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~Photos~ This is a place where we can share pictures of anything we'd like too. It could be pictures of our EDS braces, family, friends, memories, drawings, web creations, etc. * No pornographic pictures or anything inappropriate* NOTE: Images can be uploaded to the gallery before being posted!

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 01-11-2008   #1
Johnna
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Is it really EDSKids until I've littered it with pictures?!

Yup! I'm here once again to overwhelm everyone with my life!








Yup... finally got my senior pictures back!



Who doesn't enjoy a good ghetto Santa?!?



...It's L!



What would you do if you went downtown and saw this???



Just something to show off my sexy wrist brace, bendy fingers, and just how odd my friends and I are >_>;;;



...yeah.

Okay! I'll stop now before I get yelled at XD

:star: Johnna
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Old 01-11-2008   #2
ReineDeLaSeine14
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Your pics are necessary to LIFE!!!!

I love the sock...how you are a man...and yeah i'd hug those people downtown!!!!

your senior pics are GORGEOUS!!!

Stephanie like...
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Old 01-11-2008   #3
Johnna
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Thanks And btw... those people with the "FREE HUGS" sign, are my friends Risa and Jez. XP
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Old 01-11-2008   #4
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We would never yell at Johnna!!!! Now, unless you were a spammer.......

Anyway, I LOVE, LOVE, LOVE your senior pictures!!! Can I have one !? I still need to get ones done. I know, I know, I graduated last year but if you remember our school just did sucky ones, nothing like you got done and I ended up crashing horribly because of the bright lights and flashes of the camera. So we're going to make an appointment somewhere proffessional and explain it to them.
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I am beginning to learn that it is the sweet, simple things of life which are the real ones after all.
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The best and most beautiful things in the world cannot be seen or even touched. They must be felt within the heart.
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Old 01-11-2008   #5
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I had to get senior pics done...and the place was AWESOME about the lights (seriously photophobic b/c of eyes) and with positions...they let me sit A LOT.

So if you explain your needs beforehand...they really can still make fabulous pics...I'll have to post some of my senior pics soon...I just have to dig them out.
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Old 01-11-2008   #6
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Well see I had never had my pictures taken professionally (after getting sick) so I had no idea it would do that to me...now I know lol.
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I am beginning to learn that it is the sweet, simple things of life which are the real ones after all.
~Laura Ingalls Wilder


The best and most beautiful things in the world cannot be seen or even touched. They must be felt within the heart.
~Helen Keller

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Old 01-12-2008   #7
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I LOVE the senior pics. You look gorgeous in them!!
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Old 01-12-2008   #8
Johnna
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Thanks for the comments, everyone!

Isn't this adorable?



And no... believe it or not, the cat doesn't want to eat the turtle! He raised the turtle himself. :LOL:



Mischief doesn't wanna eat her either ^_^

-Johnna
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Old 01-12-2008   #9
xxBrittany
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this is sooo cute.
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Old 01-12-2008   #10
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So, I got some new metal finger braces. Thought I'd post this picture... you can kinda see them.



They're pretty comfortable... after a while, I actually forget I'm wearing them! :P

That's my friend Morgan and I at the mall. XP

-Johnna
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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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