এই পডকাস্টটি সম্বন্ধে 🔗
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!
আপডেট ফ্রিকোয়েন্সি:
biweekly
গড় অডিও দৈর্ঘ্য:
34 minutes
ইংরেজি
মার্কিন যুক্তরাষ্ট্র
120 পর্ব
12 ফেব্রুয়ারি, 2015থেকে
episodic
স্পষ্ট বিষয়বস্তু
এই পডকাস্টে 🔗
সাম্প্রতিক এপিসোড 🔗
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…
অতীতের এপিসোডগুলি অনুসন্ধান করুন
FUMS: Giving Multiple Sclerosis The Finger এর অতীতের এপিসোডগুলি অনুসন্ধান করুন।
পূর্ববর্তী এপিসোডসমূহ 🔗
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…
দাবি পরিত্যাগ: এই পৃষ্ঠায় এম্বেড করা পডকাস্ট এবং আর্টওয়ার্ক Kathy Reagan Young থেকে এসেছে, যা এর মালিকের সম্পত্তি এবং Listen Notes, Inc দ্বারা অনুমোদিত বা অনুমোদিত নয়৷
পডকাস্ট সার্চ ইঞ্জিন
আপনি আমাদের ওয়েবসাইট ব্যবহার করতে পারেন3,822,650পডকাস্ট এবং195,582,889পর্বগুলি মানুষ, স্থান, বা বিষয় দ্বারা অনুসন্ধান করতে৷
জ্ঞানেই বিনিয়োগের সর্বোত্তম ফল মেলে, তাই আমি পডকাস্ট শুনি।
‐ Benjamin "Llamacorn" Franklin
অতীতের এপিসোডগুলি অনুসন্ধান করুন
FUMS: Giving Multiple Sclerosis The Finger এর অতীতের এপিসোডগুলি অনুসন্ধান করুন।
পডকাস্টটি দাবি করা হয়েছে
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@k409
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