  Hello everyone! So I finally did it and made a Blog. Ladysarajane is impressed. She is warming my feet underneath my computer desk, as I type this. As summer approaches, Ladysarajane and I are getting braced for it. Summer tends to be our worse months for our Lupus. She hates the sunscreen and I hate having to reapply it on her every 5 minutes. For people unfamiliar with Lupus, it is an autoimmune diease, that is made worse by ultraviolet light. That includes sunlight, and fluorescent light. It has a different course in each person that has it. Diagnosis can be difficult. Ladysarajane was lucky, her's was diagnosed by the time she was 5 months. For myself, the doctor believes I had it as a teen and it wasn't diagnosed until I was 32. By that time, the accumulative damage was starting to show.
So 10 yrs later, now that I am on disability, I have decided to write about our journey together, so others can understand how someone that looks healthy may actually be fighting a chronic illness. Hopefully some questions will be answered about the diease as I describe what happens to us day to day. I think that is enough for tonight, I am writing a journal, not a book! 
