I'm glad you got such great news. Know that getting checked every 6 months, really is a good thing. If they were really concerned, he'd be in there a lot more. It might help for you to know, my Cameron has been extremely sick, and before his 2nd, 4 month hospitalization, he was seen at least every 2 weeks by his CT surgeon and seen every month by his cardiologist. Every 6 months for your Cameron really is great! My Cameron may need a transplant in the not too distant future (we're not sure at this point), but you really can't spend every day worrying. You have to have hope that your child will be taken care of. I have to remind myself every day that I can control none of this and that God has a plan.
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Cameron is born 11/10/07 FINALIZED!!! 4/3/08
Cameron is diagnosed with Hypoplastic Left Heart Syndrome 11/10/07
Heart Moms develop iron wills – they will go to the ends of the earth for their child, and if that’s not far enough they’ll tie a rope and drag the earth with them. (Steve~the Funky Heart)
A heart defect doesn’t just break one heart... it breaks three. -Supporting the Congenital Heart Futures Act
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