How photography made our invisible symptoms visible Recently, I was apart of a campaign that started in Melbourne Australia called Seeing MS. It is a global photographic project that visualises the invisible symptoms of our disease. Nine... By lynn-p1 min readBookmark for laterReactions0reactionsComments3 comments
Overlooking to turn the water off, anyone??Hello everyone, This is just one story that happened during the middle of the night, but it scared me so badly I have to talk to someone. I'll try to... By nirmal1 min readBookmark for laterReactions0reactionsComments1 comments
I used to be one of 'those' peopleI would see someone pull into a handicap spot and look perfectly fine as they walk into a store. I would assume they were cheating and shake my head in... By herigstl1 min readBookmark for laterReactions0reactionsComments2 comments
I LOVE THESE GUYSHaving been absent from the bi-weekly meetings of the HP Support Group since December, I felt a real loss - missing the group get togethers. I've re-discovered the value of... By ellj1 min readBookmark for laterReactions0reactionsComments0 comments
What's really true and what really matters?In July I will have been diagnosed with RRMS for 27 years ago. I went to the emrgency room at the NYU Med Center in Manhattan. The first suggestion from... By mr-stoneguy2 min readBookmark for laterReactions0reactionsComments3 comments
Multiple Sclerosis has proven to be a test of faithFaith. It means different things to different people. For me, my faith, changed from being split between the people I worked for, the people I worked with, and the undying... By robert-kolasinski7 min readBookmark for laterReactions0reactionsComments0 comments
The Beauty of BalanceHello all! My name is David and I was diagnosed 2 years ago with MS. I am 22 years old and attend college. My first few months after my diagnosis... By ow2138732 min readBookmark for laterReactions0reactionsComments1 comments
PPMS CanadaHi, 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... By brianlight1 min readBookmark for laterReactions0reactionsComments1 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... By 1 min readBookmark for laterReactions0reactionsComments0 comments
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... By fayski1 min readBookmark for laterReactions0reactionsComments3 comments
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... By ellj1 min readBookmark for laterReactions0reactionsComments1 comments
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... By kmrl1 min readBookmark for laterReactions0reactionsComments0 comments
Yes, Lucky Me, I Have MS, TooI 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... By carolrocha882 min readBookmark for laterReactions0reactionsComments3 comments
Still angryHi! 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... By rose1 min readBookmark for laterReactions0reactionsComments6 comments
Tecfidera - 4 months outOn 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... By skcullers1 min readBookmark for laterReactions0reactionsComments0 comments
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... By conundrum611 min readBookmark for laterReactions0reactionsComments0 comments
A Wonderful Life!Hi, I'm Bob from Kansas City, the city I had the great fortune to have experienced as a young man. I was an active person, however, I wasn't able to... By nosub662 min readBookmark for laterReactions0reactionsComments0 comments
Hello from IowaHi, I am Peg, from Iowa, live on a farm, with my husband, my 2 dogs, horses (yes I still ride), and cats, cattle. My MS began in 1982, and... By pegleg1 min readBookmark for laterReactions0reactionsComments0 comments
Back in the day....I gave birth to my son in 1983 when I was 23 years old. I had violent headaches for a few days after his birth, the doctor prescribed Tylenol with... By cathy-fay1 min readBookmark for laterReactions0reactionsComments1 comments
Wendy's StoryAround 6 years ago I was having issues common with a possible pinched nerve. My right arm was tingly and my back hurt. Then one day I was riding horses... By wendy2 min readBookmark for laterReactions0reactionsComments1 comments