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Hi Emma You have to do what is comfortable for you on the day. Only exercise at a level that you could still just hold a conversation at. What you can do will vary from day to day. Generally I do 20 minutes on the treadmill after warming up. As the minutes go by on the treadmill I increase the...

Hi Jenny I am really glad its helping, It has really helped me in the last 8 months. In March I had a pneumonia in one lung, Very serious. Sats down to late 70's. Everyone was very worried. After 6 weeks in Hospital I came out feeling OK but finding it very hard to breath, had to be on Oxygen...

Hi All I too have felt this way. I have gone through many tests. I was sure it was diabetes but the test (I have had many) always proved negative. I am told that Diabetes is quite hard to spot in CF as it has its own type, and the standard blood test doesn't necessarily pick it up. The type of...

Hi All Over the years I have heard of much research about whether carriers of the CF mutation can exhibit symptoms of CF. There does seem to be connections to parents and thier own health problems and CF. But as far as I know none of the studies have proved a positive link. It does make sense...

Hi Emma Thanks for the correction. It is www.model-technology.co.uk. Can you believe that I got this wrong!!!!! I blame the keyboard of course.......... I will reply to you on your email about the job so to speak. Eileen, Thanks for your reply too. It really nice to speak to people on the...

Hi everyone Jon Here again Well its really nice to see all the replies from all over the World, we truly live in a global community. Its amazing to see that CF touches so many peoples life's from so many different places. What do we all think of the quality of treatment you receive in your...

Hi Emma Nice to hear from you. Do you use the UK CF Trust forum? If not find it at http://www.cftrust.org.uk. Infact does anyone from this Forum use this other forum. Are most users of this site from America? Regards Jon

Hi My name is Jon I have just joined the forum, and I am from the UK. I was wondering from how many different parts of the World people with CF contribute to this Forum?