How You REALLY Doin'?

I’ve been on a journey of personal transformation. A journey to rediscover how I am REALLY doin’. A paradigm shift has occurred for me and in this podcast I bring a different perspective that I hope will open some eyes and begin conversation. I’ve never REALLY shared my background in my podcast and it is time for me to do so. I have gone down the rabbit hole in order to find a way to feel better. MS has never felt like me and I’m on a path to find, and define, my truth. In doing this I discovered Dr. Joe Dispenza. I’ll describe his work in my life and how it led me to my guests today. Scott Sunderland and Em Hollis are living proof of personal transformation and healing. They each have amazing individual stories and they have come together to create The Freedom Project.  I’ve been taking their course called Beyond Limits and it has stretched me to overcome my past and step into my future.   Scott Sunderland -  from paralyzed to walking! https://youtu.be/9DaHg-AUY2o Great podcasts with Dr. Joe Impact Theory w/ Tom Bilyeu - awesome explanation of how stress hormones make us sick https://youtu.be/La9oLLoI5Rc Aubrey Marcus - Dr. Joe dig deep into the science behind this work. https://youtu.be/mh-a4dpF93g Lewis Howes - Dr. Joe talked about finding love in your life https://youtu.be/YYCnOnZ7zyI London Real w/Brian Rose - Dr. Joe explains how he healed his broken back https://youtu.be/-WVu-OzCE9Y Danica Patrick - explains the four minute mile https://youtu.be/x9XvQKhzBlE Overcoming MS testimonials Sue - daily meditation and envisioning MRI with decreased lesions came true. https://youtu.be/BHDo99d9Xuo Damien - The power of the walking meditation. Walking in the sand without support https://youtu.be/3rq9dxsGlag Fiona - Amazing description of mystical experiences. At the end Dr. Joe explains in detail the process of what happens at the cellular level. Energy does the healing! https://youtu.be/TdJ69O53vrQ Overcoming Parkinson’s testimonial Tom - success through breath work https://youtu.be/ipvEyALfvR4 Dr. Joe YouTube videos Habits and emotions keep us living from the past. https://youtu.be/leqUIBDdU_c Ted Talk showing nerves growing back’1 https://youtu.be/o9K6GDBnByk Awareness is the beginning of healing https://youtu.be/BBIGGWzLo7A The Art of Forgiveness https://youtu.be/oxuiXuCZhOo My trip to  Cancun 2019 - I was interviewed after the challenge exercise https://youtu.be/L3scbos76og

How much you believe… In yourself? Can you put your feet on the ground in the morning are you focusing on your power… Or limitations? Chloe Cohen was diagnosed with relapsing remitting MS in 1998. She had a Trumatic head injury and within hours she was having tremors on her left side. She was only 20 years old and an aspiring cellist. That all changed. The early years after diagnosis were lonely for Chloe as they are for a lot of us. In order to find some people to share with, she cofounded an MS support group. And I’m so thankful she did. I’ve been involved with this group since 2007 and you can see Chloe‘s personality stamp on it because the meetings are always very positive and upbeat. Like she is. I have known Chloe for over 10 years and that time I have seen her belief, trust herself skyrocket. It hasn’t been easy, but she’s created a recipe That allows her power to shine despite any limitations the MS has brought on. Chloe knows she didn’t get MS at such a young age to cry about it. She’s here to teach and share her story. Whether it be in the gym and lifting more weight than she ever thought she could, speaking at MS events or in her writing She is a true example of how hard work, tenacious persistence and soulful desire can lead to amazing things. Chloe has written a book and the ebook comes out in May 2019. Chloe and I have been honored to be involved in the most recent national MS Society‘s awareness campaign. Through black-and-white pictures and heartfelt videos we got to tell our stories and it was profoundly touching for both of us. In this podcast Chloe mentions walking in the photo shoot while I was getting my picture taken and it brought her to tears. I think that’s the power of this campaign in that it touches our soul. For me it’s my daughters. For Chloe it’s the loss of her musical abilities.   Buy Chloe’s book - https://www.amazon.com/Making-Lemonade-out-Lemons-Story-ebook/dp/B07PGR64T7/ref=sr_1_2?keywords=Chloe+Cohen&qid=1552144568&s=books&sr=1-2   Whatever It Takes Campaign -  pics and videos of Chloe and Jim - www.nationalMSsociety.org/Chloe

Mark and Tamara Teeter are two of my favorite people. We are on the same bike team together, Team RoadKill, and Every time I see them, I feel better. Tamara is the warmest gentlest soul with the greatest laugh on earth. And Mark is a former traveling deadhead and scout master with fantastically intriguing stories and the biggest heart. They are high school sweethearts who got a big relationship test when Tamara was diagnosed. Marriage isn’t easy to begin with. Throw in a chronic illness like Multiple Sclerosis and it becomes critical to find common ground, a language you can speak together in order to remain strong together. Mark and Tamara went through a tough time after diagnosis and discovered how vulnerability and speaking the truth is a necessity and a way to ease the stresses, the uncertainty, that MS brings on a daily basis. Mark and Tamara have found a good recipe for themselves and can attest to the importance of sharing. Not only sharing struggles but the good stuff too. As a person with MS, I don’t think you can ever underestimate the power and relief that focusing on the good stuff provides. It took a while for Tamara to fully open up about her tough symptoms and what she found was that sometimes sharing the things that scare you the most is exactly what helps you the most.  As a support partner Mark was ready and willing to help, he just needed the right words to know how to do so. Have a listen as Mark and Tamara let you know how they REALLY did it to get to where they can truthfully talk about how they are REALLY doing now.

Team Road Kill is more than a MS bike team. TRK is a testament to the overall fact that people are good. Human connection and supporting the person next to you is what they are all about. Their motto is simply GO! They GO after living life fully, they GO! after bike riding and they GO! after finding a cure for MS. Ron Haye was diagnosed with relapsing remitting MS in 2010 when he committed himself to keep moving. Both physically and emotionally. Ron is the embodiment of GO!  As one of the founders of TRK he has helped create one of the largest bike teams in the Pacific Northwest with over 100 riders. The team has raised over $250,000 for the MS cause and they do so by putting the FUN in fundraising. TRK events include a casino bus, a poker night, a corn hole tournament and the big daddy of them all...BrewFest for MS. For this podcast I parked my van outside the Brickhouse Tavern in Vancouver Washington and talked to some TRK members during BrewFest. Ron Haye, his wife Terry, son Steven and two huge TRK contributors Mike Johansen and Robert Stuart.  I'm very thankful to be a part of this team and be surrounded by such amazing people. Their team motto says it all and is a reminder of what is good for all of us to do…GO!

Carol Moiso is a fighter!  She was diagnosed with Primary Progressive MS in 1991 when she was 47 years old.  She may be in a wheelchair to get around now but that doesn't stop her from challenging herself to swim across the Columbia river or ride 10 miles during Bike MS.  She's a proud grandma with a great sense of humor and a desire to do everything possible with her grandkids.  So she fights.  Fights her MS symptoms to be the best she can be. 

Andy Becker was diagnosed with relapsing remitting MS when he was 30 years old.  At that time he was a pack-a-day smoker and addicted to video games.  Sometimes playing 16 hours-a-day.  Getting his MS news was a wake up call for Andy. He is now addicted to endurance sports and knows the true meaning of self-care.  

auGi is how he spells his name, it's not a typo, and yes, I believe he is cool enough to not only pull off one name but spell it however he wants. auGi is a man of many talents… Dare I say a Renaissance man. He's a musician, a comedian, a graphic artist, a writer, a performer, he’s traveled the world and he's one helluva storyteller. He has written and performed his own one-man show, called SexyNurd, about his life’s desire to be a rock star commingled with his experience with MS.  auGi doesn't have MS but his experience runs deep as his mom lived with it for 34 years and it is in her memory that he brings all his amazingly wonderful talents to the MS cause.  auGi is the Vice President of Marketing and Events for the Oregon Chapter of the MS Society. As you’ll hear, he literally changed his career and his life’s direction because he doesn’t want others to suffer with MS like his mom did. You can also learn more about auGi on his blog at www.stopmakingthatnoise.com (spoiler alert...you will learn auGi's last name but don't let that destroy how cool I think he is)

Leslie is one of those people who you meet and walk away feeling better for doing so.  She radiates positive energy from her core.  I am a huge believer that our mindset effects and determines the course of our disease and of course our life.  When Leslie was diagnosed with Relapsing Remitting MS 4 years ago she didn't let it stop her life or positive attitude.  Today she is in better physical shape because exercise has become such a huge part of her daily routine.  Just ask her and she'll flex for you.  She did for me and I was blown away...as I was with her exuberance for life.  She is a huge Pittsburgh Steelers fan and like their Steel Curtain defense, Leslie is STRONG.

Man have I discovered a lot about myself.  Who I am and how that effects my MS on a daily basis.  Skeletons from my past along with negative self talk have NOT been helping me be the best I can be.  So I found a life coach, Angela Carey, who has helped me discover the negative pieces of me that have been toxic while exploring the good, positive pieces that I need to live a full life in the face of MS.  This is a podcast about my way of making the best of what I've got.  I believe Great Freedom comes from True Vulnerability so get ready for a ride through my mind and how it is making my MS journey beautiful. Angela Carey is my life coach that I talk so much about in this Discoverycast.  She has literally changed my life and I can't thank her enough.  Check her out at www.yourpowercenter.com

Yes I know #3 doesn't come after #14 but I had to take Nora's podcast down for technical reasons.  Now it's back.  Nora has had MS for just about a year yet she enlightens me to a new way of looking at things through her incredible sense of humor and age-defying outlook. On June 16th, 2013, at the age of 26, Nora was diagnosed with acute sudden onset of tumefactive multiple sclerosis and lost the the use of her left side over the course of a day and a half.  She spent 6 weeks in the hospital working hard to regain function and come to terms with this new way of life.  During that time she wrote a blog which is an honest, well written chronicle of her MS journey.  I suggest everyone with MS, heck everyone period, read this (msnorakb.tumblr.com) because Nora's amazing perspective can teach us all a thing or two.  

Andrea has continued to hijack my podcast to ask me questions about finding inspiration, Staying Gold and the importance of talking to others.  And of course we cover Andrea's big passion, Walk MS!  

Andrea is the Manager of Walk MS for the Oregon Chapter of the MS Society.  She has so much energy that I wish I could bottle it and hand it out as a cure for MS fatigue.  She is also that person who stands out in a crowd because of her laughter.  Andrea doesn't have MS...she has a passion for helping people with MS.  She is also an extrovert and LOVES being around people, has a great perspective on how she relates to people with MS and passes on information about the MS Society that you may not know.  And oh yeah, she knows a lot about Walk MS and must have a budding desire to have her own podcast because she takes over and interviews ME. The MS Society Information Resource Line 1.800.344.4867 

Lindsey shares more "Lindseyisms" on blaming MS and joking about MS...watch out if she ever gets a cane!!! Lindsey wants the world to know how important it is to love yourself and the benefits you can find.    Email - Lrhrasta@hotmail.com   Instagram - @lindzshot   Facebook - Lindsey R Hendershot

Lindsey Hendershot lives by a motto...Be You.  This creed is tattood on the palm of her hand and man does she live up to it.  She talks about loving yourself and your disease becaue you need to protect the thing most important...YOU.    She LOVES all of her and  talks about finding the silver lining in life by boiling down the bad things to be able to find gratitude an ANY situation.  Feed your body some good vibes instead of hate and bitterness. Lindsey has great ways of dealing with everyday situations and a positive outlook, and attitude, about life with MS. Wanna get more of Lindsey's positivity...she is on social media and welcomes anyone to contact her. Email - Lrhrasta@hotmail.com Instagram - @lindzshot   Facebook - Lindsey R Hendershot

Strength comes in many forms and Ryan Thompson has one of the most important...Strength of Character.   He is dealing with his MS daily while finding ways to help others with MS.  This takes strength.  In part 2 of our conversation we talk about Ryan's non-profit organization (Endless Pursuit), dating and even touch on sex with MS.  Ryan was diagnosed with relapsing remitting MS when he was 18 years old.  He is now 26 and some of his symptoms are neuropathy (sensitive skin), hot/cold sensations, foot drop, gait/balance, lassitude (chronic fatigue), and muscle spasms. Check out Ryan's passion at www.endlesspursuit.org

Ryan Thompson does a lot… he has a lot going on in his life with business and personal pursuits and he deals with MS...a lot. Besides starting a new business, getting his degree, co-leading a support group and running a nonprofit Ryan has many symptoms that his relapsing remitting MS doles out that he continually tries to overcome so he can hike and stay active.  Whew...that IS a lot! When I see Ryan once a month at our MS group I am always amazed at everything he does but I didn't REALLY know what he deals with on a daily basis until we sat and talked for a while.  We have the same disease yet we deal with so many different symptoms. We are both ambitious yet I still learn from how Ryan overcomes his obstacles through will, choice and faith. We both want to help people and THAT shines through no matter what differences our disease delivers.  Another thing we have in common is we like to laugh at/with our MS.  Ryan and his friends have put a face to this laughter and named it Margaret Swanson...get it...MS! Check out Ryan's passion at www.endlesspursuit.org  

Luanna was diagnosed with relapsing remitting MS in 2011 when she was 37.  She is a full time high school math teacher and mother of 3.  Luanna is very gooid and figuring out how she is REALLY doin' and says it’s important to look at your overall picture and take stock of what you have NOW, enjoying what you can do TODAY…appreciate yourself.  It’s hard to do all the time but take it easy on yourself and try to accept where you are.  Yesterday is history, Tomorrow’s a mystery and today is a gift…that’s why they call it the Present.     General Symptoms Now:  Cold temp., muscle spasms, twitching, headaches, numbness, dizziness, general "yucky" feeling.  

Lee was diagnosed with Relapsing Remitting Multiple Sclerosis in July of 2013.  She is in the process of tackling the gauntlet of issues that come with an MS diagnisis and shares great insight into the how's and why's behind some of her dicisions.  From keeping her career going to making huge changes with her eating habits, Lee does her research and is figuring out what works best for her.  She has a huge heart and is doing what she can to be the best she can be because in her words "this is my life and it is mine to mold and  develop".  You go girl! 

Ron & Teresa Haye inspire me. Ron was diagnosed with MS about four years ago and together with his wife Teresa is not only surviving but thriving in many ways.  Ron discusses his diagnosis and what he has done to keep his body moving. They are members of Team Road Kill, an amazing group of energized people who bring passion to not only the MS bike ride but for support of their fellow man! Finding a silver lining in multiple sclerosis seems impossible sometimes but Ron and Teresa explain some of their secrets for doing the best they can.

A year ago I was going through a MS exacerbation that was kicking my butt.  I had to stop working and driving.  Enter Bill Victor and a journey to getting stronger.  It hasn't been easy (when is working out EVER easy...?) but with Bill's functional training help I can now make it through my day safer and stronger.   Check him out at www.victor-fitness.com

I'm your host, Jim Fairchild, and sometimes summer and anxiety go hand-in-hand for me.  My MS body isn't able to do what my mind wants to do and it drives me crazy.  Especially when I see people having fun and I want to join in.  Come along as I chat about what I have discovered about myself.  Who knows, maybe you'll discover something about yourself as well.

Nancy and I talk about independence, the mud run, volunteering for the MS walk, knowing your body, asking for help, her sister's MS diagnosis, acceptance, medical marijuana and a whole lot more.  Nancy was on the trial that helped get BG12 approved for the market and is proud to say she's done it.

Nate and I talk about Monkey Pride, asking for help, going to work everyday, the importance of laughter and happy thoughts.  Multiple Sclerosis is different for everybody but it's always good to see how others deal with the issues MS brings on.  Nate will make you think and make you laugh.