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#31
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^ Aww I'm so sorry that you're having to endure pain on a daily basis Azalea
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#32
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#33
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Have you looked into ME/CFS symptoms and treatments? On that program about long covid the other day I think they said that for some people, long covid is ME/CFS so there could be some overlap when it comes to treatment?
https://www.health.harvard.edu/blog/...-2020101521173 |
#34
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^ Could it be something along the lines of sleep apnea? Or.....I forget what that thing is called, when you dream that you're falling and then you jerk awake and your heart's beating fast? (Edit: hypnic jerk.)
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#35
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That's ok. They do say that there are a lot of neurological symptoms that people can have due to long covid. I expect the medical community will gain more knowledge about it all over time, but that will probably take a long time unfortunately.
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#36
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^
that sounds really rough Nanuq, the night tremors, I know that tremor can be a way for your body to react if it's feeling really cold, it's the bodies way of generating heat by stimulating the blood flow, when I had a reaction after AZ Vaccination , my body was shivering at night, imagining it was somehow freezing, (but obviously it wasn't) I know that diazepam can be prescribed for body spasms, I'm surprised they haven't done that if it's a core issue you are having,... came across a short piece on Long Covid affecting women. |
#37
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AZ vaccination yesterday, spent an awful night dressed in thermals under 3 big duvets and a blanket and still shivered all night, a banging headache and sore eyes into the mix. Got up this morning feeling rough as and haven’t stopped eating.
...and they say the follow-up dose gives you worse side effects than the first!! ![]() ![]() ![]() |
#38
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^/^^ Maybe the second dose will be better for people who had a nasty reaction to the first dose!
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#39
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^^ poor you Kooky. How many days were you ill for post-vaccination? I’ve heard of people vomiting (and worse) having a whole week of feeling rough!
^ That’s my hope Dougella ![]() |
#40
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^Hello young lady, where the devil have you been?
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#41
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It's probably a good idea they've spaced out the first and second jabs as much as possible because if people do get worse affects after the second, it might put people off getting either.
As most people haven't had the second one yet, there haven't been many reports of issues. Although I did read that if you've had covid already, the first jab is bad (as it's your second interaction with covid). If you haven't had covid, then the second jab is bad (as it's your second interaction with covid after the 1st jab). |
#42
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People have been receiving their second doses in other countries for a while now despite reports of the side effects being worse after the second. I haven't heard of it putting anyone off yet. Does it still count as an "interaction" with the virus when none of the vaccines actually contain a live version of it?
I was pretty ill for almost a week after the first and I've never had the virus (to my knowledge). The side effects almost seem to be completely random in who they affect besides different vaccines seeming to have roughly the same range of symptoms (e.g. Oxford sounds like it's more fever-based illness from what people report, whereas Pfizer is more muscle/nerve pain and tiredness). |
#43
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The vaccines "contain material from the virus that causes COVID-19" so I would say it's still an "interaction" with it and does make a difference on whether you get side effects or not. https://www.cdc.gov/coronavirus/2019...they-work.html Quote:
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#44
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^^ My Mum had covid around the end of last year and had the covid vaccine last month but didn't get any severe symptoms with it, just felt a bit under the weather for a few days. But she is in her 60s, it seems like people who are younger can tend to get more severe side effects, which might be something to do with their immune system. But otherwise it does seem random as to who reacts more strongly to it!
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#45
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Yeah they say young people get a worse response as they have a stronger immune system.
So I guess if you have no response, that means you would've struggled if you got covid as you have a weak immune system? Quote:
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What reactions people get the most: https://www.cdc.gov/mmwr/volumes/70/wr/mm7008e3.htm Quote:
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#46
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I've noticed this past year since lockdown that my physical health has deteriorated abit due to not going anywhere basically just working then going home, its been a year since i've indoor climbed which i totally miss because it helps with my mental health and it gives me abit of exercise too which is always good, last few weeks my back/neck has been playing up just hope that settles down so in all its not been a good time... just hope when most things open back up and we have a new norm it can get better!
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#47
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My ear still isn’t back to normal. It feels like its trying to sort it self out. Constantly pop, pop, pop, popping, but never fully unpopping.
It feels weird and full (sensation wise, not to touch, I haven’t touched it). I keep hoping that if I yawn it will magically unpop. Maybe this is just how it will be from now on. I’m not in any pain or anything like that. It’s more of a mildly annoying discomfort. Guess I should ring the doctor tomorrow to ask for some advice. |
#48
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^ thank you, I've been sniffing one of those this week for my blocked nose. I hoped my ear would unblock when my nose did, but nope!
I kind of want to stick the inhaler in my ear to see if it will work! |
#49
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Oooh. That is good to know that there is a possible treatment. I have been to the nurse two or three times about this, so am starting to feel a bit annoying haha. They've never actually looked at my ear. It's all been over the phone. That's not a criticism, I just wonder if they will invite me in to take a look tomorrow.
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#50
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^ Oooo - had to google that nose balloon! That's really reassuring to know that your ear cleared up on its own
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#51
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I'm going to rant in here now. Since its sort of health related.
I had a CT Scan on Feb 16th - I've heard nothing. I went to doctors on Feb 24/25th for something else and asked about the scan. They said it would take a bit longer to get any results..fine fine. Still nothing. I have major health anxiety so I avoid this sort of thing at all costs. But after several hours of pacing up and down this morning I eventually made myself an NHS app log in so I could see my own information. I finally plucked up enough courage..to find its a very limited service until your GP allows you to see more information..so I don't have anything even on there apart from some sort of allergic reaction to medication in 2008! (Which I didn't even know I had) The GP has abandoned all hope till Tuesday - if you have a problem contact 111! Fekk sake, its so hard to get any information out of anyone, and its mostly self inflicted because I referred myself to a private cardiologist so I don't think they knew where to send the test results back to. ![]() |
#52
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^ there's nothing more anxiety inducing than waiting for results
![]() Is there any chance you chase up the private place that you went to for the tests to see where they sent the results and when they'll be ready? Hopefully their lack of urgency means it's good news ![]() |
#53
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I just sent an email to one of his secretaries
It's a very weird letter, hes either got 4 secretaries all to himself or theres a pool of them that deal with a couple of consultants at the private hospital. I'd like to think if my heart was knackered they wouldnt wait 6-7 weeks to tell me but ![]() It's a very weird issue. When a consultant tells you he doesn't think theres anything serious going on but then in the letter goes on to list various things that aint right..its slightly concerning. I've had some shocking experiences with the NHS in the past so although I don't want to get on the hating bandwagon..I'm still quite concerned they either never pressed record/they lost my results or they are still sat on a desk somewhere waiting to be shredded. ![]() I'd convinced myself no news is good news, I don't know why I've woke up today convinced I'm about to need heart surgery ![]() |
#54
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Aww Toxic. I get exactly the same - health anxiety is a horrible feeling.
At least with this digital age, you can rest assured that your results will be stored somewhere so they will be retrievable if they've been sent to the wrong place or if if they have accidentally not been sent off. Hope they get back to you soon so you can have some answers. In the meantime make sure you do some distracting things for a little bit. |
#55
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I've picked the wrong time to get brave and try and get some answers for all this, Easter is like the only time aside from xmas when things close!
The secretary I picked claims anything NHS related would never go back there, he has a private secretary and an NHS secretary (lardy da!) I either have to try my GP again or try his other secretary who would at least know if "something" exists..but because its easter your not allowed help ![]() |
#56
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^ oh no! Let’s hope they can get it sorted on Tuesday.
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#57
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I went to the nurse about my ear. She was luffly. She had a good rummage around in my ear hole and said there’s no sign of infection anymore. She suggested I try some olive oil ear drops. If it’s not back to normal by the end of next week, she says they’ll have to syringe my ears
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#58
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^ Delayed good luck on the ear front..its a weird one, its something I've never really had a problem with yet you hear of pretty much everyone having some sort of ear infection at some point!
I'm pretty miffed. I spent all the weekend bracing myself to find out what was going on. I send the e-consult message thing at like 7:55am and run off to work expecting to get some sort of phone call this week..but it was fine it wasn't at that exact minute I could put it off for a while. 10 minutes later I get one back saying they have no idea about any CT scan, it still must be at the hospital and I should contact them. I spend most of the morning bouncing between the hospital and a secretary not answering me. I finally get through to the CT department who says my report went back to the cardiologist on the 23th of March and my best bet is trying her again. Eventually in the afternoon someone answers. It's not her, shes not at work today..I get what sounds like a 15 year old on work experience filling in. Oh yes, I can see a scan here..I'll leave them a reminder tomorrow to actually consider looking at it/writing a report. 7 weeks..7 weeks and no ones even looked at it yet. I'd told myself no news is good news..but now I'm back to the start..no news is ..no news because no ones been arsed to even look at it ![]() I know he said the NHS would be fine..I don't think he was aware how much I've got myself in a state over this, I should have just paid the £400 for the CT scan (but he told me it would be an MRI which was £1700) ..Sigh |
#59
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^ oh no, that's terrible! Maybe you could ring them again today and ask for the doctor to ring you back to explain the results because you've had to wait 7 weeks and it's making you worry. Hopefully someone can speak to you about them. A few moments of phone anxiety will hopefully be more endurable than waiting for a letter to be written.
I'd like to think that because they're taking their time over it that it's not anything bad because they would have referred you ![]() Hope you get some answers soon. |
#60
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^^ It's absolutely terrible the way you've been waiting for so long for your scan report Toxic. One wonders if they would have ever gotten around to looking at it and getting back to you! Hopefully now that you've started chasing them up they will get back to you sharpish with the results and it will be good news.
I've been suffering with constant pain in both my legs particularly around the lower half and the ankle area. I also get twinges in my arms but it's not as bad. I'm now taking painkillers every day - paracetamol, Ibruprofen, Aspirin, and I've even tried Co-codamol - but none of them give me any relief. The pain is hellish at night. The pain feels like it's deep in the core of my bones. I won't bother seeing a GP because if I do eventually get an appointment with one I won't get anywhere. Last time I went for something different I was treated like a silly neurotic woman and ended up having to go private where the Doctor found a physical cause. I'll rather put up with the constant pain than risk the humiliation of seeing my GP again. |