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Episode Info: 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. 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.Read more »

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