Bronchiectasis
Posted , 20 users are following.
Hey..I have bronchiectasis and live in the UK..is there anyone else on here who lives in UK as I have never spoke to anyone about it before..
3 likes, 54 replies
Posted , 20 users are following.
Hey..I have bronchiectasis and live in the UK..is there anyone else on here who lives in UK as I have never spoke to anyone about it before..
3 likes, 54 replies
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fantasticjudyan sarah20056
Posted
I was diagnosed as “mild” just before Christmas following a dry cough for 8 months.
I am quite new here so you will get more information and questions answered by others.
But if I can help at all , I will.... just post.
Good luck
Julesb47 sarah20056
Posted
Hi Sarah
I’m in the Uk Warwickshire, had BX now for about 5 years.
It’s rubbish I won’t lie... the fatigue from my point of view is by far the worst because I’m often dragging myself around, but the coughing when it starts causes all sorts of issues in its self, I’m at the moment recovering from a chest infection that I had over Christmas and new year which has resulted in me displacing a rib which had caused me awful problems with pain in my neck shoulder and arm!!
Take each day as it comes is my motto 😁
Good luck xx
sarah20056 Julesb47
Posted
Hi
I was born and grew up in Warwickshire. If u read my other post in the discussion it gives u a bit more of my history with bronchiectasis. It's so frustrating that for the most time I don't know I have the disease and can lead a normal active life...work..travel..run etc and then I end up in hospital on IV antibiotics and now very breathless..hoping to get back to normal before long.
sally38016 Julesb47
Posted
After a spell in hospital with chest infection and partially collapsed lung. Ive had 5 chest infections since October and had 5 different types of antibiotics and was getting nowhere and after numerous trips to my doctor and after loosing 6 stone i asked for to be seen properly. So only last week i seen the chest consultant and he thinks i have bronchiectasis. I have constant cough bringing up lots of phlegm chest pain just feeling horrible and so out of breath. Ive to go for a ct scan to confirm. I come across this site and was looking for any info on this condition. Im just do tired is it going to be like this all the time im half way through another 2 week course of antibiotics andbdont seem to be getting any better. So any info on this condition would be greatly appreciated.
pam81116 sally38016
Posted
Take care Pam
margiesgirl Julesb47
Posted
Hello
just joined the group today , came home from hospital 2 days ago after a 2wk admission on IV antibiotics
a CT scan has shown mild onset bx lord if this is mild :-(
Had an undiagnosed productive cough for a little over 2yrs , it's miserable isn't it, coughing is exhausting,
it makes my head thump, ears hurt, and a whole other myriad of symptoms
Oh and I'm in Southampton (hampshire uk)
sally38016 pam81116
Posted
margiesgirl sally38016
Posted
Hi Sally
I am in a similar situation the infection is just not clearing , I'm waiting for gp to call as I'm not right
I came out of hospital last week but don't feel right at all...I struggle with the breathing exercises that respiratory physio showed me , today I am depressed tearful and very down ....I'm newly diagnosed too
sally38016 pam81116
Posted
sally38016 margiesgirl
Posted
janet24 sarah20056
Posted
I'm in the UK too Sarah...
I was diagnosed last year and have learned a lot on here from others experiences.
irishrob sarah20056
Posted
Hi Sarah I dont live in the UK but Dublin Ireland Which isnt to far
l
I have Bx the last 8 years i am 59 and take various meds Singulair tab seretide inhaler every day I also take azithromycin 25o mg antibiotic every mon wed & fri and my chest doc says i will be on for life
I work as well and try not to get infections, which is hard to do I know quite an amount about this problem
so feel free to ask me
Cheers Rob
margiesgirl irishrob
Posted
Hello Rob
I'm newly diagnosed after a 2wk stay in hospital on IV antibiotics
I was given Azithromycin last March (2017) and ended up in ICU
after experiencing an allergic reaction to it...(Steven-Johnsons Syndrome)
a rare complication to that antibiotic , look it up it may help should you
experience any funny symptoms while taking it
andrew64587 sarah20056
Posted
Sarah, I too live in the UK and have had bronchiectasis for many years. I have devised my own successful treatment regime which is to inhale an unusual essential oil (added to near boiling water) daily, together with my own exercises in the gym and swimming pool. Whenever possible I use a sauna and add olbas oil. I didn't find antibiotics much good; physio exercises from my local hospital department very elementary and difficult to follow regularly.
andrew64587 sarah20056
Posted
I am in the UK like you.