Advocacy Training - More information coming soon

Advocacy Training - More information coming soon

Education Program - More information coming soon

Advocacy Training - More information coming soon

NHF’s Washington Days is an opportunity for people affected by bleeding disorders to advocate for issues that are important to them. In 2020, Washington Days had more than 450 volunteer advocates from 45 states that met with legislators and staff to discuss federal funding for bleeding disorder programs and access to skilled nursing facilities (SNFs). The issues and priorities for 2021 Washington Days will be announced later this year.

Please note that Washington Days 2021 will be a virtual experience. Washington Days programming will take place during the dates of March 1-5. More programming details will be announced soon.

Education Program - More information coming soon

State advocacy days are one of the major highlights of local chapter advocacy programs. NHF Nevada's State Advocacy Day occurs in odd numbered years and includes volunteer representatives from the entire state of Nevada. Volunteer representatives include individuals with a bleeding disorder and/or their families members, community volunteers and other organizations. We come together to host a day at the state capitol. The event usually consists of a training session where we provide talking points and engage in role-playing activities. Training is followed by a day at the capitol where volunteers meet with their elected officials to educate them about hemophilia, von Willebrand disease and other related bleeding disorders. Constituents may visit representatives for various reasons, including to educate them, build relationships, thank them, and advocate for or against a piece of legislation.

State advocacy days give elected officials the opportunity to learn firsthand from affected individuals and families how expensive treating bleeding orders can be, and how important it is to have access to comprehensive care and continuity of care. Legislators learn how not having access to the proper treatment can be detrimental to the health of someone with a bleeding disorder, and potentially cost the state a lot of money in the long run.

More information

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

Winter Wine Fest is Now Wine Fest!

Wine Fest 2021 is Saturday, April 17th. We can't wait for you to join us on World Hemophilia Day for a day of tasting, sipping and doing good for Nevada's Bleeding Disorders Community.

Stay tuned for updates!

Education Program - More information coming soon

Education Program - More information coming soon

Education Program - More information coming soon

If conditions are not safe to offer an in-person experience, camp will be a virtual experience with a combination of live zoom cabin chats, at-home activities, camp challenges, and more to teach communication, build confidence, and develop problem solving skills.

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. More details coming soon

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