Eight Month update…
Thursday, January 23rd, 2003Mary, you have an incredibly wonderful positive attitude. It’s great
to see your joy and optimism, in spite of the setbacks.
I have a friend with this same disorder. He’s managing pretty well
with his treatment, but there are a few things you need to watch with
the coumadin therapy. He’s now taking Foxomax for osteoporosis; I
don’t remember whether the bone thinning is caused by the coumadin or
the disorder (though I believe it’s the coumadin), but it’s something
you’ll want to watch out for. He jokes about taking medicine for
“postmenopausal women”, but the Fosomax is supposedly pretty
effective–though probably tricky to take after WLS, since it’s tough
on the stomach, so you’ll want to ask your doctor about possible
alternatives.
You’re right about this disorder being inherited. He has two kids,
and one has tested to not have the disorder, the other hasn’t been
tested yet. His father evidently had it, he died from a stroke
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