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~Site Help & Support~ Not sure how to do something on the site or how to use a certain feature - ask away!

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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01-15-2008	#1
xxBrittany *Amazing Administrator Join Date: Jan 2008 Location: Maryland, USA. Posts: 737 My Mood:	Logo. Ok, so I need some help from the internet techs. I have a logo for EDSkids that I would like to put up. How would I do that? Any help would be wonderful. Thanks! -Brittany.

01-15-2008	#2
Timeless Tech Admin Join Date: Jan 2008 Country: Location: somewhere in the UK Posts: 209 My Mood:	well if you drop it my way l can upload it to the server, l'll pm you my email address ;) __________________

03-10-2008	#3
xxBrittany *Amazing Administrator Join Date: Jan 2008 Location: Maryland, USA. Posts: 737 My Mood:	Hey there! Could you PM me your email address, pretty please with sugar on top!? __________________ 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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