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Objective tinnitus help please.
Not me, my 90 years old next Monday mother in law! She has tinnitus and everyone can hear it when within earshot. We are 40 miles away and hear it when we phone her. She did have a UTI a couple of weeks ago and took Nitrofurantoin for it but became extremely unbalanced, and stopped it after four days
Not me, my 90 years old next Monday mother in law! She has tinnitus and everyone can hear it when within earshot. We are 40 miles away and hear it when we phone her. She did have a UTI a couple of weeks ago and took Nitrofurantoin for it but became extremely unbalanced, and stopped it after four days
jointpain
in
Tinnitus UK
1 year ago
Thank you
Big thanks to everyone who commiserated with me on my recent fall. Especial thanks to those who related their own stories of falling, mostly making them funny. We're a brave lot on Health Unlocked. It's taking me longer to recover than I thought it would. My shoulders still ache a bit, making it hard
Big thanks to everyone who commiserated with me on my recent fall. Especial thanks to those who related their own stories of falling, mostly making them funny. We're a brave lot on Health Unlocked. It's taking me longer to recover than I thought it would. My shoulders still ache a bit, making it hard
Alberta56
in
Lung Conditions Community Forum
1 year ago
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
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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
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
Cosopt eye drops
is anyone having trouble getting hold of Cosopt eye drops. These are single use drops which are preservative free. My pharmacist just says to ask consultant for an alternative drop but these are the only ones that lower my pressure slightly and I think I’ve had just about every glaucoma drop that’s available
is anyone having trouble getting hold of Cosopt eye drops. These are single use drops which are preservative free. My pharmacist just says to ask consultant for an alternative drop but these are the only ones that lower my pressure slightly and I think I’ve had just about every glaucoma drop that’s available
Charliecat123
in
Glaucoma UK
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
Monopost eye drops .
I wondered if anyone had any experience of using these at all . I do think they’re helping with my closed angle Glaucoma . Not quite sure if it’s acute or chronic as 2 different consultants that I’ve seen have different opinions . Unfortunately the clinic I go to is an American owned one and used by
I wondered if anyone had any experience of using these at all . I do think they’re helping with my closed angle Glaucoma . Not quite sure if it’s acute or chronic as 2 different consultants that I’ve seen have different opinions . Unfortunately the clinic I go to is an American owned one and used by
Junep
in
Glaucoma UK
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
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