In this episode of the <a class="PrimaryLink BaseLink" href="https://www.ifopa.org/advocacy_series_2022" target="_blank" rel="noreferrer noopener">2022-2023 Advocacy Series</a>, IFOPA Family Services Coordinator, Karen Kirchhoff speaks with FOP community member, Steve Eichner about his experience using a Vocational Rehabilitation program to provide financial assistance for the modifications on his new van.

In this episode of the 2022-2023 Advocacy Series, IFOPA Family Services Coordinator, Karen Kirchhoff speaks with FOP community member, Steve Eichner about his experience using a Vocational Rehabilitation program to provide financial assistance for the modifications on his new van.

In this episode of the&nbsp;<a href="https://www.ifopa.org/advocacy_series_2022" rel="noopener noreferrer">2022-2023 Advocacy Series</a>, IFOPA Family Services Coordinator, Karen Kirchhoff speaks&nbsp;with&nbsp;FOP community member, Steve Eichner about his experience using a Vocational Rehabilitation program to provide financial assistance for the modifications on his new van.

Adaptive Driving and Transportation

The International Fibrodysplasia Ossificans Progressiva (FOP) Association (IFOPA) serves families living with the ultra-rare genetic disease fibrodysplasia ossificans progressiva, as well as researchers and health care providers studying and treating this disease. The IFOPA is a US-based nonprofit organization whose mission is to fund research to find a cure for FOP while supporting, connecting and advocating for individuals with FOP and their families, and raising awareness worldwide. You can find us online at ifopa.org.

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Adaptive Driving and Transportation

Adaptive Driving and Transportation