Help With Progression...I need some help. Being direct, does anyone know if there HAS to be new lesion activity in order for there to be any progression, changes or a major flare...Reactions0reactionsComments5 repliesCoping
Intimacy and Multiple Sclerosis...One of the benefits of being a member of an extraordinary blogging community is meeting strong, vibrant women who write about a wide array of topics. One niche that I...Reactions0reactionsComments4 comments
PPMS Canada...Hi, I'm Brian, I'm 61 (2014) and was active when younger. I'm still active now doing 25 exercises a day only now from bed or my wheelchair. I have 8...Reactions0reactionsComments1 comments
Fight The Good Fight......Diagnosed in 2005, and still find myself trying to adjust to my life with MS. Never knowing what to expect, but am always expecting. A change, a sign, some news...Reactions0reactionsComments0 comments
Confused...From one of our community members: I have had MS FOR 4 YRS THAT I KNOW OF. MY DR. THAT DX. ME SAID I HAD, CARRIED IT FOR ABOUT 5...Reactions0reactionsComments2 repliesCoping
The Dark Black Dog & His Master....I was diagnosed with MS 3.5 years ago. I think its only been the past few months that I have finally come to terms with that fact. A fact, that's...Reactions0reactionsComments3 comments
questions to ask a neurologist for newly diagnosed...Hi, I've gone to an er twice in 5 weeks and they are sure that I have ms. Due to insurance problems I haven't been able to see a neurologist...Reactions0reactionsComments10 repliesHealthcare Team
When did my MS arrive?...My name: Laurence Janisse (Larry) DX 1997 PPMS @ age 55 - must have had MS long before diagnosis. I can recall at various times, prior instances of occurring MS...Reactions0reactionsComments1 comments
Support a boy’s Swim for MS!!...Hi, my son is a 6th grader in an elementary school. He is doing a service learning project by participating in the national Swim for MS fundraising activity to help...Reactions0reactionsComments1 repliesCoping
Life with MS...The impact of MS is undeniable. Everyone responds to the diagnosis differently. In addition to the impact of MS on our own lives, MS also impacts our relationships with family...
Life as it is now..........I was diagnosed at age 34, now 49. I've been on social security disability since 2001 after employment with a non-profit. Many of the symptoms, I've experienced and believe MS...Reactions0reactionsComments0 comments
Yes, Lucky Me, I Have MS, Too...I was diagnosed with Relapsing Remitting MS in 2005 at the age of 48. However, my neurologist and I believe I had my first MS relapse or "event" at the...Reactions0reactionsComments3 comments
Still angry...Hi! I'm new on this site but not new to ms. I was dx in 1992 with rr. I worked full time as a supervisor for Development disable adults. Had...Reactions0reactionsComments6 comments
Safety First: It's Time To Get A Handicapped Placard...The time had come. I finally had to give in. My legs weren’t behaving, and one of my hands was giving me trouble. Overall, I felt weak, tired, numb, dizzy...Reactions0reactionsComments14 comments
Great north run ms fundraiser...Hello all, I am running the great north run to raise money for m&s research. Please can I ask you to help me raise my target by sharing this message...Reactions0reactionsComments0 repliesCoping
"Unaffordable Health Insurance"...Wow, were to start! Back in November I was informed by my employer that as of the end of December he was dropping our health insurance. Supposedly, with the ACA...Reactions0reactionsComments2 repliesCoping
Tecfidera - 4 months out...On copaxone for 14 years. Tired of shots and about 2x a year had nasty reactions which included 10 fever, shaking for 1/2 hour and pounding heart. Started tecfidera in...Reactions0reactionsComments0 comments
MS fundraiser...From one of our community members: I started a fundraiser in honor of my grandfather Richard Kurtz who had Multiple Sclerosis (MS) and my friend Aaron Morse who has MS...Reactions0reactionsComments0 repliesCoping
MS-tshirt fundraiser...I started a fundraiser in honor of my grandfather Richard Kurtz who had Multiple Sclerosis (MS) and my friend Aaron Morse who has MS. Please help out, click on the...Reactions0reactionsComments0 repliesCoping
Feeling Deserted!...A little over three years ago I was diagnosed with MS. I was put on Copaxone, and about 9 months later had a relapse. At the time my MS Docter recommended...Reactions0reactionsComments0 comments
