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Dionis Angelic Warriors Lupus Survivors Foundation hasn't added a story.
Lupus is a awful disease. My daughter Dionis and I (Dorothy) know why it's sometimes called the cry of the wolf when it attacks a person's body as mean as a big gray wolf. Our autoimmune system fights against itself, side affects from the medication are difficult, we are hoping a cure is found soon. We are raising funds to assist the underserved lupus patients and continue to share lupus awareness material. I had no idea what was wrong me? Lupus has really screwed up my lungs, digestive system,and kidneys. I have been on supplemental oxygen around the clock since 2010. I'm in pain all the time my feet hurt so much it's hard to walk. I get weird rashes on my face? I get sudden fevers? my hair fall out? For years I kept my illness to myself because I didn't want pity just a cure. My daughter Dionis began complaining of lupus issues around the age of 5 years old. However, she was not diagnosed until she was 25 years old. Dealing with lupus is difficult anyway I look at it. But to watch my child suffer through the years with this dreadful disease really grieves my heart. I can't ease the torture she is enduring. On top of her illness her grandchild has a autoimmune disease and we pray that life will be much better for her. Since I stopped working I began digging into my family's health history. Shocking as it may seem my mother had rheumatic fever as a child. I'm wondering is this where lupus started in my family!
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