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EDS type III
Information, Symptoms, Treatments and Resources
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Posts on EDS type III
accommidations @ school? - Ehlers-Danlos Syndrome Community
- Aug 25, 2011
what types of accommedations have any of you with EDS, hypermobility type found most helpfu...
Genetician consultation to diagnose EDS type III? - Genetic Disorders Expert Forum
- Jun 04, 2008
Is it true you can't have a genetic test for EDS type III (hypermobility type)? And if it'...
Ehlers Danlos III - Genetic Disorders Expert Forum
- Feb 22, 2008
I have joint hypermobility and my PCP thinks I may have Ehlers Danlos. Since there is no s...
Hypermobility and ehlers danlos III - Chiari Malformation Community
- Mar 21, 2012
Just got back from a dr appt with my 10 year old daughter. She has hypermobility or as the ...
Opinions on MRI Please!!!! - Neurology Community
- Mar 12, 2014
I would like opinions on my MRI before I see neurologist Wednesday. I have EDS type 3. Seve...
18 year old son has no life - Neurology Community
- Mar 07, 2012
My son is 18 yrs old and is having medical problems. He has been diagnosed with EDS III and...
Post op cataract complications. - Eye Care Community
- Jan 24, 2015
Hello, Six months ago, I had IOL implanted to the left eye because of cataract. For a mo...
ehlers danlos type 3 - Chiari Malformation Community
- Nov 04, 2012
selma- can u tell me anything about this? saw nl today and hes almost positive i have it an...
Dont know what to do anymore - Pain Management Community
- Jul 12, 2015
I have been on heavy narcotics for my EDS type 3 for 5 years... I have become dependant on ...
CM type 1 and P.A.D - Chiari Malformation Community
- Aug 21, 2011
Has anyone experienced a link between Chiari Malformation type 1 and Peripheral Artery Dise...
Chiari 1 and related disorders - Chiari Malformation Community
- Jan 05, 2013
I was diagnosed with Chiari 1 malformation about three years ago (december of 2009). SInce ...
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