Dont know what to believe.

ALivingMiracle

New member
When i was two years old, i was diagnosed with CF by Doctor Stewart Adair, And after that i was diagnosed again, by Dr. Green. I am 16 years old, and was just hospitalised for a week, with pnamonia and fluid on my lungs. But now all of a sudden they are saying that i do not have CF. But when i was two, everything was there. I have all the inner cimptoms but none of the outer apperiane, except that i am pale and very small. I do not have clubbed fingers, but my skin does taste like salt. Im so confused and hurt. I have put up with the teasing because of the way i had to take meds at school. I have been harrassed for missing too much school, and gone through very tough times, for a doctor to tell me that i do not have this illness. 18 years ago my brother Adam passed away, we were told it was CF. But if i dont have it, then maybe he didnt have it, and im starting to wonder, if he didnt pass of CF, what did he pass of? Im so confused, i dont know who to believe, the first doctors or this one. The first doctors did all the tests, and it came back positive that i have CF, and now these new doctors did the same tests and they came back negitive. Im so confused, what should i do? My moms upset, my dads upset, im hurt, i dont know where to turn.

Jacky
16 years old
 

ALivingMiracle

New member
When i was two years old, i was diagnosed with CF by Doctor Stewart Adair, And after that i was diagnosed again, by Dr. Green. I am 16 years old, and was just hospitalised for a week, with pnamonia and fluid on my lungs. But now all of a sudden they are saying that i do not have CF. But when i was two, everything was there. I have all the inner cimptoms but none of the outer apperiane, except that i am pale and very small. I do not have clubbed fingers, but my skin does taste like salt. Im so confused and hurt. I have put up with the teasing because of the way i had to take meds at school. I have been harrassed for missing too much school, and gone through very tough times, for a doctor to tell me that i do not have this illness. 18 years ago my brother Adam passed away, we were told it was CF. But if i dont have it, then maybe he didnt have it, and im starting to wonder, if he didnt pass of CF, what did he pass of? Im so confused, i dont know who to believe, the first doctors or this one. The first doctors did all the tests, and it came back positive that i have CF, and now these new doctors did the same tests and they came back negitive. Im so confused, what should i do? My moms upset, my dads upset, im hurt, i dont know where to turn.

Jacky
16 years old
 

thelizardqueen

New member
I was diagnosed at 6 weeks of age, and then 10 years later the docs didn't think I had CF because I didn't look like a CF person, my lung fucntions were perfect, etc. They did another sweat test on me, and I did have CF. Get your doc to do a sweat test on you. That is how you will find out for sure. If two docs diagnosed you as CF, and one didn't - you would think majority wins. Just because you don't show "outward" signs, does not mean you do not have CF. I do not have clubbed fingers either, I don't cough at all when I'm not sick etc. You could very easily have very mild form of it. Do you take enzymes to digest your food?
 

thelizardqueen

New member
I was diagnosed at 6 weeks of age, and then 10 years later the docs didn't think I had CF because I didn't look like a CF person, my lung fucntions were perfect, etc. They did another sweat test on me, and I did have CF. Get your doc to do a sweat test on you. That is how you will find out for sure. If two docs diagnosed you as CF, and one didn't - you would think majority wins. Just because you don't show "outward" signs, does not mean you do not have CF. I do not have clubbed fingers either, I don't cough at all when I'm not sick etc. You could very easily have very mild form of it. Do you take enzymes to digest your food?
 

anonymous

New member
hi
i'm doing a school project on cf becasue i had an uncle who had it and i am now a carrier. i was wondering if there was anything that you want kids to know about cf?
and i hope that you feel better!!!<img src="i/expressions/heart.gif" border="0">
 

anonymous

New member
hi
i'm doing a school project on cf becasue i had an uncle who had it and i am now a carrier. i was wondering if there was anything that you want kids to know about cf?
and i hope that you feel better!!!<img src="i/expressions/heart.gif" border="0">
 

ALivingMiracle

New member
Thankyou all. I have had the sweat tests done. When i was two they did a sweat test, thats how they determined that i had it. But now all of a sudden those tests are coming back negitive. I take, enzymes, nebulizers, the vest, albuteral inhalors. I just dont see how the tests from 14 years ago could be different then ones from now.
 

ALivingMiracle

New member
Thankyou all. I have had the sweat tests done. When i was two they did a sweat test, thats how they determined that i had it. But now all of a sudden those tests are coming back negitive. I take, enzymes, nebulizers, the vest, albuteral inhalors. I just dont see how the tests from 14 years ago could be different then ones from now.
 

Emily65Roses

New member
Let me give you a piece of information that I've heard here before:
You CAN get a false <b>negative</b> for CF.
You CANNOT get a false <b>positive</b> for CF.

In other words, if you've had a positive sweat test, just because it's false now doesn't mean anything. If you had a positive CF sweat test done as a child, you are indeed a CFer regardless of how you look or how your health is. A lot of us look and act pretty healthy a lot longer than docs think we will. They just don't know any better. Are you going to a CF center, or just some doctor? If you're not going to an accredited CF center, I suggest you find one, because they'll be a lot more knowledgable than your current doc seems. You can find a CF center near you with this link:
<a target=new class=ftalternatingbarlinklarge href="http://www.cff.org/chapters_and_care_centers/">http://www.cff.org/chapters_and_care_centers/</a>
 

Emily65Roses

New member
Let me give you a piece of information that I've heard here before:
You CAN get a false <b>negative</b> for CF.
You CANNOT get a false <b>positive</b> for CF.

In other words, if you've had a positive sweat test, just because it's false now doesn't mean anything. If you had a positive CF sweat test done as a child, you are indeed a CFer regardless of how you look or how your health is. A lot of us look and act pretty healthy a lot longer than docs think we will. They just don't know any better. Are you going to a CF center, or just some doctor? If you're not going to an accredited CF center, I suggest you find one, because they'll be a lot more knowledgable than your current doc seems. You can find a CF center near you with this link:
<a target=new class=ftalternatingbarlinklarge href="http://www.cff.org/chapters_and_care_centers/">http://www.cff.org/chapters_and_care_centers/</a>
 

thelizardqueen

New member
Like I said - 2 doctors diagnosed you as CF, one did not. I'd go with the first two. You can't possibly get two positives, and then suddenly have CF dissapear and have a negative test. I would imagine because you've had CF this long, that you would be going to a CF specialist right? If not, you should be getting yourself one. Doctors who do not deal with CF on a regular consistant basis cannot do for you, what a specialist can.
 

thelizardqueen

New member
Like I said - 2 doctors diagnosed you as CF, one did not. I'd go with the first two. You can't possibly get two positives, and then suddenly have CF dissapear and have a negative test. I would imagine because you've had CF this long, that you would be going to a CF specialist right? If not, you should be getting yourself one. Doctors who do not deal with CF on a regular consistant basis cannot do for you, what a specialist can.
 
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