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Hooray for Lori!
If you go back and read some of your own posts here you'll find some of the same concerns, before and after transplant, that other forum members are currently expressing. You've done what many want to do - fight and succeed.
My wife no longer has MDS but like you she has after-effects of her transplant. She also has the rest of her life ahead of her, and I'm so glad that you do too. Keep taking care of yourself and thanks for being part of this community.
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