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Post by lymeangel on Jun 12, 2006 10:31:55 GMT -5
There is a new web site for Lyme Patient Stories. It is located at: www.lymeleague.com. It is called the Lyme League of America. We currently have over 200 members, all lyme patients and nearly half as many stories, from 36 states and Canada. Please post your name and/or personal story today. Legislators are READING THESE STORIES!Don't think you can't make a difference---you CAN! I met with my representative Tom Petri for 15 minutes, gave him my Lyme story and a packet of info. And now he is the only Rep. from Wisconsin currently co-sponsoring the ALERT ACT Lyme bills!!! Talk to your Senators and Representatives, they do listen. And post your story to this web site. Together we CAN make a difference. PJ Langhoff, author and founder
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Post by earlene on Jul 1, 2006 0:35:52 GMT -5
So many people don't know what is going on. I didn't know I had it untill 3 weeks ago. It is horrendous!!!
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Post by ANTHILL on Jul 1, 2006 1:42:24 GMT -5
So many people don't know what is going on. I didn't know I had it untill 3 weeks ago. It is horrendous!!! Welcome to lymebusters earlene it sure is horrendous
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