S.L.E. Lupus Foundation
LupusNY's Channel
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Life Without Lupus 2011
Night for the Fight 2011
New York Bag Ladies Luncheon April 14, 2011
Lupus Research Institute Comments on BENLYSTA
Get into the Loop, New York!
Lupus LA
Fighting Back Against Lupus
Toni Braxton at Lupus LA's Orange Ball
Life Without Lupus
What's Lupus? (1999)
Lupus LA (2009)
Life with Lupus (Part 3)
Life with Lupus (Part 2)
Life with Lupus (Part 1)
S.L.E. Lupus Foundation Visits the Today Show
Could I Have Lupus?
Lupus LA Orange Ball
Lupus LA: Supporter-created PSA (2009)
Life Without Lupus (2008)
Lupus LA 2008
S.L.E. Lupus Foundation: Life Without Lupus
Lupus Cooperative of New York
Lupus Research Institute
Entra al Circulo
Get into the Loop - LUPUS
SLE Lupus Foundation 2006
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LupusNY
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Profile
 
Name:
S.L.E. Lupus Foundation
Channel Views:
10,923
Total Upload Views:
148,084
Joined:
Dec 1, 2006
Latest Activity:
2 months ago
Subscribers:
312
The YouTube channel for the S.L.E. Lupus Foundation, its West Coast division Lupus LA, and its national partner, the Lupus Research Institute.
Country:
United States
Channel Comments
digitizedgirl (9 months ago)
Greetings from London..great channel! How are you?
sjohn6d (9 months ago)
What is Lupus Cerebristis
jackson1321@comcast.net
funnyrawfood (1 year ago)
Nutrition is the answer to all these problems. Rhumetologists never address this, they just give us pills that make us more toxic....i've had lupus and nephritis for the last 10 years...I managed to get off all of my 8 drugs....without drugs!

thanks,

-Vlad The Raw Comedian
liferegenerator (1 year ago)
:D
lovelife1265 (1 year ago)
This is a good site my mom and a friend has Lupus. I have RA for 8yr now.
Thank You!!!
Ghazivh (2 years 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 years 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 (2 years ago)
It's good to know their are people out there who know what you are going through
theleepchatchannel (3 years ago)
Thanks so much for subscribing!
luckyhayyul (3 years ago)
hey... i'm from malaysia! i'm a boy! i've got lupus since 1993!
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