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Lyme Lies

LymeBrave founder Susan Pogorzelski has partnered with leading Lyme organization Global Lyme Alliance as a regular contributor to their #MyLymeLife essay series.

"The day I discovered self-compassion in the face of this illness was the day I learned that Lyme lies.

It lies when it tells you you’ll never get better. It lies when it tells you you’ll never be independent again. It lies when it tells you you’re without purpose in the world. It lies when it tells you this disease is all that you are.

You are more than this disease."

Read the full essay, "Lyme Lies," on the Global Lyme Alliance blog.

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Have something to say?
Are you a patient or caregiver to someone with Lyme disease?

 

Become a contributor to the Being LymeBrave Blog by submitting your essay to: info@lymebravefoundation.org!

Being LymeBrave Blog

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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