tconz, I see where Tina said they sent someone to have a consultation with the CF department for her, but that was not the case for me. I just got back from there at the end of April. In my case, the plan is talk with the CF dept there on a return trip in a few months if the genetic test comes back confirming the sweat test diagnosis (or at least that was the plan the last time I spoke to my doc). Hope your trip gives you answers and a good treatment plan whether it is tweaking something current or starting over.

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