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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.
Listen in as we talk to Dr. Levoe about what he has discovered in his research and why we could be looking at something new,
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.
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