Gosh I don't know...have you been CFRD tested? I've always been super-healthy but last year I was sick for MONTHS. I just didn't know why and assumed I had caught everything from people on campus. I was diagnosed with CFRD in May. It's a pain in the butt but I really enjoy the healthy time.
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i'm going to just put this out there...*small update*
- Thread starter krisgabes
- Start date
Gosh I don't know...have you been CFRD tested? I've always been super-healthy but last year I was sick for MONTHS. I just didn't know why and assumed I had caught everything from people on campus. I was diagnosed with CFRD in May. It's a pain in the butt but I really enjoy the healthy time.
Gosh I don't know...have you been CFRD tested? I've always been super-healthy but last year I was sick for MONTHS. I just didn't know why and assumed I had caught everything from people on campus. I was diagnosed with CFRD in May. It's a pain in the butt but I really enjoy the healthy time.
Gosh I don't know...have you been CFRD tested? I've always been super-healthy but last year I was sick for MONTHS. I just didn't know why and assumed I had caught everything from people on campus. I was diagnosed with CFRD in May. It's a pain in the butt but I really enjoy the healthy time.
Gosh I don't know...have you been CFRD tested? I've always been super-healthy but last year I was sick for MONTHS. I just didn't know why and assumed I had caught everything from people on campus. I was diagnosed with CFRD in May. It's a pain in the butt but I really enjoy the healthy time.
This isn't an answer but just a suggestion. I've recently started asking for a copy of EVERY test they do on me. If the results aren't available straight away I ask at my next appointment. When they print out my PFTs, I get them to photocopy it for me, I get a copy of my sputum results each time, etc.
Perhaps this would help in the future so that instead of having to ask and get mixed responses, you have most of it right in front of you as proof <img src="i/expressions/face-icon-small-smile.gif" border="0">
Perhaps this would help in the future so that instead of having to ask and get mixed responses, you have most of it right in front of you as proof <img src="i/expressions/face-icon-small-smile.gif" border="0">
This isn't an answer but just a suggestion. I've recently started asking for a copy of EVERY test they do on me. If the results aren't available straight away I ask at my next appointment. When they print out my PFTs, I get them to photocopy it for me, I get a copy of my sputum results each time, etc.
Perhaps this would help in the future so that instead of having to ask and get mixed responses, you have most of it right in front of you as proof <img src="i/expressions/face-icon-small-smile.gif" border="0">
Perhaps this would help in the future so that instead of having to ask and get mixed responses, you have most of it right in front of you as proof <img src="i/expressions/face-icon-small-smile.gif" border="0">
This isn't an answer but just a suggestion. I've recently started asking for a copy of EVERY test they do on me. If the results aren't available straight away I ask at my next appointment. When they print out my PFTs, I get them to photocopy it for me, I get a copy of my sputum results each time, etc.
Perhaps this would help in the future so that instead of having to ask and get mixed responses, you have most of it right in front of you as proof <img src="i/expressions/face-icon-small-smile.gif" border="0">
Perhaps this would help in the future so that instead of having to ask and get mixed responses, you have most of it right in front of you as proof <img src="i/expressions/face-icon-small-smile.gif" border="0">
This isn't an answer but just a suggestion. I've recently started asking for a copy of EVERY test they do on me. If the results aren't available straight away I ask at my next appointment. When they print out my PFTs, I get them to photocopy it for me, I get a copy of my sputum results each time, etc.
Perhaps this would help in the future so that instead of having to ask and get mixed responses, you have most of it right in front of you as proof <img src="i/expressions/face-icon-small-smile.gif" border="0">
Perhaps this would help in the future so that instead of having to ask and get mixed responses, you have most of it right in front of you as proof <img src="i/expressions/face-icon-small-smile.gif" border="0">
This isn't an answer but just a suggestion. I've recently started asking for a copy of EVERY test they do on me. If the results aren't available straight away I ask at my next appointment. When they print out my PFTs, I get them to photocopy it for me, I get a copy of my sputum results each time, etc.
<br />
<br />Perhaps this would help in the future so that instead of having to ask and get mixed responses, you have most of it right in front of you as proof <img src="i/expressions/face-icon-small-smile.gif" border="0">
<br />
<br />Perhaps this would help in the future so that instead of having to ask and get mixed responses, you have most of it right in front of you as proof <img src="i/expressions/face-icon-small-smile.gif" border="0">
Sheanna, yes I have been diagosed w/ CFRD. I totally forgot to put that up there in the explanation of my situation. Being on insulin has ABSOLUTELY helped me out so much, but unfortunately it hasn't done anything for my pulmonary problems that I've been having.
Wuffles, that is such a great idea, I intend to do that from now on.
Thank you guys for your input!!
Wuffles, that is such a great idea, I intend to do that from now on.
Thank you guys for your input!!
Sheanna, yes I have been diagosed w/ CFRD. I totally forgot to put that up there in the explanation of my situation. Being on insulin has ABSOLUTELY helped me out so much, but unfortunately it hasn't done anything for my pulmonary problems that I've been having.
Wuffles, that is such a great idea, I intend to do that from now on.
Thank you guys for your input!!
Wuffles, that is such a great idea, I intend to do that from now on.
Thank you guys for your input!!
Sheanna, yes I have been diagosed w/ CFRD. I totally forgot to put that up there in the explanation of my situation. Being on insulin has ABSOLUTELY helped me out so much, but unfortunately it hasn't done anything for my pulmonary problems that I've been having.
Wuffles, that is such a great idea, I intend to do that from now on.
Thank you guys for your input!!
Wuffles, that is such a great idea, I intend to do that from now on.
Thank you guys for your input!!
Sheanna, yes I have been diagosed w/ CFRD. I totally forgot to put that up there in the explanation of my situation. Being on insulin has ABSOLUTELY helped me out so much, but unfortunately it hasn't done anything for my pulmonary problems that I've been having.
Wuffles, that is such a great idea, I intend to do that from now on.
Thank you guys for your input!!
Wuffles, that is such a great idea, I intend to do that from now on.
Thank you guys for your input!!
Sheanna, yes I have been diagosed w/ CFRD. I totally forgot to put that up there in the explanation of my situation. Being on insulin has ABSOLUTELY helped me out so much, but unfortunately it hasn't done anything for my pulmonary problems that I've been having.
<br />
<br />Wuffles, that is such a great idea, I intend to do that from now on.
<br />
<br />Thank you guys for your input!!
<br />
<br />Wuffles, that is such a great idea, I intend to do that from now on.
<br />
<br />Thank you guys for your input!!
Theres a very high chance that it's the goo in your sinuses draining into your lungs while you sleep, and causing this cycle of re-infection. It's the main reason they think I have any real CF lung symptoms. Hence my desire to go get surgery soon. Look into the sinus issues.
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