Mucus at back of thought can't sleep
I now have mucus back of throat difficult to sleep breathless each time I get up
Hot drink and move around a bit...more blue inhaler if needed
Honey n lemon.
I to suffer with bad mucus in throat making me cough all the time. Been prescribed Flixonase and fostair inhalers help a bit but still get it all the time.I keep Potters mucus lozenges with me and they help a lot
It's not too bad does fostair inhaler help I am on fostair 100/6 2 puffs twice a day
Plenty of fluids and moving around if possible. Pete has mucus in his throat most of the time and I encourage him to drink plenty. Xxxx
Lots of warm drinks. Sometimes steam helps me but not too much. xx 🌿
I realise I clearly had this before diagnosis and mobilised worked had head baby cleaned my house. Studied visited parents sister.
Now having diagnosis I feel I am no longer me.
Having a diagnosis of asthma I put my breathless down to that..went on first holiday abroad in 23 years Rome. Walked everywhere..did dementia walk with grand kids daughter not once breathless.
Now struggling to see that person since diagnosis.
I spent most of last night looking at old post of people who have had a diagnosis and the feelings fears have been the same. So that made me feel a little better. Not much though.
Next I looked for any stories where people where able to continue to working...found very few...broke my heart crying.
I do not want to manage my feelings anxiety depression with anti depressants so that's one decision I have made so far.
Feel so so ungrateful because I need to not continue to feel like this.
Having to go off sick has made me feel defeated. The deputy in the job I am leaving also has copd and asthma and she is still working. Was petrified to ask what stsge as this seems to be the important factor.
57 years of age this was the year I was going to experience life. Travel do my degree. Reduce my work hours for 40 to 31.5. Have my grand daughter on days off so son and daughter on law could have more time to selves. Decorate lounge and one wall of my bedroom.
Join a tai chi class. Zumba class.
Non of these seem possible as I hear progressive disease progressive and I can not move past that if honest.
I want advise on how I can stop..slow this disease down.
So hear I sit ungrateful angry at myself because I smoked and dreading a life of breathlessness and being on Oxygen not being able to work....that is so so important to my mental well being.
So desperate to move to move forward because I can't not carry on like this
I want this to be a nightmare but I know it's my reality.
That is how I feel...scared to move in case I become breathless. Looking at my course work and not being able to start it. Please God help me. I had so much of my blue inhaler yesterday it was unreal. Is that going to be my life until it's time for oxygen....no one truly knows.
There just needed to get this off my chest. Thank you in advance for reading this
This condition diagnosis has certainly hit you like a bolt from the blue leaving you in such turmoil you can't sleep function eat and your left reeling with it .
Its easy to let things grind you down and easily so as desperation takes over leaving you with all types of mixed emotions on a daily basis.
It's all new to you and you need to take one day at a time small steps before jumping head long into years down the line.
I was diagnosed stage 3 copd two years ago I was well aware for years I had it but choose to ignore it .
Since my diagnosis I have become a self employed dog walker I can walk up to 12kms a day I exercise I have my grandaughter regularly I go on holiday I go on date nights with my hubby .
So there is light at the end of a tunnel you just need to find yours and start with a day at a time.
Plenty of people work live survive for years without any oxygen . Don't be despondent it will unravel itself in the wash and you will find a way of accepting your health and condition you need to care of you walk a little eat a good diet build yourself up slowly and you will find you will be pushing yourself and wanting more . Don't let it take control of you ...you get control of it ...I'm going to shut up now I'm not preaching at you in any way but fully understand where you are right now
I do not feel lectured at all I am grateful for your response...hopefully when I actually get to grips with my condition I hope to revisit all the support comments made as I am sure they will all make sense.
They will in time and you will realise it's not as bad as you think at the moment take care of you ps I do zumba and tai chi also 😂
I know I do not have a crystal ball ...it's my future I am worried about. Do you find tai chi helps
Absolutely there is a few on you tube worth a browse very gentle stretching ones worth a look lol x
Ok thank you....just which I could get breathing and mental state under control
It helps with that also pursed lip breathing technique will help you calm down if you feel your building up any angst . Sniff the roses blow out the candle find that on you tube I use it a lot when walking and exercising try and enjoy your weekend do you have family support around you xx
My children but donr want to bother them...my husband but he does not understand my fear ...so no not really ....he thinks I will be fine....so does not understand why I am not helping myself
Eldest daughter understand but donr want to bother her
So feel alone
My friend recommended breathing device but don't know
Sat in bedroom all day since respiritory nurse visit
Want to go to daughters tomorrow but scared to go out in the cold and I drive
First port of call YouTube have a chat with your friend and your children explain your fears to them all . It's a long road ahead but chip away slowly and in your time but dont lock yourself away . Xxx
Feel I have done this to myself have no right to be moaning to my kids ....the eldest knows the news had rocked my world she just keeps say well you know what you need to do now mom ....actually I don't...I am so sorry to keep nothing you
We all have to a degree I smoked for years so self blame at this point in time is natural. This time in 3 months when you have worked through how to deal with it you will feel better with yourself. Write a list make goals so by the end of next week you are being more positive about things ... you will get through this in your own mind either way xxx
My goal is to get breathing under some control...get back to work next week Thursday start research for my assignment and do the baking for my grand daughter and daughters birthday gathering next Saturday oh and have a good night's sleep.
Making goals already thats positive ...What assignment are you doing for your work ??
So when you cook and do your assignment focus on making more goals... try the breathing technique when your trying to sleep x
Hi no started open university psychology and counselling degree...what breathing technique
counselling degree is fantastic .
Sniff the roses then blow out the candle pursed lip breathing technique.
Breath in for 4 seconds through your nose hold and blow out through your mouth nice and slow .
If you have another student that you know on the counselling course could you chat to them just a thought x
No becsuse its distant learning. I Trying the smell the roses now..Thank you
Hopefully we progress very very slowly
Try it a few times a day you will soon get used to it and there's examples of it on you tube you can practise along with people demonstrating it for you might be easier than me describing it to you lol xx
They gave me 1 mg of Lorazapam for breathing/panic attacks and my physio told me to look at a square and hold my breath on the shortest part and take short pant breaths on the longest sides of square worth a try it helps me sometimes also put me on 5 ml of liquid oramorph for when my breathing is bad but my hubby hates me taking it xx
Hi my mucus not that bad...does the square thing work...I think I an fearful of my future really am oramorph why oramorph
Oramorph is to settle down your breathing Consultant says they give it on chest wards. Also square excercise works if you haven’t got your self into a deep panic works for me if I catch it at the beginning xx
Ok thank you...when was you diagnosed
I do panic breath I know have you tried potters lozenges
No but will definitely get some to try anything is worth it x
It helps to shift mucus apparently mine just arrived today so trying one..
So do I. Tai chi is great. AndI do zumba and walk a lot. It all helps, but the shock of first diagnosis is awful. You will find a way to do what you want in life still. Good luck.
Thank you just seen this
Hi can I ask have stayed at stage 3 or has it progressed ...I understand if you don't answer
Any suggestions as to what I ask consultant on the 25th have a few questions but not sure what I should be asking...given a few ideas on here just want to be armed with a list
I was diagnosed stage 3 with a lung function of 46 % . I stopped smoking day of diagnosis and my last spirometer check my percentage had increased to 68 % ...So very much still stage 3 it will progress as we get older I'm 60 .
You need to eat a decent diet get yourself referred to a pulmonary rehab class which is really beneficial exercise within your limits stop and rest if you need to .
As for consultants I have never saw one but write a list of question you feel the need to ask and if you get answers it's part of the puzzle sorted for you .
Main thing is don't let it eat you up inside go for walks occupy your mind and just focus on the positive xx
Hi thank you... I gave up smoking 1st December....I was in hospital 1st December unable to breath was so frightened it was accute bronchitis...so so scared of that unable to breath situation...thought I was going to die so was poorly until around 25th Christmas..thought that's it need to look after myself and get this diagnosis....so just feel
Great your lung function increased
But that's you over step one knowing you have to look after yourself and you will in the long run once you have put things in order with your inner self you will make conscious decisions to benefit from them ...
What area will you practise in whrn your degree is final have you thoughts on it as yet x
Not thought I have always want to do the degree told kids at 57 it was to late for me but they encouraged me...I am a learning disabilites nurse love love that field...currently working 2 days a week elderly dementia care ...love the residents but service to big and there is not the time to spend with them...that's what I like doing...so going back to my field ...doing degree as I love to understand people...hoping to do some ..was hoping...to do some voluntary work when qualified
See these are my hopes and dreams
And well done you for taking that challenge . I think you have said your field to practise in without thinking . You could easily counsell families of dementia sufferers your knowledgeable in that field already with the condition and you develop learning curves with the family of the clients your looking after now .
Xxx and there is no reason not to fulfil your hopes and dreams is there?
Only just stated but could be ...and a long term goal...Thank you so much for communicating with me
Your more than welcome anytime lovley lady have a glass of wine later 😍😍
Thank you so much...I so so appreciate if ...I rather speak to someone who actually understands....how did you feel when first diagnosed...
I knew I had it for a few years prior to booking my lung function tests .
I was feeling chesty and smoking wasn't helping so I booked an appointment off my own back and the rest really is history . Knowing I had it made it easier that when I was told I suppose I had already been in denial for some time so it enabled me to focus from that day stopping smoking getting myself sorted wasn't as hard as I thought it could be it's self awareness and realisation that what good you do you will benefit from in the long run ...and your very welcome x
How proactive I wish I could be as strong as you I am just a gibbering reck ...you have spent good part of you Saturday talking me down.
I just wish I could talk and breath eat and breath....I know I am stressed and anxious...I don't even know when I need my rescue pack...what professional support did you get after diagnoses
You will get through the worst and your strong enough to fight your way back out of the way your feeling right now.
The education will develop in time with pulmonary rehabilitation as well as exercise your educated in your meds your breathing your needs and wants and how you benefit from things .
Take any support you can see a GP and if you feel you need counselling sessions take them we both know it's sounding off mechanism and they are around to listen .
If having a rant on here helps do it there's always somone to help or ring the BLF support network...
Just don't go back on the ceiling now lol xx
I hope I am thank you so so much...I hope I am going to be able to breath soon when I am walking....I know it affects your breathing but get scared flash back...respiritory nurse good bless her has organised PR for me after Dr saying no so that's something
Your so welcome and things will come right . Always ask for help when you need it somone will help you out x
Your really welcome there is a few support groups on facebook if you choose to go that route they are all private once a member just type in copd support on its search bar and join enjoy your weekend
Oh thank you and you will look now....I don't think you will ever know what you did today xxx
Nothing that you didn't already know. You just had to get a perspective on it and to keep going with the flow now enjoy your day today go see your daughter and have a gossip with her 😊
Blackbird, the support you’ve given Emily today epitomises what’s so great about this forum. Thank you for being there for her. I don’t have copd so can’t help with the sort of advice you’ve been able to give.
Emily, when first diagnosed with bronchiectasis (already had severe asthma) I was really ill at the time. I went home & made a will. But I’m still here 25yrs later. I’m having a difficult time just now, but for most of that 25yrs I’ve been stable, worked until age 60 & had a full life. What made this possible was getting on the right drug & treatment regime. I went from really ill at diagnosis to really quite well in just a couple of months! You’re not on the right regime yet. The consultant will decide the best way forward for you, and it might be that your medication needs tweaking along the way, but once you’re on the right regime for you I’m sure you’ll improve a lot.
Reading your posts, I feel the most important thing at the moment is to tackle your anxiety. Stress is terribly bad for asthmatics, or indeed any breathing difficulty. I know I can go from ok to incredibly wheezy & breathless in minutes, if I’m really wound up. On Monday you could phone the BLF helpline, and/or the Asthma UK one. I’m sure they can help talk you down from this panicky state you’re in. Things WILL get better, they really will. Just take one day at a time for now 👍 You’ll get there x
Hello and so right blackbird has spent most of Saturday with me..and that has been unbelievable. And I know my anxiety is not helping nor is my lack of sleep...I am trying and honestly blackbird has made a major difference to my stress level...do you know up until joining asthma UK and this forum I never knew there was varying types of asthma
The fear of the unknown the fear of another hospital admission
But one positive had I not had this diagnosis of COPD on top of asthma I would not have encountered such strong compassionate people
Thank you again and I will phone asthma UK and BLS Monday
How wonderful you’ve been with your support Blackbird and I agree with Hanne62, it’s people like you that help make this forum the great place it truly is.
Hang on in there Emily, you will be ok and we’re here for you. Xxxx 😘
Thank you and I will
That’s is such an encouraging post for our new friend.
Well done hun x
Hi Emily can I just tell you my coping mechanism I tell myself look you are lucky you don’t have lung cancer so you can manage this condition and do everything in life you planned it’s a challenge but you can do it . Take care xxx
Thank you....I am still just scared
Hi Christine I hear what you say i just need time to process this don't understand the condition...I may have some calm once I see consultant on the 25th...I don't want this to limit me and what I do....today I can walk up and down the stairs and breath...
Aww know exactly how you feel soooo depressing can’t arrange anything not even to do simple jobs around the house. It’s an awful desease I did same smoked for years and now paying the price but we have to carry on someone out there a lot worse off love and big hugs hope your clouds soon lift Jo xx
Hi When was you diagnosed I still work but so worried won't be to continue to work
Diagnosed 5 years ago also same year collapsed while walking the dog 🐶 an ambulance was called and they diagnosed Addisons Desease. Then a brain tumour wasn’t a good good year at all so work was stopped. Xx
Oh my dear you are amazing what is Addison disease
No not amazing I was completely terrified until I digested it all Addisons is when your Adrenal Glands which sits on top of each kidney stop working. They make steriods among other things your body needs to keep you alive. Mine failed because of all the steroids I had been given Tablets for chest injections and injections for my back knees and other body parts. I had a very bad car crash in early 90s. That was the start of it all. X
Oh my goodness for you to take the time to comfort me ...you are amazing do have you got asthma copd as well as this
No Emily it’s not Ashma just COPD and to Chat to someone always helps we don’t always have the energy level to do it but it does help we lose a lot with this illness friends can go out when they want to but our lives change. I even dread early morning appointments. Think the holidays have ended we went to Cape Verde xmas 2017/18 and I ended up in hospital for 5 days with sickness and diarrhoea if I get anything like that I have to have a 100ml injection which I carry but if that doesn’t stay in me it’s hospital and that was a hell of an experience that I wouldn’t Lille to go through again and I know my husband definitely will not chance again it happened 3 yrs ago in Cuba also so it’s a definite no from now on xx
You have a lot to contend with and it does help...have just phone community respiratory nurse awaiting call back as can't be living on fostair spiriva and still need to be reliant on blue inhaler ...is Addisondisease a form of COPD or as a result of
No neither is completely seperate but can be born with or as a result of being given steroids either in tablet or injections which is what happened to me was a complete shock and nightmare x
Wow I still find you Amazing really I do I feel honestly so humble
Honestly I feel so lucky 🍀 to have a good hospital round the corner and a good family there are people who have to cope with so much worse have just learned to give in if I can’t do a job I leave it for a better day . Take care hun smile you WILL get there this site is so good 😊 xx
God bless you xxx
You too Emily will remember you in my prayers tonight hun xx
I will pray for you also ...God is good he has introduced me to some amazing people
😇😇😇have a peaceful restful night Emily nite God Bless lovely lady xxx😇😇😇
Good night God bless
Hi Emily, believe it or not I went through a period just like you when first diagnosed. Maybe even worse, because I actually had suicidal thoughts, stupid I know. I can tell you with certainty that coping with it does get easier and better, at the moment you sound like you are in bereavement for the old you. It really is not the end of the world no matter what you may think now. You really will get used to getting breathless, even the young, fit and healthy get out of breath, it is just we get puffed out quicker that is all. You will recover your breath, there is nothing to be frightened of, in fact, exercising to get out of breath is really good for you.
The reason that you can only find a few of us still working is probably down to age, the vast majority of members here are retired. I have been self-employed for 33 years, it is up to me just when I retire, which is not in the foreseeable future. I will not say it is easy for me as my body is a medical wreck but I do still manage.
Give yourself time to adjust, time for your inhalers to build up to their most beneficial. Your Ventolin, try to keep it's use to the prescribed 2 puffs 4 times a day, using more will start to make your heart race and probably the increased pulse rate will also affect your anxiety level too. You just have a lot to learn on how to manage your condition.
Thank you and I can honestly say if it was not for here I had very stupid thoughts running through my head
Another great post for Emily61. Very good advice.
In 2016 there were 251 million people worldwide diagnosed with COPD, and probably at least the same undiagnosed, so we'll say 500 million to save arguments.
Now, on this forum going on past and present members, there are probably 200 regular posters. Of them 200 posters, lets say 50 have a different lung condition altogether, 10 have a genetic link, 10 still smoke (no blame, we all know how hard it is to give up),10 have never smoked, 10 have other conditions that prevent them from exercise, 30 have retired (brilliant point by 2greys) .
That leaves 80 ( not great with maths so may be wrong) people telling their story . Thats 80 people out of 500 million..... a very small proportion of the COPD community I would say.
That is a fascinating analysis roey123. It is something to think about . No doubt ! I see your point and I will personally refer to it when needed . Thank you . The only figure I would love to hear is how many of the folks with COPD/emphysema are over 75 ? I mean Emphysema only not asthma or Bronchitis or Bronchiectasis or overlaps but just Emphysema?
I am sure once I stop feeling sorry for myself I will be able to process this information
That looks promising but thought it couldn't be established see I have no understanding of my disease
hi Emily61-im in the same boat don't understand any of this, I have had all the test done in October at my pulmonlolagist and everything was ok-went to my doctor I see in my own town and told her I was really stressing over the blood oxygen levels dropping so she had a ct scan done with this red dye stuff and said it showed just a stace of emphysema but everyone says you can not be mild if you have blood oxygen drops you have to be in a bad stage so here I am a basket case cant even sleep and cant see my pulomolagist until march 5th so I am also like you don't know what to do! hope you do well soon!
Hi this is so the best place to be the BLS nurses are fantastic have you got their number...only today I spoke to one of them as I was getting very anxious ...March is a while away phone and see if there are cancellation...
And who is everyone...I don't know about bloods ....had bloods whilst in hospital from arm don't know outcome of that please phone as if not for her asthma UK BLS Nurse I don't know where I would be...don't get me wrong scared still but ask phone
thank you Emily61-im from the US and there information is VERY scary so I say away from googling anything on there! I stay here cause I read such positive stuff and right now I need this! thank you for responding!
Absolutely no thanks required and yes stay away from Google I did that on more than one occasion and was absolutely fell apart...this site is beyond brilliant I was told over the phone by my doctor I have asthma which I knew and COPD...that was it googled and all I saw was a death sentence....that was days ago ...I know how you feel ...please keep posting. I am a newbie but there are some experienced people here who are so so full of compassion
As Ski says , my diagnosis felt like a kind of bereavement for the life I had planned. At first I was in denial, then angry, then very depressed .
But I managed to get my degree through the OU......they are excellent for dealing with people who may have health challenges.
I do gentle yoga, have joined an art class....three of us have COPD/ asthma..., the WI....again a few with the same cough, a church group ( also coughers) . I used to go to a rehab gym class and Breathe Easy group.
I just learned to adapt.
I do still mourn sometimes for the life I had planned, but I think I have gained more insight and compassion in some ways, and less guilt about doing nothing sometimes, just cloud watching!
I also learned which medications suit me and which don't ...trial and error.
That is very important.....learn to read your body and its needs.
And a huge help to me has been Mindfulness and Meditation. Have a look at online Future learn courses from the OU . I have just finished a three week one called Intergrating Care: Depression, Anxiety and Physical Illness.
Learning to breathe in a relaxed, comfortable way....nose not mouth breathing to warm and filter the air. Relaxed GENTLE belly breathing with relaxed upper chest muscles and relaxed diaphragm area. Low GENTLE breaths....low and slow.
I noticed you said you were using a lot of your blue inhaler, if you are getting increasingly breathless, contact your health professional and see if your preventer needs adjusting.
Sending best wishes....
Hi community respiratory nurse came out to see me, as breathing not to great. Totally fell apart was totally honest with how I was feeling...she advised me to read leaflets which not got around to...but I am going to try doing...told her that I have felt unsupported apart from here....I explained I don't know what type of COPD I have...my results still mean nothing to me...she was lovely and said she would go back to the office and try and find my results...and phone me...
She has since phone said prior to inhaler spirometry test results 66% after inhaler 77%...total her that meant nothing to me..she said she would get respiratory nurse who is calling tomorrow to go through it with me...
I will I am sure take a lot of what is said for example how do i find a breath easy class.
She respiratory nurse is going to refer me to pulmonary rehabilitation class. Feel at least I am getting some practical support from health care professional.
Please bare with me as it is early days and had horrid set back yesterday
Hi again Emily was just reading your post are you under Pennine LUNG TEAM by any chance ? Glad you got to talk to your response nurse because it is frightening I had 2 really bad bouts this eve. Been on my nebuliser twice with ventolin. I still get panicky it’s so hard not too I have now turned down oxygen twice I see my constant on the 20/2 only a couple of weeks and I have decided that if it’s brought up again which it will be as he put some results of latest lung function test said that he would like me to see oxygen team also. I had a chest MRI scan so he will have those results also but I am now at the point of giving in.. I was in hosp for day last wed for facet joints injections in back of my neck and have had an operation there 10 years ago and it’s giving me a lot of pain so they take me in theatre and do them every 9 mths or so but my lung is killing on left side so feeling bad At moment I will put a sputum specimen in at my G P surgery tmorrow if no better just to be sure it’s not infection . Sorry for late night moan everybody going to cuddle my little dog 🐶 and then hop into bed
Nite god bless you all here is to a good nights sleep 💤 sleep 🛏
Hi no I am based in Birmingham under sandwell hospital first visit 25th not really sure who team is...how you doing now. You are going through a lot so you are definitely not moan..not gone through as much as you yet I am moaning
I hope you sleep well good night God bless
No your not moaning just trying to get used to an illness that you need to be in control of and it will happen it’s a lot to take in and understand love Stay strong and positive this lovely site helpssuch a lot the people make it x
How are you today
Only test I have so far x-ray on admission December bloods outcome of those I don't know and spirometer test very hard very hard
Hope you have had a good night and day and things have been a bit easier. It’s so confusing all these numbers and terms I write things down now to ask consultant as I forget when I get there. Just had a really lazy day today. Stayed in as it is wet and damp here not ideal to treck around in . Have a peaceful evening hun big hugs 🤗 xx
Thank you so much and cooked dinner went to see my parents and sister resting going to wash up then have some rest 😘 thank you again
Glad to hear you been to see parents and sister will do you good Emily. Am definitely not as bad as last night pain in left lung was awful but haven’t done a lot today I rested all day Hubby done some shopping for me and did tea . Didn’t put specimen in will give it a couple of days I have coughed that much. Am sure that’s where my lung pain is happening. Hope you are doing better. Do your ? List and ask away don’t be worried hope you get a good peaceful sleep 💤 tonight in my prayersxx
Glad you feel a little better you haven't got infection have you? Please take care good night God bless
I am going to do my list of questions started but need to complete
How are your lungs today
One thing to remember — if nobody has mentioned it yet — is that this is a support group. Usually people who post in support groups aren’t at their best or are having problems, and if someone’s doing great they’re unlikely to post. When I’m well I sometimes forget I even have this app!
You’ve had some perfect advice this morning, Emily, from valued members of this forum. I do hope they help you to adjust your thinking.
Meditation can be very useful to calm your mind....no pills needed. Lots on YouTube.....and you don’t need to be ill to join in!
Thank you I still feel the same but crying is helping
I’m so glad blackbird has been able to help you today, Emily. You’re on the right path now, I’m sure.
Good luck with your OU work. I did a degree with them some years ago. It was hard work but very very interesting.
Speak soon 🌸
Oh my so you’re waking up feeling like you’re choking on mucus then you get breathless from that struggle or you wake up breathless then choking on mucus? I use to suffer from that most often and I’d have the heater at my feet and the AC blowing in my face that felt like the only way I could breath. You really better ask the doctor good luck hope you get better soon
Try singing. It helps you learn to control your breathing and when you sing your body releases natural feel-good chemicals called endorphins. The British Lung Foundation website lists singing for lung health groups all around the country. The group I run uses singing for exercise and fun and doesn't bother about whether members can sing well or not - we're an exercise class, not a choir.
Thank you can't find anything but will look again tomorrow thank you
Hi again Emily61. I am staggered at how many responses you are getting. It is indicative of the support we all want to give you and you have been given some solid and inspiring advice.
Remember to do your breathing exercises because they really help and they move your attention in a different direction.
I can’t add anything more of use but I am thinking of you and wishing you well because you are going to get through this.
You are still in shock and this is just a temporary rock in the road.
And if you can’t climb over a rock you can always go around it😊
Sincere good wishes.
Hi Emily - has anyone mentioned reflux to you? Silent reflux (where you dont tend to have heartburn but stomach liquids get into your airways) can cause a lot of mucus in the throat. It can cause asthma like symptoms but with the difficulty being with breathing IN, not breathing out as in asthma. Lots with copd, including myself, have this. Might be worth discussing possibility with your GP/consultant.
Do hope you are a little calmer now and have been able to take in the wonderful advice and support you've had. This awful time will pass. Good luck
Yes I am a lot calmer and when I have rubbish day moment hours I come here still scared but thank you will ask about mucus 25th thank you so much
By the way, just to let you know, I was diagnosed around the same stage as you are now. That was 18 years ago and Im still going strong at 73. And there are many more like me
Thank you I don't know what any of it means but that's promising to read
hi there Im new on here not sure how everything works did you get to read my post?
Hi just let please know who you are and what support you need and keep posting...
just need help trying to figure things out about a trace of emphyasema showing up ona ct scan and not kowing what that means
Can your Dr not explain what professionals are supporting you at present ....please keep posting because I have not been on here that long but there are loads of people on here who can offer great advise
thank you I will take advise from any one!
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