Stories

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...

I 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...

Having 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...

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...

Faith. 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...

Hello 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...

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...

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...

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...

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...

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...

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...

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...

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...

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...

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...

Hi, 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...

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...

Around 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...

I should preface this story with a little history on myself. I served in the US Navy as a Hospital Corpsman. In 2009 I was assigned to working with the...