Guest guest Posted February 5, 2004 Report Share Posted February 5, 2004 I am not sure about the number of kids with larger heads who do not have RSS. I don't do the measurements for Dr. H. at the convention. And that is not the only qualifying characteristic for RSS, so it's hard to tell. I know you are looking for that name of whatever he has and I wish I could help you out. Having a name, whatever the name may be, is a comfort - it gives you something to hold onto. Your best bet is to go to Chicago in July and see what Dr. H. says. She will still give you her best advice no matter what the diagnosis. In fact, I've seen her literally walk a child and the parents to another doctor at the convention if she thought that the child did not have RSS or SGA, but the other doctor could help. Jodi Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 5, 2004 Report Share Posted February 5, 2004 I am not sure about the number of kids with larger heads who do not have RSS. I don't do the measurements for Dr. H. at the convention. And that is not the only qualifying characteristic for RSS, so it's hard to tell. I know you are looking for that name of whatever he has and I wish I could help you out. Having a name, whatever the name may be, is a comfort - it gives you something to hold onto. Your best bet is to go to Chicago in July and see what Dr. H. says. She will still give you her best advice no matter what the diagnosis. In fact, I've seen her literally walk a child and the parents to another doctor at the convention if she thought that the child did not have RSS or SGA, but the other doctor could help. Jodi Quote Link to comment Share on other sites More sharing options...
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