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8

The Lyme Times

drove all the way to Maine with fear and desperation and left with

tears of joy and a new found sense of hope. That is the feeling

that so many experience when they finally connect with a Lyme-

literate doctor and are being heard and believed for the first time

— when they are given hope that they can get better.” People from

Maine and other parts of New England came with questions and

left with answers.

Among the speakers were Pat Smith, president of the Lyme

Disease Association; Eva Sapi, PhD, researcher at the University

of New Haven; Bob Giguere, IGeneX Laboratories; Beatrice

Szantyr, MD; and Katina Makris, author and Lyme Light Radio

host. A 2-DVD set of the conference is available. Send an email to

midcoastlymediseasesupedu@gmail.com.

Massachusetts Foundation conference draws 450 patients

Connecticut LLMD Steven Phillips proved to be a strong draw

for the 450 New Englanders who braved snow and icy roads

to attend the Central Massachusetts Lyme Foundation’s first

conference in Worcester in March. Phillips, a former president of

ILADS, was the keynote speaker in the morning; in the afternoon,

Eva Sapi talked about her research on biofilms and antibiotics.

Sapi is an associate professor of Biology and Environmental Science

from the University of New Haven in West Haven, CT. The day-long

event also held break-out sessions covering topics ranging from tick

prevention, nutrition, herbal treatment, Lyme disease testing, and

patient advocacy.

Central Massachusetts Lyme Foundation is a non-profit

organization created to help those battling Lyme disease as well

as other tick-borne illnesses. Ken and Michele Miller started the

organization in memory of Michele's mother, Jeanne Cloutier,

who passed away in 2013 as a result of late-stage Lyme disease.

For more information on the Central Mass Lyme Foundation and

their upcoming events, visit their website at

CentralMassLyme.org

.

Connecticut Lyme Connection honors LDA President Pat Smith

An enthusiastic crowd gave Lyme Disease Association president

Pat Smith a standing ovation when the patient advocacy group

Lyme Connection presented her with their first Courage in

Advocacy Award at their patient conference and health fair inMay.

Several Lyme luminaries attended in Smith’s honor, including CT

pediatrician Charles Ray Jones; Columbia Lyme Research Center

Director Brian Fallon; NY LLMDs Ken Liegner and Dan Cameron,

who is also president of ILADS; CT LLMD Steven Phillips; and

family counselor Sandy Berenbaum.

Lyme disease specialist and author Richard Horowitz, MD,

the keynote speaker, talked about his book "Lyme Disease: Why

Can't I Get Better? Moving from Symptoms to Solutions." Other

speakers were New Haven University

Borrelia

researcher Eva Sapi

and Dr. William Cowden, author of the Cowden Protocol. All of

the speeches from the event are available on YouTube.

Lyme Connection collaborated with the Ridgefield Health

Department to develop BLAST, a nationally recognized tick-borne

disease prevention program that is offered free to the public at

health fairs, schools and community events. The program engages

health professionals and trained educators to teach prevention

and early symptom identification. The CT legislature is currently

considering a bill to fund BLAST. It is now funded by private

donations and grants.

Visit the Lyme Connection website at

lymeconnection.org.

Ticked Off Music Fest lights up Los Angeles

The Ticked Off Music Fest made its first foray to the West

Coast, touching down in Los Angeles at the iconic House of Blues

on the Sunset Strip in West Hollywood on March 28. The concert

series is dedicated to the prevention, awareness and cure of Lyme

disease and other tick-borne illnesses.

The Ticked Off Music Fest was founded in 2012 by Gregg Kirk,

who currently lives in the NYC metro area. Kirk is the lead singer/

songwriter for the band The Zen Engines and former publisher of

the Philadelphia/Delaware-based publication Big Shout Magazine.

He has also been dealing with chronic Lyme for almost a decade.

“The fest really picked up momentum in 2014,” said Kirk, “I

contracted Lyme disease almost 10 years ago and spent years

being too sick to play. Once I got better, I decided I'd rather play

music in situations that help people instead of banging my head

against the wall and playing the bar circuit trying to make it big.

I hooked up with Pat DiNizio of the Smithereens who played a

festival in Jacksonville, FL, and have also been working with Les

Stroud from the Survivorman TV series who has played festivals

with me in Florida andMaryland.”The first three festivals were held

in Wilmington, Delaware; Jacksonville, Florida; and Annapolis,

Maryland.

Produced by Gregg Kirk alongside line producer Sandi Bohle,

the Los Angeles fest was the largest one yet — a full six hours

Lyme Connection co-founder Karen Gaudian presents Lyme Disease

Association President Pat Smith with the first Courage in Advocacy

Award at their conference and health fair in May.