Reborn: Finding Yourself Post Diagnosis...I feel like this is a big issue that most of us have dealt with or are still dealing with it. Once...reactions10comments
Keep Finding My Way Just to Lose It All Over Again...I had my first symptom of blurry vision in the right eye back in later 2013/early 2014, when I was still living...reactions2comments
Ms or not?...Hello. I'm Patrick. I would really like for someone to read this and help me to determine whether or not my symptoms...reactions1replyHealthcare Team
Why I Do What I Do...If nothing less, COVID-19 and the protests have highlighted systemic inequities faced by Black Americans. Multiple sclerosis research is no different. That...reactions6comments
Forced Into Tysabri Rebound...Hi. I'm new to the community, but not MS. I was raised with it. My mom had it. She wasn't as lucky...reactions1comment
At-Home Exercise with MS...During this time of quarantine and social distancing, it can be hard to know how to stay active. For those with MS...reactions18comments
Hives outbreak...Has anyone experienced hives that seem to appear suddenly? I’ve recently been struggling with very itchy hives, along with swelling so bad...reactions2repliesSymptoms
Can you help define this symptom?...Hi all, Firstly, thank you all for being such a great resource. I’m currently awaiting diagnosis for some odd symptoms I’ve been...reactionsrepliesSymptoms
Has anyone found a way to manage a manual w’chair after mastectomy?...Been managing all regular household tasks - laundry, cooking (including bread making) in my manual w’chair (RGK) but now I need breast...reactions5replies
Dangerous Mind...I am 63 years old. I have been diagnosed with MS for over three years. I also have a neuromuscular disorder called...reactions3comments
At Long Last...About 25 years ago my 2nd husband and I began designing a garden I could navigate with MS. My SPMS was diagnosed...reactions3comments
MS and COVID 19...I was diagnosed with MS in 2016 but I had the first signs in 1996 overseas. In spite of these signs, I...reactions1comment
Diagnosed as a Teenager...3 years ago, I was 15 and was diagnosed with MS when my right arm went numb. Followed by that my right...reactions2comments
Used to the Notion of Lockdown...I never thought that people would need to get used to isolation. I have friends doing online zoom sessions with me. They...reactions1comment
Give Yourself Permission to Take A Nap...Why is it so hard to just sit down, close your eyes, and allow yourself to sleep, meditate, daydream, or whatever, in...reactions25comments
My Story...I was diagnosed in late 1978 about 3+ months after the birth of my oldest daughter. I won't go into everything but...reactions1comment
Having Multiple Sclerosis in the Heat of a Pandemic...I have had MS for 17 years and my symptoms are stable, manageable and invisible to most. The COVID-19 pandemic has made...reactions1comment
My Invisible Friend...4 years ago I made a new invisible friend full of troubles and pain, but I decided to accept because I don’t...reactions1comment
MS Comic: How I Describe the MS Hug..."MS hug" sounds like a pleasant sensation, doesn't it? It's definitely misleading because this MS symptom can range from slightly uncomfortable to...reactions6comments
Lost...I was diagnosed with RRMS in 1998. I was 20 years old with a 9mo old son. I woke up the day...reactions7comments
