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Mouth Taping
I have been a ' mouth breather' all my life . ( 70 yrs old now). I would say it became problematic as I entered by 50's. Waking up in the middle of the night with extreme dry mouth/throat. Then waking in the morning with a slight headache and low energy. I somehow landed on a 'mouth taping' site (
I have been a ' mouth breather' all my life . ( 70 yrs old now). I would say it became problematic as I entered by 50's. Waking up in the middle of the night with extreme dry mouth/throat. Then waking in the morning with a slight headache and low energy. I somehow landed on a 'mouth taping' site (
Manor607
in
Asthma Community Forum
3 years ago
Odd sensation of pressure difference between ears?
Hi I have; High pitched T constantly in left ear, occasionally in the right (I think) Full / heavy ears, Odd tingling in head and face around mouth Intermittent spells of a sensation i can best describe as a heavy ball rolling around in my head. Also a sore jaw, temples and an occasional fluttering
Hi I have; High pitched T constantly in left ear, occasionally in the right (I think) Full / heavy ears, Odd tingling in head and face around mouth Intermittent spells of a sensation i can best describe as a heavy ball rolling around in my head. Also a sore jaw, temples and an occasional fluttering
RobWG
in
British Tinnitus Association
3 years ago
ME exercise therapy guidance scapped by Health watchdog Nice
[i]ME exercise therapy guidance scapped by Health watchdog Nice[/i]
[i]Victory for campaigners as graded exercise therapy they rated ‘harmful’ is taken off list of recommended treatments[/i] [i]A disputed therapy that encourages people with ME to gradually increase physical activity will no
[i]ME exercise therapy guidance scapped by Health watchdog Nice[/i]
[i]Victory for campaigners as graded exercise therapy they rated ‘harmful’ is taken off list of recommended treatments[/i] [i]A disputed therapy that encourages people with ME to gradually increase physical activity will no
helvella
Thyroid UK
in
Thyroid UK
3 years ago
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UK pharmacies in dark about ministers’ plan to maintain drug supplies
The headline might be a bit overdone but, as you read, it is clear that we simply do not know what is happening. Nor what will happen. This follows at least one post about delays in getting Teva levothyroxine - which must be one of the most common thyroid medicines.
[i]UK pharmacies in dark about
The headline might be a bit overdone but, as you read, it is clear that we simply do not know what is happening. Nor what will happen. This follows at least one post about delays in getting Teva levothyroxine - which must be one of the most common thyroid medicines.
[i]UK pharmacies in dark about
helvella
Thyroid UK
in
Thyroid UK
3 years ago
Chinese herbs - so far, so good!
We are in lockfdown here in UK so I searched online for suppliers of Chinese herbs and mail-ordered the three that are recommended: white peony, black cohosh and
cramp
bark
. The author of the article recommends 20 drops of each, three times a day, specially at bedtime.
We are in lockfdown here in UK so I searched online for suppliers of Chinese herbs and mail-ordered the three that are recommended: white peony, black cohosh and
cramp
bark
. The author of the article recommends 20 drops of each, three times a day, specially at bedtime.
Skysgal
in
Restless Legs Syndrome
3 years ago
Onset of T
I had moderate T for about 3 months, apparently triggered by SSNHL. Then, 2 weeks ago out of the blue the T exploded in my head. I now have a very loud high frequency tone continuously in my right ear and more irregular noises in my left ear. When I say loud, I mean on a par with sitting in a car
I had moderate T for about 3 months, apparently triggered by SSNHL. Then, 2 weeks ago out of the blue the T exploded in my head. I now have a very loud high frequency tone continuously in my right ear and more irregular noises in my left ear. When I say loud, I mean on a par with sitting in a car
Greenandblue
in
British Tinnitus Association
3 years ago
Firstly why do my legs feel like jelly, (now on 11mg) and secondly what is the threshold for referral to a rheumatologist?
I was first diagnosed with PMR at the start of lockdown and the euphoria triggered by pred was amazing but since then 3 attempts to get below 7mg haven’t succeeded. I walk my dog daily for about 1 hour so I don’t understand why my legs feel so weak. I am in a constant battle with tiredness but I don’
I was first diagnosed with PMR at the start of lockdown and the euphoria triggered by pred was amazing but since then 3 attempts to get below 7mg haven’t succeeded. I walk my dog daily for about 1 hour so I don’t understand why my legs feel so weak. I am in a constant battle with tiredness but I don’
AnniesRyder5
in
PMRGCAuk
3 years ago
Is it worth doing 'internal stretch' or muscle exercises?
Hi - a strange question perhaps. When diagnosed with Limited Systemic Scleroderma a year ago, I was sent info sheets with hand stretching/ flexing exercises and the need to do them often was reinforced in verbal advice. I am now aware I am finding it hard to swallow some things more often so I wondered
Hi - a strange question perhaps. When diagnosed with Limited Systemic Scleroderma a year ago, I was sent info sheets with hand stretching/ flexing exercises and the need to do them often was reinforced in verbal advice. I am now aware I am finding it hard to swallow some things more often so I wondered
LadyTrundle
in
Scleroderma & Raynaud's UK (SRUK)
3 years ago
Pain management consultant
Hello , I was told yesterday I have fibromyalgia , I also have severe Ankyolosing Spondylitis. My GP who is excellent said there is not really any treatment for it. I am on Adalimumab for the AS which doesn't really help. I ache all over have muscles that are too sore to touch and have severe fatigue
Hello , I was told yesterday I have fibromyalgia , I also have severe Ankyolosing Spondylitis. My GP who is excellent said there is not really any treatment for it. I am on Adalimumab for the AS which doesn't really help. I ache all over have muscles that are too sore to touch and have severe fatigue
Stephanie6637
in
Fibromyalgia Action UK
3 years ago
changed diagnoses
been told i have ataxia for 5 years but they think i have primary lateral sclerosis, is there anyone out there with the same
been told i have ataxia for 5 years but they think i have primary lateral sclerosis, is there anyone out there with the same
golfingsue
in
Ataxia UK
3 years ago
REFINING MY PREVIOUS QUESTION (,,, food for thought): should it be preferable in PSP to take phenylalanine instead of tyrosin supplements?
REFINING MY QUESTION (,,, food for thought...) Tyrosine is a dopamine percursor and as such appears to be a good option for supplementation in PSP. “Tyrosine hydroxylase” is the enzyme responsible for catalyzing the conversion of the amino acid L- tyrosine to L-DOPA. Tyrosine can also be made of phenylalanine
REFINING MY QUESTION (,,, food for thought...) Tyrosine is a dopamine percursor and as such appears to be a good option for supplementation in PSP. “Tyrosine hydroxylase” is the enzyme responsible for catalyzing the conversion of the amino acid L- tyrosine to L-DOPA. Tyrosine can also be made of phenylalanine
BluesHealer
in
PSP Association
3 years ago
Speech Recognition
I had a speech recognition test which came back very low in one ear. In that same ear I have tinnitus and hyperacusis. I would appreciate any advice or help with this or further tests that can be done I had an MRI which came back clear
I had a speech recognition test which came back very low in one ear. In that same ear I have tinnitus and hyperacusis. I would appreciate any advice or help with this or further tests that can be done I had an MRI which came back clear
jojomac23
in
Tinnitus UK
3 years ago
Greater Understanding of PV, ET Drives Potential New Treatment Options
“Continued high-impact research may soon foster the development of disease-modifying therapies for PV and ET and satisfy this need for the optimal management of patients with these MPNs,” they said. Researchers are also determining how to best optimize current treatment options, including JAK inhibitors
“Continued high-impact research may soon foster the development of disease-modifying therapies for PV and ET and satisfy this need for the optimal management of patients with these MPNs,” they said. Researchers are also determining how to best optimize current treatment options, including JAK inhibitors
Manouche
in
MPN Voice
3 years ago
Jakavi. - PV
Hi … can anyone tell me “why” jakavi is easily accessible and affordable in the U.K. ??? Or even Europe????? Would really like to know … I’m in Ontario Canada and my hematologist is close to preparing to plead with our government to allow me to have jakavi on compassionate grounds because my “pinching
Hi … can anyone tell me “why” jakavi is easily accessible and affordable in the U.K. ??? Or even Europe????? Would really like to know … I’m in Ontario Canada and my hematologist is close to preparing to plead with our government to allow me to have jakavi on compassionate grounds because my “pinching
Hidden
in
MPN Voice
3 years ago
Polymorphic light eruption?
Hi all, hope you are all keeping ok, can I ask your advice please? Got blisters/hot/itchy skin on arms and feet only. I had sun cream on arms but not on feet and both areas affected the same. Where my flip flops had been there is no rash/blisters. Never had this before, only just finished an 8 week
Hi all, hope you are all keeping ok, can I ask your advice please? Got blisters/hot/itchy skin on arms and feet only. I had sun cream on arms but not on feet and both areas affected the same. Where my flip flops had been there is no rash/blisters. Never had this before, only just finished an 8 week
bathouse
in
Hughes Syndrome APS Forum
3 years ago
Time running out?
I have lots of health issues but last week was given the latest,upper spine cancer with floating tumours.how the hell does anyone cope with being told that? Now with pain management clinic to try to help.im in pieces!
I have lots of health issues but last week was given the latest,upper spine cancer with floating tumours.how the hell does anyone cope with being told that? Now with pain management clinic to try to help.im in pieces!
Caz4
in
Pain Concern
3 years ago
ANXIETY SUFFERER ALONG WITH LUPUS
Hi All, is anyone suffering with Anxiety?(that's probably a dumb question.most of us have it. I has diagnosed late in life about five years ago. My problem is that I suffer ANXIETY big time. Which I can't sleep without an Aid.Even before I has diagnosed with Panniculitus. I didn't't sleep without a
Hi All, is anyone suffering with Anxiety?(that's probably a dumb question.most of us have it. I has diagnosed late in life about five years ago. My problem is that I suffer ANXIETY big time. Which I can't sleep without an Aid.Even before I has diagnosed with Panniculitus. I didn't't sleep without a
Goinglong10
in
LUPUS UK
3 years ago
Permanently semi-conscious state
Hi I'm new here. My dad has had PSP for about 7 years now and it certainly now feels like he's entering his last days/weeks. One thing we're all very confused about is that he seems to be almost permanently sleeping or semi conscious. He does occasionally open his eyes, he's actually lost all ability
Hi I'm new here. My dad has had PSP for about 7 years now and it certainly now feels like he's entering his last days/weeks. One thing we're all very confused about is that he seems to be almost permanently sleeping or semi conscious. He does occasionally open his eyes, he's actually lost all ability
Ado78
in
PSP Association
3 years ago
Advice for when GP won't act?
Hi guys, I've now had a second intrinsic factor antibody test (privately). Both my private tests came out positive for IF, but the middle test I took, which was with the NHS, came out negative. The GP though thinks I have chronic fatigue syndrome as my cells are normal size and B12 blood levels are coming
Hi guys, I've now had a second intrinsic factor antibody test (privately). Both my private tests came out positive for IF, but the middle test I took, which was with the NHS, came out negative. The GP though thinks I have chronic fatigue syndrome as my cells are normal size and B12 blood levels are coming
JSD100
in
Pernicious Anaemia Society
3 years ago
My Son has Hyperacusis...
Hi, My son has Hyperacusis and he is only 13yrs of age and its really effecting his way of life, makes him very anxious and withdrawn. we come from Kent and looking for any kind of help or support...? Many Thanks
Hi, My son has Hyperacusis and he is only 13yrs of age and its really effecting his way of life, makes him very anxious and withdrawn. we come from Kent and looking for any kind of help or support...? Many Thanks
Tomuchnoise
in
British Tinnitus Association
3 years ago
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