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I posted this last week <a target=_blank class=ftalternatingbarlinklarge href="http://www.cysticfibrosis.com/forums/messageview.cfm?catid=6&threadid=53586&enterthread=y
">http://www.cysticfibrosis.com/...d=53586&enterthread=y
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And afterwards I vented my frustrations with our long wait for...
I want to thank you all for your support during the last year during both of our investigations into whether our daughter had CF.
The hospital for Sick Kids in Toronto just called and gave us the results which were negative.
We had a positive result before and one that we were uncertain of...
We got the collection device "watch" put in place and were sent to sign in on the 4th floor where the CF clinic is, I waited in line and was told to sign in at the GI clinic, they said that they don't sign in sweat test patients but they did anyway.
When we went down to have the "watch"...
I went to my GP today and talked to him about genetic testing and he said to wait and do another sweat test.
Blah, blah, blah <img src="i/expressions/face-icon-small-frown.gif" border="0">
That is booked for the 2nd of March.
The reason we were there was to find out the results from tests Shea...
Hi all, I am grateful to have found this resource and am looking for some direction.
My daughter Shea was a heathy baby until 2 when i stopped nursing her, then came oily, bulky BM's. We had a positive sweat test (78) and then a second test in the 40's.
We were told no CF and sent to a...
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