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One thing I think it that there will be advances in the dx process. And, more mutations and more knowledge about what mutations are linked to which symptoms. And finally, there will be a larger, better body of knowledge about "atypical" CF.

One thing I think it that there will be advances in the dx process. And, more mutations and more knowledge about what mutations are linked to which symptoms. And finally, there will be a larger, better body of knowledge about "atypical" CF.

One thing I think it that there will be advances in the dx process. And, more mutations and more knowledge about what mutations are linked to which symptoms. And finally, there will be a larger, better body of knowledge about "atypical" CF.

An article sent through Johns Hopkins parent's email --<br><br><a target="_blank" title="" href="http://www.telegraph.co.uk/health/healthnews/8589765/Dishwashers-harbour-killer-bugs.html">http://www.telegraph.co.uk/health/healthnews/8589765/Dishwashers-harbour-killer-bugs.html</a><br>

An article sent through Johns Hopkins parent's email --<br><br><a target="_blank" title="" href="http://www.telegraph.co.uk/health/healthnews/8589765/Dishwashers-harbour-killer-bugs.html">http://www.telegraph.co.uk/health/healthnews/8589765/Dishwashers-harbour-killer-bugs.html</a><br>

An article sent through Johns Hopkins parent's email --<br><br><a target="_blank" title="" href="http://www.telegraph.co.uk/health/healthnews/8589765/Dishwashers-harbour-killer-bugs.html">http://www.telegraph.co.uk/health/healthnews/8589765/Dishwashers-harbour-killer-bugs.html</a><br>

My son went through quite a lengthy dx process--started with persistent diarrhea--8-10x a day. This did not begin until he was 13. Every inch of his digestive system was scanned and biopsied. He became too weak to go to school for several months. I finally persuaded his doc to order CF full...

My son went through quite a lengthy dx process--started with persistent diarrhea--8-10x a day. This did not begin until he was 13. Every inch of his digestive system was scanned and biopsied. He became too weak to go to school for several months. I finally persuaded his doc to order CF full...

My son went through quite a lengthy dx process--started with persistent diarrhea--8-10x a day. This did not begin until he was 13. Every inch of his digestive system was scanned and biopsied. He became too weak to go to school for several months. I finally persuaded his doc to order CF full...

My son had normal fecal elastase and was still dx with pancreatic insufficiency. He has gained 15 lbs since starting enzymes. His fecal fat was high.

My son had normal fecal elastase and was still dx with pancreatic insufficiency. He has gained 15 lbs since starting enzymes. His fecal fat was high.

My son had normal fecal elastase and was still dx with pancreatic insufficiency. He has gained 15 lbs since starting enzymes. His fecal fat was high.

Dear moms/grandmas of children with CF, Everyday, you are an inspiration to me.  Motherhood is a unique journey.  For moms of children with CF, that journey is even more unique and special.  Your strength is admirable.  Your dedication to your child/ren is awe-inspiring.  YOur tireless advocacy...

Dear moms/grandmas of children with CF, Everyday, you are an inspiration to me. Motherhood is a unique journey. For moms of children with CF, that journey is even more unique and special. Your strength is admirable. Your dedication to your child/ren is awe-inspiring. YOur tireless advocacy is...

<p>Dear moms/grandmas of children with CF, <p>Everyday, you are an inspiration to me. Motherhood is a unique journey. For moms of children with CF, that journey is even more unique and special. Your strength is admirable. Your dedication to your child/ren is awe-inspiring. YOur tireless advocacy...

Hi--We went through a very similar process. Two borderline sweats in Feb. 2010 and got a definitive dx in Feb. 2011. DS does have two mutations but we were told by one CF clinic that they were "benign" --meaning they were asymptomatic. But--we started down this whole path because he was...

Hi--We went through a very similar process. Two borderline sweats in Feb. 2010 and got a definitive dx in Feb. 2011. DS does have two mutations but we were told by one CF clinic that they were "benign" --meaning they were asymptomatic. But--we started down this whole path because he was...

Hi--We went through a very similar process. Two borderline sweats in Feb. 2010 and got a definitive dx in Feb. 2011. DS does have two mutations but we were told by one CF clinic that they were "benign" --meaning they were asymptomatic. But--we started down this whole path because he was...

DS, 15 years old, 6'1" 142 lbs up from 122 a year ago

DS, 15 years old, 6'1" 142 lbs up from 122 a year ago