Treatment I Research I Advocacy
Treatment I Research I Advocacy
The Lyme Treatment Foundation, Inc. is an all volunteer, 501(c)(3), non-profit organization that was created to provide grants to people of all ages in the United States and Canada, to fund diagnostic testing and treatment of Lyme disease and the associated tick-borne illnesses.
We provide grants up to $4,000 to those in need to help pay for blood tests and long-term treatment of Lyme disease and other tick-borne diseases.
Since launching in 2019, we have awarded over $125,000 in Lyme disease treatment grants to people living in the United States and Canada.
Lyme disease and the associated co-infections can be devastating both physically and financially and our goal is to help those who are suffering get an accurate blood test, so that they may receive a proper diagnosis and appropriate treatment from a Lyme disease specialist.
Testing for Lyme disease is not 100% accurate, and many with Lyme disease do not test positive with the typical blood tests given in a doctor’s office. Without a positive blood test, doctors are unable to treat these patients. Many suffer for years before being referred to a Lyme disease specialist for private testing and treatment.
While these private labs are much more accurate, they are also very costly and many cannot afford to get a proper diagnosis and appropriate treatment on their own.
Our goal at the Lyme Treatment Foundation is to fund diagnostic testing and treatment for as many as possible, so that those suffering from Lyme disease and the other tick-borne illnesses may go on to live healthy, happy and fulfilling lives.
In April 2021, we launched our biomedical research granting program. Lyme Treatment Foundation is dedicated to funding research that will directly impact those suffering from Lyme disease and other tick-borne illnesses.
We are interested in funding research projects that aim to find better treatments and/or therapies to alleviate the suffering of those battling chronic Lyme disease and other tick-borne illnesses.
We will begin funding Lyme disease research in October 2021.
Please consider making a donation. Many are in need of life saving treatment. Many more are unable to work, raise their families, or go to school because of this debilitating disease and they all need our help!
Thank you for your generosity and support! Let's achieve our goal of Lyme treatment for all!
Lyme Treatment Foundation, 2021
Read our Founder's story here and learn how she contracted Lyme disease and two co-infections while hiking in Vermont and why she started the Lyme Treatment Foundation!
The CLyDRN is hosting a month long virtual event from May 1st- May 31st, 2021! Hear from some incredible Lyme disease researchers, physicians, patients and our own Executive Director, Wendy Phillips this May! Learn more below!
Lyme Treatment Foundation
Mighty Well is a wellness wear company that makes face masks and products for those battling tick-borne diseases, like picc line covers. Use code: LYMETREATMENTFOUNDATION10 at checkout to support our treatment grant program! 10% of proceeds when using the above code will be donated to LTF!
Our Founder, Wendy Phillips provided public comment to the Tick-Borne Disease Working Group in November 2020 that was featured on the Health and Human Services website! Read her comments by clicking below.
Your generous donation will help those in need of Lyme disease and tick-borne illness treatment. Together, we can make a difference! Thank you for your donation.
The Lyme Treatment Foundation is a 501(c)(3) non-profit organization and donations are fully tax-deductible. Tax ID: #83-1423577. Thank you for your support!
All information, content, and material of this website is for informational purposes only and are not intended to serve as a substitute for the consultation, diagnosis, and/or medical treatment of a qualified physician or healthcare provider.
Copyright © 2018 Lyme Treatment Foundation, Inc. - All Rights Reserved.