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Life Without Lupus

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Category: Health, Wellness, Fitness

Type: Public Membership
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Founded: Jan 30, 2007
Location:: New York,
New York - US
Members: 215




Group Leader:
S.L.E. Lupus Foundation

This is the MySpace group for the S.L.E. Lupus Foundation. Our members represent the Voices of Lupus -- the more than 1.5 million Americans affected by this devestating disease. We are spreading awareness and supporting research that will one day realize our dream of a "life without lupus."

Visit www.LupusNY.org - the website of the S.L.E. Lupus Foundation - for the latest information on lupus research, education programming, support services, and more!

With headquarters in New York City and offices in Los Angeles, the S.L.E. Lupus Foundation is one of the nations leading lupus organizations. It provides patient services, education, public awareness, and funding for lupus research.

Founded in 1970, the Foundation helps people with lupus, as well as their families and friends, cope with the anxieties and frustrations that often accompany daily living with a chronic illness. Sharing information and networking among patients and their families further helps dispel myths and provides daily support to those learning to live with lupus. We invite you to take full advantage of our comprehensive resources.

Life Without Lupus (215 Members)
**~Brandi~**


JAMIE


Zondre'e Lupus Awareness


-Dead Memories-


Lissy


The Future Is Not Ours To See


Ms. Durant


Lupus Research Institute



 Forum Post a New Topic   View All Topics » 
 Forum Topic Posts Last Post Topic Starter
blood counts?? 0
07/01/2008 6:41 PM
by: Michelle
07/01/2008 6:41 PM
by: Michelle
motherhood w/ SLE 4
05/31/2008 3:51 PM
by: Penelope
04/06/2008 3:39 PM
by: )PaganFairie(
Session 33 - Insomnia relief - Better Sleep Session (42 min) 0
05/04/2008 4:37 PM
by: Jason Newland - www.jasonnewland.com
05/04/2008 4:37 PM
by: Jason Newland - www.jasonnewland.com
LFA responds to Dr. PHIL! 2
04/06/2008 3:53 PM
by: )PaganFairie(
03/06/2007 7:31 PM
by: Jayne
The answer to the million dollar question: 0
03/30/2008 1:05 PM
by: Linda
03/30/2008 1:05 PM
by: Linda

View All Group Bulletins»   Bulletins

From Subject
Kathy 05/03/2008
09:13 PM
Flare Ups
joe. 03/24/2008
10:17 AM
I am riding in the 5 Boros Bike tour to Raise money 4 Lupus
Karen 09/10/2007
06:14 AM
Information Wanted
ava2203 06/24/2007
09:31 PM
If you have SLE, I would appreciate your help!
APS or Antiphospholipid Antibody Syndrome 06/12/2007
08:32 AM
Antiphospho....what?! Video