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RareDiseaseDay_Collage2016

The FH Foundation Goes to DC!

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FH Foundation volunteer Advocates for Awareness, Tom Weiser, and Michelle and Jason Watts, were with Cat Davis Ahmed, Director of Outreach at the National Institutes of Health and on Capitol Hill in Washington, DC for Rare Disease Week representing those in the FH Community with Homozygous FH (HoFH). … Read More


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FH and Personalized Medicine

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The Personalized Medicine Coalition has recognized FH treatments among those approved in 2015 by the FDA as personalized medicines.
“More Than 25 Percent of the Novel New Drugs Approved by FDA in 2015 are Personalized Medicines The transformation of health care from one-size-fits-all, trial-and-error … Read More