What do you want others to know about lupus?
I was diagnosed with Lupus by my PCP in 2011 after 2yrs of skin sores, extreme fatigue, joint pain, and then I began to have seizures, and a mini stroke..to name some of the issues. I am seeing a rheumatologist who is awesome, but I am having to go through the entire diagnostic process again, and it is weighing on me.
Why is lupus a cruel mystery to you?
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