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S.L.E. Lupus Foundation
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LupusNY
Joined: December 01, 2006
Last Sign In: 3 days ago
Subscribers: 113
Channel Views: 4,732

For more than 35 years, the S.L.E. Lupus Foundation has helped people with lupus
and their families, funded lupus research,
and raised awareness of this chronic illness.
City: New York, NY
Country: United States
Website: http://www.LupusNY.org
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Life Without Lupus (2008)
5:50
Visit www.LupusNY.org to learn more about the S.L.E. Lupus Foundation.
7 months ago 2,989 views LupusNY
Lupus LA 2008
4:48
[TRANSLATED] Lupus LA 2008
[TRANSLATED] Lupus LA 2008
Lupus LA, the west coast division of the S.L.E. Lupus Foundation founded by renown...
1 year ago 3,357 views LupusNY
Lupus Research Institute
7:14
The Lupus Research Institute is the only organization exclusively funding novel lu...
2 years ago 12,399 views LupusNY
Channel Comments (8)
Ghazivh (2 days ago)
Todas las debilidades del organismo como; Lupus, esquizofrenie, alzheimer, parkinson, anemias falciforme, cancer tumorales, del osos, piel, son tratables con la regeneracion del las CelulasTronco cual somos hospedeiros, sin embriones, solamente la regeneracion del las CELULAS-TRONCO por Jorge Guedes
MrsSlumdog (2 months ago)
Thank you so much for all your hard work overseas! I live in the Netherlands and people doesn't take me serious at all. Even doctors can be so ignorant! It's often so frustrating and I feel very lonely because people always start to talk about other diseases and almost never let me talk about my lupus....So I feel "comforted" in a way I can "share" things with all these people I do not know at all.....
Love ya all xxx
darklovely98 (4 months ago)
It's good to know their are people out there who know what you are going through
theleepchatchannel (4 months ago)
Thanks so much for subscribing!
luckyhayyul (5 months ago)
hey... i'm from malaysia! i'm a boy! i've got lupus since 1993!
blackmesa2Gfreeman (8 months ago)
what is lupus ?
LALupusLady (1 year ago)
Lupus Research Institutate and the SLE Lupus Foundation are an essential part of a great team working for Lupus patients.




I am so happy that I was able to be a part of the LRI's 2008 Capitol Hill Advocacy Day. (which inspired me to create videos for youtube...)
I hope you enjoy my latest videos from Lupus LA's 2008 Orange Ball. Thank you so much for all of your hard work!

Amanda
LALupusLady
bouchrouge (1 year ago)
Thank You so much!