hi i just wanted to introduce myself to the group. I'm 54 and was diagnosed 14 years ago and more recently with bronchiectasis and a giant bullae in each upper lobe of my lungs
i came across the group while looking for information on my own copd and i'm so glad i did. although i haven't posted i have been reading the tips, advice and support you all offer each other even if someone just needs to vent.
thank you
Written by
dmf64
To view profiles and participate in discussions please or .
Hello dmf64 I’m fairly new here too. This forum has been a great help to me with lots of good advice. I don’t post much but do read the comments and advice given. Fab and friendly group of people x
Hi Iris30, I’m exactly the same. It’s such a relief to know others are in the same situation, and that you’re not the only one.Illness is scary sometimes, and more so when you feel isolated.
Welcome. It’s a comfort to be able to ‘talk’ with people on here who understand. I don’t post often, but i read posts and i know there’s always someone who will reply when we have worries. Don’t feel alone.
Hello to you.You will find this a very friendly forum where there are many people living with lung conditions always willing to share their personal experience and offer support. I have copd and large lung bullae myself but not bronchiectasis but others here do.Welcome xx
Hi and welcome to the forum, we tr to share our experiences and what helps us as individuals, we are not medically trained but we know what works for us.
I was told I have clusters of bullae at the time I was working and never understood what they were on about. I had to Google it and even then nearest I got was disappearing lung. If doctors had explained in a more simple way and earlier I might have tried harder to do something. It took a day when I couldn't breath at all to walk and thought I was going to die. I think they should sit people down for a good hour and explain what it really means and what can happen. It was explained to me so quick and casual I just thought well I feel OK. I still need it explained 6 years later. I do know I am disabled now can't do much without being out of breath.
Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.
Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.