tag:blogger.com,1999:blog-1770279115036019606.post4582566140367308874..comments2023-12-08T21:09:50.173-08:00Comments on Hypochondroplasia kid: Christmas 2010Kristenhttp://www.blogger.com/profile/17878779315510872778noreply@blogger.comBlogger2125tag:blogger.com,1999:blog-1770279115036019606.post-1027204294317099242011-01-03T18:44:38.317-08:002011-01-03T18:44:38.317-08:00Well, although I have been much smaller than every...Well, although I have been much smaller than everyone around me all my life, everything else about me is "normal" I have never had any aches/pains and I don't have swayback. I am 4'10 and can do just about anything that everyone else can do. As a child I was diagnosed with "short stature", but now am questioning that. I haven't been tested yet, but I will be going in for a skeletal survey soon to determine if I have the characteristics of hypochondroplasia, and then we go from there with the DNA test to look at the specific genes. Your son Coleman is adorable. I'm doing as much research as possible before Adam's next appointments in March and April. I am hoping for the possibility of GH as well, but still need to do more research and speak more with his doctors. When did Coleman begin GH and how long will he be on them? Thanks for all your help!erin923https://www.blogger.com/profile/14008346761492257489noreply@blogger.comtag:blogger.com,1999:blog-1770279115036019606.post-76488752467184980372010-12-29T07:46:57.982-08:002010-12-29T07:46:57.982-08:00Hi Kristen. I would love to chat with you about y...Hi Kristen. I would love to chat with you about your early experiences with Coleman and his doctor visits and such. I'm still somewhat confused as to what our next steps should be or what our options are. Maybe we could chat through email or facebook? <br />Thanks<br />Ernerin923https://www.blogger.com/profile/14008346761492257489noreply@blogger.com