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Gentamicin
I have Bronchiectasis and have had it a long time .I have a New Consultant and she has put me on inhaled Gentamicin one month on ,one month off ,which I have just started..My main concern is hearing loss which they say c an happen. .I wear hearing aids already which is a recent experience.My Consultant
I have Bronchiectasis and have had it a long time .I have a New Consultant and she has put me on inhaled Gentamicin one month on ,one month off ,which I have just started..My main concern is hearing loss which they say c an happen. .I wear hearing aids already which is a recent experience.My Consultant
cat50
in
Lung Conditions Community Forum
2 years ago
Excessive sweating
With Parkinson’s, it’s common for the skin on your face to become very oily, especially on your forehead and on the sides of your nose (this is known as seborrhea). You may also notice that your eyebrows and scalp get oily too, resulting in flaky skin (dandruff). It’s also fairly common to experience
With Parkinson’s, it’s common for the skin on your face to become very oily, especially on your forehead and on the sides of your nose (this is known as seborrhea). You may also notice that your eyebrows and scalp get oily too, resulting in flaky skin (dandruff). It’s also fairly common to experience
Farooqji
in
Cure Parkinson's
2 years ago
Oily, flaky, or inflamed skin
With Parkinson’s, it’s common for the skin on your face to become very oily, especially on your forehead and on the sides of your nose (this is known as seborrhea). You may also notice that your eyebrows and scalp get oily too, resulting in flaky skin (dandruff). It’s also fairly common to experience
With Parkinson’s, it’s common for the skin on your face to become very oily, especially on your forehead and on the sides of your nose (this is known as seborrhea). You may also notice that your eyebrows and scalp get oily too, resulting in flaky skin (dandruff). It’s also fairly common to experience
Farooqji
in
Cure Parkinson's
2 years ago
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Meds after spinal fusion
My fusion was 11 weeks ago and I still need an occasional dose of my prescription medication. I have heard that otc meds such as aleve and ibuprofen can interfere with bone grafting, so I have been avoiding them. Surgeon said the otc's were okay to take at this point but I would rather wait until I
My fusion was 11 weeks ago and I still need an occasional dose of my prescription medication. I have heard that otc meds such as aleve and ibuprofen can interfere with bone grafting, so I have been avoiding them. Surgeon said the otc's were okay to take at this point but I would rather wait until I
Jeaniem130
in
Pain Concern
2 years ago
Will grommets help tinnitus?
Been diagnosed with EDT and potentially grommets will help but tinnitus has increased since Feb this year. Impacting on my balance and well being. Hoping this operation may help.
Been diagnosed with EDT and potentially grommets will help but tinnitus has increased since Feb this year. Impacting on my balance and well being. Hoping this operation may help.
Nitramp
in
British Tinnitus Association
2 years ago
CT Colonoscopy
I'm going for a CT colonoscopy next week I'm really apprehensive. I have long covid and contracted diffused vasculitis through this. Looking for reassurance really. TIA ❤
I'm going for a CT colonoscopy next week I'm really apprehensive. I have long covid and contracted diffused vasculitis through this. Looking for reassurance really. TIA ❤
M3LZY
in
Vasculitis UK
2 years ago
Effects of melatonin prolonged-release on both sleep and motor symptoms in Parkinson's disease: a preliminary evidence.
https://pubmed.ncbi.nlm.nih.gov/35536495/
Results
: Sleep latency significantly decreased from T0 to T1, but no other significant differences were found in PSG parameters. Melatonin PR treatment significantly reduced the ESS scores from T0 to T1, while the PSQI scores presented a trend of improvement
https://pubmed.ncbi.nlm.nih.gov/35536495/
Results
: Sleep latency significantly decreased from T0 to T1, but no other significant differences were found in PSG parameters. Melatonin PR treatment significantly reduced the ESS scores from T0 to T1, while the PSQI scores presented a trend of improvement
Hidden
in
Cure Parkinson's
2 years ago
Curcumin Real Clinical Study, Anti Inflam
Came across this one. I think it's a rare Curc study using real people, vs animal or lab tests. It's looking for benefits in kidney disease. I was looking to find whether Curc might be a negative for kidney but positive implications come up for reasonable doses. https://clinicaltrials.gov/ct2/show
Came across this one. I think it's a rare Curc study using real people, vs animal or lab tests. It's looking for benefits in kidney disease. I was looking to find whether Curc might be a negative for kidney but positive implications come up for reasonable doses. https://clinicaltrials.gov/ct2/show
EPguy
in
MPN Voice
2 years ago
New to the group but not the noise!
Hi, I've just been fitted with Oticon 'engage' hearing aids by my local audiology dept. after a referal from my GP. This was following being in a motorcycle collision in July 2021. I hit the side of a large car that pulled out of a line of stationary traffic. Luckily I was not seriously injured and
Hi, I've just been fitted with Oticon 'engage' hearing aids by my local audiology dept. after a referal from my GP. This was following being in a motorcycle collision in July 2021. I hit the side of a large car that pulled out of a line of stationary traffic. Luckily I was not seriously injured and
Charcoalcharlie
in
British Tinnitus Association
2 years ago
Flecainide converted my fibrillation to flutter
I started on 50mg X 2 Flecainide a few months ago after 10 years of no treatment and the effects have been life changing. However the fibrillation had now been replaced by flutter and I'm beginning to feel almost as bad again. My RHR had always been in the low 50s and BP at 125/75 but now they are prescribing
I started on 50mg X 2 Flecainide a few months ago after 10 years of no treatment and the effects have been life changing. However the fibrillation had now been replaced by flutter and I'm beginning to feel almost as bad again. My RHR had always been in the low 50s and BP at 125/75 but now they are prescribing
MisterMagoo
in
AF Association
2 years ago
Maybe Meniere`s Disease? (my hearing loss and dizziness)
I saw the ENT consultant last week - he said it may be Meniere`s disease causing my sudden dizzy spells - he prescribed Betahistine 16mg . More research for me to do ... (I really do not like to take drugs, so I`m reluctant to try something for a `maybe`). Just letting others on here know about my
I saw the ENT consultant last week - he said it may be Meniere`s disease causing my sudden dizzy spells - he prescribed Betahistine 16mg . More research for me to do ... (I really do not like to take drugs, so I`m reluctant to try something for a `maybe`). Just letting others on here know about my
DizzyLizzyYorkshire
in
Acoustic Neuroma Support
2 years ago
Low TSH and T4
I know you guys are great at understanding results. So please advise as I’m totally confused. I’m am taking 100 micro grams of levothyroxine daily and have been on this dose over a year. 2 months ago my thyroid results where; TSH 0.07 (0.27 4.2) T4 19.9 (12-22) T3 4.5 (3.1-6.8) and I was happy
I know you guys are great at understanding results. So please advise as I’m totally confused. I’m am taking 100 micro grams of levothyroxine daily and have been on this dose over a year. 2 months ago my thyroid results where; TSH 0.07 (0.27 4.2) T4 19.9 (12-22) T3 4.5 (3.1-6.8) and I was happy
Bubbles789
in
Thyroid UK
2 years ago
Where is a Cerabellar pontine angle acoustic neuroma positioned ?
Is the CPA acoustic neuromas in line with our mouth / jaw line ? I had an X-ray back in 2018. Nothing untoward was reported. If I had my CPA Acoustic neuroma back then would it have shown on this as I was only diagnosed in January 2021 measuring 4cm x 2.5 cm
Is the CPA acoustic neuromas in line with our mouth / jaw line ? I had an X-ray back in 2018. Nothing untoward was reported. If I had my CPA Acoustic neuroma back then would it have shown on this as I was only diagnosed in January 2021 measuring 4cm x 2.5 cm
Steve_04
in
Acoustic Neuroma Support
2 years ago
Hyperacousis and T from loud band. almost 3 months ago. Still not sure what I should do.
me (43 /male/musician/dj/construction) well I saw 15 minutes of an insanely loud metal band and now I have fullness that comes and goes in my ears, my voice and others voices sound loud most times, just a bit. I have some ringing but it is the H I am more confused about. I don't know if : 1`. I should
me (43 /male/musician/dj/construction) well I saw 15 minutes of an insanely loud metal band and now I have fullness that comes and goes in my ears, my voice and others voices sound loud most times, just a bit. I have some ringing but it is the H I am more confused about. I don't know if : 1`. I should
letshealthis
in
British Tinnitus Association
2 years ago
Radiation twice anyone?
Good morning. I had radiation four years ago for an acoustic neuroma and it did shrink to start with but unfortunately grew back so had to have gamma knife again. The first time I had gamma knife I was pretty much back to “normal” after a couple of days but this time is ten days later and my head still
Good morning. I had radiation four years ago for an acoustic neuroma and it did shrink to start with but unfortunately grew back so had to have gamma knife again. The first time I had gamma knife I was pretty much back to “normal” after a couple of days but this time is ten days later and my head still
Skybean1
in
Acoustic Neuroma Support
2 years ago
betahistine Dihydrochloride
Hi, ent doctor has put me on Betahistine tablets 16mg 3 times a day, been on them for two weeks now and no effect what’s so ever, if anything it’s made the tinnitus worse. I have Suffered for a year with bad tinnitus in left hear only and have no hearing loss at all when They did hearing test. Driving
Hi, ent doctor has put me on Betahistine tablets 16mg 3 times a day, been on them for two weeks now and no effect what’s so ever, if anything it’s made the tinnitus worse. I have Suffered for a year with bad tinnitus in left hear only and have no hearing loss at all when They did hearing test. Driving
Juz9876
in
British Tinnitus Association
2 years ago
ENT appointment left me feeling confused
Hi people. It's been a while since my last past as I've been dealing with a back injury on-top of this T spike. Someone up there has it in for me I swear!! 😂 So I finally had my ENT appointment this week and was left feeling utterly confused. For clarification I first had an ent appointment back in
Hi people. It's been a while since my last past as I've been dealing with a back injury on-top of this T spike. Someone up there has it in for me I swear!! 😂 So I finally had my ENT appointment this week and was left feeling utterly confused. For clarification I first had an ent appointment back in
Am3ient
in
British Tinnitus Association
2 years ago
RA and loss of hearing
Hi there. I wondered if anyone had experienced a loss of hearing, potentially due to their RA. I developed RA a year ago, and am currently on MTX and prednisolone after Sulfasalazine didn't help. Six months ago I lost hearing in one ear, literally over a couple of days, and developed tinnitus. My
Hi there. I wondered if anyone had experienced a loss of hearing, potentially due to their RA. I developed RA a year ago, and am currently on MTX and prednisolone after Sulfasalazine didn't help. Six months ago I lost hearing in one ear, literally over a couple of days, and developed tinnitus. My
Sebastian247
in
NRAS
2 years ago
Can being overmedicated cause anxiety and headaches?
Hi I wrote a couple of weeks ago that I felt I was on too much Levo as I was feeling hot, headaches, not sleeping well, a bit hyper etc. I tried to test but unfortunately couldn't get enough blood out and the test failed. Got a replacement one free of charge. But now I've dropped my dose there's no
Hi I wrote a couple of weeks ago that I felt I was on too much Levo as I was feeling hot, headaches, not sleeping well, a bit hyper etc. I tried to test but unfortunately couldn't get enough blood out and the test failed. Got a replacement one free of charge. But now I've dropped my dose there's no
Sparklingsunshine
in
Thyroid UK
2 years ago
Had 1 tinnitus noise now another has joined - help
Hello all, My first post in 3 years. I was diagnosed with high frequency hearing loss 3 years ago after getting high frequency tinnitus which I still have. My question for this group is - the last 2 weeks I have a low pitched intermittent hum now as well - has anyone else suffered this , and how do
Hello all, My first post in 3 years. I was diagnosed with high frequency hearing loss 3 years ago after getting high frequency tinnitus which I still have. My question for this group is - the last 2 weeks I have a low pitched intermittent hum now as well - has anyone else suffered this , and how do
ears1011
in
British Tinnitus Association
2 years ago
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