Noemi Acosta
Noemi Acosta

IS IMPORTANT TO ME BECAUSE MY DAUGHTER IN LAW HAS IT.I WILL WALK FOR THE FIRST TIME AND WLL KEEP WALKING TILL THEY FIND A CURE GOD BLESS EVERYONE WITH LUPUS NEVER GIVE UP HOPE.

Amanda Davis
Amanda Davis
  • Noemi Acosta

Sweet

Darrell Cortez
Darrell Cortez

I lost my older sister to LUPUS in 2001. I remember the exact time of the onset of her symptoms of fatigue, that attacked her and left her bed-ridden for an entire weekend when I was still in high school in 1983. I have been always willing to make a stance to support the cause in her memory. I've donated to the organization before, but this will be my very first walk for the cause. VERY EXCITED.

Terrie Williams-Hickerson
Terrie Williams-Hickerson
  • Darrell Cortez

It's good people like you make a difference ...Thank you

Donnalynn Hoffman
Donnalynn Hoffman

Living With Lupus Afraid Of Whats To Come Tired Of Being Tired
Not Willing To Take The Meds That Might Make My Hair Thin Or Might Make My Liver Fail
Wondering Why The Pills That Are Supposed To HelP Could Affect My Eye Sight??

Charity Mandona
Charity Mandona

I have been going to the doctors for the past four years.And doctors didn't know what it was.I should be sad coz I was told what I have now.But I am happy coz my disease has a name.It could be bad but I am positive and I will try and do the best I can about it.I am learning a lot about it everyday.The are so many disease in this world.The key to it is taking your time to learn more about and care for your sefe.Right now iam drinking nopalea which is helping me with the inflammation.

Charity Mandona
Charity Mandona

It's important to me coz I do have lupus..

Twanna Autry
Twanna Autry

Living with Lupus presents very challenging at times but I refuse to let it beat me. Join me in support for a cure!

Sharon Spero
Sharon Spero

The cause is dear to me as my family autoimmune disease that has affected almost every member of my family with Lupus affecting three members. One of these is my precious daughter who had symptoms beginning at age 16 and diagnosed with SLE at 17. It is not just a physically devastating disease but the difficulties go way beyond this. It is so difficult because the disease is not physically apparent all the time and people have no idea the suffering it causes. The attitude of many people who...

The cause is dear to me as my family autoimmune disease that has affected almost every member of my family with Lupus affecting three members. One of these is my precious daughter who had symptoms beginning at age 16 and diagnosed with SLE at 17. It is not just a physically devastating disease but the difficulties go way beyond this. It is so difficult because the disease is not physically apparent all the time and people have no idea the suffering it causes. The attitude of many people who operate under the premise that if it is not apparent at the time it does not exist and so making it so difficult for the patient and the family members all to deal with it. So in addition to the physically devastating problems and damage from the disease the inability of friends and family to understand and deal with it make it increaseingly difficult emtionally as well. It is a very lonely disease and my heart goes out to all Lupus patients -it takes a tower of strength to deal with this too. My daughter has fought a major battle with this from the time she should have been enjoying her teen years on up to now. We really need to fight a major battle to bring awareness to more of the public. It has become more so in recent years as more patients have become more public, especially high profile patients but the disease still remains such a mystery and education regarding what we do know and promoting research in every way possible needs to be promoted in every way posssible. Imagine having to deal with the pain, the breathing problems, the joint issues, kidney issues , neurological issues and seeing the blank espressions when you try to explain what is happening because of the mystery and lack of knowledge of the disease. Please, those of you who can walk, please do so and try to recruit so we can began to bring this forward.

Aida Nieves
Aida Nieves

The cause is near and dear to my heart I have lost many freinds to this illness and it seems that it doesnt get better , I was DX in 08 with SLE along with diabees, RA, asnd osteoarthritis. I will walk for the first time this year ..... Awareness

Cheryl Roop
Cheryl Roop

I was diagnosed in 2010. I am just learning my way through the disease and the effects.
Trying to find a "Help Group" in the Eastern Ky area.

Barbara Moore
Barbara Moore

I was diagnosed in 2004.

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