A list of non-profit organizations aimed at helping adults with Lyme disease in the realm of financial assistance, social security and disability education, and support groups.

A list of non-profit organizations aimed at helping families with children who are battling Lyme disease. These organizations may offer grants to help circumvent the high cost of treatment.

A list of national non-profit organizations leading the fight for Lyme disease education and awareness while supporting Lyme research and support through fundraising initiatives.

A list of support group resources from around the web.

A growing list of resources for adults and children with Lyme disease and other tick-borne infections.

Crisis Lifeline

Lyme patients are at-risk of suicide due to the accompanying decrease in quality of life. If you or someone you love is suffering from depression or suicidal ideation, contact your physician immediately or call the
National Suicide Prevention Lifeline




LymeBrave Foundation, Inc. is an education and support services 501(c)(3) non-profit organization created by patients, for patients. The material found herein is for informational purposes only and is not a substitute for the medical services or advice of professionals. While we aim to provide emotional support resources to patients and caregivers, LymeBrave Foundation, Inc. makes no representation of warranties with respect to the context of the information herein. LymeBrave Foundation, Inc. is not liable for any damages, including the health and wellbeing of individuals, arising herefrom. LymeBrave Foundation, Inc. is not responsible for third-party content, nor does it recommend or endorse third-party content.

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