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Does anyone else have Lupus and, if so, how do you cope?A year ago my Dr. told me I had Lupus, I was shocked. I wasn't even sure what it was. I already had Hepatitis C, which I got while in the Army after getting a blood transfusion, so I felt like, Great what else can happen, lol. Then I found out what else could happen and I had Heart Failure, this happened 6 or 7 times in one month so I was in the hospital for a month. They told me that Lupus attacks your heart among other things. I had fluid built up in my lungs and around my heart. They finally came up with a new drug, new for me anyway, that is used for blood pressure, and as a diuretic, so the water went away, and so far has stayed away. I was so sick this last 6 months that I lost almost 100 lbs. I definitely needed it, lol. Now my problem is that my skin hands down under my arms and a bit on my face. Does anyone know if that will go away or do I have to have surgery? I can't afford surgery anyway since I am now disabled and unable to work. So, my art, painting and now scrapbooking have been what really helps me feel better. I can stay busy and ignore the pain and sickness because I get so involved in the art that I forget everyting and time just flys by. Is anyone else disabled? I am single and wonder how people can afford to live on disability, because it is just next to nothing. So, if anyone has any ideas on making money while disabled I would love to hear from you. Ciao! Linda
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