MS Connection

I saw this on the MS UK site. https://www.youtube.com/watch?v=6groGL9p3z8&feature=youtu.be Read More

During this Friday’s — May 29 at 1pm ET — Ask an MS Expert program we’ll look at the additional challenges of the COVID-19 crisis in maintaining health and wellness with MS, including maintaining emotional wellness during this time and handling the additional stress and the potential impact it may have on… Read More

I was diagnosed with MS in 2015. Ive had no flare ups since diagnosis. Ive been on Tecfidera 240 mg. No other health related issues, although I did get shingles last year on my face. (Boy, was that painful) Any way, I lost about 60 lbs through diet and exercise 2 years ago and although Ive put a little of it… Read More

This Friday — May 22 at 1pm ET — our MS expert will tackle treatments for COVID-19 that are being explored, including news about the impact of Vitamin D and antibodies. We’ll look at the duration of symptoms and whether multiple sclerosis impacts the severity of symptoms, and discuss questions such as if we… Read More

This Friday’s — May 15 at 1pm ET— live broadcast of the Ask an MS Expert series addresses questions that those living with MS have about treating their MS during this time, especially as it relates to the use of disease-modifying therapies (DMTs). We’ll also look at the latest research to stop MS in its tracks,… Read More

My mother has MS, I've always been worried I would have it to. My mother's mood swings are overwhelming and a source of a lot of stress, which I've been dealing with for 33 years. As long as I could remember.  Recently (May 2nd) I went to my Uncles house to clean it out with the family being he passed away… Read More

This Friday’s — May 8 at 1pm ET— live broadcast of the Ask an MS Expert series provides answers to questions related to a potential COVID-19 vaccine, emerging from the crisis as businesses begin to open and other developments around Coronavirus. You’ll also hear about MS research and treatment developments… Read More

I have been battling ms since 2010 with good success but after taking treatment I am now diagnosed with breast cancer.  Is there anyone here with me.  I am trying to be positive but t unknown is scary.  Any advice? Read More

Ok so my MS has been a roller coaster up and down there's been days I can get around so so then days all I can do is lay in bed. And I kinda gave up for awhile. Between depression then stress it's been tuff. What happened was I had my sister helping me when I was with my x who was abusive. And I checked out so… Read More

Anyone know a receipy or how to make epsom salt rub or what to do? Been taking my vitamins and just starting to take magnesium 250 mlg I believe. Do I need to take double that? Can't stand this it never goes away once it starts. Read More

Hi, I'm new here and I'm still learning how to use this website so I'm really sorry if I've posted this in the wrong place.I just thought that what with the current situation where most of us are having to stay at home, we could talk about the hobbies we have.I have a lot of hobbies, but over the years, I've… Read More

MS experts will answer common questions about managing symptoms of multiple sclerosis, the role of nutrition, vitamins and supplements, and the impact of stress on MS this Friday, May 1 at 1pm EST during our Ask an MS Expert series.We'll also look at common symptoms of COVID-19, new drugs being tested for COVID… Read More

Yes, having MS sucks. Three decades of it have taught me that. And yes, being gimpy/disabled/no-energy during a time of crisis sucks. Having a health risk factor with Covid-19 certainly sucks. And those of us on DMTs that increase our risk factor with Covid-19 most certainly sucks! But enough sucking. We with… Read More

Get the latest information related to coronavirus – including home testing kits, MS registries, updated MS DMT guidance, and the reopening of businesses in some states, on Friday, April 24 at 1pm EST during our Ask an MS Expert series. You'll also hear from our expert physical therapist on how to incorporate at… Read More

Hi, I am just looking to find connections with other caregivers. I am Also a young adult (27 years old) and it's hard for that age bracket specifically to understand what I go through.  Read More

Join us this Friday at 1 p.m. EDT for the Ask an MS Expert series. Hear from MS experts on COVID-19 and MS, as well as the CARES Act and what it means for people living with MS. Sign up here Read More

Hello all, I am curious if there is a social meet in the inland empire in CA to meet others with MS.  I am alone on this and diagnosed in the 90's.  I don't know anyone, and family does not understand.  I was told to go to the support groups, which I have, but majority are married and do not go through what I… Read More

I was diagnosed at age 20 Doctors considered my first attack on my eyes at age 15 was MS Read More

As a general rule, I find moderate-to-cooler temps in low humidity climates the best for my MS.  But that sweet spot exists nowhere ALL THE TIME.  The earth spins/tilts, ya know.  Yet, in the US, some places are pretty good.  If you start with the idea that most people with MS like low humidity days, then you… Read More

We know many people living with MS have questions about COVID-19 and MS treatments. Join us for our Ask an MS Expert series this Friday, April 3 at 1 p.m. EDT, featuring leading MS experts who will share the latest information on COVID-19 and MS treatments and answer your questions.Register here. Limited space… Read More