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Otomize ear spray
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Relapse after 4 years
I was diagnosed with PMR after having a Erythrocyte sedimentation rate of 31mm/hr in 2017 Went on steroids and managed to come off when the rate dropped to 19mm/hr in early 2019 I play golf and was diagnosed with a blood clot in June 2022. So on medication for 12 weeks to clear. Advised not to play
I was diagnosed with PMR after having a Erythrocyte sedimentation rate of 31mm/hr in 2017 Went on steroids and managed to come off when the rate dropped to 19mm/hr in early 2019 I play golf and was diagnosed with a blood clot in June 2022. So on medication for 12 weeks to clear. Advised not to play
Starman53
in
PMRGCAuk
1 year ago
Bad episode of Vertigo and blood tests
Hello everyone, I used to have subclinical Hashimoto for more than 10 years and was on 25 or 50 mcg of Levothyroxine. Several months ago I started to take Tirosint gel capsules 50 mcg. I did not feel the difference, just maybe my tinnitus became a bit louder and started effecting my hearing. Recently
Hello everyone, I used to have subclinical Hashimoto for more than 10 years and was on 25 or 50 mcg of Levothyroxine. Several months ago I started to take Tirosint gel capsules 50 mcg. I did not feel the difference, just maybe my tinnitus became a bit louder and started effecting my hearing. Recently
Gal_Ka
in
Thyroid UK
2 years ago
Expiration date
After reading about the (supposed?) shortage of B12 in UK, I, too, am wondering if PanPharma’s shortened expiration date from 2 years to one year has contributed to this perceived shortage. Have we gotten the final answer on why PanPharma shortened their expiry date? Does anyone know if the inactive
After reading about the (supposed?) shortage of B12 in UK, I, too, am wondering if PanPharma’s shortened expiration date from 2 years to one year has contributed to this perceived shortage. Have we gotten the final answer on why PanPharma shortened their expiry date? Does anyone know if the inactive
EiCa
in
Pernicious Anaemia Society
2 years ago
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Dizziness and vertigo
Hi I've got PA and self inject for 1 year, generally 1 monthly. I have started suffering dizziness and vertigo. Laying down makes the room spin and I'm walking like I'm drunk. I'm wondering if this is a symptom or something else? I am trying to get GP Appointment as I can't drive or get to work! Any
Hi I've got PA and self inject for 1 year, generally 1 monthly. I have started suffering dizziness and vertigo. Laying down makes the room spin and I'm walking like I'm drunk. I'm wondering if this is a symptom or something else? I am trying to get GP Appointment as I can't drive or get to work! Any
Hidden
in
Pernicious Anaemia Society
2 years ago
Somatic Experiencing Success?
I'm curious if anyone has had any success utilizing somatic experiencing. In principal it makes sense, but in all honesty, my symptoms seem too "severe" to find success in such a mild approach... I am trying to stay positive. My therapist downplays the FND "diagnosis", not from a "i dont believe you
I'm curious if anyone has had any success utilizing somatic experiencing. In principal it makes sense, but in all honesty, my symptoms seem too "severe" to find success in such a mild approach... I am trying to stay positive. My therapist downplays the FND "diagnosis", not from a "i dont believe you
seamuspg
in
Functional Neurological Disorder - FND Hope
2 years ago
Tmj and tinnitus
Has anyone with tinnitus and tmj feel numbness on that side of head?
Has anyone with tinnitus and tmj feel numbness on that side of head?
Doxiemom1
in
Tinnitus UK
2 years ago
SUDDEN increase in Sed rate, or erythrocyte sedimentation rate (ESR
Hello, I want to thank everyone that shared their personal insights replying to my post "ANCA MPO and Systemic sclerosis positive - Sudden ESR 93". Your comments are invaluable and I appreciate every word. Thank you, This post is focused on ESR. This is copied directly from the Mayo Clinic web site
Hello, I want to thank everyone that shared their personal insights replying to my post "ANCA MPO and Systemic sclerosis positive - Sudden ESR 93". Your comments are invaluable and I appreciate every word. Thank you, This post is focused on ESR. This is copied directly from the Mayo Clinic web site
irishponies
in
Scleroderma & Raynaud's UK (SRUK)
2 years ago
SUDDEN increase in Sed rate, or erythrocyte sedimentation rate (ESR)
Hello, I want to thank everyone that shared their personal insights replying to my post "ANCA MPO and Systemic sclerosis positive - Sudden ESR 93". Your comments are invaluable and I appreciate every word. Thank you, This post is focused on ESR. This is copied directly from the Mayo Clinic web site
Hello, I want to thank everyone that shared their personal insights replying to my post "ANCA MPO and Systemic sclerosis positive - Sudden ESR 93". Your comments are invaluable and I appreciate every word. Thank you, This post is focused on ESR. This is copied directly from the Mayo Clinic web site
irishponies
in
PMRGCAuk
2 years ago
Sed rate, or erythrocyte sedimentation rate (ESR) SUDDEN increase
Hello, I want to thank everyone that shared their personal insights replying to my post "ANCA MPO and Systemic sclerosis positive - Sudden ESR 93". Your comments are invaluable and I appreciate every word. Thank you, This post is focused on ESR. This is copied directly from the Mayo Clinic web site
Hello, I want to thank everyone that shared their personal insights replying to my post "ANCA MPO and Systemic sclerosis positive - Sudden ESR 93". Your comments are invaluable and I appreciate every word. Thank you, This post is focused on ESR. This is copied directly from the Mayo Clinic web site
irishponies
in
Vasculitis UK
2 years ago
Definitely a flare. Stiffness now making itself known. Increase dose to where and for how long?
Morning all. Those of you who replied to my post 27th will have the background.It did not seem to be a flare but after 3 days at 9mg the bilateral stiffness is there. Also feeling my knees. The dead head and fatigue has lessened a lot in last few days. I feel I am back to where I was 2 years ago! I increased
Morning all. Those of you who replied to my post 27th will have the background.It did not seem to be a flare but after 3 days at 9mg the bilateral stiffness is there. Also feeling my knees. The dead head and fatigue has lessened a lot in last few days. I feel I am back to where I was 2 years ago! I increased
Ebiker
in
PMRGCAuk
2 years ago
Drinking more water
I often see advice on this site, regarding tinnitus/dizziness/vertigo, to drink more water and wiuld like to know how this helps. I've currently got a momentus spike in tinnitus - same happened this time last year- i started Betahistine again to curb the vertigo (which is hovering in the background again
I often see advice on this site, regarding tinnitus/dizziness/vertigo, to drink more water and wiuld like to know how this helps. I've currently got a momentus spike in tinnitus - same happened this time last year- i started Betahistine again to curb the vertigo (which is hovering in the background again
noisynora
in
Tinnitus UK
2 years ago
11yo son with facial palsy following surgery
Hi there. My son has just been diagnosed with facial palsy following ear surgery and it’s a weird feeling - maybe numbness is the best way to describe it. So I just wanted to say hi.
Hi there. My son has just been diagnosed with facial palsy following ear surgery and it’s a weird feeling - maybe numbness is the best way to describe it. So I just wanted to say hi.
JBops
in
Changing Faces
2 years ago
Dizziness and weirdness
Hi everyone, thank your kind comments. I have had this dizziness for a while now,I told one doctor about it and he thought it was labrynthitus. I keep feeling like I am tilting to one side, and moving when I am not, it makes me feel a bit weird. As one person mentioned it might be bppv a form vertigo
Hi everyone, thank your kind comments. I have had this dizziness for a while now,I told one doctor about it and he thought it was labrynthitus. I keep feeling like I am tilting to one side, and moving when I am not, it makes me feel a bit weird. As one person mentioned it might be bppv a form vertigo
fibrogirl41
in
Fibromyalgia Action UK
2 years ago
Back to Square One.
So my ESR has gone from 8 to52 and CRP has gone from 6 to 20 since August last blood test. I'm back on 30 mg pred and due more tests. GP hopes that the symptoms I am suffering from including collapsing legs, pain in lower ribs and back plus loss of balance might now improve. Amen to that because I have
So my ESR has gone from 8 to52 and CRP has gone from 6 to 20 since August last blood test. I'm back on 30 mg pred and due more tests. GP hopes that the symptoms I am suffering from including collapsing legs, pain in lower ribs and back plus loss of balance might now improve. Amen to that because I have
cycli
in
PMRGCAuk
2 years ago
perforated septum - RArelated
anyone here developed perforated septum (hole in nose cartilage) with their RA? if so, any advice on management or treatments? Hospital gave me antibiotic cream and didn’t want to advise/consider other treatment or advice. When II first noticed it was there I thought I must have caused it myself
anyone here developed perforated septum (hole in nose cartilage) with their RA? if so, any advice on management or treatments? Hospital gave me antibiotic cream and didn’t want to advise/consider other treatment or advice. When II first noticed it was there I thought I must have caused it myself
Barbara_Stark
in
NRAS
2 years ago
Another 6 month checkup done
Hi all. I just thought I would share my good news. After the last 6 months of having a tooth removal, a root canal, 7 crowns and a bridge all under a general anesthetic and finally getting to go on our postponed dive holiday to South East Sulawesi Indonesia from 2020, it was more good vibes with all
Hi all. I just thought I would share my good news. After the last 6 months of having a tooth removal, a root canal, 7 crowns and a bridge all under a general anesthetic and finally getting to go on our postponed dive holiday to South East Sulawesi Indonesia from 2020, it was more good vibes with all
Dragonspen
in
CLL Support
2 years ago
tinnitus first post
hi all Matthew here. Thought I’d do my first post as I’m struggling. I have had a high pitched ringing mainly in left ear for about a month, see ent in a few days. It’s not hearing loss or an ear infection. Also found out from blood test I’m hypothyroid so started meds for that last week. Apparently
hi all Matthew here. Thought I’d do my first post as I’m struggling. I have had a high pitched ringing mainly in left ear for about a month, see ent in a few days. It’s not hearing loss or an ear infection. Also found out from blood test I’m hypothyroid so started meds for that last week. Apparently
mra1984
in
British Tinnitus Association
2 years ago
Weight Gain with IVF meds (FET)
Hi everyone, I started my first round of IVF back in March, I had a BMI of 29 so only just within the NHS requirements, and was told ideally to lose weight if possible. I seemed fine with the drugs for egg collection, obvious hormonal fluctuations and a few aches/tiredness, but nothing weight gain related
Hi everyone, I started my first round of IVF back in March, I had a BMI of 29 so only just within the NHS requirements, and was told ideally to lose weight if possible. I seemed fine with the drugs for egg collection, obvious hormonal fluctuations and a few aches/tiredness, but nothing weight gain related
IVFtrip
in
Fertility Network UK
2 years ago
Artane
I was on Artane [Trihexyphenidyl ] for stiffness and within 2 weeks of taking it I had severe hallucinations , I thought the doctor would of decreased my dosage , but she increased it. I really wish I did not do that. It was a mistake and it took some time to get over it.
I was on Artane [Trihexyphenidyl ] for stiffness and within 2 weeks of taking it I had severe hallucinations , I thought the doctor would of decreased my dosage , but she increased it. I really wish I did not do that. It was a mistake and it took some time to get over it.
Annie81963
in
Cure Parkinson's
2 years ago
Incessant itching driving me crazy
I was diagnosed with SLE and APS around 25 years ago ; although I reckon I've had both for most of my life ; I'm 74. Over the years I've had a number of DVT's and a PE and I'm on life long Warfarin. I was on Hydroxy. but was taken off this due to it causing vision problems. The most persistant problem
I was diagnosed with SLE and APS around 25 years ago ; although I reckon I've had both for most of my life ; I'm 74. Over the years I've had a number of DVT's and a PE and I'm on life long Warfarin. I was on Hydroxy. but was taken off this due to it causing vision problems. The most persistant problem
jamesroybuck
in
LUPUS UK
2 years ago
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