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Acupuncture, thoughts?

If I had your symptoms I would definitely seek out a good osteopath, one familiar with cranial work. The amount of problems I've experienced from impinged nerves in my upper vertebrae is pretty long but did include teeth grinding and jaw alignment.
Best wishes with it...👍🏻
Cheers Mark, someone else sent me a DM saying the same.
Again though this isn't bloody straight forward because I went to see a Chiropractor about 10 years ago and it was him who gave me my chronic tinnitus, now I have this second tinnitus with a billion other symptoms. Needless to say I would be terrified of seeing an osteopath in case he made my 2 x tinnitus worse.
Having said that, I will see the dentist first, then go from there, If I get no joy I need someone who knows what the hell they are talking about rather than someone who just wants my money.
 
Kermit: Have you had Covid?
Some of what you are describing could be as a result of long Covid - especially the tinnitus.
 
Kermit: Have you had Covid?
Some of what you are describing could be as a result of long Covid - especially the tinnitus.
I couldn't agree more and I was shocked when neither of the Drs nor the ENT specialist asked me this as I thought this would be their first question.

As far as I know I haven't had Covid but of course it is possible I did and was asymptomatic. I'd be shocked if I have had it but as I say anything is possible.
 
Have you had any other symptoms of long Covid? Chest pain? Muscle ache? Fatigue? Sudden hearing loss?
 
Have you had any other symptoms of long Covid? Chest pain? Muscle ache? Fatigue? Sudden hearing loss?
No none of those.
Give it another month though and who knows!
 
It's sounding more and more like your dentist solving it.
Tinnitus is not much fun is it?
 
It's sounding more and more like your dentist solving it.
Tinnitus is not much fun is it?
Oh I hope so.

I hate to admit it but on many occasions 10 years ago when I first got this high pitched hissing tinnitus I thought I was going to have to kill myself. I managed to get through it.
Now this second one has popped up but it is so different, it is more like a hearing issue as if I close my ears it will go, whereas of course my 'proper' tinnitus never ever goes whatever I do.
It's almost like a symptom of Meniere's where my ear is hunting for a low sound. If a car drives past the house it relieves the noise. It's all very odd.

So yeah tinnitus is vile, having 2 of them is err horrific.

Sounds like you have it, not cool.
 
I have I think four different noises but it's hard to tell. First one was like a very low frequency hum, next ones were the high pitch whistle and hiss due to hearing loss and also have now the pleasure of hearing the blood flowing through my head which is a low pitched roar. I think what happens is the brain turns up the volume when your hearing starts to fail and picks up noises that it would have previously ignored.

It used to bother me continually but I eventually accepted that it's not actually doing me any harm and have learnt to live with it. More of a problem for me now is the hearing loss, especially now having to listen to and understand a foreign language, I can barely make out English sometimes.
 
I have tinnitus , but not all the time.
I got Covid very mildly last February and then long Covid reared its ugly head at the end of August. The muscles at the top of my arms and legs ache all the time and I have an almost constant pain in my chest. Then I got the 'low buzz' tinnitus.
Last Tuesday I got sudden hearing loss in both ears. I went to A7E as this can be a warning that a stroke is on the way. I was sent to ENT and told that there was no blockage or infection. I went to see a nurse practitioner at my GP's surgery and she said that if it's not a blockage or infection it must be because I've had high blood pressure for some time.
I've lived with Heart Failure for a few years now so I check my weight, blood pressure, heart rate and oxygen saturation most days and I do NOT have high blood pressure. 135/82 today with a resting heart rate of 62 and oxy of 99%.
So, as usual, I've done my own research and found that my muscles ache because the enzyme that tells the muscle how much oxygen to take out of the blood flowing through it has been affected by Covid. My heart is a muscle so that explains that too. Lack of oxygen to the arteries in the ear can cause sudden hearing loss (and tinnitus) so I think I've got Long Covid.
Reasonable assumption? Trying to get any sort of help for long covid is a waste of time. Clinics have been set up - but all they do is gather information from you and offer no help.
I've had a chest X-ray, blood tests, ECG and Echocardiogram but I've had to push hard to get these and I am awaiting the results.
Like you, Kermit, I have no faith in the NHS because of their incompetencies causing the death of a loved one so I use the NHS to gather information and then find my own natural solutions where possible. My heart failure was caused because my GP gave me Tramadol for arthitic pain. He didn't tell me that it could cause arrhythmias that could cause heart failure. He didn't monitor me and let me use Tramadol for more than two years leading to HF at level four. I could write a book about the NHS errors and omissions that my family have endured.

I try to work along with Mother Nature now and I use Earthing to reduce inflammation and to keep my cells properly charged. I use light therapy for most other things. A friend and I decided to do this a few years ago and designed our own 300watt light with LEDs that are from 415nm to 1070nm wavelength. Blue light sets the body clock if used on a morning so it knows when to do various things. It also kills germs - including viruses. Green help with pain. Red and near infra red penetrate deepest and help with pain, healing, and they also energise the cells to produce ATP (energy).
Well worth the research if you have the time.
 
I have tinnitus , but not all the time.
I got Covid very mildly last February and then long Covid reared its ugly head at the end of August. The muscles at the top of my arms and legs ache all the time and I have an almost constant pain in my chest. Then I got the 'low buzz' tinnitus.
Last Tuesday I got sudden hearing loss in both ears. I went to A7E as this can be a warning that a stroke is on the way. I was sent to ENT and told that there was no blockage or infection. I went to see a nurse practitioner at my GP's surgery and she said that if it's not a blockage or infection it must be because I've had high blood pressure for some time.
I've lived with Heart Failure for a few years now so I check my weight, blood pressure, heart rate and oxygen saturation most days and I do NOT have high blood pressure. 135/82 today with a resting heart rate of 62 and oxy of 99%.
So, as usual, I've done my own research and found that my muscles ache because the enzyme that tells the muscle how much oxygen to take out of the blood flowing through it has been affected by Covid. My heart is a muscle so that explains that too. Lack of oxygen to the arteries in the ear can cause sudden hearing loss (and tinnitus) so I think I've got Long Covid.
Reasonable assumption? Trying to get any sort of help for long covid is a waste of time. Clinics have been set up - but all they do is gather information from you and offer no help.
I've had a chest X-ray, blood tests, ECG and Echocardiogram but I've had to push hard to get these and I am awaiting the results.
Like you, Kermit, I have no faith in the NHS because of their incompetencies causing the death of a loved one so I use the NHS to gather information and then find my own natural solutions where possible. My heart failure was caused because my GP gave me Tramadol for arthitic pain. He didn't tell me that it could cause arrhythmias that could cause heart failure. He didn't monitor me and let me use Tramadol for more than two years leading to HF at level four. I could write a book about the NHS errors and omissions that my family have endured.

I try to work along with Mother Nature now and I use Earthing to reduce inflammation and to keep my cells properly charged. I use light therapy for most other things. A friend and I decided to do this a few years ago and designed our own 300watt light with LEDs that are from 415nm to 1070nm wavelength. Blue light sets the body clock if used on a morning so it knows when to do various things. It also kills germs - including viruses. Green help with pain. Red and near infra red penetrate deepest and help with pain, healing, and they also energise the cells to produce ATP (energy).
Well worth the research if you have the time.
George, I am so sorry you lost someone you love due to the incompetence of the NHS, it really makes everything worse doesn't it? I get intrusive thoughts regularly now thinking 'I should have got Mum off that ward and she'd still be here' It really is painful isn't it.

And wow your GP caused your heart failure, incredible, I really do not know what to say, that is scary stuff. Makes my problems seem so silly.

It is ridiculous that so many of us are left to Google our issues. I knew more than the ENT when I saw her. She didn't even ask me if I was taking any regular medication. Since then after Googling I have stopped taking Cetirizine which I had been taking for 20 years as this can cause brain fog, since stopping the medication this is getting much better. I had thought it was due to being perimenopausal but the HRT wasn't helping, I was also told after blood tests that I had low folate so started taking folic acid but after many months the brain fog was still with me. So yep I was left to Google that. How can you not even ask a patient if they are on any medication? I could be on all sorts as far as she is concerned.

It is a scary time now, if anyone in my family gets ill I will probably go straight into cardiac arrest because I will panic so much from fear that the NHS is 'too busy to help'

Many thanks for taking the time on this, George, much appreciated. xxxxxxx
 
More questions for you Kermit.
Is your tinnitus in one ear or both?
When did the new type of noise start?
Is it there all the time or does it lessen or go sometimes?
Did it coincide with anything else at the time? (eg new phone, new microwave oven.)
 
Here's a chart that shows how to keep your brain happy, which then helps with other issues such as tinnitus.


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More questions for you Kermit.
Is your tinnitus in one ear or both?
When did the new type of noise start?
Is it there all the time or does it lessen or go sometimes?
Did it coincide with anything else at the time? (eg new phone, new microwave oven.)
Just one ear, my left which is the same ear as my chronic T.
Started last summer, about August maybe.
It's there all of the time.
Nothing new at the time, but I'd had a tooth out a few weeks before after 3 lots of antibiotics for an infection.
 
That's interesting as high dosage antibiotics are known to damage the cell in the inner ear.
 
That's interesting as high dosage antibiotics are known to damage the cell in the inner ear.
Ah interesting.
Wouldn't explain everything else but interesting anyway
 
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