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This Is Lupus

Lupus Pain/Problem Video Site
Lupus Pain/Problem Video Site Lupus Pain/Problem Video Site
Lupus Pain/Problem Video Site

Lupus affects millions.Individuals whose lives have been greatly affected by lupus describe the suffering caused by disease and offer ways that you can help find a cure. With nearly 300 chapters, branches and support groups in 32 states, the Lupus Foundation of America (LFA) is the nation's leading non-profit voluntary health organization dedicated to finding the causes and cure for lupus. Our mission is to improve the diagnosis and treatment of lupus, support individuals and families affected by the disease, increase awareness of lupus among health professionals and the public, and find the causes and cure. Research, education, and patient services are at the heart of LFA's programs.

Channel: People & Blogs
Uploaded: November 30, 1999 at 12:00 am
Author: LupusFoundation

Length: 07:23
Rating: 4.8314605
Views: 80234

Tags: lupus  debilitating  disease  SLE  Autoimmune  Erythematosus  Women  Health  Gala  Foundation  LFA  LupusFoundation  

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Video Comments

babygirl91580 (November 30, 1999 at 12:00 am)
omg im will add all that suffer to this in my prayers, i just found out a close friend has this, and i knew nothin about it, she has to have a kidney removed, im afraid for her!
penmart127 (November 30, 1999 at 12:00 am)
Both my daughters' have SLE.....My youngest has had to undergo the chemo treatments for her kidneys...My oldest nearly died in August 2009....she has heart damage as a result and both have permanent kidney damage.....
tracywen55 (November 30, 1999 at 12:00 am)
Great video!!! I have lupus too. I made a personal choice and switch my diet to vegan diet to see if it helps. I've only taken Prednisone (60mg/day) for 12 days and my doctor is already tapering it down for me. Just for your information.
Weisenheimer78 (November 30, 1999 at 12:00 am)
I wish you all peace and health, really trully, I hope the little moments bring you joy.
jjacela (November 30, 1999 at 12:00 am)
i was diagnosed with lupus at the age of 7 (luckily). i was in & out of the hospital with complications, such as thrombocytopenia (low platelet count & extreme bleeding). i didnt get to enjoy life until i turned 12 & went into remission... 3 years later i had a flare up and my SLE advanced to lupus nephritis. im 20 now and in college and working on my degree in biochem. i'm losing hair and i have joint pain everyday, but Lupus doesn't have to hold me down. i really do pray for a cure one day!
luisnitro91 (November 30, 1999 at 12:00 am)
I just found out that my wife have lupus, my God I'm all here by my self thinking of this and geting all the info I can gather together with tears on my eyes. Sorry I just had to take this out of my chest a bit please someone help I just found out today.
bbrenda17 (November 30, 1999 at 12:00 am)
I am a 19 yo. I have been diagnosed with a blood mutation, meaning bloodclots. I had DVT and PE and theres a possiblity I also have Lupus. I also have Juvinile Rheumatoid arthritis. I...Im very scared of Lupus. I hope theres a cure because Ive had enough of pain already...
briandaniel39 (November 30, 1999 at 12:00 am)
Hi, my name is J. Daniel Bracamontes and i have LUPUS since like 8 months, i feel happy for a fundation like this, trying to help people with LUPUS, I want to Know more about Lupus coz here in mexico theres not alot of information... Sorry but my english is not hat good...
sandraaaa4 (November 30, 1999 at 12:00 am)
my heart goes out to all lupus patients young and old i was just diagnosed with this disease last april ! i wish you all health love and happiness ALWAYS!!<3
LovelornBabe17 (November 30, 1999 at 12:00 am)
Lupus hair is how your hair looks from affects of the disease.. not a type of hair that shows up that tells u that you have it.

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