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There are ways I hate this time of year, because I hear about all these

possibly great fixes available, and invariably some get my hopes up,

unnecessarily.

First, I have to remember that doctors are going to put things as positively

as possible at a conference. They're defending their livelihood, after all,

and on top of that, want to give us hope.

Second, I have to remember that EDS, while an inherited, family syndrome, is

incredible individual. Just because it works for one, or even most, it doesn't

mean it's a guaranteed fix. And most of these techniques have been assessed

and rejected for me -- although that's no reason to reject them out-of-hand,

either.

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