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See how you can help support Kendall, Scarlett, and the thousands of other affected patients and families UMDF serves this holiday season.

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FIND A MITO DOC 

UMDF maintains a list of 200+ doctors treating and researching mitochondrial disease.

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WE CAN’T DO IT ALONE  

Your involvement is critical to find a cure for mitochondrial disease.

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VIEW UMDF EVENTS 

Find a virtual support meeting or UMDF fundraiser in your hometown.

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BE AN ADVOCATE  

Use your voice to impact legislation affecting the mitochondrial community at the federal and state level.

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Get helpful resources, educational info and caring support.

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READ IMPACT REPORT 

The work done through UMDF is making a global impact.

UMDF Connect

Advocacy Update – April 2022

White House Releases Fiscal Year (FY) 2023 Budget Request - Big Proposed Increases for Research On Monday, March 28, 2022, President Biden released his proposed fiscal year (FY) 2023 budget. The president’s budget request starts the Congressional budget process. The...

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Symposium 2023 – Keeping You Safe

Symposium 2023: Patients and Families - Keeping You SafeUMDF Mitochondrial Medicine 2023 COVID-19 Protocols as of February 13, will include: At this time, we are not requiring attendees to attest to being vaccinated.  Although COVID cases are lower than 2022, most...

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Symposium 2022 – Keeping You Safe

Symposium 2022: Patients and Families - Keeping You SafeUMDF Mitochondrial Medicine 2022 COVID-19 Protocols as of March 25, will include: Attendees must attest to being fully vaccinated per the CDC. Attendees must wear masks within all of the UMDF meeting space. We...

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