MS Has Been My Greatest TeacherAs a personal belief, we are spiritual beings, souls, light, whatever you believe or choose to call the energy that runs all...reactions7comments
Hard to Explain but Then Again Why Bother!When I was 57 years old I was told my brain was that of a much older person's. Admitted for a spinal...reactions10comments
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
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
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...reactions4comments
Please HelpFor 20 years I have been dealing with weakness, numbness, tingling, unable to use my arm or legs for periods of time...reactions2comments
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
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
The Silver Lining?Having lived with Primary Progressive MS for 20+ years, I’ve experienced most of the symptoms that make this disease often horrifying. Somehow...reactions1comment
Really?After falling down and laying in the hallway for 3 hours too dizzy to move, I made it to doctor's and all...reactions5comments
