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The Hemophilia Foundation of Nevada (HFNV) is Nevada's only not for profit, community based service and advocacy organization serving the health, education and peer support needs of Nevadans with inherited bleeding disorders and their families.

Friends of the HFNV





VOLUNTEERS - WE NEED YOU

The Hemophilia Foundation of Nevada (HFNV) is made up of many people who donate their time, and in many instances money, to ensure the HFNV is able to continue to deliver its programs and services to Nevadans with inherited bleeding disorders. Have you received services from the HFNV? Educational materials or sponsorship of your child to bleeding disorders camp?  None of these programs would exist  if not for the existence of the Hemophilia Foundation of Nevada  and the HFNV would not exist were it not for the generosity of its volunteers. Have you volunteered to serve on any HFNV committees or to help at any fund raising events such as the Golf Tournament, Motorcycle run, 1 Mile Walk?  Have you attended events and meetings sponsored by the HFNV? Have you given the HFNV a donation or asked your family, co-workers or employer to do so?  If not, now is the perfect time to start a new habit, the habit of giving back to the bleeding disorders community. If you don’t then who will?

Be sure to check the Calendar of our upcoming events. We have many opportunities for you to volunteer.  The success of these fund raising events is very important to the HFNV’s programs, services and especially  the Summer Camp program. It takes not only volunteers but funds to sponsor summer camp each year. Please give us a call at the HFNV office 702.564.4368 or send us an e-mail and tell us of your desire to help.

If you have volunteered at any events, summer camp or made a donation, we would like to say “Thank You”. Your continued support is what keeps your foundation successful and serving the bleeding disorders community of Nevada.

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HFNV Services

Help to support comprehensive hemophilia care in the state of Nevada.
Assist with ensuring emergency factor availability in hospitals statewide
Sponsorship of educational programs for consumers and healthcare providers
Sponsor youth ages 7-17 to Hemophilia Summer Camp
Distribution of educational materials Publish informational newsletter
Assist clients with insurance denials and reimbursement problems
Host Consumer Social Events such as picnics and Holiday Parties
Telephone peer support network and youth group

HFNV Goals

• Improve consumer and healthcare provider education about inherited bleeding disorders
• Promote and support comprehensive hemophilia care in Nevada
• Raise the awareness of bleeding disorders
• Serve as a resource center for distributing educational and informational materials
• Diminish geographic and insurance/reimbursement barriers to receiving adequate care

HFNV Mission


“To improve the quality of care and life for people with hemophilia, von Willebrand disease and other inherited bleeding disorders, through education, peer support and advocacy.

 

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