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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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Old 11-27-2009   #1
SophieeBabessxo
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blink Pictures.

I know how to put a hyperlink to a picture. But how do you get the picture appear in your thread? x
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Ehlers-Danlos Syndrome Hypermobility
Caffeine intolerance
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Old 01-12-2010   #2
xxBrittany
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I usually go to www.photobucket.com and then click the picture I want or upload my own, and it's usually to the left but there will be a little box with all sorts of ways of uploading your image to different websites and use the forumn code and your picture should appear..

If not you may have to have Ai or Timeless guide you through it.
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Old 01-12-2010   #3
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Okay, I will try it when I have some pics
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Ehlers-Danlos Syndrome Hypermobility
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Old 01-12-2010   #4
xxBrittany
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Ok! Hope I helped! I'm not sure good with all of that yet!
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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 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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