This is topic If you're going to San Francisco... in forum General Support at LymeNet Flash.


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Posted by Robin123 (Member # 9197) on :
 
...be sure and wear your screen name there...

yes, you can sing the above two lines...

Really, very important, actually - we want to be able to meet each other at the conference, don't we? yes, we do! no more square heads...
 
Posted by LittleLymie19 (Member # 15610) on :
 
I was told that the conference was only for doctors!! We can go too?!

Who is speaking?

I know of a doctor that's holding a "workshop" but it sounded like it was for other doctors.

Is there a site where I can read about what's going to take place?
 
Posted by CaliforniaLyme (Member # 7136) on :
 
I am in charge of name tags and ROBIN you and everyone else who wants your email or online nameon the nametag you are supposed to EMAIL ME
with WHAT YOU WANT ON YOUR NAMETAG!!! (Robin!!!
email me*)!

[email protected]


Hey Peoples*)*!))!!
 
Posted by Robin123 (Member # 9197) on :
 
The conference is open to the public!!

See the following for agendas and sign-up:
www.lymedisease.org
www.lymediseaseassociation.org
www.ILADS.org

I think today may be the last day to sign up for the activist workshop on Thursday.

Yes, ma'am, Sarah, emailing you -- *)!*)!!!**

[ 12. October 2008, 03:25 PM: Message edited by: Robin123 ]
 


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