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Thank you. <img src="i/expressions/face-icon-small-smile.gif" border="0"> i am searching on european forums. But after hospital i will tell you how we are going. <img src="i/expressions/face-icon-small-smile.gif" border="0">
Hi! It is so interesting. Today i had 3 long discussions with our doctor. She told that we have another equipment for sweat tests and thats the reason our results is borderline. I said her if we can do those tests like all the world. She said no we have only this equipment. After that i was...
Hi! It is so interesting. Today i had 3 long discussions with our doctor. She told that we have another equipment for sweat tests and thats the reason our results is borderline. I said her if we can do those tests like all the world. She said no we have only this equipment. After that i was...
I know - from side it can listen like fantastic (that anyone paid attention to their sweat tests but it is true - after negative del 508 everybody became calm) - but please believe me - every word i say is true. I am so bad feeling right now. <img src="i/expressions/face-icon-small-sad.gif"...
I know i am bad mother i was not find information earlyer. I have also son 10 years old. He also had big coughing problems till his 8 years. He also has chronic rhinitis but very, very little. But he had big problems after big coughing problems with his stoma. He had 2 endoscopies - both showed...
I know i am bad mother i was not find information earlyer. I have also son 10 years old. He also had big coughing problems till his 8 years. He also has chronic rhinitis but very, very little. But he had big problems after big coughing problems with his stoma. He had 2 endoscopies - both showed...
And i will go to our only cf doctor and will try she will pay more attention to our situation. <img src="i/expressions/face-icon-small-smile.gif" border="0">
Wow, great! Thank you very much for link. <img src="i/expressions/face-icon-small-smile.gif" border="0"> i would study, try and look what will happen. I have once more question about my daughters stomache (yes, it is rare but she has lying at bad at those moments and saying me "mommy, hurts!")...
Aboveallislove, thank you for your answer! <img src="i/expressions/face-icon-small-smile.gif" border="0"> it is so great i can speak to anyone for my situation (in our county is only 20 cf patients and in our forums anyone does not know anything about this illness). Can you please tell me once...
I am from Latvia - it is near Baltic sea - small country with only less then 2 million population. Well, i guess so i should go to another country because i am reading this information and begin worrying very. I believed our doctors and did not find any more information. I even did not know that...
I am reading this forum (it is so great that i found it!) and read that one user says that cough is good for cf - stopping cough is bad. Is it so really? I am begin worrying more. Can it be?
I am from very small country - we have only one old cf doctore and i can not go to another one. But i am very, very worrying for my daughter! Should i pay attention on her stomache? I know that our family doctore says - it is from her nerves (she has also neurological problems).
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