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CAREGIVER RESOURCES

Below is a list of national organizations dedicated to providing support for long-term caregivers.

Know of another resource? Get in touch!

LymeBrave Foundation, inc. is unaffiliated with the listed organizations unless otherwise noted.

Lyme Organizations

LymeBrave Foundation
www.lymebravefoundation.org
That's us! We provide resources and tools, support programs, and healing workshops to help caregivers help their loved ones on this journey through Lyme disease. Coming soon!

 

Caregiver Action Network
www.caregiveraction.org
A national non-profit organization providing education, support, and resources to family caregivers, including caregivers of those with chronic illness. Be sure to check out their CareCommunity for additional support.
 
Family Caregiver Alliance
www.caregiver.org
A leading non-profit organization addressing the needs of families and friends who serve as caregivers. providing long-term care for loved ones at home. Family Caregiver Alliance provides services, educational programs, and resources to help caregivers manage the demands of caregiving.  

National Alliance for Caregiving
www.caregiving.org
A coalition of non-profit organizations focused on improving the lives of family caregivers through awareness of caregiving issues, research, and national programs. 

National Caregivers Library
www.caregiverslibrary.org

Providing comprehensive resources and tools for caregivers, including how to care for yourself and others with specific illnesses and disabilities. Additional resources include homecare, legal matters, medical care, and financial tools.





 

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 & Crisis Lifeline

 

1-800-273-TALK

(1-800-273-8255)

OR

988

Disclaimer

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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