Dec 7, 2022 | Diane Hunter
When I was diagnosed with multiple myeloma in January 2017, my daughter was a sophomore in college. The last thing I wanted for her was to be worried about me. When I asked my oncologist if I should tell her in person, he told me, “Your daughter is stronger than you...
Dec 7, 2022 | Becky Bosley
It’s almost here! The excitement is palpable! This is my second year attending the American Society of Hematology (ASH) Annual Meeting and Exposition as a social media correspondent for the International Myeloma Foundation (IMF). I am honored to once again be able to...
Dec 6, 2022 | Teresa Miceli
Hello Myeloma community! It is that time of year again – the 64th American Society of Hematology (ASH) annual meeting, being held in New Orleans, LA (NOLA) from December 10-13, 2022. The Support Group Leaders (SGLs) are back at it for the first Hybrid IMF SGLs@ASH....
Dec 5, 2022 | Sheri Baker
For me, 2022 has been a fun year. Things started to feel a little back to normal. I traveled with my husband for vacations and to visit family. I also traveled for myeloma conferences. I was so excited to be back in-person at the International Myeloma Foundation (IMF)...
Dec 5, 2022 | John DeFlice
To improve is to change, to be perfect is to change often. Winston Churchill Treatment of multiple myeloma (MM) has changed drastically in the last ten years with proteasome inhibitors, immunomodulatory drugs, monoclonal antibodies, and CAR T-cell therapies. The...
