Emily, if you have anything specific I would be more than happy to answer what I can for you. It makes a differece if there's a little more background that people provide us with (like you did-thank you) and some specific questions. Even if they are about therapy and such. There is a lot of ipersonal and daily activity nformation that is not readily avilable-even on the internet and a lot of us realize that. A lot of the questions most of us get frustrated with are, "what is CF, exactly" because that shows me they have done NO research. Now if they came on the board and were like, "i am doing a project, did some research and understand CF is a genetic disease, how do parents pass that on then (or even, what exactly does the "genetic" part mean-some people really don't know) and what is the probability of a child having CF..." or "I see mention of the therapy vest, what is that, how does that work, would you say that is more/less beneficial than conventional chest PT? How long do you do your chest PT for? Something, anything to show they have done a little bit of research, even if it's on this website and they just want some clairification of things. I remember what it was like to have no clue about Cf so I put myself in their shoes, but I also remember doing my research first. I think that's the point we are trying to make.
Please do feel free to post your questions though, our intentions are not to discourage anybody from seeking knowledge.
Julie (wife to Mark 24 w/CF)
Please do feel free to post your questions though, our intentions are not to discourage anybody from seeking knowledge.
Julie (wife to Mark 24 w/CF)