Victoria Wilcox's LYME NY lyme walk

victoria and sarah are 2 high school seniors who have organized this 1st AWARENESS LYME WALK IN NYC...

THEY NEED YOUR HELP! actually a closeup of your face and a brief paragraph 2" VERTICALLY MAXIMUM so it can be pinned to the back of those WALKING for us!!

all details are here!! to date, they have had only 20 FOLKS SEND THIS INFO, and have working many months on this!

please help them and us out by PARTICIPATING.

DEADLINE IS: MAY 15, 2008

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http://flash.lymenet.org/ubb/ultimatebb.php?ubb=get_topic; f=3;t=019567

THANK YOU ALL for reading and hopefully your participation.

Vic recently was in the hospital again; twice since she started organizing and was in a self-induced COMA to get her lyme symptoms under control; so she is having severe health problems too like us!

she asked me to post this on any LYME groups; so there you go; your invitation to participate!

acc......

sorry, i really don't know or more than likely, have FORGOTTEN due to my severe neuro lyme the answer on that. but if you go to her link above; you could ask her yourself!

i hope you/OTHERS on this board will participate! its so easy to!

Otherwise, I'll call in my personal geek squad, if necessary.

Thanks again!

Connie

connie, fantastic!! try this!

Please feel free to email us at lymesucks2@yahoo.com with any questions, comments or concerns you may have about the walk.

victoria can then give you her home address so it can go SNAIL mail!!

thanks for your willingness to educate others on our lyme disease!!

I am feeling so much better and ready to raise

awareness and bring attention to this disease. It is

truly horrible to suffer from Lyme and his friends,

babs, bartonella, ehrlichia, brucellosis,etc. The most

horrible part of the suffering is not knowing what's

causing the pain and the uninformed doctors who don't

even know to look for Lyme as a possibility. Meanwhile

Lyme and his friends are having a party in our brains

and bodies at our expense. We are stuck cleaning up

the mess! I believe

it is so common that it needs to be a standard 'rule

out' diagnosis. That's my story and I'm sticking to

it!

lymie,

" That's my story and I'm sticking to it!"

i use that expression ALL the time; you must have seen it somewhere!!

wonderful; vic will be so happy to get yours.

do you know of others to participate in her LYME WALK by just submitting 2" long info on themselves and a face photo IF possible!? one of the easiest projects i've ever worked on!

best wishes on your lyme journey!

That's weird they only have 20 or 30 pictures so far.

I wonder what the problem is?????

Keep us posted

Connie