Help Samuel Fry Beat HLH
Donación protegida
Three-month-old Sam has hemophagocytic lymphohistiocytosis (HLH), a very rare and potentially fatal disease of his immune system. He is currently at Children's National Medical Center in Washington, D.C., where he receives a cocktail of steroids (to arrest the HLH) and chemotherapy (to break down and eventually disable his immune system). These treatments are expected to take 6-8 weeks.
If the treatments are successful, the next step--the only available step if we're going to cure Sam--is to replace his immune system with a bone marrow transplant.
Please help Sam's family cope with medical bills and lost work time.
To follow Sam's progress, see http://samuelhfry.blogspot.com/
If the treatments are successful, the next step--the only available step if we're going to cure Sam--is to replace his immune system with a bone marrow transplant.
Please help Sam's family cope with medical bills and lost work time.
To follow Sam's progress, see http://samuelhfry.blogspot.com/
Organizador
Friends of Sam Fry
Organizador
Silver Spring, MD