What does HPPS mean in UNCLASSIFIED

Hemophilia Patient and Program Support (HPPS) is a non-profit organization that works to provide individuals with bleeding disorders access to the resources and support they need to live healthy lives.

HPPS works primarily to serve individuals with bleeding disorders as well as their families. This includes people living with hemophilia, von Willebrand disease (VWD), rare factor deficiencies, Gaucher disease, and other inherited bleeding conditions.

HPPS works to provide the bleeding disorder community with comprehensive programing that helps address physical, mental, financial, social, and emotional needs. Examples include education programs on topics such as finances and nutrition; access to grants for medical supplies; online discussion groups; emergency response plans; crisis counseling; volunteer opportunities; op-eds related to public policy reform; emergency financial assistance; transportation aid; camp scholarships for children living with hemophilia; mentoring programs; patient navigation services; webinars on various topics related to hemophilia care management; patient advocacy initiatives at both local and national levels; scholarship opportunities for students pursuing post-secondary schooling or academic studies related to healthcare fields involving bleeding disorders; employment training programs specifically tailored towards helping those living with a diagnosis of a bleeding disorder obtain gainful employment in healthcare settings where they can help others.

Yes! You can visit HPPS's website at www.hppsusa.org or contact them via telephone at 888-530-8555 for more information about all of the services offered by this organization.