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Hydroxychloroquine/Plaquenil and Tinnitus
I started hydroxychloroquine about 4 weeks ago for lupus, and have a noticeable increase in tinnitus (ringing in the ears). I had originally tried hydroxychloroquine back in 2017, which lead to onset of tinnitus - when I had stopped taking it, the tinnitus decreased although never fully went away. I
I started hydroxychloroquine about 4 weeks ago for lupus, and have a noticeable increase in tinnitus (ringing in the ears). I had originally tried hydroxychloroquine back in 2017, which lead to onset of tinnitus - when I had stopped taking it, the tinnitus decreased although never fully went away. I
Heather_16
in
LUPUS UK
3 years ago
update
My diverticulitis turned into a bowel perforation. I managed to avoid surgery (for now at least), but did manage to develop brachycardia (extremely low heart beat) while there. Seeing the cardiologist first thing Monday morning. Honestly, what's it going to be next?
My diverticulitis turned into a bowel perforation. I managed to avoid surgery (for now at least), but did manage to develop brachycardia (extremely low heart beat) while there. Seeing the cardiologist first thing Monday morning. Honestly, what's it going to be next?
winfong
in
PMRGCAuk
3 years ago
Hearing loss and Lupus
Hi all. I am just wondering if anyone with lupus have any issues with their hearing. My GP thought during recent continuous flares this is affecting my hearing. I went for a hearing test and was told I had 40% less hearing and I could either buy a hearing aid for £500 or get referred to GP. I went for
Hi all. I am just wondering if anyone with lupus have any issues with their hearing. My GP thought during recent continuous flares this is affecting my hearing. I went for a hearing test and was told I had 40% less hearing and I could either buy a hearing aid for £500 or get referred to GP. I went for
Jamaica21
in
LUPUS UK
3 years ago
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Urgent Postive Help needed. Tinnitus now in both ears. (may be Stess related)
Male 43 Years Hello All I see a lot of Info here on this Forum, and I need some Real Honest help from the all the Experienced Members , as I summarizing very very hard 3.5 months. Loud Onset :- June 2021 , I suppose because of stress . The audiogram is the same from the last 6 years. No Exposure
Male 43 Years Hello All I see a lot of Info here on this Forum, and I need some Real Honest help from the all the Experienced Members , as I summarizing very very hard 3.5 months. Loud Onset :- June 2021 , I suppose because of stress . The audiogram is the same from the last 6 years. No Exposure
Roberto-1978
in
British Tinnitus Association
3 years ago
Who do you talk to?
Hey All, So my ranula turned into a plunging ranula (I think) but the GP has referred me for an expedited cancer check as the gland beneath is swollen too and he wants to make sure it's not cancer. I'm telling myself it's a plunging ranula for now as there is a tail and the gland hurts so all the symptoms
Hey All, So my ranula turned into a plunging ranula (I think) but the GP has referred me for an expedited cancer check as the gland beneath is swollen too and he wants to make sure it's not cancer. I'm telling myself it's a plunging ranula for now as there is a tail and the gland hurts so all the symptoms
Insomniacette
in
LUPUS UK
3 years ago
Hyperreflexia
I would love to hear others' experience with hyperreflexia as result of PA. I have periods (often in the last days before my injection), when I get low-level random muscle twitches, mostly in my arms and back, then they subside. I have been found to be hyperreflexive in reflex tests since my PA diagnosis
I would love to hear others' experience with hyperreflexia as result of PA. I have periods (often in the last days before my injection), when I get low-level random muscle twitches, mostly in my arms and back, then they subside. I have been found to be hyperreflexive in reflex tests since my PA diagnosis
Bellmore2089
in
Pernicious Anaemia Society
3 years ago
Ankles.
I am new to this forum. 56 year old male and had RA for 16 years. Was under control in the early days, however last five years has got steadily worse. I take Biologics MTX and steroids when needed. I had an MRI on my feet a couple of weeks ago with a follow up last week. My hind foot and ankles are
I am new to this forum. 56 year old male and had RA for 16 years. Was under control in the early days, however last five years has got steadily worse. I take Biologics MTX and steroids when needed. I had an MRI on my feet a couple of weeks ago with a follow up last week. My hind foot and ankles are
property2
in
NRAS
3 years ago
Convergence Insufficiency
I've seen CI mentioned a few times here, sometimes in association with migraine so this might be of interest to some people here: https://pubmed.ncbi.nlm.nih.gov/25313120/ Balance issues also get mentioned here so if you haven't already seen them the Life Rebalanced Chronicles, made for VeDA by an award
I've seen CI mentioned a few times here, sometimes in association with migraine so this might be of interest to some people here: https://pubmed.ncbi.nlm.nih.gov/25313120/ Balance issues also get mentioned here so if you haven't already seen them the Life Rebalanced Chronicles, made for VeDA by an award
210272
in
Functional Neurological Disorder - FND Hope
3 years ago
ABout The A And E
Hello to everyone who has wrote to me about A and E. The update is now my cancer Lung Nurse has brought my 1st CT Scan forward from December 2021 to October 5th at 1.15pm and check for blood clot and cancer etc. My breast scan went well it was just cysts thank goodness. I still have my pain and on medication
Hello to everyone who has wrote to me about A and E. The update is now my cancer Lung Nurse has brought my 1st CT Scan forward from December 2021 to October 5th at 1.15pm and check for blood clot and cancer etc. My breast scan went well it was just cysts thank goodness. I still have my pain and on medication
Jojoclown
in
Lung Conditions Community Forum
3 years ago
Tinnitus just started
I have been slowly increasing my levo (finally after many discussions and tests with endos and Gp) and recently went up to 100mcg. I am getting blood tests done to see what effect that has had on all my levels. I’m the meantime I am now suffering from tinnitus which I see can be related to thyroid dysfunction
I have been slowly increasing my levo (finally after many discussions and tests with endos and Gp) and recently went up to 100mcg. I am getting blood tests done to see what effect that has had on all my levels. I’m the meantime I am now suffering from tinnitus which I see can be related to thyroid dysfunction
doingitfordad
in
Thyroid UK
3 years ago
Meniere's?
Hi. I'm new here. Does anyone have Meniere's Disease? I am being treated for it - I had SSNHL last November in my right ear. They think its menieres or vestibular migraine. I then unluckily got shingles on my good eardrum - yup - right on my eardrum!! So I have tinnitus in both but hearing loss in my
Hi. I'm new here. Does anyone have Meniere's Disease? I am being treated for it - I had SSNHL last November in my right ear. They think its menieres or vestibular migraine. I then unluckily got shingles on my good eardrum - yup - right on my eardrum!! So I have tinnitus in both but hearing loss in my
LoveActually01
in
deafPLUS
3 years ago
Staying well on biologics…
Good evening, I’m new to biologics. I’ve been on adalimumab (and methotrexate) for about 4 months…. Had to pause today for a while due to a horrible throat infection requiring AB’s. Do all biologics make you really susceptible to infections?? If so, any advice on how to keep myself well? (Supplements
Good evening, I’m new to biologics. I’ve been on adalimumab (and methotrexate) for about 4 months…. Had to pause today for a while due to a horrible throat infection requiring AB’s. Do all biologics make you really susceptible to infections?? If so, any advice on how to keep myself well? (Supplements
EmJ79
in
NRAS
3 years ago
Vibration sounds in ears
Hi I’m fairly new at this. 3 weeks ago I started with a ear infection which caused my ear to get plugged and Amit of tenderness on my head and neck area. After the 3rd day I was able to unplug my ear but ever since then I hear kind of a vibration sound, though I don’t feel it. Sometimes it sound a like
Hi I’m fairly new at this. 3 weeks ago I started with a ear infection which caused my ear to get plugged and Amit of tenderness on my head and neck area. After the 3rd day I was able to unplug my ear but ever since then I hear kind of a vibration sound, though I don’t feel it. Sometimes it sound a like
Lalaworld
in
British Tinnitus Association
3 years ago
Implant improves Balance, Movement and Quality of Life to people with Inner Ear Disorder
Getting around without the need to concentrate on every step is something most of us can take for granted because our inner ears drive reflexes that make maintaining balance automatic. However, for about 1.8 million adults worldwide with bilateral vestibular hypofunction (BVH) — loss of the inner ears
Getting around without the need to concentrate on every step is something most of us can take for granted because our inner ears drive reflexes that make maintaining balance automatic. However, for about 1.8 million adults worldwide with bilateral vestibular hypofunction (BVH) — loss of the inner ears
wobblybee
in
Ataxia UK
3 years ago
Tinnitus and cochlear implants …do they work together?
Hi everyone i have been going through a lot lately and would really love some positive comments. I have Tinnius in my right ear. This was a result from a dr trying to put a grommet in my ear. It was taken out and put back in 3 times , then I had a stapadectomy.then I had a cochlear implant … but it was
Hi everyone i have been going through a lot lately and would really love some positive comments. I have Tinnius in my right ear. This was a result from a dr trying to put a grommet in my ear. It was taken out and put back in 3 times , then I had a stapadectomy.then I had a cochlear implant … but it was
1Dar
in
Tinnitus UK
3 years ago
New Hearing Loss and Access to Work
My hearing loss is very new and was diagnosed in July of this year. It's currently considered mild, my left ear is worse than my right due to having a perforated eardrum as a child in the left ear. I had an assessment with Audiology for hearing aids and learnt so much about it that I didn't know before
My hearing loss is very new and was diagnosed in July of this year. It's currently considered mild, my left ear is worse than my right due to having a perforated eardrum as a child in the left ear. I had an assessment with Audiology for hearing aids and learnt so much about it that I didn't know before
Yasai
in
Hearing Link
3 years ago
Ear wax
.does anyone know if putting olive oil in blocked ear make you more deaf when you have ear wax. .my ear is compleatley deaf now and my head feels horrible .nurse Told me to put olive oil in my ear to help soften the wax ready for ear to be suringged im bit worried about it as I am going through anxiety
.does anyone know if putting olive oil in blocked ear make you more deaf when you have ear wax. .my ear is compleatley deaf now and my head feels horrible .nurse Told me to put olive oil in my ear to help soften the wax ready for ear to be suringged im bit worried about it as I am going through anxiety
Dextersam10
in
Anxiety Support
3 years ago
Tinnitus getting worse
Hi everyone, I’m new here and very pleased I have found this forum. I have had tinnitus for about 20 years but was able to cope with it, now it is so bad it’s more of a roar than ringing, I have seen endless neurologists and had several scans which have all been clear, which I am relieved about as had
Hi everyone, I’m new here and very pleased I have found this forum. I have had tinnitus for about 20 years but was able to cope with it, now it is so bad it’s more of a roar than ringing, I have seen endless neurologists and had several scans which have all been clear, which I am relieved about as had
Yoga62
in
Tinnitus UK
3 years ago
Things are getting worse
Hi all I’m still here the thoughts unfortunately of just giving up are still there I’ve now come down with constant nausea from the moment I wake up till I go to bed the doctor has tried ever anti sickness they have but nothing works I called them again today and they can’t do anything else blood test
Hi all I’m still here the thoughts unfortunately of just giving up are still there I’ve now come down with constant nausea from the moment I wake up till I go to bed the doctor has tried ever anti sickness they have but nothing works I called them again today and they can’t do anything else blood test
SarahLouise84
in
British Tinnitus Association
3 years ago
The good, the bad and the ugly!
Good evening folks. I have not posted anything for a while. You may recall that I posted my journey with the neuromod device. (It knock me for six, caused nausea and put me back into depression!!) I still have to take medication for nausea as a result. Here's a thought. " Hearing loss and Tinnitus
Good evening folks. I have not posted anything for a while. You may recall that I posted my journey with the neuromod device. (It knock me for six, caused nausea and put me back into depression!!) I still have to take medication for nausea as a result. Here's a thought. " Hearing loss and Tinnitus
ade-the-pade
in
British Tinnitus Association
3 years ago
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