#177: Paula Jakson Jones & Angele Rice - 2018 Midcoast Maine Lyme Disease Conference.

In this episode you will learn:

  • Why you won’t want to miss the Midcoast Maine Lyme Disease Conference
  • How this conference is perfect for patients as well Lyme Literate Health Care providers
  • How the conference is designed to take care of people with Lyme including a quiet room and quality food

Meet this week’s guests: Paula Jackson Jones & Angele Rice

Paula was bit by a tick in October 2009 going undiagnosed for almost 18 months. In April 2011, Paula had Neurological Lyme Disease and numerous co-infections and began her three year journey back to health with a team of lyme literate doctors.

Angele Rice was bitten as a child – after growing up with numerous complex chronic health conditions – her state of health after the birth of her first child galvinized her to look for answers for why she was so sick – she was finally diagnosed with lyme at age thirty.

These women first created the Midcoast Lyme Disease Support group – and later the conference as a way to empower and educate their local community about lyme disease – and as a way to bring national expertise to their local community.

Web Links:

Midcoast Maine Lyme Conference:  Website


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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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