I'm brand new at this- hoping to reach out to others with mantle cell. My sister (58) has been fighting this ugly "thing" since last November. Sounds like MC is one of the rarest forms of lymphoma, so there isn't a lot out there, although they do know that it is on the rise. Hoping to help and share as we go through this. We have our first appt with the transplant team tomorrow. One step at a time......…
