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MS is...

by Amanda
(Wentzville, MO, USA)

MS is... "remembering to not take the small things for granted like feeling the wind blow your hair, the grass between your toes, watching the sun rise and set, and the miracle that today... today you can get out of bed by yourself."


I wanted to submit my "MS is...", I try to focus on the good things, and the good days... trust me we all know when we're having a bad day but even though, as I write to you I have double vision / vertigo / loss of balance / nausea / and fatigue and am on steroids... I have to be grateful for what I CAN do! :)

I've been diagnosed since June 2005. Started on Rebif and in the process of switching to Tysabri.

This is the first time I visited your website... Saving to my favorites!

Amanda



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MS is...

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Feb 26, 2010
Rating
starstarstarstarstar 		Like A Rollarcoaster
by: Lynn

Waking up each day is an experience in itself. With MS one never knows what lies ahead. A positive attitude will surely get you through!!!!!!!!!
Feb 24, 2010
Rating
starstarstarstarstar 		Welcome
by: Jane D.

Welcome, Lorna--Your entry was beautiful and oh, so true. MS is often so weird it's easy to just try and handle the symptoms and forget to be grateful. I hope to see you around here a lot.

Jane
Feb 24, 2010
Rating
starstarstarstarstar 		MS treatment
by: Lorna

I think that I am one of few who have never done any of the traditionally used steroids. This is because I was misdiagnosed for so long with CFS (Chronic Fatigue Syndrome), that I just read about what would be used for this condition & it helped me.

Guess this makes me lucky,
Lorna

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