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hi there, I acquired tinnitus 3 months ago and had a hearing test last week resulting partially moderate to severe hearing loss. considering hearing aids as I am only 52. they are expensive though 3k for the cheapest ones. wondering how people have found the tinnitus reduction with aids?
hi there, I acquired tinnitus 3 months ago and had a hearing test last week resulting partially moderate to severe hearing loss. considering hearing aids as I am only 52. they are expensive though 3k for the cheapest ones. wondering how people have found the tinnitus reduction with aids?
TriumphT100
in
Tinnitus UK
5 months ago
worse through exercise
I have posted before about my tinnitus. It gets worse when ill & now found out that exercise has also made it worse. Went back to the gym Saturday to get me back walking as I don’t feel safe walking outside due to having balance problems & partial deafness caused by the injury to my left ear over a
I have posted before about my tinnitus. It gets worse when ill & now found out that exercise has also made it worse. Went back to the gym Saturday to get me back walking as I don’t feel safe walking outside due to having balance problems & partial deafness caused by the injury to my left ear over a
091960
in
Tinnitus UK
5 months ago
Breast and pelvis tenderness after injecting
Hi All, I am new to the forum and grateful for all the info I have received so far. My query is: do any of you experience breast tenderness and lower abdomen/ pelvic pressure after injecting?
Hi All, I am new to the forum and grateful for all the info I have received so far. My query is: do any of you experience breast tenderness and lower abdomen/ pelvic pressure after injecting?
Jjjmmm
in
Pernicious Anaemia Society
5 months ago
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Pink cheek, ref Rapid Access for hearing loss
Hi everybody hope you are all doing well. I've NOT been diagnosed but briefly this is where I am now and wonder if anybody had similar without it being AN. Tinnitus and pulsatile tinnitus 24/7 for past 14 months or so, random vertigo. Headaches left temple and to rear of ear like the lower skull area
Hi everybody hope you are all doing well. I've NOT been diagnosed but briefly this is where I am now and wonder if anybody had similar without it being AN. Tinnitus and pulsatile tinnitus 24/7 for past 14 months or so, random vertigo. Headaches left temple and to rear of ear like the lower skull area
hollyrain
in
Acoustic Neuroma Support
5 months ago
sound distortion
hi I am new to the forum and would like to share and hear from other members on this subject I am suffering from tinnitus for many year following a me’nie’re’s disease this cause a loss of hearing as well. I have an hearing aid which helps to reduce the tinnitus. Some weeks ago I had a strange sound
hi I am new to the forum and would like to share and hear from other members on this subject I am suffering from tinnitus for many year following a me’nie’re’s disease this cause a loss of hearing as well. I have an hearing aid which helps to reduce the tinnitus. Some weeks ago I had a strange sound
Blueberry-muffin
in
Tinnitus UK
5 months ago
Improved?
Had investigations for right ear polyp that had been present for over 20 years but making routine ear micro suctioning difficult (long standing over production of ear wax). Had hearing test but waited for results (October 2023). Went to concert 3rd Nov and mistakenly did not wear ear plugs. Very loud
Had investigations for right ear polyp that had been present for over 20 years but making routine ear micro suctioning difficult (long standing over production of ear wax). Had hearing test but waited for results (October 2023). Went to concert 3rd Nov and mistakenly did not wear ear plugs. Very loud
GlenM12
in
Tinnitus UK
5 months ago
Buzzing… how do you get used to it? Or rather ignore it!
Hi I’ve had tinnitus for about 5 years. It started with the hissing sound. After trying sound therapy treatment, I became aware of a tune in one ear. It gradually faded and I was told I had wax in that ear. I think wax helped block my sound as I had it removed and 8 months on it is just starting to
Hi I’ve had tinnitus for about 5 years. It started with the hissing sound. After trying sound therapy treatment, I became aware of a tune in one ear. It gradually faded and I was told I had wax in that ear. I think wax helped block my sound as I had it removed and 8 months on it is just starting to
TishL
in
Tinnitus UK
5 months ago
Migraine and Tinnitus
Hi, I am a 64 year old man and suffered with severe migraine since childhood, about four years ago I started with Tinnitus which has been permanent since, I have tried Botox and many different migraine medications throughout the years, I have recently been given Anjovy which I am reluctant to try due
Hi, I am a 64 year old man and suffered with severe migraine since childhood, about four years ago I started with Tinnitus which has been permanent since, I have tried Botox and many different migraine medications throughout the years, I have recently been given Anjovy which I am reluctant to try due
beaverwood
in
National Migraine Centre
5 months ago
Rapid Decline - anyone experience this?
I am an 82 year old woman who was diagnosed two years ago with SCA6 which my mother and grandmother also had. For the last two years tho I was dizzy all the time, my speech increasingly slurred, and I had eye problems and issues with balance, I still walked three miles a day, drove (sometimes 1 1/2
I am an 82 year old woman who was diagnosed two years ago with SCA6 which my mother and grandmother also had. For the last two years tho I was dizzy all the time, my speech increasingly slurred, and I had eye problems and issues with balance, I still walked three miles a day, drove (sometimes 1 1/2
Hickox
in
Ataxia UK
5 months ago
Tinnitus and visual disturbances?
Does anyone else suffer from both tinnitus and visual disturbances? I don't mean synchronised in any way, just generally. I get classic visual migraines (with aura) every few weeks but get other visual disturbances more regularly that can occasionally be quite dramatic. My visual migraines pre-date my
Does anyone else suffer from both tinnitus and visual disturbances? I don't mean synchronised in any way, just generally. I get classic visual migraines (with aura) every few weeks but get other visual disturbances more regularly that can occasionally be quite dramatic. My visual migraines pre-date my
Fridays_Child_62
in
Tinnitus UK
5 months ago
Stress, again taking a comeback....
So I have been at work for 10 months and I have had to move rooms that I work in, honestly to help out that room and put the managers mind at rest I would be OK doing it. Well I thought it was lasting a couple of months but it hasn't. I ended up getting stressed out because of the noise and doing nothing
So I have been at work for 10 months and I have had to move rooms that I work in, honestly to help out that room and put the managers mind at rest I would be OK doing it. Well I thought it was lasting a couple of months but it hasn't. I ended up getting stressed out because of the noise and doing nothing
Hidden
in
Headway
5 months ago
hello 👋
just introducing myself to this fabulous group, looking forward to finding out new ways to cope with Tinnitus/dizziness
just introducing myself to this fabulous group, looking forward to finding out new ways to cope with Tinnitus/dizziness
Positivevibes24
in
Tinnitus UK
5 months ago
advice please
I am having checks for possible PMR at my request. Having suffered for the past four years with neck shoulder jaw and face pain eye disturbance and terrible drenching night sweats. I have almost self diagnosed. Although I am awaiting an appointment with Max facial as my ENT consultant said it was TMJ
I am having checks for possible PMR at my request. Having suffered for the past four years with neck shoulder jaw and face pain eye disturbance and terrible drenching night sweats. I have almost self diagnosed. Although I am awaiting an appointment with Max facial as my ENT consultant said it was TMJ
Nonameme
in
PMRGCAuk
5 months ago
Cladribine
I have recently been diagnosed as having RRMS. I have only had 2 relapses in the past year, both of which involved temporary loss of eyesight. On both occasions, my vision returned to normal by itself, without any need or medication to be prescribed. However, my most recent MRI contrast scan shows that
I have recently been diagnosed as having RRMS. I have only had 2 relapses in the past year, both of which involved temporary loss of eyesight. On both occasions, my vision returned to normal by itself, without any need or medication to be prescribed. However, my most recent MRI contrast scan shows that
max011
in
My MSAA Community
5 months ago
Mobility aid
I have fibromyalgia also suspected PoTs and just recently got diagnosed with me/cfs. I have been having some difficulty with walking and getting around the house, I am finding myself holding on to the walls and kitchen counter for some support/ balance as the pain is getting really bad, is it time for
I have fibromyalgia also suspected PoTs and just recently got diagnosed with me/cfs. I have been having some difficulty with walking and getting around the house, I am finding myself holding on to the walls and kitchen counter for some support/ balance as the pain is getting really bad, is it time for
Forgetmenot88
in
Fibromyalgia Action UK
5 months ago
Tinnutus Suddenly
So a year ago I had a virus that bought on tinnitus it seemed to go after a couple of months, though I think it was still there at some very low level and forgot about it I also have vertigo randomly for a few seconds if I roll over in bed or sit up fast and if I bend over and look under a desk say
So a year ago I had a virus that bought on tinnitus it seemed to go after a couple of months, though I think it was still there at some very low level and forgot about it I also have vertigo randomly for a few seconds if I roll over in bed or sit up fast and if I bend over and look under a desk say
Downup24
in
Tinnitus UK
5 months ago
Had my 13-YRO T-Tube grommet removed and new one put in put in last week, still feel nauseous/ill...is this normal or to be expected?
[i]
Is this normal to still be in pain / feeling like this a 9 days after?
[/i] Last Wednesday I had my old T-bar Grommet removed from my ear and another new T-bar Grommet inserted straight after. I was awake and was done with a general anaesthetic injection in the affected ear. The ear was
[i]
Is this normal to still be in pain / feeling like this a 9 days after?
[/i] Last Wednesday I had my old T-bar Grommet removed from my ear and another new T-bar Grommet inserted straight after. I was awake and was done with a general anaesthetic injection in the affected ear. The ear was
accidentalglixch
in
deafPLUS
5 months ago
wax treatments
having had an appointment with the specialist nurse yesterday I have been referred to occupational therapy for some help with my clawed hands. Really hoping I can get some positive help as I do suffer at times with pain and stiffness despite doing exercises. She also mentioned a wax bath treatment which
having had an appointment with the specialist nurse yesterday I have been referred to occupational therapy for some help with my clawed hands. Really hoping I can get some positive help as I do suffer at times with pain and stiffness despite doing exercises. She also mentioned a wax bath treatment which
Clangerscat
in
Scleroderma & Raynaud's UK (SRUK)
5 months ago
Head tingling face, legs, and arms
Hi, I am a newbie here, so hope you are all doing as well as can be expected. for the last 12 months I have had 24/7 head tingling in random parts of the head with weird sensations too, plus head pain and now headaches daily. Went to GP who sent me for an MRI and Neurologist who was absolutely useless
Hi, I am a newbie here, so hope you are all doing as well as can be expected. for the last 12 months I have had 24/7 head tingling in random parts of the head with weird sensations too, plus head pain and now headaches daily. Went to GP who sent me for an MRI and Neurologist who was absolutely useless
bubbatetley
in
Acoustic Neuroma Support
5 months ago
AF with Bisoprolol
I have been switched from Disopyramide to Bisoprolol because Disopyramide was out of stock. I am now in AF and while Bisoprolol seems to be constraining my Heart Rate, I have been in AF nearly all day, and it’s not great. With Disopyramide twice a day, the next dose would resolve any AF, the Bisoprolol
I have been switched from Disopyramide to Bisoprolol because Disopyramide was out of stock. I am now in AF and while Bisoprolol seems to be constraining my Heart Rate, I have been in AF nearly all day, and it’s not great. With Disopyramide twice a day, the next dose would resolve any AF, the Bisoprolol
DE-AF
in
AF Association
5 months ago
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