Well, at least this article includes included a speaker from Lyme Action Network and an ILADS trained doctor. But how in the world is the health depart going to take steps to "get ahead of Lyme disease?"
I wonder who the organizers are in bed with--since the government/Heath department is involved, I question if they are in bed with IDSA and are using the doctor trained in ILADS and Lyme Action Network to make it appear as if both "camps" are represented.
Along with the aforementioned paragraph, the article discusses a bill passed by the Senate which " . . . would require a state commission to submit a report on the impact of providing insurance coverage for Lyme and other tick-borne related diseases by May 1, 2017 . . . ".
So the cost of insurance provided to Lyme patients seems to be more of a concern than the cost of Lyme sufferers economically, physically, emotionally, etc.
Anyone know more about things mentioned in this article?
-------------------- Just sharing my experiences, opinions, and what I've read and learned. Not medical advice. Posts: 1431 | From USA | Registered: Mar 2015
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