Hi many of you will have seen my posts on my de mukeing saga whereas just can't seem to lessen it , I have pints of the stuff on a daily basis, when I'm ready to expel it I feel so uncomfortable and quite breathless, last week had an X-ray consultant said didn't appear to be much mucus showing in my lung, when I get that horrid tight feeling in my back and round my midriff I have to get the stuff out but it's so often it's ruling my life and wearing me out, my question is if I didn't expel it would I choke or what would happen , I Darby plan to go anywhere because of it, any advice please x
Stupid question re mucus: Hi many of... - Lung Conditions C...
Stupid question re mucus
I cant answer that sorry but wanted to suggest you going on a pulmonary rehabilitation course if you havnt already been on one...... they talk a lot about mucus and the best way of shifting it im sure you would benefit from the information and the course itself is great
Hi Mandy , thanks for replying yes I've been on one but a couple of years ago, but maybe wouldn't hurt to go again just unbelievable how much there is !!! Thanks xx
Yes ive done it twice and got much more out of it the second time because most of it went over my head the first time round,,,,, plus when you do it again you have more knowledge on the illness and how it affects you so i had a list of questions .
Hi
Some suggestions
there is an opp now that kills the nerve that produces mucus and the same nerve is also responsible for contracting the air ways. there are 4 hospital in London doing it and others over the country. People who have this opp say its like a new life, they can breath again walk again and come off oxe . Worth a talk with your doctor. good luck
@tomhatha Have you got a link to any info?
Hi tom, wow thanks for that I will have a look at your posts to see if I can read up a bit on it but I would certainly be interested in that if it were poss I've tried everything else, I do luv singing but my family don't haha but I think they would rather hear me sing than struggle on , thanks X carol
If I get the time I'll look for that one and send to you regards Tom
Hi tom ' really appreciate your help, I've been trying to get on Twitter for hours it's a site I don't use so I'm struggling to see your posts but I will keep trying , thanks X carol
I tried up till 11 30 last night and I couldn't find it I did send the address to someone on Healthunlocked but can't remember who
sorry, what it is they put the thing down your throat but instead of looking in the stomach they go down into the lung and kill the nerve that makes mucus and also makes the airways narrower regards Tom
I'm off to the Resp nurse this morning to find out how to use my new Accapella device which is for helping to shift mucous. I'll let you know what I think of it later. Perhaps it would help you.
Hi moy, I do have one of those they are good for moving stubborn Muke etc, I need to stop making so much 😞 Xx
Ah! I understand. Mine is worse in the mornings and the daily cry is 'Where on earth is it all coming from?' My poor husband cannot get over the quantity I shift when he helps me with postural drainage. I usually find that the morning 'slap' leaves me reasonably clear until the evening, but when I have and infection it's present all day.
I've got my acapella now so am hoping it might reduce the need for my husband to assist.
I used to be the same until I started using Mucodyne (Carbocisteine 375mg). The Chest consultant prescribed it. It works wonders.
You poor thing I know just how you feel I take carbocisteine do my breathing exercises and it still wears me out trying to shift it when I'm full of mucus my oxygen levels drop right down and then go up when I've coughed myself silly.
Take care carolg1