Who we are:
The Hemophilia Foundation of Nevada is a nonprofit consumer advocacy and service organization founded in 1990 to help meet the vast education and support needs of the bleeding disorders community in Nevada. In July of 2011 we merged with the National Hemophilia Foundation to provide the best possible programs and support to the community. The new Nevada Chapter of the National Hemophilia Foundation is committed to maintaining the commitment of our founder Renee Paper and continue to strive to the high standards that Renee would be proud of.
Our Mission Statement:
The National Hemophilia Foundation is dedicated to finding better treatments and cures for bleeding and clotting disorders and to preventing the complications of these disorders through education, advocacy and research.
PROGRAMS & SERVICES
Peer Support:
Resources/Referral:
For more information please contact:
Nevada Chapter of the National Hemophilia Foundation
7473 W. Lake Mead Blvd. Ste 100
Las Vegas, NV 89128
702-564-4368 Office
702-446-8134 Fax
Info@hfnv.org
- Disseminate information on inherited bleeding disorders and their complications, including hepatitis and HIV/AIDS, to consumers, health care providers and the public.
- Sponsor seminars on inherited bleeding disorders and their complications.
- Publish a newsletter, "Hemophilia Foundation News and Views".
- Maintain a large Library of brochures, books, articles, videos and audio tapes
Peer Support:
- Host picnics and social events.
- Telephone Support Network
Resources/Referral:
- Maintain listings for specialized hemophilia care and emergency clotting factor acquisition
- Sponsor youth to Hemophilia Camps.
- Financial reimbursement guidance.
- Consumer advocacy.
- Support comprehensive hemophilia care in Nevada
For more information please contact:
Nevada Chapter of the National Hemophilia Foundation
7473 W. Lake Mead Blvd. Ste 100
Las Vegas, NV 89128
702-564-4368 Office
702-446-8134 Fax
Info@hfnv.org
