November 8, 2012
It's incredibly reassuring to have this organization which provides information on DES issues of all sorts, and advocacy in many arenas for research and actions that improve our lives and health. And day to day, I feel connected to a community of real people who are going through DES-caused medical and emotional issues just like me. I don't feel bewildered, isolated and alone with my own medical problems and questions as I did in earlier years before I had DES Action and its email listserve. Would that every person with a rare medical condition had a group like this! Thanks to all who work to make it so good.
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