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This may not be the correct place for this...but I didn't see another forum that would fit, with my very tired eyes. I have a 7 year old son who was diagnosed at 2 weeks old. Recently, he cultured PA for the third time in his life. I'm not sure what changed but this has sparked absolute...

I have recently come across some startling information that was handed down by another paitient of our CF doctor. I don't want to jump to conclusions, so I'd like to research it myself...and see what I find. Does anyone know how to begin this? Would I have good results just googling the dr's...