I was diagnosed with myelodysplastic syndromes in 2017. I immediately contacted the MDS Foundation. My oncologist said, "Don't trust Dr. Google. Here is a list of suggested websites." The Foundation mailed me a packet full of information about MDS, so I learned a lot. (I had never heard of MDS.) A representative even called me!
Christina HegartyMember
, what a helpful resource—thanks for sharing! -Christina, Blood-Cancer.com Team
Yolanda Brunson-SarraboMember
This experience has been like a flower pulling back the petals in digging further for information. I remember reaching out to the top blood cancer organizations which led to other resources; I felt it did take some work in comprehending and finally make more own plan of how and where to find information.
Amanda BrunsonMember
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