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Hi all,

We all have experienced a sense of confusion and loss that Still's

creates. Also, many here were diagnosed as children back when information and

support was nearly non-existant. One of our group, has a passion for developing

better information to help children cope with such experiences. As a result, a

tri-fold brochure is being designed to help parents navigate Still's Disease.

I would like to ask everyone to support this endeavor. Please communicate

techniques that might help parents communicate with physicians, or things you

feel will aid parents in communicating with thier child about the experiences

they will encounter. I can not think of a group better equipped to voice the

needs of this special segment of our population.

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