Hello, my name is Olivia
and I am 13 years old, and I have Lyme Disease. I started the LivLyme Foundation to raise money for children that cannot afford their Lyme medication and to raise money to find a cure for all of us suffering from Lyme disease. Thank you for visiting my website and remember you are just one bite away from getting Lyme disease.
Gala & Donations Raised $340,000 to help children afford meds and to find a cure!
The annual incidence of Lyme Disease is now 1.5 times more than the estimated number of cases of breast cancer.
Estimated number of new cases of Lyme's Disease each year. 10 times more Americans than previously reported.
of Lyme Patients end up with long term health problems typically due to delayed diagnosis.
The 2017 LivLyme Foundation Grants have been awarded. We gave eleven grants to children ranging in ages of 5-20 years old & from 11 different states. These grants will help families that cannot afford their child’s Lyme medication & doctors. We will also provide...read more
The Founder of the LivLyme Foundation Spoke at the HHS Tick-Borne Disease Working Group Inaugural Session in Washington D.C. on December 11, 2017
“The Tick-Borne Disease Working Group was established by Congress in 2016 as part of the 21st Century Cures Act to provide subject matter expertise and to review federal efforts related to all tick-borne diseases, to help ensure interagency coordination and minimize...read more
On December 4th, LivLyme Foundation’s Founder Olivia was awarded “The Bravery Award” from Stanford University
On December 04, 2017 Olivia was awarded “The Bravery Award” from Stanford University School of Medicine BioADD Laboratory for her advocacy work for Lyme disease. She is the youngest recipient of this award. While at Stanford, she also gave a presentation on Lyme...read more