Search
Search
About
Log in
Join
Experiences with
Otomize ear spray
Posts
Communities
4,247 public posts
Filter results
It’s not hearing loss, it’s Eustachian Tube Dysfunction (they think)
Since having bacterial meningitis in January 2023, my ears have felt sort of blocked. After my follow up appointment a couple of weeks of coming out of hospital, they thought I had lost some hearing. I had a hearing test today- hearing is absolutely fine. They think I may have Eustachian Tube Dysfunction
Since having bacterial meningitis in January 2023, my ears have felt sort of blocked. After my follow up appointment a couple of weeks of coming out of hospital, they thought I had lost some hearing. I had a hearing test today- hearing is absolutely fine. They think I may have Eustachian Tube Dysfunction
ElephantLover2023
in
Meningitis Now
1 year ago
Menieres tinnitus
I have recently been diagnosed as having Menieres disease . Although we seem to have got the vertigo under control, for now at least, my tinnitus is driving me insane. I'm struggling more than anything withe the aural fullness and ear pain, as if it's going to burst. The pressure in my ear greatly affects
I have recently been diagnosed as having Menieres disease . Although we seem to have got the vertigo under control, for now at least, my tinnitus is driving me insane. I'm struggling more than anything withe the aural fullness and ear pain, as if it's going to burst. The pressure in my ear greatly affects
Tiggywinkle23
in
Tinnitus UK
1 year ago
Curious in the USA
I know this is a British site, and I'm a Brit permanently living in the USA, so moderators please feel free not to post if this contravenes your rules. And it's mainly for US people to answer, as I know I'm not the only one. I have moderate Tinnitus. Very annoying, but liveable, doesn't change too
I know this is a British site, and I'm a Brit permanently living in the USA, so moderators please feel free not to post if this contravenes your rules. And it's mainly for US people to answer, as I know I'm not the only one. I have moderate Tinnitus. Very annoying, but liveable, doesn't change too
PABLR
in
Tinnitus UK
1 year ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
thyroid and tinnitus
I was diagnosed with under active thyroid about 9 years ago and take 75 mg levothyroxine daily. I have been experiencing tinnitus for many years now, but wonder if there is a link between thyroid disorders and tinnitus?
I was diagnosed with under active thyroid about 9 years ago and take 75 mg levothyroxine daily. I have been experiencing tinnitus for many years now, but wonder if there is a link between thyroid disorders and tinnitus?
Rockyport
in
Thyroid UK
1 year ago
Anyone got endolymphatic hydrops but not Ménière’s?
Just curious to hear what symptoms and treatment are like? I’ve been diagnosed with chronic vestibular migraine but consultant now thinking it could be EH due to my symptoms- persistent vertigo/dizziness, constant T but fluctuating in pitch, pressure feeling in head, fullness, popping and what I call
Just curious to hear what symptoms and treatment are like? I’ve been diagnosed with chronic vestibular migraine but consultant now thinking it could be EH due to my symptoms- persistent vertigo/dizziness, constant T but fluctuating in pitch, pressure feeling in head, fullness, popping and what I call
ArtyPants46
in
Tinnitus UK
1 year ago
Carbocisteine 375mg
I’ve been taking 4 daily of this medication for several years. However last couple of weeks I’m coughing lot and not always able to get up mucus, including after using Aerobika. My physiotherapist says when she listens to chest there are more noises than used to be. The product leaflet says two capsules
I’ve been taking 4 daily of this medication for several years. However last couple of weeks I’m coughing lot and not always able to get up mucus, including after using Aerobika. My physiotherapist says when she listens to chest there are more noises than used to be. The product leaflet says two capsules
Morrison10
in
Lung Conditions Community Forum
1 year ago
Can emotional distress cause problems?
I added T3 to my Levo a few months ago and all seemed to be going well. How ever on two occasions since then I’ve received some bad news about sudden deaths of people I know ( one a very close aunt). Now I know I have PTSD so that is an added issue , but I feel like I’ve been hit by a bus! I mean I feel
I added T3 to my Levo a few months ago and all seemed to be going well. How ever on two occasions since then I’ve received some bad news about sudden deaths of people I know ( one a very close aunt). Now I know I have PTSD so that is an added issue , but I feel like I’ve been hit by a bus! I mean I feel
SarahJane1471
in
Thyroid UK
1 year ago
Deaf in one Ear but it still aches!
About 25 years ago I had an experimental grommet fitted into my left ear. Within few hours it was totally blocked, but I had to wait 7 months for it to be removed, by which time I was told that the nerve was dead and I wouldn’t be able to hear through it. However now I still get earache in it! Does anyone
About 25 years ago I had an experimental grommet fitted into my left ear. Within few hours it was totally blocked, but I had to wait 7 months for it to be removed, by which time I was told that the nerve was dead and I wouldn’t be able to hear through it. However now I still get earache in it! Does anyone
Morrison10
in
Lung Conditions Community Forum
1 year ago
phone call at last
Hello all you kind , knowledgeable people out there. Some may remember that l have posted before and that l am currently on Temgesic. At the moment l take 600mcg at 5 pm and 800mcgs at 10.30 pm. It has taken about 10 months or so to titrate up to this dosage. Although Temgesic has never fully covered
Hello all you kind , knowledgeable people out there. Some may remember that l have posted before and that l am currently on Temgesic. At the moment l take 600mcg at 5 pm and 800mcgs at 10.30 pm. It has taken about 10 months or so to titrate up to this dosage. Although Temgesic has never fully covered
bedith6
in
Restless Legs Syndrome
1 year ago
MRI/MRE
we’ll, I was stressing for nothing. The MRI was nothing. They use the 3T which is a little larger, not much, than the traditional MRI and did nit have the loud banging and clanging. It had a little noise but my country music drowned most of it out. Now the MRE is a little different story. Because I’
we’ll, I was stressing for nothing. The MRI was nothing. They use the 3T which is a little larger, not much, than the traditional MRI and did nit have the loud banging and clanging. It had a little noise but my country music drowned most of it out. Now the MRE is a little different story. Because I’
gwillistexas
in
PBC Foundation
1 year ago
autoimmune hearing problems
I’ve posted this on SRUK forum too. Sorry this goes on a bit. Along with my UCTD with systemic sclerosis gut problems I’ve developed, I’ve had hearing problems for years. I’ve never really thought it could be another autoimmune problem but recently I couldn’t hear my own voice. I wear hearing aids and
I’ve posted this on SRUK forum too. Sorry this goes on a bit. Along with my UCTD with systemic sclerosis gut problems I’ve developed, I’ve had hearing problems for years. I’ve never really thought it could be another autoimmune problem but recently I couldn’t hear my own voice. I wear hearing aids and
Halfwayuphill
in
LUPUS UK
1 year ago
autoimmune ear problems?
Sorry this goes on a bit. Along with my UCTD with systemic sclerosis gut problems I’ve developed, I’ve had hearing problems for years. I’ve never really thought it could be another autoimmune problem but recently I couldn’t hear my own voice. I wear hearing aids and have just got new ones and thought
Sorry this goes on a bit. Along with my UCTD with systemic sclerosis gut problems I’ve developed, I’ve had hearing problems for years. I’ve never really thought it could be another autoimmune problem but recently I couldn’t hear my own voice. I wear hearing aids and have just got new ones and thought
Halfwayuphill
in
Scleroderma & Raynaud's UK (SRUK)
1 year ago
Please, help. Eustaquian tube obstruction instead of tinnitus?
I was almost surely diagnosed with tinnitus after seeing a couple of doctors but I'm experiencing things that make me positive I instead just have my Eustaquian tube closed either by wax or mucus from a large series of un-properly cured colds. 1. I've been having this mucus sensation in the back of
I was almost surely diagnosed with tinnitus after seeing a couple of doctors but I'm experiencing things that make me positive I instead just have my Eustaquian tube closed either by wax or mucus from a large series of un-properly cured colds. 1. I've been having this mucus sensation in the back of
Mirror665
in
Tinnitus UK
1 year ago
Pulsatile tinnitus, headaches and sleep!
Hello Had my audiology test. No deafness but ENT referral that he said could take 18 months, on the pulsatile tinnitus. I spoke to him about the headaches but he said what I described wasn't a red flag. So now we wait. Can I please ask about these headaches and sleeping? I read to try to sleep with
Hello Had my audiology test. No deafness but ENT referral that he said could take 18 months, on the pulsatile tinnitus. I spoke to him about the headaches but he said what I described wasn't a red flag. So now we wait. Can I please ask about these headaches and sleeping? I read to try to sleep with
hollyrain
in
Tinnitus UK
1 year ago
Yawning so much! 🥱
Hello all, Quick question for you to help with if possible. Why, oh why do I yawn 🥱 upon doing any exercise? My Wk 1 R2 run was interspersed with so many yawns! But then I remembered I yawn if I ever go for a walk with steep inclines and yawn when I climb the hospital stairs at work. I do
Hello all, Quick question for you to help with if possible. Why, oh why do I yawn 🥱 upon doing any exercise? My Wk 1 R2 run was interspersed with so many yawns! But then I remembered I yawn if I ever go for a walk with steep inclines and yawn when I climb the hospital stairs at work. I do
Wonderland1
in
Couch to 5K
1 year ago
Advice on RLS as a reaction to medication?
Hello, I currently have long covid and vestibular neuritis, and have had these conditions for around six months. The vestibular neuritis is causing considerable vertigo symptoms. Just over a month ago, my GP gave me Betahistine to try and ease the vertigo. Within a few days of this, I began getting
Hello, I currently have long covid and vestibular neuritis, and have had these conditions for around six months. The vestibular neuritis is causing considerable vertigo symptoms. Just over a month ago, my GP gave me Betahistine to try and ease the vertigo. Within a few days of this, I began getting
RiversofLondon
in
Restless Legs Syndrome
1 year ago
Light headed.
A couple of times this week I have felt light-headed for a few minutes. I do have AF. I take Warfarin and Bisoprolol. I usually feel well. I wonder is this with having AF? I haven't experienced this before. My AF was diagnosed about 4 years ago.
A couple of times this week I have felt light-headed for a few minutes. I do have AF. I take Warfarin and Bisoprolol. I usually feel well. I wonder is this with having AF? I haven't experienced this before. My AF was diagnosed about 4 years ago.
benmaise
in
AF Association
1 year ago
Pulsatile Tinnitus and Hypertension
Hi,Anyone else suffering from pulsatile tinnitus and high BP? I'm currently waiting ENT and CT scan for further investigation. I'm struggling to sleep at night when the tinnitus is really loud, tried headphones, but can't sleep with the noises playing in my ear.
Hi,Anyone else suffering from pulsatile tinnitus and high BP? I'm currently waiting ENT and CT scan for further investigation. I'm struggling to sleep at night when the tinnitus is really loud, tried headphones, but can't sleep with the noises playing in my ear.
Pinkutd
in
Tinnitus UK
1 year ago
bystolic vs metropolol
has anyone had wheezing and shortness of breath on metropolol? Pulmonary dr just switched to bystolic?!
has anyone had wheezing and shortness of breath on metropolol? Pulmonary dr just switched to bystolic?!
Jancam1943
in
AF Association
1 year ago
Is this a breakthrough - I'm going to try it ASAP
Hi All, I have had various levels of Tinnitus for a number of years, over the last few weeks it has got worse and louder so I did some more research. https://www.otologie.com/about-lenire/ This looks promising, will get a hearing test tomorrow and then either do an online consultation or pop over
Hi All, I have had various levels of Tinnitus for a number of years, over the last few weeks it has got worse and louder so I did some more research. https://www.otologie.com/about-lenire/ This looks promising, will get a hearing test tomorrow and then either do an online consultation or pop over
Django1
in
Tinnitus UK
1 year ago
1
...
20
21
22
...
100
Next page
10
20
30
40
50
60
70
80
90
100
Filter results
Clear filters
Posted in
All communities
British Tinnitus Association
574 results
Thyroid UK
371 results
Tinnitus UK
336 results
View top 10 communities
Sort by
Most Relevant
Newest