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My Lungs Part 6

996 replies

TheDrsWife46 · 05/04/2020 21:03

New thread here let me see if i can link back and forth...

OP posts:
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Kim82 · 06/04/2020 15:22

Oh and I have a metallic taste in my mouth that won’t go no matter how much I try to get rid of it.

Bornfreebutincovidchains · 06/04/2020 15:24

How can any doctor or a and e tell when it needs antibiotics? Or its moved to a secondary infection?

simplekindoflife · 06/04/2020 15:26

@AnythingPecan totally agree! And all NHS advice advises that it's not COVID unless you've got a fever and a persistent cough... which this board seems to have completely disprovedConfused

AvonCallingBarksdale · 06/04/2020 15:39

Hi all. Hope it’s ok to jump in here. I’m feeling increasingly nervous - developed dry cough last Monday, ie 8 days ago. It’s got progressively worse and is now really rattly, painful just to the left of my breastbone, coughing up some white/yellow phlegm (sorry). I’m also achey and shivery and a bit hot overnight (but that’s usual for me). Extremely tired too. I just don’t feel any better at all and although I’m propped up at night I’m struggling to rest.
I’ve done the NHS111 online questions and have the Ask NHS app but I’m a bit confused as to what next Confused. It’s been over a week. Thank you from a rather scared exhausted MNetter.

GrapefruitsAreNotTheOnlyFruit · 06/04/2020 15:41

Ok updating everyone. Day 25, I have still got a fever. Spoke to GP. They said they are hearing from lots of people with prolonged symptoms though they said 25 days of fever is a lot even so. They prescribed antibiotics in case of a secondary infection and told me to call back on Thursday if I am not better.

Taffyapple8 · 06/04/2020 15:43

Has anyone had bad sinus pain? The pain around my eyes is so intense at times and usually precedes a spoke in temperature x

WorriesomeDad · 06/04/2020 15:50

@mumlurker @AnythingPecan I know exactly what you mean. I’ve been struggling with it too. Breathlessness with good Sats doesn’t make much sense. Either it’s psychosomatic or the virus somehow messes with the bodies receptors that measure it. The former would certainly be better than the latter!

Taffyapple8 · 06/04/2020 15:50

The squits are back now. This is relentless. Thought I was having a better day

TheDrsWife46 · 06/04/2020 15:55

Just dropping in to say that I just went on the C-19 tracker webinar thats collating all the symptoms. If you’re not already on it, download it as they are producing a far more detailed and flexible view of symptoms than the nhs snapshot symptom checker. You can go online and see their research that shows that people of symptomatic covid are more likely to report loss of sense of smell, fatigue, shortness if breath etc rather than the nhs partyline of cough and fever.

covid.joinzoe.com/

OP posts:
AnythingPecan · 06/04/2020 15:58

@TheDrsWife46 thanks for this. I've always wondered how they can collate such data if they're not 100% sure it's covid. If nobody's testing, then won't their data be inaccurate if nobody can be sure it's covid?

Meltedwellie · 06/04/2020 16:03

@Bornfreebutincovidchains 111 sent me to A&e. Doctors there could tell I had a secondary bacterial infection through blood tests.

Tangledyarn · 06/04/2020 16:04

@Runnerduck34 I've got a sick note from my gp as I'm going into week 5 of being unwell now.

onlinelinda · 06/04/2020 16:10

@user, your symptoms are consistent-they vary. I have had chills rather than temperature too.

I'm on day 22 and , after a really good weekend, was really chilled again for 2-3 hours later this morning . I spoke with the duty GP, who told me that after 6 weeks of taking with COVID patients all day, that my symptoms are not unusual. Also the long time span comes up reasonably often, and that there is a spectrum of timescales . He also advised that I drink plenty of fluids-at least 2 litres. The fact I'm no longer breathless means I have probably turned a corner, even with continued on and off chills. I hope that reassures some other long term sufferers.

That Winnie the pooh cartoon is lovely @jackjacktheincredible and thank you
💕

Porcupineinwaiting · 06/04/2020 16:13

Hi @AvonCallingBarksdale

What is next is rest and drink, rest and drink - and keep an eye on your temperature and your breathing. The bad news is that you could easily be ill another week or so but it will pass. Just hang in there.

onlinelinda · 06/04/2020 16:13

@pinkoneblueone, antibiotics can't hurt, I
Would think? I was given them in week 1, which surprised me, but they do knock any underlying or secondary infection on the head. Also you have to treat the asthma as well as the covid.

Runnerduck34 · 06/04/2020 16:14

@ tangledyarn, just spoke to GP who has signed me off for a week, big relief that i now know i can rest.
Think i did too much yesterday and have noticed if my symptoms ease and i start to do normal stuff i very quickly crash back down again

Runnerduck34 · 06/04/2020 16:21

@kim82
I think there a lot of us on here that have had similar symptoms to those you list but most have also had either a cough and/ or a temperature.
It could be the virus or another virus or something else entirely but take care of yourself and take it easy.

KatySun · 06/04/2020 16:22

Avon if your symptoms are getting worse, call 111 to speak to someone. I was triaged through to a clinician also on day 8 and found it reassuring.

pinkoneblueone · 06/04/2020 16:22

Most of us have had symptoms like this to be honest

longshot · 06/04/2020 16:22

@Runnerduck34 yes I am the same, do a lot and pay for it the next day! I’ve resigned myself to 6 weeks of very little. I do however feel well enough to work a bit on my laptop and homeschool a bit so I guess it’s not that bad. I just can’t sort my house, garden or exercise!

musicposy · 06/04/2020 16:27

Hi everyone, checking in on day 28 (I think!).
I’m feeling a bit better as though the antibiotics are kicking in - certainly breathing better.

tangledyarn, letsbesensible, stayathomegardener and anyone else I missed with CFS, this is my next big worry. I am so weak. My legs are like jelly, I can barely get beyond the bathroom and even my arms ache if I type or hold a book. Im looking at the garden longingly because I can’t even begin to get down there.

I was diagnosed with ME in my 20s at a time when a lot of people still dismissed it. My doctor at the time said “a lot of doctors will dismiss you as if it’s not a real illness but I think you have something very real which we don’t yet understand called ME”. I’d had a pneumonia and I just could not recover. I remember the first time I managed to walk to the corner shop at the end of my road - 6 months later - and I was triumphant. Then I started to improve a lot and, in a move people thought was utter stupidity at the time, got pregnant with DD1. After the first trimester everything suddenly felt miles better, possibly due to pregnancy hormones!

In the years since I’ve definitely had relapsing remitting episodes, usually brought on by viruses and autoimmune diseases. Last time was three years ago when I got viral meningitis which in turn triggered coeliac disease. I was so ill with that it was 6 months of a gluten free diet before I was able to go out properly and live a “normal” life. The doctors have termed it as bouts of Post viral fatigue rather than CFS but it’s nothing for me to be 6 months after these episodes to even begin to get back to any kind of normality.

Since the coeliac I’ve worked really hard to gently build my fitness and health and I was doing pretty well before this, though I’ve never been up to working more than 3 days a week since (which is a worry as DH has lost his job and daren’t get a new one until I get an antibody test).

In some ways I’ve done this before and so I know I can do it again. In other ways I know exactly what the next few months might look like and that’s scary. I desperately need to get back to teaching and earn some money. At least the government self employment scheme will help for a couple of months.

In some lovely news I told my pupils I couldn’t teach them online this week as I was on antibiotics now and too weak. This is the fourth week and I know a lot have been very concerned for me. One of my lovely pupils makes kefir for a living and as it’s probiotic I asked if she had some spare she could sell me. She came round and dropped two bottles off as a gift. This is just one example of how amazing people have been during this.

JackJackIncredible that was a lovely picture and much needed.

Love to everyone still suffering and all those I haven’t mentioned. I’m keeping up with all your stories. You can beat this! Flowers

pinkoneblueone · 06/04/2020 16:28

I think I am experiencing pay back for cutting our grass yesterday 😔

Standrewsschool · 06/04/2020 16:29

Avon - your symptoms do seem similar to the mn-strain of the virus. I had a really rattle cough that made me almost heave. I ended up phoning the dr after ten days or so and got antibiotics.

Fatigue is a key element of the disease. Basically, you have to ride it out, and try not to do too much. If you feel you are deteriorating, then contact Gp/111. However, a lot of us seemed to ‘coast’ at the same level of illness, not severe, but not mild. Then you start to feel better, and then have a relapse, and then improve again.

Sorry, hope this isn’t too depressing. Keep posting how you feel and we’ll support you (and everyone).

stayathomegardener · 06/04/2020 16:31

@onlinelinda that's reassuring that a lack of breathless despite chills indicates turning a corner.

JackJackIncredible · 06/04/2020 16:37

Has anyone else been vomiting a lot? Can’t keep anything solid down, really. :( This has been new over the past couple of days.

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