On Tuesday we heard many sad testimonies on Lyme disease, the tick born illness, from Mainers affected by the disease. Changes need to be made to allow for prevention, proper diagnosis and adequate treatment options in Maine and beyond. I met Paula, an inspirational advocate who is providing education and support to our community, who shared her story fighting Lyme disease. She is a 5-year Chronic Neurological Lyme Disease survivor. She is the co-founder of Midcoast Lyme Disease Support & Education (MLDSE) which provides much needed support and education to people affected in midcoast Maine and advocates treatment and diagnostic changes at all governmental levels. I fully support this bill, which will help the well-being of Mainers suffering from this awful disease.
Angele Rice & Paula Jackson Jones, local Lyme disease advocates, educators, supporters and very inspirational women. Great work ladies!
Photo credit: http://www.midcoastlymediseasesupport.blogspot.com/
For more information on their mission and Lyme disease in Maine see the links below:
Midcoast Lyme Disease Support and Education
Lyme Disease - Infectious Disease Epidemiology Program - MeCDC; DHHS Maine
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