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Welcome To EDS-Kids
EDS Kids is a support group and community dedicated to helping children and young adult who suffer from chronic pain resulting from illnesses and genetic conditions like Ehlers Danlos Syndrome and Fibromyalgia. Ehlers-Danlos Syndrome (EDS for short) is a genetic connective tissue disorder which primarily causes chronic joint pain and joint dislocations. EDS Kids is a community dedicated to helping not only sufferers of EDS but their family and friends too.
My name's Brittany and I'm a 17 year old girl living in Maryland.
I have Ehlers Danlos Syndrome types 1 & 3, Chronic Fatigue Syndrome, Wacky Blood Levels, POTS, Juvenille Arthritis, Depression, etc.
I love meeting and talking to new people with other syndromes and just plain so called Normal? That's so stereotypical but you know what I mean, I think? Anyways, kudo's for Gwen making a new and improved website, it looks amazing but there will probably be some other changes.
Crafting and Art is just one of my passions as well of music.
I also love working on computers, and designing graphics and such.
But due to brain fog that's all I can think of right at this moment. So I cannot wait to talk to each and everyone of you and if you ever need anything please let me know, dont hesistate to ask, I don't bite
Steph - it is JRA. I just got diagnosed with it. They knew I had arthritis but wasn't really what category I fell under.
Johnna - I missed you too! How are you!? Thanks for making the incredible youtube videos by the way. I showed them to my home teacher and she really learned what we go through everyday.