My son was born May 20, 2000 and was diagnosed with CAH when he was only 6 days old. We feel very blessed that this disorder was caught so early and treatment begun so quickly, but I am having good days and bad days with dealing with this. I don't know anyone else who has a child with CAH and have a hard time explaining how I feel sometimes. My son was also born with club feet affecting both feet and we have been casting since he was less than 1 day old. I have heard the first year is the hardest with CAH and I am wondering if anyone could give me some advice on how they have dealt with the constant ups and downs.