Guest guest Posted December 17, 2003 Report Share Posted December 17, 2003 Hi Hari, Welcome to the list, and congratulations on the birth of your son. I have a few suggestions: 1. Contact n Norbury (www.chargesyndrome.org) and get a copy of the Manual as soon as possible! CHARGE Syndrome Foundation, Inc. 2004 Parkade Boulevard Columbia, MO 65202-3121 Phone: or Contact: n Norbury n Norbury: (Executive Director) marion@... Meg Hefner (Genetic Counselor): meg@... 2. Track down Brown at California Deafblind Services (San Francisco) - tel , also as soon as possible - he's brilliant and compassionate and will be a wonderful resource for you and your family! 3. Take a deep breath and try to get some rest ;-) As others on the list have said, it all gets less overwhelming after a while (most of the time)... 4. What about Mihir's vision? Is there any evidence of Coloboma? That should be checked out by a specialist (ie. a genetic ophthalmologist who is familiar with the condition) as soon as possible... 5. It's not too early to start reading, singing, talking to your son. Stimulate, stimulate, stimulate all the senses - vision, hearing, touch, taste, smell etc. Even if some of the senses are compromised or incomplete, you can connect with whatever is present. BTW - how do you know he " failed " his hearing test - were they able to quantify his hearing deficit, and did they use an ABR test? My daughter had two heart defects at birth; the 4mm PDA didn't close by itself so after several rounds of prophylactic antibiotics for dental work etc. at 3 1/2 years old she had a catheterization to install a coil in the duct to close the hole. It appears to have been successful. Don't hesitate to ask this list all your questions... I am sure that SOMEONE has already been there! Best wishes, Anne, mom of Penina (CHARGE, 7) Montreal, Canada Quote Link to comment Share on other sites More sharing options...
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