MS for 40+ yearsMS has been a big part of my life for many years. First "episode" 1974 when my daughter was born. Officially diagnosed in 1996. Now I am 61 years old... By maggie-mae1 min readBookmark for laterReactions0reactionsComments1 comments
New Diagnosis of Remitting/Relapsing Multiple SclerosisI started experiencing numbness in my hands and then it went into my arms. I went to a physiotherapist thinking it was a pinched nerve in September 2014. Numbness increased... By skaet32 min readBookmark for laterReactions0reactionsComments0 comments
Just DiagnosedHi I was just diagnosed with MS about a month ago and it was very stressful getting diagnosed for it. It took me 5 months to get diagnosed. At first... By 3 min readBookmark for laterReactions0reactionsComments4 comments
Newly diagnosed with Relapsing/Remitting MSFirst, I would like to introduce myself. My name is Michele. I am 45 years old, and was officially diagnosed with Relapsing/Remittng MS on September 30, 2015. I have been... By 1 min readBookmark for laterReactions0reactionsComments3 comments
MS THE NEVER ENDING BATTLE!!I was diagnosed on April 1,2011 after fighting through 10 years of tests, MRIs, LPs and several neurologists. I was so worn out from all the above I quit going... By tmbb6x2 min readBookmark for laterReactions0reactionsComments1 comments
Horrible disease but don't stop fighting!Hi everyone! So I have a long story which I try to compress to make it not so long to read. I am 36 years old guy and everything was... By 1 min readBookmark for laterReactions0reactionsComments0 comments
I wonder, "why me"?So when I was 14 years old, a freshman in high school I something told me there was something different about me, but I didn't know what that "something" was... By 2 min readBookmark for laterReactions0reactionsComments0 comments
55 Life LessonsI read Maria Shriver’s 60 best life lessons in honor of her turning 60. So, I thought in honor of me turning 55 - I will write my own life... By ldg12304 min readBookmark for laterReactions0reactionsComments0 comments
The struggle is real.I was diagnosed 12 or 13 years ago. I can't remember really. Tragic events get blurry in my memory. But it gets worse. I was standing in church, eyes closed... By tlve5y2 min readBookmark for laterReactions0reactionsComments1 comments
Silence is my nameWhat is in a name? My name is not really Silence, but Benjamin Franklin used it as a pseudonym, so can I. I am Silence and I have Multiple Sclerosis... By 4 min readBookmark for laterReactions0reactionsComments4 comments
M.S., my evil partnerYears ago I got epilepsy out of the blue and it took me a while to learn how to make decisions on my own proper! I got a brain operation... By 3kbwwk1 min readBookmark for laterReactions0reactionsComments3 comments
MY WIFE HAS M.S.Hi, Lorraine has MS and is taken Tecfidera, so much better than the shots. Gradually she is becoming worse and uses a scooter most of the time. Lately, she is... By rainy19591 min readBookmark for laterReactions0reactionsComments2 comments
MS was the only thing I focused onI was diagnosed in 2007 with RRMS. I worked 12 hr days 5-6 days a week as a QA Supervisor in a food plant. The only doctor I made time... By 2 min readBookmark for laterReactions0reactionsComments2 comments
It is what it is & I am slowly dealing with it...I am 37 & finally got diagnosed with RRMS after a year of tests and trials. It was a relief to finally know that I was dealing with some very... By 6tlnk1 min readBookmark for laterReactions0reactionsComments3 comments
Makes us strongerI am determined not to let this disease define who I am, but it does define what I am fighting through my diet and exercise regimen. I love baseball (the... By alpatetta1 min readBookmark for laterReactions0reactionsComments2 comments
StrengthI was diagnosed several years ago with the illness. It's funny because if you didn't know me you would think I'm the picture of health. Well, the funny thing is... By 1 min readBookmark for laterReactions0reactionsComments8 comments
How MS Helped Me See What the Holidays are Really AboutLiving with MS, there are always three things that I think about whenever I have to go somewhere for any length of time: 1) What will the temperature be? 2)... By sp6g44 min readBookmark for laterReactions0reactionsComments2 comments
New at this. Trying to figure it outI am new at MS. PPMS is now in my vocabulary. Part of my job is being a researcher so research on MS I have done. I thought, no problem... By 1 min readBookmark for laterReactions0reactionsComments2 comments
Well Meaning Words, "But, You Look So Good!"After living with RRMS for almost 30 years now, like others that have heard this said to them (But, You Look so Good) I am sure they are tried of... By CommunityMember35291 min readBookmark for laterReactions0reactionsComments6 comments
Dying yet living with Love.My story begins very early stage. I will give a short version, as I'm writing a book. No one could understand, why I was accident prone. Fire prone. Mum used... By yc68eo2 min readBookmark for laterReactions0reactionsComments1 comments