O TYM PODKAŚCIE 🔗
A podcast providing information, inspiration and motivation for living your best life with Multiple Sclerosis. Learn to speak to this disease as it deserves - tell it FUMS every day!
Częstotliwość aktualizacji:
biweekly
Średnia długość dźwięku:
34 minutes
Język angielski
Stany Zjednoczone
120 odcinków
od 12 lutego 2015
episodic
wyraźne treści
W TYM PODKAŚCIE 🔗
NAJNOWSZY ODCINEK 🔗
Being a podcaster can be a lonely life. So what better way to begin the holiday celebrations than getting some of your favorite MSers together to talk about our plans for the season?
Alongside my guests, we talk about some of the things that can play on our minds during this time of year, particul…
WYSZUKAJ MINIONE ODCINKI
Wyszukaj minione odcinki FUMS: Giving Multiple Sclerosis The Finger.
POPRZEDNIE ODCINKI 🔗
Brooke Pelczynski's life with Multiple Sclerosis is an inspiring example of someone taking their diagnosis and turning it into something great. Most recently, her varied career has led to her working for Marvel Comics!
Brooke was undertaking her BFA in Illustration in New York when the fatigue…
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 psy…
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 i…
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 podc…
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 l…
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 in her la…
The truth has been out for a long time - exercise is good for MS and other neurological conditions. But of all of the programs suggested for us, how many of them really know what it's like to live with MS?
My guest today is Mariska Breland. She was a video producer living a very high-stress li…
I don't know about you, but when I was diagnosed with MS my medical care team couldn't answer all of my questions. Although, to be honest, the stress and cog fog meant that I forgot most of the questions I wanted to ask anyway. And the pamphlets that were forced on me just didn't cut…
I've talked before about diet and lifestyle as a way to manage Multiple Sclerosis. It's an exciting area, with more research being done all the time!
If you've been researching this for any time, you've probably heard about Intermittent Fasting (IF). But what is it? And how coul…
Zastrzeżenie: Podcast i grafika osadzone na tej stronie pochodzą z Kathy Reagan Young, który jest własnością jego właściciela i nie jest powiązany ani wspierany przez Listen Notes, Inc.
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I have no special talent. I am only passionately curious, and
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‐ Albert "Llamacorn" Einstein
WYSZUKAJ MINIONE ODCINKI
Wyszukaj minione odcinki FUMS: Giving Multiple Sclerosis The Finger.
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