The HPS Network does not charge membership dues, but relies on donations from it's members and outside parties to fund research and operational costs.
Join the HPS Network in our pursuits and friendship. We are in frequent communication with researchers and will make any developments available to its members.
Get out the word about HPS and help raise money to find a cure at the same time! Find out more about how you can help out here.
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Join one of the HPS Network listservs on Yahoo! Groups and stay in touch with the HPS family all year long!
El propósito de esta página de Internet es el de proveer información acerca del Síndrome de Hermansky-Pudlak. No es nuestra intención la de ofrecer diagnóstico o consulta médicas. No tome ninguna decisión o acción sobre su condición actual de salud basada en la información presentada sin consultar primero con su médico.


