Cycling through MS...It appears to take an approach to MS information, management and peer involvement which has the potential to add... By amfadventures2 min readBookmark for laterReactions0reactionsComments4 comments
I have ms since 2006...I have used copaxone and rebif now I am on Tecfidera and doing great my husband divorced me as soon as By dianna241 min readBookmark for laterReactions0reactionsComments1 comments
Why Are You Always Talking About MS?...You can’t pick me out of a crowd most of the time and say…”oh poor thing she has... By msgypsyfay4 min readBookmark for laterReactions0reactionsComments3 comments
Karen MS story...I had been told that I had peripheral neuropathy for a few years, and finally a neurologist changed the diagnoses By karenlenn1 min readBookmark for laterReactions0reactionsComments1 comments
Dancing With MS...I have watched as the system has complicated a very simple virus and have tried my best to share all By 1 min readBookmark for laterReactions0reactionsComments0 comments
Uncharted Waters...I have osteoarthritis as well so joint pain has added to daily challenges, but I am also a cancer survivor... By kimberlyerin1 min readBookmark for laterReactions0reactionsComments4 comments
MS: Mighty Strength...Hi. My name is Dorcas. I was diagnosed with MS in 2003. With all the aches, pains and aggravating symptoms, ... By 2a3l541 min readBookmark for laterReactions0reactionsComments0 comments
Primary Progressive MS...I was diagnosed in 1990 with PPMS but had to go on long term disability a year and a... By redfeatherwoman1 min readBookmark for laterReactions0reactionsComments8 comments
Kristi's MS Story...I've been here almost two years and am fairly happy. I saw a neurologist for the first time in many... By kristiivie2 min readBookmark for laterReactions0reactionsComments2 comments
Bill's MS Story...Right now I can only walk a very short distance on my walker and only stand a very short By william-berger1 min readBookmark for laterReactions0reactionsComments0 comments
Betty's MS Story...I have had double vision since coming down with MS in 1962, and my vision has very much, become blurry.... By bettyjmendoza1 min readBookmark for laterReactions0reactionsComments5 comments
Lois's MS Story...I just see primary Drs now as the MS Drugs do not seem to agree with me. From what I... By psanders71 min readBookmark for laterReactions0reactionsComments2 comments
Traveling with MS: I learned more in 15 minutes while waiting for a train at Union Station....So I took my cards out of my purse to "prove" that I have MS (and I've been on... By pamisue213 min readBookmark for laterReactions0reactionsComments4 comments
MS through a Teenager's Perspective:...I endured through the pain though during the MRI and eventually it went away. After my docs looked at the... By gabbywilson3725 min readBookmark for laterReactions0reactionsComments2 comments
Possibly Have MS But No Official Diagnosis Yet... I'm Scared...I've been to doctors and told them these symptoms and three doctors told me they think it was MS... By veromana4 min readBookmark for laterReactions0reactionsComments2 comments
MS Hug...I have been diagnosed since 1997 and regularly going to our MS Clinic as well as using Avonex for 5 years... By 232ismq1 min readBookmark for laterReactions0reactionsComments4 comments
Singin' With MS...Back to doctor one week later and he gave me the news. Mine is relapsing/remitting. Had had balance, numbness, By zingbeck1 min readBookmark for laterReactions0reactionsComments5 comments
How do you MISS MS on an MRI?...I am a 46 year old man, and have been diagnosed for 2 years this month.... By aub521 min readBookmark for laterReactions0reactionsComments0 comments
MS, no way!...I read and searched MS blogs and sites on the computer. It took me a while to agree to... By dianedee3 min readBookmark for laterReactions0reactionsComments0 comments
What MS Has Taught Me about Strength...Jim has a BS and MS from the University of Wisconsin, Madison.... By sp6g43 min readBookmark for laterReactions0reactionsComments0 comments