2019 Race for FH Banner

FH Can’t Wait!

It is life threatening.

People with familial hypercholesterolemia (FH) are in a race against time. Join the Race for FH to help raise funds that will find every person with FH, increase understanding of FH and ensure optimal care to save lives. 

The 2019 Race for FH kicks off on April 8 and crosses the finish line on May 4 — Race for FH Challenge Day.

Help us reach our goal of raising $200,000

Worldwide FH Awareness Day

FH Awareness Day

FH Awareness Day was established in 2012 by the FH Foundation to raise awareness of familial hypercholesterolemia worldwide during Cholesterol Education Month. Together, we raise our voices in our local communities, in clinics, and on social media in order to help people #KnowFH.

How will you Race for FH?

Walk a mile a day during the #Race4FH (April 8 through May 4)
Run a 5k on May 4 – Race for FH Challenge Day
Ride a total of 1000 miles between April 8 and May 4
weight lifting
Do a Crossfit WOD every day

Visit Race for FH to sign up today. http://give.theFHFoundation.org/2019RaceforFH.

You will then be able to set up a personal fundraising page; add your own photos, videos and stories; and send emails right from your page asking people to support your efforts.

FH Foundation Global Call to Action Summary

A Global Call to Action: Summary

A 4-page summary of the Global Call to Action on Familial Hypercholesterolemia is available now.

Every gift matters

Early and accurate diagnosis and effective treatment can dramatically increase life expectancy for people with FH. Every dollar donated through the Race for FH helps improve diagnosis rates, increase understanding of FH and ensure optimal care to save lives.

 $25 connects a person with FH with a community of others affected by FH. 

$100 provides educational programs and materials to people with FH to help them understand their treatment options.

$250 trains a volunteer to raise awareness of FH in their community.

$500 supports advancing technology that can identify the 90% who don't know they have FH.

$1,000 helps fund the CASCADE FH® Registry -- the only ongoing research that shows how individuals with FH are diagnosed and treated in the U.S.  

Register Today

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