May 4th National Lyme Awareness Flash Mob Event!

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Twystoflyme
New Member


Date Joined Feb 2013
Total Posts : 3
   Posted 2/1/2013 9:00 PM (GMT -6)   
www.facebook.com/events/219802911488696/


Hi,
I'm new around here. :-)
I'm hoping to spread the word of the mob and gather more Lyme troops across the country. There is a map on the Facebook event page I hopefully linked above. I am working really hard to kick off Lyme Awareness month of May with a good start. We have 17 states so far.

I am doing this all from my bed. I even have a flash mob event planned for my local farmers market (big deal in my small town).
If I am too sick at the time it can happen without me. As I am undergoing iv therapy for neuro Lyme, babesia, bartonella, and erlichia. Took me like many too long to get a diagnosis. Which is why I am so motivated. My husband has it along with our 4 yr old. :(
The CDC and IDSA are letting us down and the LDA and ILADS can only do so much. We have to find our strength and gather all we can and rise up and make our voices heard to protect the future to make doctors be educated about Lyme to educate the general public. I was so clueless before I got sick, like most everyone.
Please join in!
If you would like more info check out the link

Post Edited By Moderator (Traveler) : 2/4/2013 11:15:24 AM (GMT-7)


Traveler
Forum Moderator


Date Joined May 2007
Total Posts : 14752
   Posted 2/4/2013 1:16 PM (GMT -6)   
Hi Twyst!
I just made corrections to the link so that it became the hyperlink you were trying for.

What a great idea!! I'm pretty locked down at home now, taking care of my FIL, but we can sure spread the news to others!!! Thanks! :-)

May I copy and paste your post here into an email to send off to a Local group here?
Treating with Acupuncture, Traditional & Modern Chinese Medicine & Western Herbs. Before tx, I had all but 20 of the symptoms on the "Master Symptom List" for Lyme disease.

"Absence of proof is not proof of absence" - Dr. Edwin Masters, great LLMD & researcher -RIP

Questions about what I've posted or just have questions? Please email me!!! Click on the blue envelope under my screen name

Twystoflyme
New Member


Date Joined Feb 2013
Total Posts : 3
   Posted 2/4/2013 4:16 PM (GMT -6)   
Thank you Traveler!
Share Away! We need the rest of our United States represented on the map! We even have MT, and I was reapetedlytold, "there is no Lyme in MT. So, if its here in MT, it definitely MUST be everywhere!
;)

Traveler
Forum Moderator


Date Joined May 2007
Total Posts : 14752
   Posted 2/4/2013 5:03 PM (GMT -6)   
Thank you so much!! Sharing away!! smilewinkgrin
I'll be watching for the results!
Treating with Acupuncture, Traditional & Modern Chinese Medicine & Western Herbs. Before tx, I had all but 20 of the symptoms on the "Master Symptom List" for Lyme disease.

"Absence of proof is not proof of absence" - Dr. Edwin Masters, great LLMD & researcher -RIP

Questions about what I've posted or just have questions? Please email me!!! Click on the blue envelope under my screen name

samjones
Regular Member


Date Joined Jan 2013
Total Posts : 355
   Posted 2/4/2013 11:56 PM (GMT -6)   
I can't believe there is nothing going on in Ct!! What can I do to get something started??
Undiagnosed lyme, bartonella, anaplasmosis, babs for 25 yrs with a 16 year old that I passed lyme and coninfections to daughter through pregnancy. We both began treatment 1/6/11. Still treating. Daughter will be a success story hopefully in 2013!
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