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.

Jared was ill for several years but found a turning point when he finally faced the reality of Lyme disease and took responsibility for his health. He took a step back from medical treatment to focus on the mental and emotional roadblocks that were preventing him from getting healthy.

Aaron was actually inspired by the Lyme Ninja Radio podcast, and has made his own called Lyme Voice. Dedicated to those who are suffering and living with Lyme Disease, they explore the often complex social and emotional aspects of Lyme that impact households across the country.

Mytrae Meliana is a Soul purpose coach, women's workshop leader, spiritual teacher, and holistic psychotherapist. Mytrae's spiritual path, which she's had for most of her life, has wound through Integral Yoga, Tantra, mysticism, and metaphysics. She was miraculously healed of Lyme Disease on her first visit to John of God, a spiritual healer in Brazil.

Susan Luschas, PhD, is an MIT-trained scientist and engineer. Her eldest daughter was bitten by a tick. They went to a doctor, who told them because it had been imbedded for less that 24 hours she didn’t have lyme disease.

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