Join the Policy and Advocacy Taskforce

Are you passionate about rare diseases and public policy? Are you interested in getting more involved in federal or state policy, or both? Our National and Regional Policy and Advocacy Taskforces provide forums for volunteers to be more deeply involved in grassroots advocacy efforts and to fight for legislative solutions. The Taskforces are open to all, including experienced advocates and new volunteers, and we will offer you all the training and tools you need to be successful!

Our National Policy & Advocacy Taskforce is focused primarily on federal policy. We host four National Taskforce meetings per year, each aimed at providing rare disease advocates with new skills to add to their advocacy toolkit. Our four Regional Policy & Advocacy Taskforces each focus on improving state-level policy for rare disease patients and families across the country. Taskforce members have the opportunity to collaborate with and learn from advocates in neighboring states during five Regional Taskforce meetings throughout the year.

Get started by telling us a little bit about yourself:

Sign up using the form below to receive more information about the Policy & Advocacy Taskforces and register for our first National Taskforce meeting!


Policy & Advocacy Taskforce Events

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Today

Region A: Washington, Oregon, California, Idaho, Nevada, Utah, Arizona, Montana, Wyoming, Colorado, New Mexico, Alaska, Hawaii, Guam, American Samoa, Northern Mariana Islands

Region B: North Dakota, South Dakota, Nebraska, Kansas, Oklahoma, Texas, Minnesota, Iowa, Missouri, Arkansas, Louisiana, Wisconsin, Illinois

Region C: Michigan, Indiana, Ohio, Kentucky, West Virginia, Tennessee, North Carolina, South Carolina, Mississippi, Alabama, Georgia, Florida, Puerto Rico, US Virgin Islands

Region D: Virginia, District of Columbia, Maryland, Delaware, New Jersey, Pennsylvania, New York, Connecticut, Rhode Island, Massachusetts, Vermont, New Hampshire, Maine

 

Policy Taskforce Map


Meet Our Taskforce Co-Chairs

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Kellie H.

Rare Mom

Region A

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Melanie F.

Rare Disease Patient

Region A

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Nick K.

Rare Dad

Region A

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Andrew L.

Rare Disease Patient

Region B

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Breana B.

Rare Disease Caregive

Region B

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Nicole I.

Rare Mom

Region B

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Aaron B.

Rare Disease Patient

Region C

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Jeron H.

Rare Disease Patient

Region C

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Pam J.

Rare Mom

Region C

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Julie R.

Rare Mom

Region D

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Tai P.

Rare Disease Advocate and Researcher

Region D

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Barbie Ann S.

Rare Disease Patient and Rare Mom

Region D