Anyone currently being treated for HCL?

I was diagnosed  with HCL last November 2020 and have since had bone marrow biopsies and cladribine.

HCL didn’t clear after 1st treatment, so have undergone my second round.
Would love to talk to any other sufferers, to compare notes, it is quite rare I believe, especially in women.

anyone out there in remission and for how long?