing mini episodes each Monday to highlight important topics for a healing journey. These Factors In Action episodes will share insightful ways that you can bring the healing factors into your life. This Week - Empowerment with a New Diagnosis Start from an Empowered Place. First, take a deep breath. Determine if you are in an emotional emergency or a physical emergency. Many cancers have been growing for some time and therefore are not a physical emergency. Most of us have time to research, get second opinions, and make informed decisions. Tell your doctor you do not want to hear the “prognosis” or the statistics. You are not a number and should insist from the start on being treated like an individual not as a number or diagnosis. The statistics and prognosis will not help you and may only upset you more. No one, not even the smartest doctor, can possibly know YOUR outcome. There are so many stories of people who have outlived the prognosis! You can be one of them! _____ To learn more about Liz and Karla's private practice, The Health Navigators, A Virtual Cancer Wellness Community, visit www.HealthNavs.com   Click here, to learn more about health coaching and our Overcome the Odds Coaching Program and schedule your free Discovery Call.   Follow the Health Navigators on Social Media: Facebook, Instagram, YouTube    ______ Follow Radical Remission on Social Media: Facebook , Instagram, YouTube

It's not unusual to have difficulty finding the right word or remembering where you put things. But persistent problems with memory or the ability to perform everyday tasks might be signs of something more serious. An "Early Onset of Dementia" or "Mild Cognitive Impairment" diagnosis can be a sudden blow to any family. In this case and on this episode, gospel musician, Josh Singletary, shares about his Mom with a recent diagnosis of dementia. His honesty of the unknown road ahead makes this a vulnerable story of a family trying to pull together for their loved one.  Josh's love for his Mom, his knowledge of music and faith in the Lord and his family's desire to walk this unknown territory with their eyes wide open, is encouraging for any family walking this dementia journey.   www.verandaministries.org www.joshsingletary.com

Today Laura joins us on the podcast to talk about their recent BPD diagnosis and how they're moving forward with life given this. They also had some spidey senses that perhaps they struggled with ADHD so we administered the ADHD self-reporting tool and spoke about the results. It was so fun to have Laura join us on the pod. You can find them on Twitch @glomdi or right here: https://www.twitch.tv/glomdi Support the showYou can find Laurie and Sara on Instagram to follow their day to day lives even further @laurieanned and @saraswellnessway. You can also find the podcast on IG @boldbeautifulborderline Leave us a voicemail about your thoughts on the show at boldbeautifulborderline.comRegister for our free peer support group at https://www.eventbrite.ca/e/the-super-feelers-club-tickets-145605434775Register for our low-barrier drop-in DBT group at https://www.thewellnesswayllc.comPurchase the Exploring Your Borderline Strengths Journal at https://www.amazon.com/Exploring-Your-Borderline-Strengths-Amundson/dp/B0C522Y7QT/ref=sr_1_1?crid=IGQBWJRE3CFX&keywords=exploring+your+borderline+strengths&qid=1685383771&sprefix=exploring+your+bor%2Caps%2C164&sr=8-1 If you like the show we would love if you could rate, subscribe and support us on Patreon. Patreon info here: https://www.patreon.com/boldbeautifulborderline?fan_landing=true ...

There's no doubt that our blood sugars affect our mood and cognitive function, and in this week's episode, I'm joined by Brea Di Dato, a family and psychiatric nurse practitioner in Oregon, for a conversation that is chalk full of wisdom. Our conversation includes her story of being diagnosed at age 38, her experience with neuropathy, anxiety, and more. She paints a vision of how our joy can coexist with suffering and that the goal of life is NOT an end to suffering. Brea also shares her expertise on the role between blood sugar, cognitive function, mood, and how to effectively communicate your “grumpy space” needs to your partner.Time Stamps:  (04:56) Weight Loss and Brain Fog: Her Diagnosis at 38 Years Old (08:20) Her First 6 Months of Diagnosis(10:05) Neuropathy (12:05) How She Approaches Her Patients Now Post Diagnosis (13:04) The Slippery Slope of Single Data Points (14:53) Safety & Taking Control of Anxiety With a New Diagnosis (17:43) Barriers to Living (19:40) First Steps: Validate the Grief (20:48) The Coexistence of Joy and Suffering (22:42) A Dead Person Goal(23:45) Growth, Change, and Discomfort (26:22) Distress and Burnout (30:15) Reaching Out for Help (33:18) Diabetes, ADHD, Blood Sugar and Cognitive Function(35:49) Blood Sugar and Mood (38:41) Creative and Effective Communication of Your Needs(42:32) I Don't Need You to Fix ThisWhat to do now: For any person with Diabetes in Oregon who would like to talk to someone about their mental health, check out Brea's business website https://www.pbh.health/Follow me @lauren_bongiorno and @riselyhealth on Instagram to stay in the loop for when new episodes drop.Learn more about our coaching programs HERE. Disclaimer: Nothing you hear on the Reclaim your Rise podcast should be a substitute for personalized professional medical advice. Please always consult your physician or other medical professional before making any changes to your diet, insulin dosages, or healthcare plan.

Today we're joined by Meagan Chorney, mother, entrepreneur, and mental health advocate. Meagan spent most of her life believing she had anxiety, only to discover at the age of 29 that she had been misdiagnosed. With a new diagnosis of Autism and Bipolar disorder Meagan is relearning herself and her coping mechanisms. Today we're covering how diet, structure, and the right community can impact your mental health journey, as well as the shame that seems to follow a mental health diagnosis. We talk about the need to advocate for yourself in our current healthcare system, the misconceptions around Bipolar disorder, and the small steps to take when wanting to make big life changes. Meagan is committed to breaking to stigma around mental health and is doing so one conversation at a time. Follow the HER podcast on IG here ->⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ ⁠⁠⁠⁠@its.her.podcast⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠   Check out all our links here -> ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠HER links⁠⁠⁠⁠⁠⁠ Follow Meagan on IG here -> @mmeaganicole Follow Jessica Janzen on IG here -> ⁠@thejessicajanzen⁠ & ⁠@loveforlewiston⁠ Book a FREE discovery call on her website here -> ⁠https://jessicajanzen.ca⁠ Mention the HER Podcast when booking 3 or 6 month coaching packages with Jessica & receive 10% OFF! Follow Glam Lash on IG here -> ⁠@glamlashstudio.yxe⁠ Visit their website here -> ⁠www.glamlashstudioyxe.com⁠ Use code "HER10" to get 10% off your next appointment!

I lay out my story as it unfolded over the past year and some change. You get some raw me as far as emotions go. I'm feeling good! I'm not numb. The emotions have come back, kinda in my face, as far as intensity and control at times. I give you every bit of me. The good, yeah there is good! The bad, I sunk low at times. Did I mention the good? It feels great feeling good and I want to share this hope with you in the realest real way I can. Let's Go!

In this episode, I am joined by Rachel Zukose at the ASHA Convention. Rachel Zukose, MA, CCC-SLP, TSSLD,  is an ASHA certified and New York State licensed Speech Language Pathologist in the Hudson Valley who assesses and treats a diverse range of communication disorders.  Rachel has experience with assessment and treatment with both pediatric and adult patients within a variety of areas including: articulation, language, feeding, voice, fluency, cognitive communication, social communication, alternative and augmentative communication, as well as Childhood Apraxia of Speech. Rachel is PROMPT trained and LSVT certified and has a special interest in working with children with Childhood Apraxia of Speech and cognitive communication patients including: patients with Traumatic Brain Injury, Dementia, and Parkinson's Disease.  Rachel believes it is important to advocate for her patients and provides education and collaboration with parents, spouses, clients, and other professionals to best suit her patients' needs.  Rachel is passionate about the field of speech-language pathology and takes a personal interest in the success of each and every one of her patients.  Visit Speechie Side Up to learn more about this episode.

Although our primary focus on the podcast is Multiple Sclerosis, we're well aware that the diagnosis journey for different conditions can be very similar. For one thing, people often have no prior knowledge of their condition before they're diagnosed.In this episode, I talk to my friend Victoria Garner about her experience of being diagnosed with Chikungunya Virus. This is a viral disease that is spread to people by the bite of an infected mosquito. The most common symptoms of infection are fever and joint pain. But as you'll hear, Victoria also experienced brain fog and neurological issues, which will be all too recognizable to people with MS. And her initial symptoms were brushed off as being stress-related. Sound familiar?Victoria talks about when she first realized that something was wrong, her struggle to get a diagnosis, and the anger she felt at having to adapt to her new reality. She also talks about how much happier she is now that she has worked to make her life better than she ever could have imagined.DISCLAIMERThe information in this podcast is for informational purposes only and is not intended as a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified healthcare providers with any questions you may have regarding a medical condition or treatment.Links and resources:If you're interested in having Kathy speak at your event, learn more hereFind out more about the DMAT Fitness Training programYou can find Kathy Chester at:msdisrupted@gmail.comdisruptfitnessgym@gmail.com moveitorloseit109@gmail.com Connect with @msdisrupted on Instagram, Facebook, TikTok Here are some additional products that help Kathy deal with beating the Heat and Migraines.  Take advantage of the coupon code.Koldtec - Cool Head WrapKOLD10To save $10 off every item in-store:2 items = $20 savings3 items = $30 savingshttps://www.koldtec.com/ Cold bean bag Releafpack. 15% discount use code Disrupt15https://www.releafpack.com 

Evelyn O'Rourke, RTÉ Reporter

Welcome back to Hope for Parents with Struggling Teens. Today we're joined once again by Brittany Johns, LMFT to talk about some recent trends in the mental health world and a few of the dynamics we've been seeing recently in many families of struggling teens.We address some new diagnostic terms that are growing in popularity, as well as a couple of phrases that aren't actually real diagnoses at all.First, we address the term “school avoidant.” Many of our listeners will draw different conclusions on how helpful this phrase is or isn't. I talk about the potential downside of labeling common behaviors that fall within the middle of the bell curve of common teen issues as disorders or terms that sound like diagnoses. I share a little bit about my own personal experience with ADHD, and how it's still important to encourage teens to lean into personal responsibility as they learn how to work hard in school and develop tools for success, wherever they find themselves on the list of learning challenges and possible cognitive deficits. Next, Brittany and I talk about the importance of walking alongside a teen when they experience failure, and how that looks very different than rescuing or protecting them from potential failures. We look at troubleshooting together with your child, helping them process failure as part of living, and reframing the adverse experience as a learning opportunity. Then, we discuss some common traps that parents tend to fall into when their teen is struggling. These include enabling, excusing, fudging on boundaries, and failing to grieve unmet expectations in order to accept the season they find their family in.We address video game use and addiction, and whether or not it's accurate or helpful to call the behavior self-medicating. Brittany explains the appeal of predictability in games versus the unknown outcomes of taking real-life risks.We talk about the modern medical landscape we find ourselves in, and how many health insurance companies' emphases on getting a diagnosis right away can pose challenges for therapists. I also explain the possibility of incorrect diagnoses being made to move through a system lacking nuance for less common cases. I hope today's episode encourages you to think about new ways you can walk alongside your teen through the normal failures of life, and live free from the common traps of over-diagnoses, excuses, and unnecessary complications in the healing process of your family.

Moe has been focusing a lot on his health lately, and has a new diagnosis...let's talk about it. Learn more about your ad choices. Visit megaphone.fm/adchoices

Trauma expert Stephen Regel discusses what Stephanie went through mentally later life. Stephanie also explains some of this in her interview with Andy Whittaker before she died. Also, former police officer Ellie Baker explains the significance of Michael Sams' typewriter and there's a dive into the true crime archives to look at other kidnappings where a stranger was taken. Producer: Andy Whittaker. Online Producer: Rachael Smith. Executive Editor, BBC Radio Nottingham: Chris Pegg. Executive Producer: Kathryn Morrison.

On the new June Sitting Down with Dr. Dan bonus episode, host Dr. Dan and audio engineer Phil have a great conversation about your listener questions including: tension between a mom and son, financial challenges, a new autism diagnosis, and more.Each month Dr. Dan answers questions listeners submit about parenting (and sometimes adulting, too!) on our Sitting Down with Dr. Dan bonus episodes. Please email your parenting questions to us at podcast@drdanpeters.com or DM us on social media. We read every question and we want to consider yours for a future bonus episode.Our brand new bonus episodes drop in our regular podcast feed that last Tuesday of every month.Follow us @parentfootprintpodcast (Instagram, Facebook) and @drdanpeters (Twitter).Listen, follow, and leave us a review on Apple Podcasts, Wondery, Amazon Music, or wherever you like to listen. Remember you can hear every episode one week early and ad-free by subscribing to Wondery+ in the @WonderyMedia App.For more information:www.exactlyrightmedia.comwww.drdanpeters.comFor podcast merch:www.exactlyrightmedia.com/parent-footprint-shopDr. Dan's expertise and wisdom is not a diagnosis or treatment. The information provided on the Parent Footprint podcast should not be used for diagnosing or treating a health problem or disease. Anyone seeking medical advice should consult with a licensed physician. Please reach out to your doctor for advice or a qualified health provider regarding medical conditions, questions, or situations. The information provided on Parent Footprint and by Dr. Dan is for entertainment purposes only, and does not substitute for professional medical advice. Dr. Dan does not know your child, is not your child's doctor, and has not treated your child.See Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

In this episode, I update you on my new diagnosis and where I have been hiding this year. Think surgeries, mental breakdowns etc, all the fun stuff! ❤️ the podcast?Why don't you give it a review/rating on this podcast platform!

Moe has been focusing a lot on his health lately, and has a new diagnosis...let's talk about it. Learn more about your ad choices. Visit megaphone.fm/adchoices

In today's solo episode, Karrie discusses her relieving, angering, and surprising diagnosis. Make sure to listen for the lesson she has for you from her deeply personal experience. •Karrie shares how she had to go with her gut and advocate for herself as a woman who went unheard. •Karrie talks about how this had been an issue since childhood and went unnoticed.•Karrie talks about why advocating for yourself is important in every area of your life, even when you are being blown off by people in white coats. NEW QUIZ - Take The High Functioning Anxiety Quiz Here Want to connect? karrieoutloud.comInstagram: @karrieoutloud Pinterest: @karrieoutloudcoachingp.s. Just in case you haven't heard this today...I see you. I love you. And I'm rooting for you. Always.

This episode is a chat about Bryce's results from his recent auditory testing at the Nova Southeastern University in Davie, Florida.  Bryce endured three hours of audio testing that confirmed that Bryce has an auditory integration deficit. We talk about how this resulted in poor testing results with his recent speech evaluation as well as recommended ways to help Bryce's brain correctly process sounds. We are still digesting all of this information and will be working with "Team Bryce" to help him overcome these learning obstacles.   Bryce is a funny, mechanical, HAPPY little guy who was diagnosed with autism at age two and is now nine years old. His pure joy makes this world a much better place!If you are enjoying the show, please take a quick moment to give us a rating and review to help other families find our podcast, too. We are humbled and honored to follow our calling and be Autism Ambassadors while helping others understand our world a little more than they did before listening to the podcast. We also feel called to bring light to a community that has experienced dark days after the "diagnosis". (Luke 1:79) You can follow us on our Parenting Autism Youtube Channel (Parenting Autism Show) and our Facebook & Instagram pages to see stories, pictures, and videos of our autism journey. You can also contact us through Facebook, Instagram, or by email: parentingautism@att.net. We also give an update on Chris' foot surgery along with other highlights from the past week. Support the show

On today's Celiac Project Podcast:Part 2 of Winter News and Notes is a jam packed episode filled with great stories and advice! Mike and Cam comment on an incredible email from a newly diagnosed listener with a house full of teenagers and a whole lot of unanswered questions. They also share lists of some of the top gluten free ballparks and some of their own tips on how you can be prepared and stay safe when heading out to a sporting event. You will also find out about the intriguing saga of KC Potato Girl and so much more!Listen to the full episode here: https://celiacprojectpodcast.libsyn.com Hosted on Acast. See acast.com/privacy for more information.

We're back!! Sorry we missed last week, but Darren was out of town.  Today we dive into the specifics of his third brain surgery and where we are today. MY BOOK: https://www.amazon.com/dp/1685156126/ref=cm_sw_em_r_mt_dp_ZYMQ0QJ4YHRRYRY0V2DS GROUPS TO JOIN: * Not Today Cancer Club - STRONGER TOGETHER - Cancer group for women you can request to join: https://www.facebook.com/groups/womeninpink MY FAVORITES: To help with sleep Sleepi Gummies: https://glnk.io/z2pl/jendelvaux15 * Pique Tea: Favorite Tea:  https://www.piquetea.com/?rfsn=5818415.d1d969a&utm_source=affiliate * ORGANIFI Chocolate:  https://www.organifishop.com -> Use JEND at check out to save 15% off * HEAT HEALER:  https://heathealer.com/?sscid=c1k6_11m8gb&

Hello Moms,  Can you believe we are in the last day of 2022? I can't believe I am 1 week away from meeting my new bundle of joy. Pregnancy during these last weeks before the due date has been painful. I do not remember this with the other 3 and  I don't like it here. The pressure, the heartburn, and the feeling like I can't do nothing is enough for me. Please pray for me and baby boy if you think of us. In this week's episode, I'm discussing the devastating news that comes with finding out your baby will not live a "normal or perfect " life.  We don't realize it but we are so hurt because we have to mourn the life we expected for our baby and this is very similar to the 5 stages of death. Don't worry Mom these Tips will help you take everything one day at a time. You will soon have a " New Normal" that you will adapt to and you will feel so thankful and blessed. Remember you are not alone and it's okay to feel angry and frustrated but always remember to put your hope in God.  So Grab Those Medical Supplies and Check- In for Your Weekly Dose of Encouragement! Come hang out with us in the Facebook Group https://bit.ly/3z77IAG Download our DIY Important Facts Slide Template-This DIY Template Slide lets you discuss your child's diagnosis, how to care for them, important contacts, what to do in case of emergency, and more. It gives you Peace Of Mind while your child is at school, with a caregiver, or doing sports. Anyone will feel more equipped when watching your warrior. https://bit.ly/3fAKSJN Connect=>info@youareresilientmom.com

Diabetes Core Update is a monthly podcast that presents and discusses the latest clinically relevant articles from the American Diabetes Association's four science and medical journals – Diabetes, Diabetes Care, Clinical Diabetes, and Diabetes Spectrum. Each episode is approximately 20 minutes long and presents 5-6 recently published articles from ADA journals. Intended for practicing physicians and health care professionals, Diabetes Core Update discusses how the latest research and information published in journals of the American Diabetes Association are relevant to clinical practice and can be applied in a treatment setting. This issue will review: Long-term Weight Training and Mortality in U.S. Male Health Professionals With and Without Type 2 Diabetes Trajectories of Cognition and Daily Functioning Before and After the Diagnosis ofDiabetes The Portfolio Diet and Incident Type 2 Diabetes Racial Disparities in Access and Use of Diabetes Technology Among Adult Patients With Type 1 Diabetes Deficits and Disparities in Early Uptake of Glucagon-Like Peptide 1 Receptor Agonists and SGLT2i Among Medicare-Insured Adults Following a New Diagnosis of Cardiovascular Disease or Heart Failure Sleep Duration and Risks of Incident Cardiovascular Disease and Mortality Among People With Type 2 Diabetes Outcomes For more information about each of ADA's science and medical journals, please visitwww.diabetesjournals.org. Presented by: Neil Skolnik, M.D., Professor of Family and Community Medicine, Sidney Kimmel Medical College, Thomas Jefferson University; Associate Director, Family Medicine Residency Program, Abington Jefferson Health John J. Russell, M.D., Professor of Family and Community Medicine, Sidney Kimmel Medical College, Thomas Jefferson University; Director, Family Medicine Residency Program, Chair-Department of Family Medicine, Abington Jefferson Health

On episode #39 of All Ears at Child's Voice: A Hearing Loss Podcast, Wendy and Haley sit down with Carrie Balian about her advocacy work supporting other parents of children with hearing loss. Carrie is a mom to five, whose oldest son Jack was born deaf. She is a coordinator of the Illinois Guide By Your Side Program, and serves on both the Illinois Universal Newborn Screening Advisory Committee and Illinois Hands and Voices board. Guide By Your Side provides free one on one support through providing trained parent guides to families with kids who have been diagnosed with hearing loss. Wendy, Haley and Carrie discuss how to support parents going through a new hearing loss diagnosis and the resources that are available to everyone.

Agoraphobia, online yoga, pregnancy, and vaccines are all on the table as Drs Anne Cross and Scott Newsome discuss the COVID-19 pandemic and how it affects their patients with MS. Relevant disclosures can be found with the episode show notes on Medscape (https://www.medscape.com/viewarticle/977031). The topics and discussions are planned, produced, and reviewed independently of advertiser. This podcast is intended only for US healthcare professionals. Resources Coronavirus Disease 2019 (COVID-19) https://emedicine.medscape.com/article/2500114-overview Multiple Sclerosis https://emedicine.medscape.com/article/1146199-overview COViMS Registry https://www.covims.org/ An Italian Programme for COVID-19 Infection in Multiple Sclerosis https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7191287/ Paxlovid Emergency Use Authorization https://labeling.pfizer.com/ShowLabeling.aspx?id=16474 Bebtelovimab Fact Sheet for Healthcare Providers https://www.fda.gov/media/156152/download Remdesivir Prescribing Information https://www.gilead.com/-/media/files/pdfs/medicines/covid-19/veklury/veklury_pi.pdf Evusheld Fact Sheet for Healthcare Providers https://www.fda.gov/media/154701/download New Diagnosis of Multiple Sclerosis in the Setting of mRNA COVID-19 Vaccine Exposure https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8656147/ COVID-19 in Patients With Neuromyelitis Optica Spectrum Disorders and Myelin Oligodendrocyte Glycoprotein Antibody Disease in North America: From the COViMS Registry https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8407145/ Neuro-Ophthalmologic Manifestations of Multiple Sclerosis https://emedicine.medscape.com/article/1214270-overview

I'm back today after a looong break with Part 1 of our PANDAS journey. I wasn't planning on making this a two parter but there is SO MUCH to discuss with this story. This episode is extremely raw and vulnerable. I had wanted to wait and share all this til we had some kind of resolve with this situation, but as time goes on, I realized I might be waiting forever. So this episode covers the lead up to Logan's PANDAS diagnosis. Once I had recorded almost an hour of audio and barely scratched the surface of this saga, I realized it would take more than one episode to explain everything. So stay tuned for Part 2! I want to say again a very heartfelt THANK YOU to this incredible community. I have truly felt all your support, love and prayers over these last several weeks and it means so much to me and our family! This podcast is sponsored by BetterHelp To get 10% off your first month go to: https://www.betterhelp.com/adventuresinautism Connect with Megan: IG: @adventuresinautismpod & megan.carranza FB: @Adventures In Autism Podcast Email: adventuresinautism2018@yahoo.com Enjoying the show? I would so appreciate your rating & review! --- Send in a voice message: https://anchor.fm/megan-carranza/message

It's evidently clear that Americans are overwhelmed with loss. Grief is a new norm. Covid-19 not only put us on a fast track to a new age of virtual existence, it also ushered in a new era of isolation, heightened fear and persistent grief among other things. Mindfulness For The Soul takes a look into how and why this trend had been building since the onset of the pandemic in 2020. A new diagnosis from the APA offers hope for many. --- Support this podcast: https://anchor.fm/john-tsilimparis/support

About Mallory Mallory Brown is wife to her college sweetheart, Tom, and mother of 2 blessings (Julie 7, Adam 4). She is an accidental stay-at-home mom, occupational therapist, and lover of outdoors and hiking. She is also the creator of Open Door Encouragement and Bible-grams.   Related Links Instagram: @opendoorencouragement (for daily bible grams, notifications for blog posts, and sharing Favorite Soul Shaping Things) Website: www.opendoorencouragement.com (for all of the Bible-grams created, in a digital format. All housed by topic. )   *Theme music and editing by Open Mic Studios. https://openmicrecordingstudio.com/  

When we hear a new diagnosis, whether it is weight-related, mental health, behavioral, or physical, a lot of questions come up for us as parents. How do you learn to ask questions that actually help you and your child, now? Full show notes available here. --------------------- I ask a favor of you: if you liked this episode, please subscribe, rate and review on your favorite podcast service, and share with your friends so they know that there is a different way to stop struggling with worries about weight. It's easy and fun! And when you're ready to start applying this in your own home, check out www.wendyschofermd.com for more information about how the Family in Focus program can help you and your family create lifelong healthy relationships with food and body, now and at every weight. Disclaimer: While Wendy Schofer, MD discusses health and wellness, this is not medical advice and she is not your doctor. Optimal health is achieved in combination with your physician, who collaborates with you for your individual health. Talk to your doctor. And tell them about Family in Focus. Mwah!

It's Q&A time! In today's episode, Lissie sits down and answers all of YOUR questions. Join us as she discusses: Her best advice to someone recently diagnosed with diabetes 1.5 as an adult Her go-to Dexcom and Omnipod sites Wedding planning with type one Adhesive reactions from diabetes devices and so much more. SHOW NOTES ⏰ (1:04): My TED talk. ⏰ (2:38): Overview of the episode ⏰ (3:28): Question 1: What is your first piece of advice to somebody that was just diagnosed with type 1.5 at 30 years old? ⏰ (9:03): Question 2: Wedding prep and diabetes ⏰ (12:53): Question 3: I need new Dexcom sites. Tummy and arms are tired. ⏰ (14:50): Question 4: How long have you had diabetes? ⏰ (16:44): Question 5: Preventing skin issues with Dexcom and Omnipod. Mine are completely ruining my skin
- Check out @mary.type1 (https://www.instagram.com/mary.type1/) on IG for her adhesive tips ⏰ (20:08): Thanks for hanging out today, let me know if you like the Q&A style podcast @needlesandspoons_ (https://www.instagram.com/needlesandspoons_/) Disclaimer: Nothing inside of Keeping it 100 Radio or our resources is intended as medical advice. Always consult a physician before making changes to your insulin doses, diet or general wellness.

So-called long Covid may now include a new diagnosis of diabetes, a recent study shows. Diabetes expert Rita Kalyani at Johns Hopkins says this study follows participants over 12 months after their Covid infection. Kalyani: It was really in a national database. Almost 200,000 participants who had a positive Covid-19 test between March 2020 when […]

For some, getting a new diagnosis causes a feeling of relief to wash over them.  "I'm so happy it's this and not that!" or "thank goodness they finally found something!" But, often a new diagnosis isn't something we were hoping for. It can be hard to figure out how to deal with a new diagnosis. It might be IBS, migraine, or fibromyalgia. Or maybe you just got diagnosed with something like MS or cancer.  For someone who's always been healthy, it can be a shock. There are no rules, and there is no "normal" way of feeling. Everyone is a little different, even when they have the same diagnosis.   How to deal with a new diagnosis in 7 steps. Take the time you need to take it in. It's ok to focus on yourself for a few days, or weeks. Do your research and find out what to expect, but don't waste hours a day googling your diagnosis. You'll learn more as time goes on, and you might find misinformation out there. Locate the best doctor in your area who specializes in your diagnosis, or the system it affects.  Ask friends and family, or others with the disease. Ask your doctor who they would see, and get a referral there. Find a support group.  If you can get out, a medical center by you might have a specialized support group.  You can join a local group, or an online support group. WARNING - please don't give away personal information in an unsafe place.  ALSO, many "support" groups can bring you down by only discussing the negatives of what they're going through.  Find a place that is both honest and positive. Allow yourself to feel.  In the beginning you might have all kinds of feelings.  Be aware of those 5 stages of grief, and communicate how you feel with those around you so they can support you in the way you need it each day. Do not succumb to guilt.  This is not your fault. You didn't bring it on yourself.  You will still be able to have a satisfying life. You are still the parent your children were meant to have.  Feeling guilty doesn't make things any better, it just sucks your energy.  Find ways to enjoy your life.  You may start doing things differently, but you really can find joy no matter what's happening around you. There is so much more on the website! Check out HardyMom.com/new-diagnosis Thank you for joining me today!  Want more? Go to HardyMom.com and you'll find ways to live well, grow, and enjoy your life again -with any health challenges. I'd love to hear what you think about this episode! Send me a message at HardyMom.com/contact Have a blessed week, Jen

Hi, friends! In this episode I go into the beginning of the third trimester. I briefly touch on one of the disagreements with my surrogate, but it's mostly about my mom's new cancer diagnosis. There's no blog post for this one, but I hope you enjoy listening! :) Ps: If you or a family member have experienced cancer that has spread to the brain, you might get triggered by this episode so feel free to skip it! ❤️

In this episode we will answer the question that almost no one dares to ask.... How does it feel to receive the news that your child has a disability and that your family life will never be the same? In yet another brutally honest episode, Alma and Iris reveal their personal experience (which years of professional experiences didn't really help prepare them for...).  

On this episode of Food Allergy Talk, I welcome our special guest, Dr. Alan Khadavi, board certified allergy and immunologist out of Los Angeles, California.  Dr. Khadavi is an experienced allergist assisting both adult and pediatric patients who suffer from chronic allergies, asthma, and other respiratory conditions.Dr. Khadavi recently enjoyed the privilege of being named a Rising Star in the Los Angeles edition of Super Doctors in the field of Allergy and Immunology.  He was also named Most Compassionate Doctor by the Patient Choice Awards in 2013 and 2014.  In 2013, 2014 ,2015, 2019, 2020 and 2021, he was named to Castle Connolly's list of Top Doctors. He was given the Vitals Patients' Choice Award for physicians who provide excellent care and the On Time doctor award as well. Los Angeles Magazine recently named him a “Top Doc” for its 2019-2021 editions.In this episode I sit down to chat with Dr. Khadavi about:Signs and symptoms of food allergySigns and symptoms of new additional food allergiesDifferent ways food allergy presents (hives and some "typical" presentations vs other less obvious presentations)What method to go through pediatrician and primary care physicians to investigate underlying health issuesThe top 9 allergens, multiple food allergies, and rare food allergiesIncrease in food allergy diagnosisVegetable and fruit allergy vs Oral Allergy SyndromeHow food allergies are diagnosed with focus on individual historyDifference between IgG and IgE blood testsSkin prick tests and comparison to blood tests and individual historyWhen are food challenges looked at as an optionNo such thing as a mild allergy, past reactions cannot dictate severity of future allergic reactionWhen to administer epinephrine?Epi first, and epi fastWhen requesting prescription, how many for home and elsewhere to request, expiration date and genericsExpired epinephrineFind Dr. Alan Khadavi online at: https://allergylosangeles.comYou can also follow him on Instagram: https://www.instagram.com/dralankhadavi/Listen online anytime: https://foodallergypi.com/the-food-allergy-talk-podcast/ or on any podcast player. 

Receiving a neurodivergent diagnosis can be confusing. Especially when you get it later in your life as a teen or adult. You may not know how you feel about it or what it means. In this episode, Jason has some perspectives to share with you to help you going forward. Get full show notes here: https://JasonDebbie.com/46

Receiving a neurodivergent diagnosis can be confusing. Especially when you get it later in your life as a teen or adult. You may not know how you feel about it or what it means. In this episode, Jason has some perspectives to share with you to help you going forward. Get full show notes here: https://JasonDebbie.com/46

In this episode I open up about a new diagnosis we have received for our clubfoot cutie, and how her clubfoot treatment journey has changed the way I have approached her new diagnosis. While I don't go into specifics about this new diagnosis, I talk about the impact her clubfoot diagnosis has changed the way I approach this new diagnosis. I talk about the different ways I researched the new diagnosis and it's treatment, to how I explain it to others, and how I have allowed myself more grace while I emotionally process the change this new diagnosis brings to our lives. It wasn't until we were faced with something entirely new to us again that I began to notice how much I have grown since her clubfoot diagnosis, and how this treatment journey has had a lasting impact on the way I interact with the medical world and how I allow myself time and space to process new changes.

On this episode of The Food Allergy Talk Podcast, Lisa Horne interviews her son, Stetson, a 14-year-old teen with food allergies. Stetson was anaphylactic to peanuts and shellfish since he was just a baby. In the past 6-8 months of this podcast interview Stetson began having symptoms that appeared at first glance to perhaps mimic potential Celiac, Crohn's and Colitis, IBS or other potential digestive issues. We had no idea that what was lurking behind these symptoms were added anaphylactic food allergies that appeared over a decade since his original diagnosis. What was even more confusing is that they were similar to food allergies by way of symptom, but also appeared to be other issues. Listen into our experience detailed in hindsight to see what we learned as we navigated this new terrain, as well as the feelings and emotions that can go along with a new food allergy diagnosis. While Stetson has had anaphylactic food allergies since he was a toddler, Stetson is much more than his food allergy. He is a video gamer, plays both piano and guitar, plays golf, and has recently taken up archery. There may be some things that Stetson cannot eat, but he hasn't let his food allergies top him from living and enjoying life. Even with this latest curve ball adding an additional 7 allergens: pecan, walnut, oat, garlic, sweet potato, watermelon and pear.Listen to hear about his experience and finding the the silver lining living a life with food allergy, and making the most out of it. Food Allergy Info Card referenced in this episode was made on www.vistaprint.com using the following verbiage (feel free to copy and use this verbiage), and then listed respective allergens:I have anaphylactic life-threatening food allergies to the following foods and should I come in contact with them would require emergency medical attention. This includes cross-contact. Freshly cleaned prep and cooking surface is appreciated as well as any utensils used to prepare and serve food. Thank you for helping me to dine here safely.(Insert own allergens)Listen online anytime: https://foodallergypi.com/the-food-allergy-talk-podcast/ or on any podcast player. 

A young mother presents puzzling symptoms when she arrives at the ER. Tune in for a few minutes to test your medical diagnostic skills.(00:00) Introduction(00:22) The Case(02:23) The Evidence(03:53) The Diagnosis(04:09) The Return(04:40) Additional Evidence(05:15) New Diagnosis(05:55) But Why? 

After my diagnosis with T1D, it took me a while to be open about it. Not only to friends, family and old high school peers - but to social media. Even 2-3 years after my diagnosis, you couldn't pay me a million dollars to post about being type one diabetic. That's what makes Liv different. Being diagnosed a little over six months ago, she quickly brought her journey to Tiktok. Not expecting it to be found, she accidentally gained 45,000 followers on her account. Inside this episode, we talk all about the realities of being diagnosed at 27 years old, how her diagnosis away from home shifted her relationships, and most of all how she takes comfort in sharing her journey with others on TikTok. Here's whats inside today's episode: Liv's diagnosis at 27 years old Being diagnosed during the pandemic The highs and lows of a T1D diagnosis Her social media experience and how her TikTok grew almost overnight The good, the bad and the ugly of sharing online Her plans for her acconunt RESOURCES: - Apply for the Skin Grip Diabetes Scholarship - Hangout with Liv on TikTok! 
SHOW NOTES
 
⏰ (3:39): Do you mind introducing yourself Liv?
 
⏰ (5:50): How was that experience being diagnosed a little bit later in life?
 
⏰ (7:58): What made you initially say, Okay, I need tests run?
 
⏰ (9:16): How's the transition been?
 
⏰ (12:58): What has been the biggest learning curve for you so far with the diagnosis? 
 
⏰ (16:39): What made you say like no to MDI and go on to like a pump and CGM?
 
⏰ (18:09): What has been the best part of the diagnosis and what has been the worst part? 
 
⏰ (21:01): Your TikTok journey…
 
⏰ (28:05): Have you ever gotten those people who maybe don't understand diabetes too well, or like made assumptions or you know, like those, the troll accounts?
 
⏰ (32:16): Do you have a bigger vision for this account?
 
⏰ (35:12): What would you tell somebody else who was just diagnosed? And what would you tell somebody who isn't sure how to support their loved one who was just diagnosed?
 
⏰ (39:13): Have you given yourself the space to grieve? Like, do you feel like it was hard to give yourself that space?
 
⏰ (42:16): Where can people find you on TikTok, Instagram?
 

- TikTok - liv_violette

 
- IG - @olivia_violette
 Disclaimer: Nothing inside of Keeping it 100 Radio or our resources is intended as medical advice. Always consult a physician before making changes to your insulin doses, diet or general wellness.

In September of 2018 Antra Boyd [a veteran nurse and experienced professional RN Patient Advocate] RN, BSN, MSN was told she had a 8cm mass on her left ovary. In a matter of minutes she went from advocating for patients with complex medical diagnoses to being a patient herself. Things got FREAL very quick (if you are not yet schooled in the RNegade glossary of terms, FREAL = f@cking + real). When the gynecologist/oncologist told her that her best option was to have a total robotic hysterectomy and that the surgery was scheduled to be in 3 weeks, Antra hopped on the ‘urgency train.' She was a hot, blithering mess. When faced with a cancer diagnosis, that big ol' C-word sends people into complete fear mode, and not even this whiley veteran nurse was spared. Luckily, Antra had the where-with-all to gather her support team and ‘phone a friend.' Karen DiMarco reminded her that the urgency train was a ride she DEFO did not want to be on for peace and clarity of mind, and that the three weeks until the proposed surgery was plenty of time to research the particulars regarding the recommended ‘STEP 1' course of action (surgery). ‘STEP 2,'the possibility of chemotherapy and/or radiation, need-not yet bugger her brain until after STEP 1 was completed. During those 3 weeks, Antra was like the ‘dog with a bone' she is for her own clients, and tracked down all the information she could find to make an informed decision. Along the way she made curiosity her superpower, and learned how to be engaged in her care simply by asking questions (lots of questions). THIS IS ESSENTIAL: in spite of the fact that we are conditioned to NOT doctors - but if we don't engage and don't question, we cannot be fully informed of ALL of our options. We can't know what we don't know unless we look… and ask. Cancer treatment in the US is big business so there is no incentive for allopathic doctors to suggest possible treatments outside of the conventional care toolbox: cut it out (surgery), poison it (chemotherapy, burn it (radiation.) Finally, even when Antra was armed with all the information she needed to make an informed decision, her decision about what to do came from the place of her own inner knowing. The medical team is there to guide you, but not decide for you, and this clarity enabled Antra to take control of her own course of action, and ultimately make the right decisions for her own health and healing. RNs get a CE for this course on RNegade.pro.