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Thank you all for the reply. I truly do appreciate it. I'm doing a bit better. It is still very hard to accept.
My dad goes in tomorrow for his first session of chemo. We are meeting with his hematologist beforehand. We don't know much of anything besides the fact that he has MDS. We were caught so off guard that we really didn't know what to ask when he was first diagnosed. Hopefully tomorrow the doctor will talk more about the severity of his MDS and his subtype. I'll definitely be posting tomorrow night once we get some more information. We don't even have a copy of his BMB report!
My dad is being seen at Stanford in California. Does anyone know of any exceptional MDS specialists in California?
Thanks again
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