Coughing a lot through night
Posted , 8 users are following.
Not long found out I have bronchi ecstasies the hospital had known over a year I have a bad chest infection I am cough all night had bad ones before but this seems really bad do you cough a lot in the night xx
0 likes, 21 replies
thomaschan72383 judy09425
Posted
judy09425 thomaschan72383
Posted
cofalot judy09425
Posted
I am assuming since you have been diagnosed with bronchiectasis you have had a ct scan and are now under the care of a respiratory specialist - you should be. Consulstant should have referred you to a physio.
I don't generally like to suppress a cough in bronch if it is productive, as it is basically doing the physio for you. I have over the years, however had those nights of constant cough cough cough.
I have recently found from a bronchiectasis forum, and this is going to sound crazy but give it a go, you might be surprised: Use good old Vicks vapour rub, not on your chest but, wait for it (on the soles of your feet) and cover with a pair of socks.
I occasionally have steroids and do have a steroid inhaler but these are not for my bronchiectasis but for my asthma. I try to keep the orals to a minimum.
Try the loony sounding Vicks thing. It does work for some.
love cx
judy09425 cofalot
Posted
judy09425 cofalot
Posted
cofalot judy09425
Posted
cx
judy09425
Posted
steve62514 judy09425
Posted
Keep a diary of how you feel and go discuss it with your chest consultant (regular GPs do not have the experience and if you can afford a session at a private hospital with a reknowned lung defence unit - getting one of them on public healthcare or insuance is a bonus) is then absolutely essential to make sure:
1. The best antibiotic is found (antibiotics do control my cough as well as placating the other bacterial effects of wheezing, flash fevers, tiredness/exhaustion); needs a thoroughly analysed sputum sample in a big hospital lab; several days cooking is required - too many cheap clinics/hospitals come up with a same day result which will not have captured the deep-seated bug if one is affecting you
2. Other supplementary drugs are tailored for you - cortiscosteroids (as an inhaler like Symbicort, or as a pill like Prednisolone on a carefully tailored dosage over a few weeks including a declining tail; anti inflammatories/longer acting breath relievers like theophylline; mucus thinning agents like carbocysteine/acetylsteine: releivers like 'Berodual' for breath shortness. Some of these are primarily for asthma or COPD but I have found them very helpful in keeping a good comfort level. I suspect some doctors do not prescribe all those cos the books do not associate them with B treatment
3. Don't be afraid to pop a couple of paracetemol if your coughing gets bad. They have an anti-nflammatory effect and sometimes when I wake at 4am and feel that inflammatory hoary feeling in the chest and an involuntary cough the paracetemol will quieten it down and give me a refreshing few more hours of sleep.
I am not a medical pro - just a sufferer whose diagnosis progressed over 32 months from acute bronchitis to early stage lung cancer (discounted) to non-aggressive lung lymphoma (treated with radiotherapy) to bronciectasis. I've been given a whole load of differing medications over that time by several different specailists in the UK and Thailand. Check everything out with a medical pro and make sure that, if you are taking a cocktail of differing drugs, that the doctor/pharmacistr has considered clashes and side effects.
I'm lucky in that I seem to be ok on my regimen of 'Symbicort', Puroxan (a third world alternative to theophyline and much better IME) antibis when needed and occasional puffs on a cheap releiver or occasional paracetemol. Once I drop the antibis its only a matter of time before the next infection comes along and needs jumping on. My consultants allow me to be my own best prescriber for comfort.
[Just for completion I very occasionally take on an as required basis Ozemaprole for gastric effects and pill side effects and a hay fever nose spray to clear my sinuses (one of my ears will infrequently block up with mucus). It's not as bad as it sounds - most days I am only taking 3 different things!]
judy09425 steve62514
Posted
cofalot judy09425
Posted
You don't say if you have been taught lung clearance or how to use many of the gadgets available - the flutter: acapella choice. All bronchs are different and prefer different methods.
One thing we all have to be is our own advocates with bronch. So learn all you can. I would put up the British Thoracic Guidelines up for you but links take so long on here it would be quicker for you to google it.
cofalot judy09425
Posted
The guidelines advise that a sample is sent in at the beginning of an infection but that abs should be started straight away and changed if sample shows the pet you are growing is not sensitive to it. This works for me and if I waited for a sample to come back I would be hospitalised. I have less orals now (and am intolerant to many) as I now nebulise abs for 28 days on and 28 days off.
Wishing you well and that you will finally get the treatment you need and deserve.
love cx
steve62514 cofalot
Posted
cofalot steve62514
Posted
love cx
sylvia91360 judy09425
Posted
cofalot sylvia91360
Posted
Respect to one very strong lady.
love cx
judy09425 sylvia91360
Posted
sylvia91360 cofalot
Posted
take care sylvia
cofalot sylvia91360
Posted
I am so very sorry to hear of your partner's daughter's passing. How devastating - cf is a nasty cruel condition.
Take care
love cx