Episode 153: Tending the emotional side of Lyme disease.

In this episode you will learn:

  • How for Susan the worst part of being sick with Lyme Disease was the isolation
  • The launch of the Lyme Brave foundation, a national support resource center for patient
  • Why Susan is passionate about making sure Lyme patients and caregiver stories are heard

Meet This Week’s Guest, Susan Pogorzelski:

Susan was born in Pennsylvania, where she graduated from college with a BA in English. In 2012 she was diagnosed with late-stage Lyme Disease after being sick with little explanation for nearly 15 years. After being in remission for nearly a year, Susan relapsed in 2015. Her new book, The Last Letter is closely based on her own struggles with Lyme Disease.

Web Links:

Lyme Brave Foundation Website: lymebravefoundation.org
Lyme Brave on Facebook: Lyme Brave Foundation

So glad you joined us this week. Want to subscribe to Lyme Ninja Radio? Have some feedback for us? Connect with us on iTunes! iTunes not your thing? You can also find us on SoundCloud.

Mackay Rippey

I practice acupuncture in Clinton, NY, a small village in the geographical center of the state. Once I became aware of Lyme and other insect carried diseases, I started seeing my chronic patients in an entirely different light. Join me as I speak with the the most fascinating people in the Lyme community. If you know someone I should interview, let me know.

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