Truth Be Told MS

When we first spoke to James we were impressed by his own brand of “the new normal” We loved speaking with James and hearing of his Full Family life and Work life while being victorious one step at a time.

A long trip to Moscow with encouraging results.Steve reached out to us to ask “have we ever covered HSCT”? Well we have. However, Steve’s candid recount of his trip to Moscow and his experiences before and after shines a light on how far Stem Cell Treatment has evolved.

Listen in as Guest Host Bruce Elliott interviews the Truth Be Told Team.We talk medications, exercise, hope and TBT plans going forward.

When we first interviewed Carolyn, we were amazed at her graceful ability to Ballroom Dance. This episode we share updates about award winning Dancing and her re-certification in her EMT work.

Dr. Beaber Speaks with us today about rebuilding myelin and hypothesises about directions away from Auto-immune suppressants to DMT’s which re-build and strengthen myelin.

Dr. Brandon Beaber talks about positive attitude, grief and acceptance in building resiliency when living with M.S. He discusses the case studies referenced in his new book. A must read for anyone living with M.S.

Diagnosed at Eleven years old Tevin has used acceptance and awareness to manage his M.S. Symptoms. From Coffee to Oranges hear what gives Tevin that bust of much needed energy.

We welcome Dee back to discuss her journey from those M.S. Funnies to a "A Dose of PositiviDee"

We hope you have had a happy and productive year, and wish you the warmest feelings as we usher in the holidays together.

Vitamins, yes, we know about M.S. and but what do we know about minerals. In todays show we break it down with Nina Eubanks. Listen in as she literally dishes the dirt on how we are missing out on Disease Modifying Natural Elements

The Face of Pharmacare (Bill Swann) after the election that wasn’t Listen in as Bill Swann breaks down why Pharmacare lost out to more commercial and face-saving issues.

91 episodes, 2 years and many revelations and unanswered questions. On today’s episode our co-host Jana interviews Marie on her reflections over the past 2 years of hosting Living with M.S. - Truth be Told.

Jess – Generation M.S. Gen – Next. I love interviewing newly diagnosed people. They are the new Generation to usher in the Protocols over the next 20 Years. Read her inspiring Jess has just started her own Podcast. Listen to her “disabled to enabled podcast”

After following this M.S. Facebook warrior TBT had the honor of interviewing this fearless young man. Whether you’re a M.S. veteran or newly diagnosed Causo’s story will inspire you. mystrugglemystrength.org.

Listen in as Mary tells us how Journaling has helped her manage her symptoms. Have you ever journaled? Me either, but Mary speaks to the cathartic effects of self journaling.

Pharmacare. Canada will be heading to the polls in October for our Federal Election. All Parties will have a policy on Pharmacare. Listen in as Bill Swann (Faces of Pharmacare) outlines what is on offer. What it might look like and most importantly; how to self advocate.

Living with M.S. for more than 30 years. Robin shares with us the results of her research and unpacks some real truths about her dealings with M.S., Neurologists and Systemic Barriers. There are no “sacred cows” as we discuss the business model of illness and missed Return on Investment Opportunities when no investing in wellness.

Shift M.S. is a global network of supporters who have just celebrated their 10th year. Started by a Man living with M.S. who saw a need, this organization reaches out and provides “human services” to people living with M.S.

Here at Living with M.S. we strive to bring new kinds of diet and exercise to our listeners. Listen in as Jody talks about Kettle Kickboxing and its positive effects on Balance. Jody does discuss modifications and safety.

Today we get a chance to speak with another hard-working Patient Advocate. Listen in as we discuss “pushing through” and the importance of knowing your body when gauging work and life balance with M.S.

Always wanting to cover all things about living with M.S. this week we talk to a Mother and Daughter about their journey to diagnosis. We applaud Amber for her college graduation. We also touch on Racial in-equality in diagnoses and care. And lessons passed from Mother to Daughter.

As a Chiropractor Bill often worked with Patients with M.S. So, when he was diagnosed he had a great fear of the worse case scenario. Fearing he would lose the ability to communicate with his daughters he started his Blog: From Daddy with Love. Please join us and listen to Bill’s Journey and how he is living with M.S.

When David starting researching HSCT, he didn’t find many reputable associations or societies to help him make an informed decision. David wanted information not opinions. Listen and learn how David’s Path to HSCT has led him to start a community to better educate people living with M.S. about the mosconceptions.

Lets’ catch up with former guest and award-winning distance swimmer, Susan as we hear about what she has been up to since we last spoke. Learn about the new M.S. Health and Wellness Centre and the Human Services they Provide to People living with M.S. Also, hear about our golf tournament and how you can join us in raising funds to support the great work being done by Susan and her group.

Today we speak with Ron, a 61-year-old man living with M.S. He recently underwent the HSCT Treatment. We discuss the good, the bad, and why Ron is pleading people to Research before commitment.

We often marvel at how we, those living with M.S. “Trip over thin Air” or do we? I spoke with Pat Aquistino about how to safe proof your home to prevent falls. We also discussed the need for esthetically pleasing “grab” bars and no, Towel racks are not safe.

Listen in to my conversation with Dr. Casey Farin as we discuss new DMT’s for Secondary, Progressive M.S. Dr. Frain, explains her view of the evolution of M.S. Care and Compassion.

After 15 years of living with M.S., Patient Advocate and Nurse, Jana discusses her choice to move from Medication to an Holistic approach when managing her M.S.

Listen in as myself and new co-host, Jana Bartley interview Dave. A practicing chiropractor, Dave uses a combination of Diet, Exercise and mindset to manage his M.S. Follow his Health Detour Tips and listen to his journey.

Dr. Beaber had posted a link on his Social Media Account about a Swedish study on “Benign” M.S. Listen in as we discuss the intricacies of this type of M.S.

Melinda had always been strong she had suffered and powered through migraines all of her life. She is no stranger to pain and medication. But when she walked into a Brick Wall, she decided the time had come to see a neurologist. Listen in to hear her tale.

When Tim married his wife she had already been diagnosed with M.S. and she already had a child. While many partners “bolt” when faced with the news. Tim rolled up his sleeves and went about the business of building a life for his new Family.

Let’s share Chris’s Journey from near wheelchair to full on Action Man. With a Grim prognosis to a self evaluation as result of seeing himself on video. Listen as Chris shares his journey of living with M.S.

On today’s show we interview M.S. Pals contributor Mary Pettigrew.  Mary walks us through Mind Plasticity. And talks about retraining her brain as a way to manage her M.S.

Listen in with Dr. Beaber as we discuss Body Mass index and what it means for managing M.S. We discuss BMIs and why it’s not about being thin. Listen in and enjoy.

“There’s something wrong with my eye…” Listen to how those three words propelled Jay and his wife on a journey of insurmountable odds to find the best treatment for his wife’s M.S.

On today’s episode we speak with Dr. Ron Girard. After serving in the military and obtaining his medical degree there was simply no explanation for the fatigue, sluggishness and speech problems. Post M.S. Diagnosis, Dr. Girard adopted the “no pill for all ills philosophy”. Listen in to Dr. Girard’s journey of self discovery of diet which took him from a wheel chair to total mobility.

On today’s show I interviewed Nancy, an avid hockey mom from the Toronto area, whose personal story is featured on a really great, new app called Aby. Aby is a free app that just launched in Canada and it’s completely dedicated to helping people with MS manage their health and everyday life. One of the best features is the personal journal, where you can track your symptoms, appointments and treatments, set up reminders, and even export reports to share with your Neuro!Have a listen to my conversation with Nancy and check out the app here: https://aby-app.ca

When Carolyn was referred to us by a former guest, we were thrilled. Listen to Carolyn’s inspiring story of hope, positivity, laughter and caring.

When Yvonne reached out to us here at Living with M.S. Truth be Told we were thrilled. Listen as this Author, Advocate, and M.S. Chats participant shares her truth about living with M.S.

What can you say about woman with M.S. who is recognized as a point of light by the British Prime Minister. In this interview with Trishna, listen to her story of advocacy, determination and sheer positivity.

Matt was enjoying a sunny day playing soccer. Then his head started swirling. Listen in to hear about a teenage diagnosis and the power of family when living with M.S.

Listen to Julies Story of being diagnosed in her teens. And her commitment to writing to inspire.

For Gina, being diagnosed with MS at 27 was almost like it never happened. Her symptoms became docile and she didn’t share her disease with friends or family. It wasn’t until a few years had gone by that Gina decided to “come out” about what was going on with her body. Now with more support than ever, Gina has become an advocate for MS. She’s even written a novel, Stumble To Rise, which is set to release early next year and she speaks at different venues to share her story with others.To hear more about Gina and her journey with MS click the link below.

When Kristy was in her third year of University, she started feeling more and more tired but such was the life of a student, right? When the fatigue persisted and her vision started to blur Kristy was diagnosed with MS after numerous tests.Kristy was set back but determined to finish University. During her final year, for her final project, she submitted designs inspired by her MS symptoms. Her designs were so beautiful people across the UK started to take notice.Kristy now runs Charcot, where she uses her MRI scans to create breathtaking designs from the lesions on her brain..Check out her story by clicking the link below.

When Meisha was diagnosed with MS in April 2017, she had no idea that when she got her results back from the doctor’s that it would come up as MS. Unsure of what would happen or how she would now go forward living with MS.Meisha took to different exercises to help with her MS symptoms. Taking part in different activities like seated yoga and different mind stimulating activities, Meisha tackles everyday with a positive attitude.With the support of her family, newly diagnosed Meisha shares her new journey with us.Click the link below to hear her story

This past year we’ve had so many amazing guests and a lot of them, believe it or not, become guests from writing in and telling us their stories. We hope you continue to reach out and share your story with us and the rest of the MS community.When former police officer Jack wrote in after listening to a few episodes and reading our posts we invited him to share his story. For single father Jack, his diagnosis came as a shock, like it does for so many of us, and he wasn’t sure how he would explain what was happening to him to his 6 year old son, Justin.5 years later, Jack and Justin tackle day to day tasks as a team. Gathering strength and support from his loving son, Jack is living in his truth, one day at a time.Click the link below to hear Jack’s story.

Resident neurologist, Dr. Beaber is back and this time we’re talking all about MS and mental health. With high rates of suicide among people with MS, Dr, Beaber addresses the mental health issues that can plague many of us. He breaks down what it means or what it takes to be “happy” while giving us different tips and insights on how to deal with depression.Often times it can feel like we’re alone and we’re the only ones dealing with things but sometimes when you reach out you just might find that you have more in common with someone than you may think and that sharing our stories with others can be a great healing mechanism.And while happiness might seem unattainable in the moment, everything takes time including healing ourselves. If you ever need someone to talk to please reach out to your friends, families, doctors and if that’s not an option you can even find comfort in some of the wonderful online communities that have been built around MS support.From your friends at Truth Be Told.