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.

Alison Perch was 27 when she was finally diagnosed with Lyme Disease. And spent years after that getting treatment, getting married, herxing, relapsing, and getting better again.

Robin Shirley, CHHC, is the Founding President of Take Back Your Health Int’l, a company that hosts internationally attended health conferences and retreats across the U.S. She speaks, consults and writes about The Take Back Your Health Lifestyle and how to reduce the symptoms of chronic illness.

Erin Murphy became symptomatic in highschool with fatigue, depression, and anxiety. When she attended college she studied psychology and then neuroscience in an attempt to understand what was happening to her.

Katina is a frequent guest on Lyme ninja radio. She is a graduate of Duke University and The Stillpoint School of Integrative Life Healing. She is a classical homeopath and author of several books on Lyme Disease.

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