Winter Wine Fest is Now Wine Fest!

Swirl. Sip. Bid. Repeat! Support the Nevada Chapter of the National Hemophilia Foundation during our annual Wine Fest featuring a Wine Tasting and Silent Auction. All proceeds raised stay right here in Nevada to provide support and advocacy to Nevada children and families with bleeding disorders.

This year's wine fest is a virtual event led by “Wine Hosts” who will register a tasting room and set a fundraising goal for their room. Team Captains and Participants will receive supplies from NHFNV depending on their fundraising level. Visit https://hfnv.org/get-involved/special-events/wine-fest.html to learn more.

Register for Wine Fest by visiting: http://bit.ly/NHFNVWineFest and clicking "Register/Create A Page"

Spark Therapeutics – Understanding Gene Therapy Research and Its Potential Application to Hemophilia.

Education Program - More information coming soon

Education Program - More information coming soon

We understand that there is much uncertainty as it relates to COVID-19. Both organizations are committed to providing an experience that helps our young people grow, build confidence, and find joy. After careful review of the facts, and with advice from our medical teams, we will be moving forward with a virtual experience for 2021. We appreciate your patience and understanding in these uncertain times.

Camper applications are now open, deadline is March 31st

If conditions are not safe to offer an in-person rafting experience, camp will be a virtual adventure with a combination of live zooms, at-home projects, and more to teach independence and skills related to transitioning to adulthood.

Education Program - More information coming soon

Weeklong education and community building event featuring live and on-demand opportunities to learn and connect. Culminates in a final event with virtual sponsor booth and special participant activities.
Details coming soon

Education Program - More information coming soon

Hosted by NHF. BDC 2021 will feature more than 90 educational sessions, poster abstract presentations, industry symposia, networking and social events, and exhibits. A lineup of dynamic speakers will provide essential information and insights on the evolving landscape in this exciting new era of treatment for hemophilia, von Willebrand disease, and rare bleeding disorders.
Some sessions not to miss this year include:
• VWD pre-conference workshop
• Gene Therapy
• Health Insurance Navigation
• Telemedicine
• Mental Health & Wellbeing
• Plus Many More!

Our Reno Walk has now gone Virtual. Register today, create a team, raise funds and walk with us in your own neighborhood!

The funds raised at this event will be used to assist our overall 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.

We can't do this walk without you! Please create a team and have your family, friends, neighbors, co-workers and anyone else you know help you not only raise funds but also raise awareness for hemophilia and other bleeding disorders. If someone you know has already created a team, join their team and support them! And if you can’t make it to the Walk at Bartley Ranch on September 12, you can still support it by creating a virtual team! Please spread the word to support the important work that chapters like us and other chapters across the country do for those affected with bleeding disorders!

PARTICIPANTS WHO MAKE A $30 MINIMUM DONATION WILL RECEIVE A UNITE FOR BLEEDING DISORDERS T-SHIRT

Thank you for your support!

Our Las Vegas Walk has now gone Virtual. Register today, create a team, raise funds and walk with us in your own neighborhood!

The funds raised at this event will be used to assist our overall 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.

We can't do this walk without you! Please create a team and have your family, friends, neighbors, co-workers and anyone else you know help you not only raise funds but also raise awareness for hemophilia and other bleeding disorders. If someone you know has already created a team, join their team and support them! And if you can’t make it to the Walk, you can still support it by creating a virtual team! Please spread the word to support the important work that chapters like us and other chapters across the country do for those affected with bleeding disorders!

PARTICIPANTS WHO MAKE A $30 MINIMUM DONATION WILL RECEIVE A UNITE FOR BLEEDING DISORDERS T-SHIRT

Thank you for your support!

Education Program - More information coming soon

Education Program - More information coming soon