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Abi's Pain Diary
Created on 2005-02-07 07:45:59 (#6045232), last updated 2005-04-22
52 comments received, 7 comments posted
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| Name: | Abi |
|---|
I have a connective tissue disorder called Hypermobility Type Ehlers-Danlos Syndrom (EDS), which was formerly called Type III. I have a variety of unstable joints, sensativity to light, sensative skin, a heart murmur and an unfortunate allergy to codine derivatives. I take a combination of Neurontin, Skelaxin, Celebrex, Nortriptyline and Inderol daily, plus Lidoderm patches and Zomig as needed to control migraines and joint and muscle pain. I tread water for excersize and still manage to get hurt, somehow.
For more info on EDS, try Ehlers Danlos National Foundation and this article.
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For more info on EDS, try Ehlers Danlos National Foundation and this article.

Come on, hug me. You know you want to.
*HUGS* TOTAL!
Give Abi more *HUGS*
Get hugs of your own
And when you're done clicking that, click these.
Save The World - One Click At A Time!
On each of these websites, you can click a button to support the cause -- each click creates funding, and costs you nothing! Bookmark these sites, and click once a day!


Click here to post this on your page or 'blog
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