For Blood Cancer Awareness Month, I went out on a limb and wrote a series of posts for LinkedIn to help spread the word and provide more insight into the journey than the paper-thin stuff some of the foundations have been posting. So far I've written about what it is, diagnosis, treatment, and the costs. I have two more planned on supporting a cancer patient (and their care partners!), and finally resources available. A former colleague was recently diagnosed with MGUS and hadn't heard about Healthtree or how/why to get a specialist. She does now. A woman I've never met offered to get tested for bone marrow transplant eligibility because her family had to deal with blood cancer. I pointed her to Blood Cancer United where I'm sure she'll be able to help. And health professionals from around the world have commented or reposted. Which is kinda cool. At least a few more people know about MM. Here's my profile if anyone wants to check it out. https://www.linkedin.com/in/tim-johnson-9152b42/ Be well, everyone.