Paula Jackson Jones is the President and Co-founder of Midcoast Lyme Disease Support & Education

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.

The Midcoast Lyme Disease Support & Education group (MLDSE) was created and exists to raise awareness, foster education, advocate for change and provide community support for those affected by Lyme Disease and other tick-borne associated diseases in the Midcoast Maine community.

Keep educating, keep organizing, keep working. Enough snowflakes and we will have a storm!

Warmly,

Mackay's Signature

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Meet Lyme Ninja’s Health Experts

As a regular listener to Lyme Ninja Radio, you will be exposed to many experts in and around the Lyme Community. It’s important to keep tabs on the latest developments in Lyme research and treatment, and it’s also important to cross pollinate these ideas with experts outside of the Lyme community. Many scientific breakthroughs happen unexpectedly. The most famous example is the accidental discovery of penicillin. By including experts from field outside of the Lyme community, I hope to keep our thinking fresh.

Below are the most recent Expert interviews.

Read Paula's moving letter to her pre-Lyme self.

Read the Letter