LymeNet Flash: Under Our Skin in Orlando Nov 20th 7pm

This is topic Under Our Skin in Orlando Nov 20th 7pm in forum General Support at LymeNet Flash.

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Posted by ThatColorGreen (Member # 16016) on :

Hey guys!

For anyone interested, Under Our Skin will be showing @ the University of Central Florida, in Orlando on 11/20 (thursday). Movie starts @ 7pm.

It's FREE!!!

PM me if you want more info. It should also be up on the UOS site

[Smile]

~Green~

[ 07. November 2008, 09:51 AM: Message edited by: ThatColorGreen ]

Posted by Tincup (Member # 5829) on :

GOOD for you!!!

Wish I were there!

Especially this morning! It was down in the 40's. YIKES!

But I am loving it to see so many people raising awareness everywhere.

And especially in Florida, where there is no such thing as Lyme disease!

Thanks Green!

[Big Grin]

Posted by ThatColorGreen (Member # 16016) on :

Thanks tincup!

I'm pretty excited about the whole thing.

I got a room conformation yesterday and I thought i was going to jump out of my skin!

[Big Grin]

~The Green One~
[group hug]

Posted by ThatColorGreen (Member # 16016) on :

^ for anyone in Fl

[Smile]

Posted by 1WearyChick (Member # 17840) on :

Sorry for the ignorance, but is that a movie about lyme?

I am near Orlando, sort of, closer to NewSymrna/DeLand (Stetson University) area

Posted by ThatColorGreen (Member # 16016) on :

Hey wearychick

yes it is.

you can watch the trailer @

www.underourskin.com

Posted by ThatColorGreen (Member # 16016) on :

[woohoo]

Posted by bettyg (Member # 6147) on :

hi green, congrats on getting it scheduled!!

our library chairs were so HARD to sit on; how is your site?

may i suggest you add NOV. 20 in subject line by editing it using pencil to do this.

i'll help you keep this up the last few days prior to remind florida folks!! [group hug]

Posted by bettyg (Member # 6147) on :

here's what i printed also and handed out to EACH attendee to let them know of dr. jones legal expenses and give a plea for donations...

Dr. Burrascano's most recent "Diagnostic Hints and Treatment Guidelines for Lyme and Other Tick Borne Illnesses" @ http://www.ilads.org/burrascano_0905.html
suggests that you discuss with your doctor continuing treatment until you are symptom free for 2 months.

this link, making the most of your LLMD visit, may help you also
http://flash.lymenet.org/scripts/ultimatebb.cgi?ubb=get_topic&f=1&t=020605#000005

please see BettyG's newbie package info on the link below; click on link at bottom of my package. Check it out as time permits for you! 149 pages of good info !!
@ http://tinyurl.com/58eyou
IGENEX ``Lyme diagnostic'' lab, Calif., 1.800.832.3200; www.igenex.com and ALL 15 protein bands are shown on lab results!! CALL THEM FOR CURRENT $$.

If you would like to send a letter of SUPPORT or thank you to Dr. Jones, please send to: Dr. Charles Ray Jones
111 Park St., 1st floor
New Haven, CT 06511
HOW TO DONATE TO KIDS LLMD DR. JONES LEGAL DEFENSE FUND:

Make Donations payable to: " Pullman & Comley
Trust Account-for Dr. Charles Jones"
Mail to:
Elliott Pollack
c/o Pullman & Comley, LLC
90 State House Square
Hartford, CT 06103-3702

Note "gift" in the memo field
http://www.youtube.com/watch?v=MNGnsAgKT8s

Posted by ThatColorGreen (Member # 16016) on :

thanks bettyg

[Smile]

~Green~

Posted by ThatColorGreen (Member # 16016) on :

^

Posted by tdtid (Member # 10276) on :

I hope you are able to get a good turn out.

One of the main "characters", Mandy Hughes was from Orlando, Florida. Wonder if that will help get the message across for those that will say there is no lyme in Florida as they say for ALL states these days.

Is this something that can be put in your Orlando paper?

Cathy