25 thoughts on “2014 Worldwide Lyme Disease Awareness Protest Locations Map”

  1. Iceland
    Hef verið að huga að stað til að vera á til að mynna á okkur Lyme Disease sjúklinganna og Boreliabakteríuna og hættuna sem því fylgir. Hef verið að spá í Velferðarráðuneytið Hafnarhúsinu við Tryggvagötu Reykjavík. Föstudaginn 23 maí kl.13.00 -15.00

  2. Guðjón Egilsson
    Hef verið að huga að stað til að vera á til að mynna á okkur Lyme Disease sjúklinganna og Boreliabakteríuna og hættuna sem því fylgir. Hef verið að spá í Velferðarráðuneytið Hafnarhúsinu við Tryggvagötu Reykjavík. Föstudaginn 23 maí kl.13.00 -15.00

  3. Hi all! My name is Steve and 4 years ago I started the Loudoun Lyme 5K. This year it will be held on May 18, 2014 in Ashburn, VA. Please help spread the word!! Our website is http://www.loudounlyme.org or you can “Like” us on facebook- Loudoun Lyme Group.

    Thanks!

  4. Hi I am from North Carolina and as we all know there is no Lyme disease here because ticks know how to read and always carry a map with then wherever they go- So they never cross state lines. RIDICULOUS!!!! I contracted LYME for sure I know in the late 90’s but was biten several times after that with CFS- memory loss- sugar problems- headaches ect.. Was told to see a psychiatrist, that it was all in my head- that they couldn’t find anything- was told by one doc whom I told I couldn’t sweat that if I’d give him all my files he’d go over them and call me back- He never did and when I called for a copy of them – was told they had been shredded. Was finally diagnosed in 2012 by my hero the LLMD. Started treatment and starting to get some of my life back.. Looking forward to the day when the world finally wakes up and realizes that ticks are everywhere because contrary to the load of bull told to them by the CDC, ticks cant read.

    1. Hi,
      I live in NC also and recently found out I have lyme from a pos Igenex test. I’m in Charlotte and would like to find others locally or a support group. Any suggestions?

      Thank you,
      Angela

  5. Hi, I am from Burnaby, BC, Canada and contacted Lyme in 2004. Despite it being a text book case, it was misdiagnosed as some strange reaction to a spider/bug bite and thus treatment was never given. As a nurse we were not taught about Lyme Disease and by June 2007 I had to go off on sick leave. Now it has been confirmed I have third stage Lyme Disease but am being denied treatment here in Canada. It’s the Aides controversy all over again, this time its Lyme Disease, from a simple bite from a tick, that can be as small as a poppy seed. College of Physicians and Surgeons in Canada, hear our cry and wake up and do something about treating those who are suffering from this severe systemic infection!!!

    1. @Susan Owen please contact Dr. Murakami, a BC native and doctor who treated Lyme he’s basically become an activist for it teaching and helping people learn and connect with those who need treatment – please contact him!

  6. Hi! I’m italian and also in Italy there’s a protest for Lyme Awareness.
    We have a Facebook page:
    Worldwide Lyme Protest Italy.
    Thank you
    Franca

    1. Buon Giorno Franco!

      Can you give the URL address for your protest in Italy? I live in the U.S. but my family is from Modena and I would love to pass this along to them! Thank you! You can email me at: alxkwriter@yahoo.com

      Ciao,
      Shantiann

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