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To become the voice of a statewide advocacy program that will provide state officials, civic organizations and Connecticut families with educational information. We will communicate the need for a better awareness and understanding of all Lyme Disease symptoms, the absolute necessity for funding in research as to quality/quantitative testing and cure, historical and more accurate collection of current statewide statistics and a clear picture of short term and possible long term effects and personal costs associated with being affected by Lyme disease and other illnesses transmitted by the same ticks.
VALD CT is a non-profit state advocacy organization dedicated to providing State officials, civic organizations and Connecticut families with educational information regarding the need for enhanced awareness and understanding of all Lyme Disease symptoms; the measures needed to prevent Lyme Disease (tick bites); and the necessity for funding of research for more accurate tests to diagnose Lyme Disease. VALD CT also advocates for further research for a cure for Lyme Disease and promotes understanding of the long and short term effects and high personal and monetary cost of this disease.
- Betty Brumberg
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