Is tinnitus an ME symptom? - Discussion of evidence

No, there is no irony in what I am saying. That is why I find it so strange that you should find it.

I am simply pointing out what is likely to be an own goal.

As far as I can se in the USA because the CDC or IOM or whoever did not stick to clear arguments things are likely to unravel back to where they were. In the UK the NICE committee did a good job but because they did not stick to clear arguments there is wriggle room for both CBT and GET. Maybe my uncompromising approach is not tactically ideal but over the years it has paid off for me. Not in financial terms but in terms of getting worthwhile things done.

 

Over the years of belonging to various ME/CFS groups, I have seen too many people attributing any new medical symptoms to ME. Anytime someone has a new symptom they should get it checked out by their GP as chances are it has nothing to do with ME.

 

By reading. I then explain why reading levels the playing field, e.g., it provides readers with knowledge of those associations where they have been documented.

 

Look up Vickie Logan. Her singular case study almost dismantled Lyme orthodoxy. Before the medical case study, her story was just an anecdote. So one patient sans statistical associations can influence in a powerful fashion medical science.

 

N = 1.
My own tinnitus is directly related to my ME symptoms. When I'm reasonably well I don't have any tinnitus.
But when I have PEM I have pronounced tinnitus in my right ear the level of which is directly related to the severity of my ME (flu like illness etc). When my ME is at it's worst I also get it it in my left ear but not as bad as in the right ear. The ringing in my right ear is the first indication of PEM onset and it is the last symptom to resolve itself (3-16 days later).
I can't separate my tinnitus from my ME, they appear to be part of the same problem, I can never have one without the other.

 

I had very mild tinnitus prior to getting ME/CFS. However my tinnitus became noticeably worse the day I came down with EBV.

Similar to @John Mac, my tinnitus ramps up when I'm in PEM. It's one of the first signs of PEM for me (along with pain in my calves) and is so reliable it is one of my warning signs that I need to immediately stop whatever I'm doing. I can usually predict the intensity and duration of a crash from the volume and pitch of the tinnitus.

A few years ago, I had a significant setback in my ME. (One doctor said it was a reactivation of EBV but I haven't seen the test results to confirm.) In addition to the standard tinnitus I get in a usual crash, I could hear a second (and sometimes a third) kind of tinnitus at a different pitch and volume from the first.

I no longer mention tinnitus to doctors after being told that reporting it was a sign that I was 'catastrophising' and was 'overly focussed on trivial symptoms'.

 

I think the problem with tinnitus is that it can be switched on or off by attention mechanisms that act both short term and long term and are not necessarily consciously controllable.

The most remarkable thing for me is that I had tinnitus for thirty years - it was always there if I asked myself if it was - until I got hearing aids. The hearing aids suppressed the tinnitus but not just when I was wearing them. Even lying in bed at night without them on I could not get the tinnitus to be there. It had gone. But there are times when it reappears even with the hearing aids on. It has been present this last week or so and that is since being ill with Covid and recovering over 6 weeks but who knows if that is relevant.

And a lot of symptoms in other places increase when one is ill for another reason - I get back or shoulder pain when I have a cold for instance. I think I would expect tinnitus to be more apparent when PWME are feeling bad but that does not necessarily mean that more PWME have tinnitus than the general population.

 

I will contribute my penny worth....
Blood flow and blood volume are issues it is often suggested for people with ME.

Husband has ME and has low background tinnitus.

He also when stressed has Pulsatile tinnitus (which it is suggested is often caused by disorders or malformations in the blood vessels and arteries, especially those near the ears.)
Can low blood flow cause tinnitus?
Blood vessel disorders.

These blood flow changes can cause tinnitus or make tinnitus more noticeable.4 Feb 2021

So ME or comorbidity,.... or both?

 

My tinnitus started well before my ME. I didn't notice any drastic change in it when I did develop ME. I think there may be a link between neuroinflammation and tinnitus, and ME seems to involve neuroinflammation, but tinnitus isn't unique to ME.

I like to blame ME for all sorts of things. Haven't cleaned the floor in a while: ME. Procrastinated over taxes: ME. Sore muscles after washing windows: ME.

 

I kept a log for a total of 434 days of my symptoms, their severity and other factors such as supplements taken, food, weather patterns and mental wellbeing. I then used machine learning algorithms to identify any factors that would differntiate the severity of my symptoms. Using a sequence mining algorithm, i managed to find my "vicious cycle" of symptoms, of which the beginning and end was tinnitus.

The graph below has been sent to a selected number of researchers in order to explain more about the vicious cycles i have been experiencing :





My vicious cycle would go as follows :

Tinnitus1 : The point in time where tinnitus is experienced (unilateral)
Red circle : It is the period in time right after the tinnitus1 incident where energy is affected, very negative mental wellbeing, several neurological symptoms at their worst.
Blue circle : Several hours after the tinnitus1 incident, i begin to experience symptoms with somewhat less severity.
Green circle : day(s) after the tinnitus1 incident , symptoms significantly better until the next tinnitus incident (tinnitus2)

When i was getting worse the time between each tinnitus incident was decreasing. From this i hypothesised that if i could stop tinnitus from taking place there would be improvement on my symptoms. This was indeed the case. The less tinnitus incidents i experienced the better i felt, ultimately leading to my recovery.

 

I developed tinnitus after a prolonged bout with bronchitis, which caused the worst cough of my life. I don't notice it much during the day, but at night I need a white noise machine.

 

I used to get a lot of tinnitus and deafness, but I think it was due to scratching and trying to clean out my ears with various things. They tended to itch a lot in the summer. Sometimes I went completely deaf until the ears were eventually unblocked. I couldn't even use the phone.

 

n = 1. Tinnitus was a symptom I had never experienced before and started exactly at the same time as my first major ME crash. Now I get it everytime I crash.

 

Interesting. One of my aunts developed tinnitus after taking statins. Seemingly it's a not uncommon side effect.

 

I don't know if this resonates for other people, but I think my tinnitus is tiny muscles in my ear shaking rapidly back and forth, or spasming. If I'm wearing ear plugs, I can feel the pressure behind it rise and fall rapidly, or a sensation like my ear is sucking on the ear plug rhythmically. I only developed tinnitus after I started experiencing fasciculations of the muscles in my scalp and face, and for the brief few months where those went away, the tinnitus was also absent.