Share your experiences and connect with others in the community. Which symptoms do you experience most often? Do you have any MS management tips to share with others? Please take a moment to share your story with us!

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Featured Stories
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Posted by alchemie - April 11th, 2014

“Multiple Sclerosis sucks… but zombies don’t want to eat my brain!” -alchemie (est. 2008) I worked for Foster Care for a little over 5 years. I’m currently working part-time at our Foster… READ MORE

stories
Posted by Queenie - April 3rd, 2014

I was always moving around. Taking care of my family and friends. This time I needed to be taking care of.  It all started in March 2012.  I was a caregiver for… READ MORE

stories
Posted by Roger Deuxmont - March 31st, 2014

Life & Times of an MS Sufferer….. These pages are dedicated to the following people, my father Leslie 1911-1980, my father was an indirect casualty of the smoking lobby, succumbing to the… READ MORE

stories
Posted by Chrissy - March 29th, 2014

Ok. So where do I start? I was diagnosed 8 years ago after a 6th nerve palsy in that left my left eye unable to turn all the way to the left… READ MORE

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Posted by Dave - March 28th, 2014

I was diagnosed with MS about a year ago. Since then my life has changed dramatically. First, everyone says (or they want to believe,) he looks normal. All I can say is… READ MORE

stories
Posted by Bob Stewart - March 27th, 2014

My first exacerbation occurred while at spring training with the Boston Red Sox professional baseball team. It started with my vision and two years later I was through playing professional baseball and… READ MORE

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Posted by Billie73 - March 21st, 2014

MS. You’re here. Not residing anywhere else but here, within me. Nine years and counting. Probably much longer if you really want to play dirty. Why did you choose me when there… READ MORE

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Posted by ellj - March 12th, 2014

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 these meetings… READ MORE

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Posted by Spritebottle - March 6th, 2014

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 can be… READ MORE

stories
Posted by Brian Light - March 3rd, 2014

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 rather dramatic… READ MORE

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Posted by nubi - March 2nd, 2014

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 confirming that… READ MORE

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Posted by Angel Hataway - March 1st, 2014

I was diagnosed with MS at the age of 28,I am now almost 37.My husband drove me to the hospital to find out what was wrong with me. I couldn’t drive anymore,… READ MORE

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Posted by Fayski - February 28th, 2014

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 it… isn’t… READ MORE

stories
Posted by ellj - February 27th, 2014

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. eg in… READ MORE

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