Central Mass Lyme Foundation is a 501c3 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 Mom, Jeanne Cloutier, who passed away on February 9, 2013 as a result of late-stage Lyme disease. Michele and Ken witnessed first-hand the devastating effects of the disease and their foundation was created to help raise awareness, educate, and provide advocacy so that the general public can be empowered to take back their health.
The Central Mass Lyme Foundation holds monthly meetings, except in December, during which they provide Lyme disease support to any and all who attend. Their mission statement is as follows.
With regard to Lyme and tick-borne diseases, the Central Mass Lyme Foundation will:
Raise awareness through advocacy and education, and provide resources and guidance that empower and help improve the quality of life of those that are suffering.
For more information, visit www.CentralMassLyme.org.
Central Mass Lyme Foundation
We make every effort to ensure the accuracy of this information. However, you should always call ahead to confirm dates, times, location, and other information.