My View Series #7

I was doing some internet research on what could trigger a lupus flare and came across a magazine called Lupus Now. It had some good articles to help lupies deal with their symptoms and learn to live with lupus. They have a section called "My View" where they have readers respond to a question. In the Summer 2011 issue, they asked, "What would you tell a friend who has just been diagnosed with lupus?" I really liked some of the responses, so I'll share some of them in a series of posts.

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Not a day goes by that something in my body doesn't remind me that I have this "lovely" disease. It's hard because people look at you and think "you look fine." Just smile and try to keep a great sense of humor. IT is what IT is, but it doesn't have to define WHAT or WHO you are!—Amy Bass

- a little lupie -