Everyone who knows my myeloma journey knows how important family is to me. Making memories with my family is what give me hope. I gained a son Friday night. I’m grateful to have experienced the marriage of my daughter, nine and a half years after dx. #foreverCarters
Thankfully the world has many myeloma heroes, including these presented at #ASH2022 last evening. Congratulations especially to @AhlstromJenny and @MyelomaTeacher. Keep knocking down diversity barriers @MYELOMAhope as you lead #myeloma pts to improved access and better therapy.
Lack of diversity in cancer #clinicaltrials means underserved populations are less likely to benefit from the best hope for cure. Listen to Dr Borno
@UCSFCancer & @MYELOMAhope discuss increasing minority representation in potentially life-saving trials.
https://t.co/wAMtLUrm6m
September is #BloodCancerAwarenessMonth. Do you #kNOwMyeloma?
During the 2022 IMF Support Group Leaders Summit, we asked patients and care partners what they wished people knew about #multiplemyeloma. https://t.co/mU6VdAHOas
Impostor syndrome isn't a disease. It's a normal response to internalizing impossibly high standards.
Doubting yourself doesn't mean you're going to fail. It usually means you're facing a new challenge and you're going to learn.
Feeling uncertainty is a precursor to growth.