Cystic Fibrosis Foundation: Sweat Test
Wednesday, February 17th, 2010 at
7:54 pm
CysticFibrosisUSA asked:
The Cystic Fibrosis Foundation created this informational video about the sweat test to inform parents about the procedure.
Tagged with: Cystic Fibrosis Foundation • Parents • Sweat Test
Filed under: Cystic Fibrosis
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No prob about the feeding tube. I got it taken out a few months ago and had surgery two days ago to close up the hole. Yes, I’m in mortal pain but it’ll get better.
He came to my church and my mom introduced me to him and told him I have CF. He talked to them for a little while, they signed some paper work, then he took some pictures of me. I’m on the trailer and everything. Oprah’s dad signed a painting of me and Miranda Lambert too. Good news about the feeding tube, I GOT IT TAKEN OUT! I had surgery a few days ago to close up the hole.
how did you become the poster child?
selenagomezfancj? how did you become the poster child? i have cf too. im 14 and i was diagnosed when i was 8 months years old. im sorry to hear about your feeding tube. i was about to get one, but now im doing better on my weight. please comment back. id love to hear from any of you all.
i really need the support
I have CFRD (cf related diabetes) and am looking for a tablet instead of insulin – do you have any suggestions? I would be very thankfull if you helped me! – I’m 14
When i was born they said i didn’t have cf but then they did another test when i was 2 and it came back positive – i’m 14 and my mum has cf. – sorry to hear about the feeding tube.
i dont have cf but my freind does accutally she was the last one to coment on this video. HI CORENE!!!!!!
I had the test done when I was 2 years old and it came back positive so I have CF too. I’m 13 now and I can’t even lay on my belly because of the feeding tube. How many of you still have it? I got it out for 2 years but they put it back in! Anyway, do yall know that guy that’s breaking bords and getting on the Oprah show. I’m the poster child of the Cf foundation. If you look up Caring Now For Kids With Cf you’ll see me on the trailer.
CF is an inherited genetic disorder, so I’m afraid moldy house or well ventilated palace, if both your parents are carriers of the gene, theres a chance you will be born with it! would help if you got your scientific facts right, before you express your opinions!!
i had this test done last year b/c i was in the hospital with phnemonia so i got the test and it came out positve so i have CF and no the test does not hurt it kinda tickles
i had this test done a couple months ago b/c i have very chronic asthma so they decided to check for cf – i found it a little bit painful but if i moved my fingers alot it didnt hurt that but but there was a kid before me that had it and the poor kid was screaming !
no its doesnt hurt, just scary really.
Does it hurt?? I read an article that said the test was painless?
This is why I am studying genetics.
i have cystic fibros
i had this done when i was 1 1/2 years old.
so i dont remember it…may i ask why this test was so bad???
I have Cystic Fibrosis I just know there will be a cure soon! I am praying and keeping the faith!
me too. i had to do the sweat test, it ******. so u have cf too?
ive had this procedure done
i hated it =[