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Welcome to the LymeBrave Blog! While we've been blogging since 2012 as part of our Lyme disease advocacy efforts, we're excited to share this new supportive space with you. We hope this will be a place where you can take comfort in the fact that you're not alone in your struggles, learn valuable tools to help you on your journey back to wellness, and begin to heal from the emotional toll of living with Chronic Lyme disease. Here on the blog, you'll find previous writings--cross-posted from our various platforms and compiled for easy reading--as well as new essays and collaborative features that will be announced soon. Stay tuned to see how you can get involved! Have something to share? Send us a quick hello or find us in one of our social spaces over on the Contact page.


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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.

© 2019  LymeBrave Foundation, Inc.