My First Year

This is all so new to me. I have more questions than answers, so my story is short. I know that every Lupus Warrior has separate and different symptoms, but one thing that seems to bind us all together is the low awareness of this disease. No one seems to understand it — my doctor included. I’m learning to live with it slowly, but I need a better support system. I have gone to the Michigan Lupus Foundation support groups, and the people are real and helpful. Without friends and a family that understands, I don’t know what I’d do. For now, I’m trying to listen to my body and discover myself all over again. Prayers please!

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