Research on ET treatments

I get periodic bulletins via email from Patient Power that track what Big Pharma is researching for MPN patients. Looks like a vaccine approach may be tried for ET-CALR patients in a few years.

I don't get too geeked up about this stuff because most treatments will be prohibitively expensive for many of us, at least initially. But the treatment research is predicated on what scientists are learning about how different forms of ET work. So info here might be especially interesting to other CALRs like me.