Guest guest Posted September 20, 2005 Report Share Posted September 20, 2005 Lace - first, take a deep breath. We are all here for you. Second, we all may be frustrated by the many things we need to do for our RSS children - and, if by reading the posts you feel overwhelmed - my apologies. There are many varying degrees of RSS, and fortunately, most of their issues can be dealt with - not that there aren't alot of them at times - but, rest assured - you have MAGIC and this support group to come to during those more demanding times. My son Ian, 2 with RSS, is an amazing boy. He's bright, sweet, friendly, outgoing, stubborn, shy, obstinate.....gosh the list goes on. But, I wouldn't change his diagnosis for the life of me. He and his syndrome are teaching me so much about myself and life itself. Do I sometimes feel in denial of my son's situation and wish he didn't have it? You bet. But, in some way, I feel almost privileged to have a son like Ian. Why? Because he reminds me of how precious life is, how unimportant being perfect is, and how there is always room to be a better person. You will be fine. The best thing I can suggest is to stay on-line here when you can, and definately go to the convention next Summer. I've noticed a very interesting thing about these moms - there is such a connection here. Not just because we have similar issues - but, we all have the same drive to help our children have the best life possible, we are all caring individuals and will do whatever it takes to keep our children as healthy as possible. Aren't all moms like that? Well, usually. But, for some reason, I see a beautiful group of woman that put their best foot forward for their children and their families. I can not emphasize how much it helped going to the convention - and belonging to MAGIC was the other wonderful thing I could do for my son, but also for me. Keep us posted. - H > > I have just been to the genetics dr with my son brayden and they are > as > > sure as can be that he has RSS. So now trying to find an endo in my > > area to deal with. I feel like I still dont know whats going on. I > > have no clue whats coming next. Could someone please give me a > little > > insight on whats coming for my boy. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 20, 2005 Report Share Posted September 20, 2005 Beautifully said, . It brought tears to my eyes. And you speak the truth. Jodi Z > > > I have just been to the genetics dr with my son brayden and they > are > > as > > > sure as can be that he has RSS. So now trying to find an endo > in my > > > area to deal with. I feel like I still dont know whats going > on. I > > > have no clue whats coming next. Could someone please give me a > > little > > > insight on whats coming for my boy. Quote Link to comment Share on other sites More sharing options...
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