The Walton Family Foundation
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The LivLyme Foundation, established by Olivia at the age of 12, is dedicated to supporting children unable to afford Lyme disease medication while also funding research for better treatment and a cure for Lyme and other tick-borne diseases. With a mission to raise awareness, the foundation provides financial assistance for medical treatments and grants to scientists working on innovative solutions in the field.
As the fastest growing vector-borne infectious disease in the United States, Lyme disease affects over 476,000 individuals annually, including 200 children each day. The foundation aims to educate the public on prevention, treatment, and the importance of early diagnosis, contributing significantly to the fight against this serious health challenge.
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