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,

Mackay's Signature

P.S. If you enjoyed the show, leave a comment below.

Clear BRAIN FOG in minutes without taking another supplement using our exclusive Lyme NinjaBrainwave Breathing Technique.

"...the benefit experienced is far greater than solely assisting to clear the horrible immersion into cognitive fog...
...it feels like it is also working to gently regulate my whole body...
...Love it!" - Janelle R.

Get My Cheat Sheet

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.

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.

Connie became passionate about medicine and healing as a result of her decade-long battle with Lyme disease, which led her on a quest to find better answers for herself and others, since the conventional medical community had failed to provide her and others she knew with real solutions for Lyme disease.

Tony Silva and Frances Martinez are a couple that loves the arts, film, photography, beauty, and the truth. They want to raise awareness about this horrible disease, but we also want the world to truly UNDERSTAND what it is like to have it and be in the middle of its madness.

Paula Jackson Jones is the President and Co-founder of Midcoast Lyme Disease Support & Education, a non-profit 501c3 organization that serves the needs of Midcoast Maine’s Lyme community since 2014.

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