Likely to be the first round of information needs. Materials describing, or (more likely), a sign displaying our region would be very valuable, as we are extremely under-represented nationally, and at large events in the Lyme community.
*If you plan to attend, please let me know here or at InvisiblyLymeMontana.com or the Invisibly Lyme Montana Facebook Page.
The more visible we can be, the more we remind our fellow patients, partner groups, and the public that Lyme is everywhere and we are in just as much need of help, and in some ways more, given our isolation from Lyme Literate physicians, organized patient groups, and broader opportunities for informed medical care.
By we, I mean our states, we as patients, and the existing groups related to our geographic areas (where applicable).
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