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Mark - Thanks for the response. I know of one other CFer with the same mutations, and he has CFRD as well.
Tom - That explains it! Thanks so much for the response, that was the missing piece of information I needed <img src="i/expressions/face-icon-small-smile.gif" border="0">
Mark - Thanks for the response. I know of one other CFer with the same mutations, and he has CFRD as well.
Tom - That explains it! Thanks so much for the response, that was the missing piece of information I needed <img src="i/expressions/face-icon-small-smile.gif" border="0">
I was diagnosed with CFRD in September, and I have gone through and read all the previous threads. It's some where between entertaining and frustrating that we all seem to be told different things about it. I do have a question though.
My dietician (who works at both my CF center, and my endo...
I was diagnosed with CFRD in September, and I have gone through and read all the previous threads. It's some where between entertaining and frustrating that we all seem to be told different things about it. I do have a question though.
My dietician (who works at both my CF center, and my endo...
I can relate. I have lows more than highs, and I have to eat ALL the time, but at the same time food makes it worse because it sends me into cycles of spiking (200) and then dropping really fast (40). I was put on 1/2 unit of novolog with my biggest meal of the day, but even that was too much...
I can relate. I have lows more than highs, and I have to eat ALL the time, but at the same time food makes it worse because it sends me into cycles of spiking (200) and then dropping really fast (40). I was put on 1/2 unit of novolog with my biggest meal of the day, but even that was too much...
I just got diagnosed in Sept. My numbers are still low, my 2 hour oral glucose test still comes back normal, and my a1c is 5.5-6.0. My highest blood glucose ever was 300.
I usually run low and have more problems with my lows than highs. They tried to put me on fast acting insulin at first, but...
I just got diagnosed in Sept. My numbers are still low, my 2 hour oral glucose test still comes back normal, and my a1c is 5.5-6.0. My highest blood glucose ever was 300.
I usually run low and have more problems with my lows than highs. They tried to put me on fast acting insulin at first, but...
My first port went bad after a year, there was no pain, it just simply wouldn't flush anymore so they gave me the one I have now. I do all kinds of exercise with it, even when it is accessed. The only pain I get from it is the tegaderm irritating my skin when it is accessed for IVs. I access it...
My first port went bad after a year, there was no pain, it just simply wouldn't flush anymore so they gave me the one I have now. I do all kinds of exercise with it, even when it is accessed. The only pain I get from it is the tegaderm irritating my skin when it is accessed for IVs. I access it...
My first port went bad after a year, there was no pain, it just simply wouldn't flush anymore so they gave me the one I have now. I do all kinds of exercise with it, even when it is accessed. The only pain I get from it is the tegaderm irritating my skin when it is accessed for IVs. I access it...
I really don't want to live alone, but I live out of state from family, so I am hoping my parents will come down for a few months, and then maybe friends so that I avoid being alone for more than a few weeks. This could be a whole seperate thread, it worries me so much.
I really don't want to live alone, but I live out of state from family, soI am hoping my parents will come down for a few months, and then maybe friends so that I avoid being alone for more than a few weeks. This could be a whole seperate thread, it worries me so much.
<BR>I really don't want to live alone, but I live out of state from family, soI am hoping my parents will come down for a few months, and then maybe friends so that I avoid being alone for more than a few weeks. This could be a whole seperate thread, it worries me so much.
Thanks for all the input! My CF doc has vaguely mentioned it possibly being arthritis, or fibromyalgia. I am starting to feel like I am just being pawned off to the next doc, but I am going to try and get the rheumotology appointment set up soon.
I am sort of the opinion that even if it's not...
Thanks for all the input! My CF doc has vaguely mentioned it possibly being arthritis, or fibromyalgia. I am starting to feel like I am just being pawned off to the next doc, but I am going to try and get the rheumotology appointment set up soon.
I am sort of the opinion that even if it's not...
Thanks for all the input! My CF doc has vaguely mentioned it possibly being arthritis, or fibromyalgia. I am starting to feel like I am just being pawned off to the next doc, but I am going to try and get the rheumotology appointment set up soon.
<br />I am sort of the opinion that even if it's...
Thanks for all the input! My CF doc has vaguely mentioned it possibly being arthritis, or fibromyalgia. I am starting to feel like I am just being pawned off to the next doc, but I am going to try and get the rheumotology appointment set up soon.
I am sort of the opinion that even if it's not...
Thanks for all the input! My CF doc has vaguely mentioned it possibly being arthritis, or fibromyalgia. I am starting to feel like I am just being pawned off to the next doc, but I am going to try and get the rheumotology appointment set up soon.
I am sort of the opinion that even if it's not...
Thanks for all the input! My CF doc has vaguely mentioned it possibly being arthritis, or fibromyalgia. I am starting to feel like I am just being pawned off to the next doc, but I am going to try and get the rheumotology appointment set up soon.
<br />I am sort of the opinion that even if it's...
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