My Journey with Two Autoimmune DisordersI am an ex-CEO, a digital professional with 19+ years of experience, and I suffer from two autoimmune disorders – MS and...reactions10comments
MS and the FighterI was always very active. I became a dancer and joined Martial Arts. It was a big part of my life. My...reactions2comments
Somewhere SmilingHi community, my name is Kawanda. I was recently diagnosed with Relapsing MS, but I have been living with this disease for...reactions4comments
Is MS Affected by Sound Waves?I have most of the "normal" symptoms I read about on the web with the exception of the one that is causing...reactions3comments
My First Flareup Was Right Before a Neuro FinalI come from a family of autoimmune disease extending back for at least three generations, and there was always a morbid family...reactions3comments
Please HelpFor 20 years I have been dealing with weakness, numbness, tingling, unable to use my arm or legs for periods of time...reactions2comments
Ex-CEO Navigating Life with MS - Now What?Hello all! At the age of 19, began to exhibit symptoms of fatigue, night sweats, pain, insomnia, and low-grade fevers. Was diagnosed...reactions19comments
RRMS to SPMS in 1 month and Losing Optimistic AttitudeI was DX in 1997 with RRMS, and since August 2018 my whole life has turned upside down. I’m having problems walking...reactions5comments
My Experience as a TeenagerI don’t have much of a story, because I’m a teenager and I was just recently diagnosed with MS a few months...reactions3comments
MS and Its Challenges!MS is a disease which is very rarely understood, as I am sure many other debilitating or terminal conditions are. Especially in...reactions1comment
It’s Not Personal… At Least I Don’t Think It Is…It’s not personal… at least I don’t think it is… When I forget what you have told me…for the umpteenth time in...reactions3comments
Finally an AnswerBrain lesions and a spinal tap with high myelin protein confirmed it. After three years of symptoms and numerous doctors, I was...reactions1comment
MS and My Personal MantraAt my age of 76 I find myself just wanting to give up and not try and fight this horrible disease any...reactions6comments
WendeeI guess I posted in the wrong spot, I started my story somewhere. Well, I’m a 49-year-old nurse that was diagnosed about...reactions1comment
Primary Progressive MSI was diagnosed in 1990 with PPMS but had to go on long term disability a year and a half after my...reactions8comments
The Journey of Having This DiseaseI realize I am not the average person suffering from this disease. I am male, 58 when diagnosed, and only been in...reactions7comments
Numbness Affecting WalkingI have been affected by numbness that deters my walking. My right knee is numb to the point that I have to...reactions3comments
Challenge of Staying Hydrated With an Overactive BladderAvoiding the risk of embarrassing myself is among many of the challenges associated with living with the MonSter. I have encountered another...reactions12comments
The Power of LaughterQuote - Lord Byron: "Always laugh when you can. It is cheap medicine." When did I first become aware of the 'Power...reactions6comments
Where to Go From Here...Well I have a long story as do many of you. I’ve been reading stories for a while now but I feel...reactions13comments
