I just tweeted it. Maybe that will help too!
Posted by jlf2012 (Member # 36002) on :
I posted it on my FB page. Shouldn't we all consider sharing/posting in order to help spread awareness?
Posted by droid1226 (Member # 34930) on :
I added story on the page, tweeted it. We can't complain about the IDSA, CDC, insurance, or Dr.s if we aren't vocal when opportunities like this arise.
Posted by feelfit (Member # 12770) on :
Infirm? Home-Bound? You can still have a voice. Pls. take the time to make yours count.
Posted by jlf2012 (Member # 36002) on :
Why are so many people afraid to be vocal about lyme disease? Is it because we think we'll be looked upon as contagious? Or is it just because many of us are too sick to care? Maybe it's because the disease is so confusing. I wish everyone on this site would share this information no matter how controversial lyme disease is. The word needs to get out there to the public. If we all share this it will help so much.
Posted by map1131 (Member # 2022) on :
Thurs night at our support meeting a new member told us she had been to see ID doctor on Wed.
She had documentation and positive tests results from filria (sp) and mongellons.
This ID ripped her up oneside and down the other. He actually said "I bet you are part of that cult of lime green t-shirt wearing group."
I guess the ID society of Louisville has become very aware of our large growing group of Lyme supporters.
I'm thrilled they know of our existence and our threat to lies.
Pam
Posted by Robin123 (Member # 9197) on :
I'd say, excuse me, the word is not cult - it's culture. We are part of a culture that wears Lyme green T-shirts...
Whatever they say, listen, then respond with the truth.
More T-shirts! Design more lime green T-shirts and wear them visibly.
So how do we keep this top google spot search going? Just by posting the link on our social networks?
Posted by jlf2012 (Member # 36002) on :
Yes, click on the link and then you can share it on Twitter or FB.