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gila
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Post subject: research shows poss assoc EDS-MS  Posted: Sat May 31, 2008 6:46 am |
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| Dessert Spoon |
Joined: Wed Apr 26, 2006 8:45 am
Posts: 676
Location: London, UK
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ReineDeLaSeine14
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Post subject: Re: research shows poss assoc EDS-MS Posted: Sat May 31, 2008 11:42 am |
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| Crystal Spoon |
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Joined: Thu Jan 11, 2007 9:25 pm
Posts: 9105
Location: Connecticut...part-time Texan...and French at heart :)
Blog: View Blog (1)
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I'd believe it.
My great aunt had MS...and my geneticist told me that AI CTDs and stuff are more prevalent in the hypermobile population...
...Mom and I are shining examples...and she suspects that I have MS as well (or Lupus that affects my nervous system...which is my neuro's standpoint as of yet) so yes I can see it.
Serafina...she's hypermobile and has MS. So is Cyndi.
_________________
~Stephanie~
Unknown genetic disorder causing EDS, Dysautonomia, Asperger's Syndrome and other wacky things (ie. seizures, vision impairments, JRA)
Also have Bipolar I, Borderline Personality Disorder, EDNOS and some other stuff.
I am rarely here so if you wish to speak to me please use my email provided in my profile. Thanks 
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gila
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Post subject: Re: research shows poss assoc EDS-MS Posted: Sun Jun 01, 2008 6:19 am |
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| Dessert Spoon |
Joined: Wed Apr 26, 2006 8:45 am
Posts: 676
Location: London, UK
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Brooke
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Post subject: Re: research shows poss assoc EDS-MS Posted: Sun Jun 01, 2008 8:08 am |
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| Serving Spoon |
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Joined: Sat Mar 01, 2008 8:14 pm
Posts: 2960
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Gila, thanks for pulling together the pdf.
I'll read it sometime today after the school graduation.
I hope you feel less head-achy and horrible later this afternoon/tonight.....
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~Brooke
Multiple Sclerosis, post-neurosurgery pituitary adenoma, rapid cycling bipolar II
"Supporting Cast of Issues":
Hypothyroidism, Scoliosis, Resolved Infertility, post- Fibroidectomy, PTSD, Facet joint, bulging disc, CTS, optic neuritis, Torn Retina, mild concussion, torn meniscus etc. knee surgery, ruptured biceps tendon surgery
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stacekins
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Post subject: Re: research shows poss assoc EDS-MS Posted: Sun Jun 01, 2008 8:26 am |
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| Soup Spoon |
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Joined: Mon Jun 11, 2007 11:48 pm
Posts: 955
Location: Michigan
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Thats a really interesting article. Thanks for sharing it.
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Staci Jo
*22*
Life's not waiting for the storm to pass, its learning to dance in the rain. (but gee I sure with the storm would go away for just a little bit!!!)
Classical EDS, Celiac Disease, FMS, PCOS, IBS, Migraines, GI problems, Bulging disk & DDD * L4-L5, Depression, Anxiety
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cynner68
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Post subject: Re: research shows poss assoc EDS-MS Posted: Sun Jun 01, 2008 1:21 pm |
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Joined: Sun Apr 23, 2006 2:20 pm
Posts: 7228
Location: New Braunfels, Texas
Blog: View Blog (2)
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Very interesting. Thanks for posting, gila. I'm looking at both Dx, myself, so it's very curious.
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Click me.> Nobody puts Baby in a corner!
~Thanks for the memories, Patrick.
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TinkerbellK
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Post subject: Re: research shows poss assoc EDS-MS Posted: Mon Jun 02, 2008 6:03 pm |
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| Dessert Spoon |
Joined: Fri Mar 16, 2007 9:14 am
Posts: 723
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this is really interesting, although I admit it doesnt make me feel all warm and fuzzy (as I am being tested for MS...) I can't wait to see this silly neuro!
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~K~
EDS: Hypermoblty, occult tethered cord, cervical-cranio instability, Chiari?, retroflexed-odontoid with pannus, CFS, CMP, Reynauds, adrenal problems...
It's kind of fun to do the impossible" ~Walt Disney
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Katiepillars
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Post subject: Re: research shows poss assoc EDS-MS Posted: Tue Jun 10, 2008 6:14 pm |
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| Dessert Spoon |
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Joined: Wed Apr 02, 2008 3:18 pm
Posts: 512
Blog: View Blog (3)
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Yeah tinkerbellk, I'm looking at both diseases too... definately not feeling all warm and fuzzy.
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People won't remember what you said or did, but they will remember how you made them feel.
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sorry peops, too nauseaous and head ached to write anything
