Living with LupusThis section is a place to share stories about Living with Lupus Below are entries of those who have already shared their stories. We hope that you find their experiences helpful to your own situation. You may also Help others by sharing your story. To quickly access health information from your website's browser, download Epilepsy I was about 6 or 7 when I was diagnosed. I had a Gran Mal seizure in class. It had been very rough, with at least a one seizure a month. Very often many more. I was very self concious of this. I always thought everyone knew,because some people who I knew about this thought I was odd. This was my cross. I finally accepted this about 16 years ago when I had my last seizure Then 1 1/2 years ago I was diagnosed with Lupus I have to have many test to find out if that was the cause of my seizures I opted against it because I delt with the unknown for all my life. Knowing the reason why wouldn’t change anything. I will be 54. Others may want those tests but it didn’t matter to me. I still take medicine for seizures because of all the years of taking it there could be terrible effects on my body if I stop and it could affect my lupus which is pretty well controled with few problems. As I said other may feel differed,but thats how I feel. Life is pretty good. Comments
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