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Long Covid

Last August I went for a lung function test...now 6 months later i got the call back....my lung function is at 70% is the bad news, the good news is they think it can be greatly improved with asthma inhalers, the positive hope based on the fact that part of the lung function test included trying breathing exercises with and without an inhaler hit and inhalers were making a difference

I haven't got the prescription yet but the prescription is for a pink inhaler, with positive effects due after 6 weeks of use....I'm hopeful. Will report back if anything good happens and maybe this is a path others might want to try
 
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It's kind of nice when you get something measurable they can address. My lung function tests were all normal so it wasn't an avenue we could explore.
 
Full paper for that is here.


31 people, very varied “LC” symptoms, and loads in the “matched controls” group getting worse for some reason. So not much to go on really. I don’t see how proposing a set of biomarkers which neatly resolve in a small cohort does anything to make those biomarkers relevant to persistent LC.
 
My friend reckons he has got rid of his 11 year olds post viral fatigue / long covid (not sure if it was ever formally diagnosed) by using some sort of iron tablets from Holland and Barrett and something called augmented NAC, combined with lots of water and dioralyte (he was told to use salt but didn’t think his daughter would manage that without vomiting so substituted). Something to do with flushing out spike proteins he said. I believe they went to a private consultant.

She went from barely being able to get off the sofa for months to being back to her old self and back at school within a month.

Not entirely sure of the science behind it and certainly not endorsing it as treatment as not a doctor I thought it worth mentioning in case it is something that can be explored.
 
It’s worth bearing mind too for any isolated case that you can’t tell whether the thing you took helped or whether the improvement was going to happen anyway.

It’s pretty much always the latter, unfortunately, at least for LC cases which meet ME/CFS criteria. Spontaneous remission is very common in year one and quite common in year two. Pretty much all patients try some kind of supplement or some other kind of intervention at some point in year one, and in most cases there will be something onto which remission can be pinned. There are no supplements or interventions which have shown consistently good results in blind trials.
 
I haven't got the prescription yet but the prescription is for a pink inhaler, with positive effects due after 6 weeks of use....I'm hopeful. Will report back if anything good happens and maybe this is a path others might want to try

Is that seretide?

I've been using it for ten years and have found it really effective

Has it helped you?
 
It’s worth bearing mind too for any isolated case that you can’t tell whether the thing you took helped or whether the improvement was going to happen anyway.
Yes I suspect an element of this too in my friends case
 
Is that seretide?

I've been using it for ten years and have found it really effective

Has it helped you?
Brand name Fostair
"The two active substances are beclometasone dipropionate and formoterol fumarate dihydrate. Beclometasone dipropionate belongs to a group of medicines called corticosteroids which have an anti-inflammatory action reducing the swelling and irritation in your lungs."

so a different thing, but probably does something simliar ?


...and yes its helping!!
 
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I got the novavax vaccine now that it's available privately, on the grounds that some people have seen improvements after it. I think it has helped, I was on an upward trajectory anyway but it seems to have noticeably reduced my mental fatigue. I feel able to do more/think more in a day without problems, and I actually feel mentally energetic sometimes. Fatigue from doing physical stuff is still very much there, though it has been slowly improving.
 
I got the novavax vaccine now that it's available privately, on the grounds that some people have seen improvements after it. I think it has helped, I was on an upward trajectory anyway but it seems to have noticeably reduced my mental fatigue. I feel able to do more/think more in a day without problems, and I actually feel mentally energetic sometimes. Fatigue from doing physical stuff is still very much there, though it has been slowly improving.

How are you feeling now? Is there much evidence online so far that it can improve LC symptoms?

I am quite tempted tbh. It's available at a local pharmacy for £65. Had Covid again 8 months ago and still recovering from what that's thrown up. On top of the stuff from before. Lots of weird foot and toe cramps and weird feelings I have every day and which tbh are slightly debilitating some days. Affecting my ability to work, do exercise sometimes just even move around the house with ease.

Luckily I'm sleeping well and able to rest enough and my brain fog and the more severe symptoms I had before are a lot better - my energy reserves feel much stronger again.. on good days been cycling swimming in river doing bar work and teaching online plus going out socialising etc. Ive realised that really hot weather can make me more fatigued, make various symptoms worse... so I do need to be careful this summer as going to Spain for 2 weeks.
 
Sorry to hear covid hit you again. Yes, I find hot weather worse than I used to.

I think it's hard to say about long term effects of the vaccine because of the ups and downs you get anyway. On balance I might guess there has been a slight improvement. I think my partner got covid recently (though tested -ve), and it's possible the recent vaccination saved me another bout. So I'm thinking I'll probably get another jab 6 mths after the first, and if it goes well, potentially every 6 mths.
 
So, the NIH in the US is currently by a massive margin the largest investor in long covid research. It’s still spending money on researching behavioural therapies, but is gradually seeing sense and allocating cash to biomedical research.

That looks deeply endangered under a Trump (and RFK?) covid denialist healthcare regime. The smart move might be to rebrand long covid as “vaccine damage”, mitigations to which would be looked at much more sympathetically by antivax and post-truth funding authorities.
 
So, the NIH in the US is currently by a massive margin the largest investor in long covid research. It’s still spending money on researching behavioural therapies, but is gradually seeing sense and allocating cash to biomedical research.

That looks deeply endangered under a Trump (and RFK?) covid denialist healthcare regime. The smart move might be to rebrand long covid as “vaccine damage”, mitigations to which would be looked at much more sympathetically by antivax and post-truth funding authorities.
Except you're looking for the wrong mechanism then, surely?
 
I took all the vaccines over pandemic and got a mild dose of COVID at very end of pandemic

Last winter I came down with several cases of colds/ flu and in end OH told me to see GP.

Sent off for X ray to check my lungs. Came out fine. And blood test.

The winter has just started and I'm on my second cold now. Feeling run down this morning.

I never used to be like this. Used to get flu vaccine and then might get one mild cold/ flu over winter.

I can only think its connected to getting COVID once. As last winter my GP said as people weren't mixing over pandemic their immune systems were weakened. Or something like that.

I've been struggling over last six weeks and its been making me irritable.

Is this some kind of slightly weakened immune system due to COVID ?

I take iron supplements anyway and have done for other reasons ( I'm platelet donor and iron levels can go down)

Also take calcium as have slightly low calcium levels

This is unconnected to the pandemic.

I'm not one to dwell on being ill and this is all starting to get on my nerves.

Nor have I believed stuff from my anti vaxx acquaintances that this is my fault for being a Sheeple and having the vaccine.

Surprising number of people I know are blaming the vaccine. Is there anything in that? What I call the post pandemic anti vaxxers who now reckon it was all over dramaticised
 
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Surprising number of people I know are blaming the vaccine.
My LC started before I’d had any vaccine doses, so in my case definitely not. I’ve had every dose I’ve been eligible for and will continue to do so.

An old friend from my younger days, whom I met at a mutual friend’s 60th, told me my LC was definitely vaccine caused, that I was misremembering the onset date, and that lockdown caused more ill effects than the pandemic, which he was skeptical about anyway.

I removed myself from his presence and sought other company.
 
I took all the vaccines over pandemic and got a mild dose of COVID at very end of pandemic

Last winter I came down with several cases of colds/ flu and in end OH told me to see GP.

Sent off for X ray to check my lungs. Came out fine. And blood test.

The winter has just started and I'm on my second cold now. Feeling run down this morning.

I never used to be like this. Used to get flu vaccine and then might get one mild cold/ flu over winter.

I can only think its connected to getting COVID once. As last winter my GP said as people weren't mixing over pandemic their immune systems were weakened. Or something like that.

I've been struggling over last six weeks and its been making me irritable.

Is this some kind of slightly weakened immune system due to COVID ?

I take iron supplements anyway and have done for other reasons ( I'm platelet donor and iron levels can go down)

Also take calcium as have slightly low calcium levels

This is unconnected to the pandemic.

I'm not one to dwell on being ill and this is all starting to get on my nerves.

Nor have I believed stuff from my anti vaxx acquaintances that this is my fault for being a Sheeple and having the vaccine.

Surprising number of people I know are blaming the vaccine. Is there anything in that? What I call the post pandemic anti vaxxers who now reckon it was all over dramaticised
vitamin D supplements?


I've not noticed a change in my illness frequency in my life except when I partnered up with a teacher and he brings all the germs home. When my child started nursery and brings all the germs home and then less in lockdown because no germs coming home...
 
Surprising number of people I know are blaming the vaccine.
There is no substantive evidence indicating LC follows from vaccination. For starters, how many of those people (with LC/PASC) have been exposed to SARS-CoV-2?

All the research evidence points to the opposite - that vaccination helps reduce incidence of LC and associated persistent symptoms.

DOI:10.1038/s41467-023-38388-7
DOI:10.1056/NEJMe2407575
 
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Yeah, there's much more evidence that covid fucks with people's immune systems long term: The immunology of long COVID - Nature Reviews Immunology
Anecdotally I know a bunch of people who didn't have major long covid symptoms but who seem much more vulnerable to viruses in general now.

Unfortunately it's all too new and emerging for your average GP to be aware of it so don't expect any sense out of them.
 
Is this some kind of slightly weakened immune system due to COVID ?
How's your diet? 70-80% of your immune cells are in your gut. If you can improve gut health, you'll have a better resistance to bugs.

Link for info here: How Gut Health Affects the Immune System and How To Boost It

Since I improved my diet and started eating fermented foods, I have had no colds at all, and my recent bout of Covid was mild in comparison to the first time, which made me staggeringly ill for 2 weeks then another week of 'just' ill.
 
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