Paws With a Cause is coming to evaluate me. - Page 2

		EDSkids Forum > EDS & Other Health Issues > ~Miscellaneous~
Paws With a Cause is coming to evaluate me.

~Miscellaneous~ Have an EDS question (or any other health question!) but can't decide where to put it??? You can place it here!

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.

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08-05-2008	#11
xxBrittany *Amazing Administrator Join Date: Jan 2008 Country: Location: Maryland, USA. Posts: 913	Aw, Staci... I am so sorry. But excuse my rudeness but who in the hell are they to tell you that they do not find enough NEED?! I think they need to seriously take a walk in our shoes. And then maybe they will actually think things through. Just like I told Johnna and almost everyone else on here and this goes for EVERYONE else as well.. Call me whenever, day/night, laughing or crying.. I don't care. I'm here for you. __________________ Brittany Lynn Stay Strong. I am a site administrator and if you ever need anything please feel free to contact me. "some of us are just trying to get through the day without falling apart." A good friend is a connection to life - A tie to the past, a road to the future, the key to sanity in a totally insane world.

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© EDS Kids 2008
EDS Kids is a support group and community dedicated to helping young adults and children who suffer from chronic pain caused by illnesses and genetic conditions like Ehlers Danlos Syndrome and Fibromyalgia. Ehlers-Danlos Syndrome (EDS) is a debilitating genetic connective tissue disorder which 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.
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