Wednesday, May 30, 2012

All SharePosts Relating To "MS Community"

Vicki

Vicki, Health Guide

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Health Guide with Secondary Progressive MS and Osteoporosis
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The Internet, MS Support and Me

I have been very quiet for the last couple of months because of my Trigeminal Neuralgia (TN). Shortly after the new year, the medication I relied on for almost three years to reduce my pain suddenly stopped working. I could barely open my mouth to eat or drink for weeks, and I slept both day and night. Bummer. During this time, several Health... Read moreChevron
posted 03/05/2012, comments (4)|
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Amy Gurowitz

Amy Gurowitz, Health Guide

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Writer, Educational Designer, Non-Profit Founder, Dx in 1988
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Question of the Week: That Auld Lang-List

This is a bizarre week, isn't it? We've survived the madness of the holidays; the shopping, the baking, the decorating, the eating, the wrapping, the opening, the eating, the smiling, the eating, the singing, the eating and finally the Alka-Seltzering. Hopefully our celebrations were enjoyed without major incident (no food poisoning,... Read moreChevron
posted 12/29/2011, comments (20)|
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Amy Gurowitz

Amy Gurowitz, Health Guide

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Writer, Educational Designer, Non-Profit Founder, Dx in 1988
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Can You Find the Funny While Living with MS: Question of the Week

MS is in no way funny.  Yet many people are able to find a way to laugh. Some of us laugh at ourselves and some of us find funny things to distract ourselves from MS. It's good to have either one. Kind of like a first-aid kit. Something that is easy access for when you need it most.   As far as distraction laughing, I like to go to... Read moreChevron
posted 10/18/2011, comments (10)|
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Cathy

Cathy, Health Guide

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I have had MS for 25+ years and am a trained Peer Resource for Shared Solutions for Copaxone. I am a recent graduate of the Alfus Patient Advocate Certificate Program from The University of Miami. My mission is to "pay it forward" by helping others with MS and other autoimmune diseases.
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Grant for people with MS for goods and services...

  Hello all!  I wanted to share with you an email I received from MS Foundation, a wonderful organization that you should familiarize yourself with if you haven't done so already.  Please read below about the possibility of a grant for people with MS in need of certain items to make their lives a little easier:   MS ADVOCACY... Read moreChevron
posted 06/08/2011, comments (0)|
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ohwhiterose

ohwhiterose

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Diagnosed with MS in 1997. Married 30+ yrs with 3 adult children.
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Senior Moment

  Us MS'rs can refer to this as an MS moment. Just remember 'The person who learns to laugh at himself will never cease to be amused'. Isn't this the truth. Share with others your most unforgetible  MS moment.
posted 06/02/2011, comment (1)|
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