I am participating in the 2026 March for Marrow: Walk for PNH to benefit the AAMDS International Foundation, an organization that represents a cause very important to me.

Paroxysmal nocturnal hemoglobinuria (PNH) is a rare, life-threatening blood disorder characterized by chronic red blood cell destruction. The only cure for PNH is a bone marrow transplant, a procedure which is very risky and is only an option for a small percentage of patients who are lucky enough to have a bone marrow match.

AAMDSIF serves and educates the patient population and health professionals and provides financial support to clinical researchers searching for better treatments and cures.

Will you please join me?