Advocating for Life Without Limits
Great Lakes Hemophilia Foundation (GLHF) provides public policy advocacy on behalf of, and in partnership with, the bleeding disorders community. We educate government officials about the impact that existing laws and pending legislation may have on someone living with a bleeding disorder.
Wisconsin Legislative Day
Join us on March 1 in Madison as we educate our legislators about bleeding disorders and access to care, fair insurance practices, and voice our support for issues important to our community. You will be armed with information and most importantly, your experiences, when meeting.
Please note, a special advocacy training will take place virtually on the evening of February 28 to prepare you for the Wisconsin Legislative Day the following afternoon.
There is nobody that can share your story better than you!
Legislative Bills To Watch
2021-22 Wisconsin Legislature Senate Bill 215: Relating to the application of prescription drug payments to health insurance cost-sharing requirements.
Learn more about Senate Bill 215.
Wisconsin Chronic Disease Program – Thank You For Your Continued Support!
For complete information about how the Wisconsin Chronic Disease Program impacts the bleeding disorders community, click here.
National Hemophilia Foundation’s (NHF) Washington Days is an annual opportunity for people affected by bleeding disorders to advocate at the national level and learn effective grassroots advocacy techniques. Join others from bleeding disorder communities across the country as we meet with legislators and staff on Capitol Hill to share stories, ask questions and voice concerns. This helps lawmakers who shape national healthcare policy better understand life with a bleeding disorder.
Washington Days Travel Grants
GLHF offers travel grants each year to cover the cost of registration, hotel accommodations and airfare for up to two advocates from the Wisconsin bleeding disorders community. If you are interested in heading to Washington, D.C. with GLHF to impact the legislative process, contact Karin Koppen at firstname.lastname@example.org for more information.
We need your voice now more than ever. If you’re interested in participating in advocacy at a local level by sharing your story and representing the bleeding disorders community, please consider joining GLHF’s Advocacy Committee. We’ll share the many ways you can get involved and help us advance our mission of advocacy. Please contact Karin Koppen, email@example.com.
You can also make an impact by contacting your Senate, House, and State Legislators directly.
Move advocacy forward for the bleeding disorders community.