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jaw pain
A few weeks ago I noticed that I couldn’t open my mouth as wide as I normally could without pain on the left side. Also, if I yawn and forget not to open it too wide I get a horrible pain and twisted feeling in my neck and throat. I went to the doctor’s surgery this week and saw a senior health practitioner
A few weeks ago I noticed that I couldn’t open my mouth as wide as I normally could without pain on the left side. Also, if I yawn and forget not to open it too wide I get a horrible pain and twisted feeling in my neck and throat. I went to the doctor’s surgery this week and saw a senior health practitioner
Gaycreasey
in
PMRGCAuk
2 months ago
Update
Hi everyone, I promised to let you know any updates. I went to audiology and ENT yesterday, had a hearing test then seen a specialist nurse then a consultant. I’m afraid I need a cochlear implant, my hearing is very poor now in my left ear, they think the cause is my sensorial hearing loss suddenly just
Hi everyone, I promised to let you know any updates. I went to audiology and ENT yesterday, had a hearing test then seen a specialist nurse then a consultant. I’m afraid I need a cochlear implant, my hearing is very poor now in my left ear, they think the cause is my sensorial hearing loss suddenly just
Numptybrain
in
PMRGCAuk
2 months ago
Vagus nerve stimulation'
I've posted here a few times to discuss gut health for those of you suffering from PA who also have gut issues. In my quest to find some relief from visceral hypersensitivity and massive intolerances (leading to malabsorption) I began acupuncture treatment this year. I am very lucky to have an anethesist
I've posted here a few times to discuss gut health for those of you suffering from PA who also have gut issues. In my quest to find some relief from visceral hypersensitivity and massive intolerances (leading to malabsorption) I began acupuncture treatment this year. I am very lucky to have an anethesist
expatkerry
in
Pernicious Anaemia Society
8 months ago
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NHS London statement on Synnovis ransomware cyber attack
I am posting this using the NHS' own website version - it is covered across news sites as well. It seems it is having a major impact on blood tests - which might immediately affect some members. As well as the rest of the impact. [i]
NHS London statement on Synnovis ransomware cyber attack
[
I am posting this using the NHS' own website version - it is covered across news sites as well. It seems it is having a major impact on blood tests - which might immediately affect some members. As well as the rest of the impact. [i]
NHS London statement on Synnovis ransomware cyber attack
[
helvella
Thyroid UK
in
Thyroid UK
2 months ago
Tinnitus and White Noise
Over the last 3 years my Tinnitus has deteriorated rapidly. It is constant and I have found one thing that makes me sleep at night is WhiteNoise on YouTube. Highly recommendable. I am getting hearing aids which the Audiologist hopes will reduce my Tinnitus. Meanwhile, it's really troublesome and affects
Over the last 3 years my Tinnitus has deteriorated rapidly. It is constant and I have found one thing that makes me sleep at night is WhiteNoise on YouTube. Highly recommendable. I am getting hearing aids which the Audiologist hopes will reduce my Tinnitus. Meanwhile, it's really troublesome and affects
Nana1944
in
Tinnitus UK
2 months ago
New to tinnitus and frightened
Hi everyone, I'm new to tinnitus, just 3 weeks in but have already been told my hearing is fine and there's no problems with my ears by an audiologist. I recently went through a stressful period at work followed by my mum being rushed into hospital and being told out of the blue that she only had days
Hi everyone, I'm new to tinnitus, just 3 weeks in but have already been told my hearing is fine and there's no problems with my ears by an audiologist. I recently went through a stressful period at work followed by my mum being rushed into hospital and being told out of the blue that she only had days
MiniRocket
in
Tinnitus UK
2 months ago
Severe tinnitus and sensorineural hearing loss
(Moderator's note - this post contains suicidal ideation, which may be upsetting to some readers) I have recently been diagnosed with granulomatosis with polyangiitis as a result of an autoimmune disorder and have been suffering with tinnitus since the 17th December 2023. The tinnitus is often raging
(Moderator's note - this post contains suicidal ideation, which may be upsetting to some readers) I have recently been diagnosed with granulomatosis with polyangiitis as a result of an autoimmune disorder and have been suffering with tinnitus since the 17th December 2023. The tinnitus is often raging
LRM001
in
Tinnitus UK
2 months ago
update on switching to digoxin from lopressor
Stopped digoxin this am and starting back on lopressor. bad heartburn and nausea just kept getting worse. Lots of hydrating and will explore ablation. Really felt sick on digoxin. Although don't feel generally great this was really not a good experience.
Stopped digoxin this am and starting back on lopressor. bad heartburn and nausea just kept getting worse. Lots of hydrating and will explore ablation. Really felt sick on digoxin. Although don't feel generally great this was really not a good experience.
farewelltoarms
in
Atrial Fibrillation Support
2 months ago
menieres
hi I’m new to group Diagnosed menieres about 8 yrs ago Suffer from severe hearing loss tinnitus Recently tinnitus just became very loud and leaving me unable to work and socially isolated Slowly loosing my confidence Anyone else feel similar as I feel alone X
hi I’m new to group Diagnosed menieres about 8 yrs ago Suffer from severe hearing loss tinnitus Recently tinnitus just became very loud and leaving me unable to work and socially isolated Slowly loosing my confidence Anyone else feel similar as I feel alone X
Bluerose57
in
Tinnitus UK
2 months ago
Hydroxychloroquine and tinnitus
I been on leflunomide and hydroxychloroquine for about ten months and have suddenly developed tinnitus, and feel as if I have a small electrical substation between my ears. From internet research I see that hydroxychloroquine can cause tinnitus and the rheumy team have suggested stopping it for just
I been on leflunomide and hydroxychloroquine for about ten months and have suddenly developed tinnitus, and feel as if I have a small electrical substation between my ears. From internet research I see that hydroxychloroquine can cause tinnitus and the rheumy team have suggested stopping it for just
spartacus101
in
NRAS
2 months ago
V + O for R/R CLL post FCR
I sent this to skyshark based on some info he posted but I was[u] hoping for the whole group to chime in.[/u] I had 3 rounds of FCR in 2018 stopped because of profound neutropenia. I relapsed exactly 2 years later and though I did not start Tx until the 5 year point in 2023, would have gladly started
I sent this to skyshark based on some info he posted but I was[u] hoping for the whole group to chime in.[/u] I had 3 rounds of FCR in 2018 stopped because of profound neutropenia. I relapsed exactly 2 years later and though I did not start Tx until the 5 year point in 2023, would have gladly started
skipro
in
CLL Support
2 months ago
GCA. Pulsatile tinnitus
May I ask what any of you good people know about pulsatile tinnitus. Do you consider my GP should see me, or at least write to me or speak to me on telephone. When I recently started hearing my heartbeat in same ear that GCA symptoms started I called my rheumatology dept & was seen. Had blood tests
May I ask what any of you good people know about pulsatile tinnitus. Do you consider my GP should see me, or at least write to me or speak to me on telephone. When I recently started hearing my heartbeat in same ear that GCA symptoms started I called my rheumatology dept & was seen. Had blood tests
CavalierKC3
in
PMRGCAuk
2 months ago
An online Study….recruiting re Speech Disorders
A new study on speech disorders in ataxias is recruiting participants Do you have a diagnosis of ataxia, and experience speech disorders? If so, you could help researchers in a study investigating speech disorders across various ataxia types. This is an online study and does not require travel.
A new study on speech disorders in ataxias is recruiting participants Do you have a diagnosis of ataxia, and experience speech disorders? If so, you could help researchers in a study investigating speech disorders across various ataxia types. This is an online study and does not require travel.
wobblybee
in
Ataxia UK
2 months ago
supplements for a fibs???
Has anyone here used magnesium or L arginine for atrial fibrillations? If yes, and you had good results, what were the dosages and how often daily? Thank you.
Has anyone here used magnesium or L arginine for atrial fibrillations? If yes, and you had good results, what were the dosages and how often daily? Thank you.
peachtreepiggy
in
Atrial Fibrillation Support
2 months ago
Musical Ear Syndrome
Hi. I've been looking through to see if anyone has posted about hearing random music with tinnitus. It is very distracting and making me feel isolated and desperate. I developed sudden hearing loss and tinnitus in my left ear in winter 2022, then recently an ear infection in my right ear made the tinnitus
Hi. I've been looking through to see if anyone has posted about hearing random music with tinnitus. It is very distracting and making me feel isolated and desperate. I developed sudden hearing loss and tinnitus in my left ear in winter 2022, then recently an ear infection in my right ear made the tinnitus
SeashellSara
in
Tinnitus UK
2 months ago
Headsets
Hi there, I have had tinnitus most of my life but since developing Meniers disease last year it is unbearable at times. I have managed to adjust but I am finding work very difficult. My job is helping very vulnerable people over the phone, calls can last anything from 20 mins to 3 hours. I wear a headset
Hi there, I have had tinnitus most of my life but since developing Meniers disease last year it is unbearable at times. I have managed to adjust but I am finding work very difficult. My job is helping very vulnerable people over the phone, calls can last anything from 20 mins to 3 hours. I wear a headset
Loveclimbing
in
Tinnitus UK
2 months ago
Ginkgo - possible adverse side effect: Nervous anxiety
It's me again. On about Ginkgo as usual... Having taken Ginkgo for over 6 months, and having planned relief from Tinnitus by doing so, I may have experienced a side effect. Recent bouts of nervous anxiety. This is not the kind of anxiety you might experience in a dentist waiting room. No, this is
It's me again. On about Ginkgo as usual... Having taken Ginkgo for over 6 months, and having planned relief from Tinnitus by doing so, I may have experienced a side effect. Recent bouts of nervous anxiety. This is not the kind of anxiety you might experience in a dentist waiting room. No, this is
Ray200
in
Tinnitus UK
2 months ago
Hearing aids and work
Hi, I started using hearing aids earlier in the year (moderate to severe loss, with profound at the highest frequencies). I’m only in my mid 50s and have close to 10 years working left. As with a lot of office workers I’m now spending an awful lot of time on MS teams. I’m really struggling with headphones
Hi, I started using hearing aids earlier in the year (moderate to severe loss, with profound at the highest frequencies). I’m only in my mid 50s and have close to 10 years working left. As with a lot of office workers I’m now spending an awful lot of time on MS teams. I’m really struggling with headphones
GillyA
in
Tinnitus UK
2 months ago
Sonitus soundbite
Hi all, Has anyone had any experience of using the Soundbite device to address hearing loss in one ear after acoustic neuroma surgery? Just looking at options as I'm struggling a bit, so it would be good to hear of others experience. Here's the website: https://www.sonitusmedical.com/the-soundbite-hearing-system-in-detail
Hi all, Has anyone had any experience of using the Soundbite device to address hearing loss in one ear after acoustic neuroma surgery? Just looking at options as I'm struggling a bit, so it would be good to hear of others experience. Here's the website: https://www.sonitusmedical.com/the-soundbite-hearing-system-in-detail
domforr
in
Acoustic Neuroma Support
2 months ago
tinnitus so loud I can’t hear in my right ear
I’m currently experiencing a difficult time owing to a family bereavement . My tinnitus has been getting worse over last few days and today my hearing is almost completely gone in my right ear . I have had an mri with clear results . Is there anything I can do to try to help calm it down ? I’m assuming
I’m currently experiencing a difficult time owing to a family bereavement . My tinnitus has been getting worse over last few days and today my hearing is almost completely gone in my right ear . I have had an mri with clear results . Is there anything I can do to try to help calm it down ? I’m assuming
Jannypetlump
in
Tinnitus UK
2 months ago
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