This is what Sandis’s biological father has.
It is hereditary.
Sandis will be following up with a cardiologist in the next few months to see if he has it, as well. Assuming things go well and his heart looks fabulous, he will follow up with a cardiologist annually or bi-annually until he hits puberty. Then he will follow up with a cardiologist annually until he is in his late twenties to ensure that he is not developing this condition.
And, of course, I don’t think this is fair.
I’m not really grieving, it could be nothing, and he could be fine.
But I’m not exactly jumping for joy either.
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2 comments:
I really hopes it turns out to be nothing for Sandis. But, the added doctor's appointments, that really sucks.
Oh man, that blows. I hope Sandis doesn't inherit it.
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