Stories

I'm I'm glad I found a site that I can get some info or maybe talk to somebody Maybe but even here it seems that all the stories are from...

My story on MS I was diagnosis in January 2016. Things are not really good for me at this time I was disabled before this with other bad troubles so...

Toward the end of my second pregnancy, I kept falling forward onto my belly. The nurses in the maternity ward always giggled when I came through the door. "Back so...

I've had MS for 20 years come May. I've had the gamut everything from losing my eyesight to partial paralyzation too many relapses I've had every kind of treatment that's...

Hello everyone! My name is Amy and I was diagnosed with RRMS in 2009. I worked in the medical field most of my life, first as a CNA, then as...

I’ve been taking Avonex since I was diagnosed with MS in November 2015. When I was told that the treatment was a once-a-week injection, I thought, “No problem! I take...

It's been 20 years since my diagnosis. Recently my neurologist retired. In looking for a new one, my insurance company informs me I have to complete another MS work up...

I have had M.S. for 30 years. It's exhausting. It has robbed me of many important relationships. My children are fed up of hearing about it. I split up with...

Well my name is Lacey. It was almost 18 years ago my son was 6 weeks old. Such a wonderful time in my life. I had just had this beautiful...

I just got diagnosed with MS in November 2015. Starting in early October, I had a strange sensation of not being able to sense cold with my left hand. I...

I'm a 67 yr. old retired nurse who has had MS since a diagnosis in 1994 after many years of doctors guessing at my diagnosis since no lesions showed on...

Thank God I am blessed to have an amazing husband. But I have one child, a daughter, left at home. I think it's the hardest on her. She tells me...

I've been living with MS for 6 years now. Short in comparison to most. I was diagnosed in 2010 at the age of 49, with an abrupt onset of double...

Most days, life it is what it is. I am a “happy go lucky” roll with the punches kinda person. I have a great life. I have accepted this hell...

Though a positive attitude is best in most, if not all matters, unfortunately, I'm constantly reminded of the cons of living with MS. I refer to those cons as the...

I met my fiancé in 1998. She told me right away that she had MS. I had no idea what that meant but she seemed perfectly healthy and we hit...

I can be the grouchiest, snidest, meanest, most outspoken, most outgoing, most self-confident and most arrogant person that you have or will ever meet……. while I’m sitting on my ass...

Hi all - I was diagnosed with MS in 2008, after living with it for easily ten years before diagnosis. I assumed I was out of shape when my legs...

Upon my diagnosis in 2004, my mom couldn't handle it. We quit talking for 7 years. We started talking again back in September 2015 due to the death of my...

By Michelle Barton I keep reading articles about things people need to know about multiple sclerosis or how to treat people with chronic diseases. What needs to be written is...