Ehlers Danlos Websites
Hypermobility Syndromes Association (HMSA)
The Hypermobility Syndromes Association - supporting people with hypermobility, Ehlers-Danlos syndromes, Marfan syndrome, sticker syndrome and more.
Meglathery MD: Coinherited CYP21A2, TNXB, C4 Genes in Chronic illness
RCCX: Co-segregating C4, CYP21, TNXB mutations may explain EDS/hypermobility, CFS/ME/FM, MCAS, POTS/OI/dysautonomia, autism/mood disorders/anxiety/schizophrenia, MS, Lyme, CVID, endocrine and pain syndromes, etc. in patients and their families
CEDSA Home
CEDSA helps patients and families who are diagnosed with Ehlers-Danlos Syndrome by providing advocacy, medical resources, and additional help.
Sincerely, Miranda Marie
Sincerely, Miranda Marie is the website of young adult author Miranda Marie, where she discusses writing, publishing, books, and her genetic condition, Ehlers Danlos Syndrome.
CEDSA Home
CEDSA helps patients and families who are diagnosed with Ehlers-Danlos Syndrome by providing advocacy, medical resources, and additional help.
APNED | Association des Patients Normands Ehlers Danlos
L’Association des Patients Normands Ehlers Danlos a pour objet principal l’aide aux personnes présentant le syndrome ainsi qu’à leurs "aidants".
Handcrafted Ring Splints | Zebra Splints | Home
Affordable high quality handcrafted silver ring splints. Made by a zebra, for zebras!
Words from a weird girl
Hi, I'm Molly, but you can just call me Mol. I use this website to chronicle my journey with rare diseases using humor, sass, love, tears, and most of all complete and total honesty. Welcome to my...
Home
At Perth Paediatric Physiotherapy we are committed to making a positive contribution to your child's physical function, general wellbeing and health education.
Home
RCCX: Co-segregating C4, CYP21, TNXB mutations may explain EDS/hypermobility, CFS/ME/FM, MCAS, POTS/OI/dysautonomia, autism/mood disorders/anxiety/schizophrenia, MS, Lyme, CVID, endocrine and pain syndromes, etc. in patients and their families
EDS International Symposium 2016 | Hosted by EDS UK and EDNF
Internet home for the EDS International Symposium 2016 in New York City, hosted by Ehlers-Danlos National Foundation and Ehlers-Danlos Support UK
Americans Disabled By Vaccines
Organization of Americans who acquired debilitating disorders after injury or vaccination
Americans Disabled By Vaccines
Organization of Americans who acquired debilitating disorders after they were vaccinated
Americans Disabled By Vaccines
Organization of Americans who acquired debilitating disorders after injury or vaccination
Ian McQueen
Ian, Novelist, EDS Type III, Former Dancer, Occasional Vegan. Curator of Invisible Things. @IanMcQn
Central Dermatology
Our expertise includes diagnosis and treatment of a wide spectrum of skin-related conditions.