First Impressions

Debi Collins is a Chittenango, NY resident who became a Lyme patient advocate after being infected with Lyme disease and Bartonella. She co-founded CNY Lyme Support in January 2011 along with three others whose lives had been affected by Lyme disease. They meet on the first Sunday of the month at Sullivan Free Library in Chittenango.

The photo above is Debi and Rod having a coffee break at Burger King on their 25th anniversary which they spent working on their 1843 home.

Debi helps run a fabulous support group and I learn more every time I go. Central New York Lyme Support email: cnylyme@gmail.com

Warmly,

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Lyme Ninjas

I’ve been talking to people with Lyme from all over the country. I am always amazed by how knowledgeable and educated they are about Lyme. Some are passionate about gathering political support. Some are passionate about alternative treatments. Some are passionate about helping others. They all share a deep commitment to make their pain and suffering a positive contribution to the world. That’s why I call them Lyme Ninjas.

Below are the most recent Lyme Ninja interviews.

Paula & Angele 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.

While you are listening, check out Debi's Support Group - Central New York Lyme Support
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