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Personally, not to sound rude to the above poster, we were told to NEVER use humidifiers as they can harbor all kinds of bacterias that will then be emitted into the air. This is what *we* were told and every center and patient has their own ways of doing things -- just not something i'd ever...
Personally, not to sound rude to the above poster, we were told to NEVER use humidifiers as they can harbor all kinds of bacterias that will then be emitted into the air. This is what *we* were told and every center and patient has their own ways of doing things -- just not something i'd ever...
<br>I agree with Bill. My son could have been one of those missed cases had we dismissed the initial concern that he did in fact have 1 common CF causing mutation. We instead did not want to take chances and risk his health so we did the sweat test, which is really a VERY EASY test, and once his...
<br>I agree with Bill. My son could have been one of those missed cases had we dismissed the initial concern that he did in fact have 1 common CF causing mutation. We instead did not want to take chances and risk his health so we did the sweat test, which is really a VERY EASY test, and once his...
<br>I agree with Bill. My son could have been one of those missed cases had we dismissed the initial concern that he did in fact have 1 common CF causing mutation. We instead did not want to take chances and risk his health so we did the sweat test, which is really a VERY EASY test, and once his...
Our son started Pulmozyme when he was 2 months old. It was a preventative treatment and still is. He just turned 1 (today in fact) and has never been sick (other than teething issues). Our clinic will hold off on HTS until he is 2 IF they can. If not they'll start him sooner but would like to...
Our son started Pulmozyme when he was 2 months old. It was a preventative treatment and still is. He just turned 1 (today in fact) and has never been sick (other than teething issues). Our clinic will hold off on HTS until he is 2 IF they can. If not they'll start him sooner but would like to...
Our son started Pulmozyme when he was 2 months old. It was a preventative treatment and still is. He just turned 1 (today in fact) and has never been sick (other than teething issues). Our clinic will hold off on HTS until he is 2 IF they can. If not they'll start him sooner but would like to...
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>violeteyes00</b></i>
I am so upset. I took my son back to the doctor today because he is yet again sick with an upper respritory virus and has been for 5 days with no improvements. I was told basically to let it run its coarse. I was...
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>violeteyes00</b></i>
I am so upset. I took my son back to the doctor today because he is yet again sick with an upper respritory virus and has been for 5 days with no improvements. I was told basically to let it run its coarse. I was...
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>violeteyes00</b></i>
<br />
<br />I am so upset. I took my son back to the doctor today because he is yet again sick with an upper respritory virus and has been for 5 days with no improvements. I was told basically to let it run its...
I believe it varies hospital to hospital (depending on if where you are going is an accredited CF Care Center) on when you get back the results. With my son we got the results the same day. Makes it nice so you don't have further waiting which is super hard.
I'll be thinking and praying for...
I believe it varies hospital to hospital (depending on if where you are going is an accredited CF Care Center) on when you get back the results. With my son we got the results the same day. Makes it nice so you don't have further waiting which is super hard.
I'll be thinking and praying for...
I believe it varies hospital to hospital (depending on if where you are going is an accredited CF Care Center) on when you get back the results. With my son we got the results the same day. Makes it nice so you don't have further waiting which is super hard.
<br />
<br />I'll be thinking and...
Like others have said, there is no correlation between high chloride levels and the severity of the disease. My sons came back at 111 on 11/15 and 112 on 11/17. So far we've had mainly GI issues. We're here if ya need us! <img src="i/expressions/face-icon-small-smile.gif" border="0">
Like others have said, there is no correlation between high chloride levels and the severity of the disease. My sons came back at 111 on 11/15 and 112 on 11/17. So far we've had mainly GI issues. We're here if ya need us! <img src="i/expressions/face-icon-small-smile.gif" border="0">
Like others have said, there is no correlation between high chloride levels and the severity of the disease. My sons came back at 111 on 11/15 and 112 on 11/17. So far we've had mainly GI issues. We're here if ya need us! <img src="i/expressions/face-icon-small-smile.gif" border="0">
I agree with everyone here to get the Genetic Testing done. 30 is fairly borderline but genetic testing will give you a clearer answer. I caution you though -- genetic testing is expensive so i do hope that insurance will cover some of it. If it wasn't for insurance i would've sat down and cried...
I agree with everyone here to get the Genetic Testing done. 30 is fairly borderline but genetic testing will give you a clearer answer. I caution you though -- genetic testing is expensive so i do hope that insurance will cover some of it. If it wasn't for insurance i would've sat down and cried...
I agree with everyone here to get the Genetic Testing done. 30 is fairly borderline but genetic testing will give you a clearer answer. I caution you though -- genetic testing is expensive so i do hope that insurance will cover some of it. If it wasn't for insurance i would've sat down and cried...
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