Well thank you Pearl! I appreciate it, but I am not associated with them, except I am a member of PACCT, the research group. I've had MDS for 8 years now, so have read a bunch and listened to many webinars. Knowledge is power; you feel more control over the disease. Yes, I am a retired RN, which makes it easier in some ways, but harder in other. At any rate, I am happy to still be around, and try to help if I can. And good luck with your journey.
Mags
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Margaret, age 68, dx MDS 5 q- 5/09- now RCMD; also MGUS. TP53 and TET2 mutations
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