Guest guest Posted April 30, 2006 Report Share Posted April 30, 2006 Hi everyone, I've been a lurker on this message board for a while now, and I was wondering how many of you out there are the sibling, parent, or child of a person with Achalasia? If so, what has it been like for you? What are some of the things that you do to help out, especially when dreaded surgeries or diagnoses come along? Have any of you had to do this long distance? Thanks! Annie Quote Link to comment Share on other sites More sharing options...
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