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Hi, all newcomers, and hi to and Jim. So glad to see all of you using

this wonderful support site. I haven't been using it long, but feel it is

an answer to prayers. I don't have anything to report about my grandson

Trey other than he seems to be doing great. said he ate a whole hot

dog and kept it all down. (I hate hot dogs - full of chemicals, blah!) Do

you all feel the same way that I do - I keep having this feeling that there

families out there somewhere that need this support site and don't know

anything about it. I cringe when I think of the children that are out there

being mis-diagnosed or not diagnosed at all. I wish there was someway to

get the symptoms of RSS on a national TV show - like Dateline, 20/20, Oprah,

etc. I did see a show of hers that showed medical miracles. One was a

little girl that had her legs and arms lengthened. They never did say what

her " defect " was, but the before and after photos were miraculous. She was

there on stage with the doctor. Could RSS kids benefit from this instead of

growth hormones? The bones actually grew! Did any of you see it? My

messages are always too long, but I can't help it. I seem to have a new

purpose in life thanks to little Trey. Bye,

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