Drugs and Hugs

FUMS 117 – Mind, Mood, and Memory in Multiple Sclerosis w/ Dr. Anthony Feinstein

MS is often described as an invisible disability. But as the disease progresses, the focus – of patients as well as medical professionals – can shift to more visible, physical symptoms, like mobility issues. However, because the majority of people with MS are diagnosed in their 20s and 30s, the psychological and cognitive effects can […]

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FUMS 116 – Managing Daily Life as MS Progresses w/Jenn Powell

My guest today is Jenn Powell. She’s an active advocate in the MS community, imparting her hopeful optimism to the real-life challenges facing those of us living with MS. Now with secondary-progressive MS, Jenn continues to elevate the patient voice to better the lives of our community. Jenn is the Brand and Marketing Manager for

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FUMS 115 – MSer Sue Casey says “Grab The Happy!”

If you’re connected with Multiple Sclerosis in any way – whether you’re a patient, or a caregiver, family member, or loved one of somebody with the disease – it’s easy (and NATURAL) to live in the what-ifs. We can all wallow in the negatives – hey, there’s a reason why this podcast is called FUMS!

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FUMS 114 – The Art of Rebellion With Kick-Ass MSer Lydia Emily

Content warning: this episode includes a discussion about Lydia’s personal experiences of Primary Progressive MS and her plans with regards to Death with Dignity, aka Suicide. Lydia Emily Archibald is an artist to her core. She was born in Chicago to globe-trotting activist parents, and this laid the foundation for her socially-conscious and politically-motivated artworks,

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FUMS 113 – An Invitation From Dr. Terry Wahls To Be Part of Her Latest Study

More and more often, we’re all hearing and talking about the use of diet and lifestyle as a way to manage chronic illness – and not just on the FUMS Podcast! In this episode, Dr. Terry Wahls (now officially our most featured guest) is here to tell us all about how we can get involved

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