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Side effects of nefopam sweats
Recently been put on nefopam due to night pains because of hip and back pain. Does anyone else suffer sweats from nefopam? I'm trying to rule them out as on other meds too.
Recently been put on nefopam due to night pains because of hip and back pain. Does anyone else suffer sweats from nefopam? I'm trying to rule them out as on other meds too.
Jackieginger44
in
Pain Concern
5 months ago
Do I declare Esophageal varices (no longer found) on travel insurance?
Hi All, I've booked a holiday for April next year and I'm looking for a bit of advice regarding my travel insurance. Due to having a blood clot in my portal vein because of my MPN I was diagnosed with having Esophageal varices (bloated blood vessels). However, I recently had an endoscopic examination
Hi All, I've booked a holiday for April next year and I'm looking for a bit of advice regarding my travel insurance. Due to having a blood clot in my portal vein because of my MPN I was diagnosed with having Esophageal varices (bloated blood vessels). However, I recently had an endoscopic examination
MarkD6701
in
MPN Voice
11 months ago
threadworm fibromyalgia link?
Morning all, I’ve recently been diagnosed with fibro and even more recently been researching if there is a link between it and thread worm as 5yrs ago I had threadworm then the other night I’ve realised they are back so was wondering if anyone else has found a link as my fibro flares have been so much
Morning all, I’ve recently been diagnosed with fibro and even more recently been researching if there is a link between it and thread worm as 5yrs ago I had threadworm then the other night I’ve realised they are back so was wondering if anyone else has found a link as my fibro flares have been so much
Emmybird2
in
Fibromyalgia Action UK
1 year ago
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Questionn
Can a Patent Ductus Aerteriosus be diagnosed with a posterlateral thoracotomy then be monitor to make sure it closes?
Can a Patent Ductus Aerteriosus be diagnosed with a posterlateral thoracotomy then be monitor to make sure it closes?
LonerIQ
in
Lung Conditions Community Forum
1 year ago
PPPD and vestibular disorders
Did you know that many of the underlying issues in dizziness are related to the autonomic nervous system? Or that sleep, diet and stress can play a role? Re-actives team program centres on an holistic approach to dizziness; an approach that includes looking at your movement, muscular factors, lifestyle
Did you know that many of the underlying issues in dizziness are related to the autonomic nervous system? Or that sleep, diet and stress can play a role? Re-actives team program centres on an holistic approach to dizziness; an approach that includes looking at your movement, muscular factors, lifestyle
Lady4
in
Functional Neurological Disorder - FND Hope
11 days ago
Cerelle desogestrel
I've been taking 2x desogestrl tablets daily since January and have noticed the past few months cramping but no period, I've had to go to hospital for morphine to calm this, could this mean my endo has grown back even thought i only had a lap in March 22?
I've been taking 2x desogestrl tablets daily since January and have noticed the past few months cramping but no period, I've had to go to hospital for morphine to calm this, could this mean my endo has grown back even thought i only had a lap in March 22?
Surfingblue
in
Endometriosis UK
1 year ago
Help!
Hello everyone. 💙It's been six months since my mother had herpes encephalitis type 1, but she still can't stand up and is physically weak. I don't know if occupational therapy is useful or not? What should I do to improve her physical condition?
Hello everyone. 💙It's been six months since my mother had herpes encephalitis type 1, but she still can't stand up and is physically weak. I don't know if occupational therapy is useful or not? What should I do to improve her physical condition?
Ftmz
in
Encephalitis International
2 months ago
tramadol
I was on tramadol for at least 10 years----100 mg. then my doc took me off because a neurologist put me on Clonazepam for REM/SBD (rapid eye movement sleep behavior disorder.) But I was also getting cervical and lumbar rhizotomies...and still do every 12-14 months or so. I am now working with the VA
I was on tramadol for at least 10 years----100 mg. then my doc took me off because a neurologist put me on Clonazepam for REM/SBD (rapid eye movement sleep behavior disorder.) But I was also getting cervical and lumbar rhizotomies...and still do every 12-14 months or so. I am now working with the VA
Shadowperson
in
Pain Concern
1 year ago
Low B6... taking a complex with pyridoxine which obviously doesn't suit
Back to the search for the best B complex (Thorne being elusive at the moment and didn't do particularly well at keeping my B12 up)... one which contains pyridoxal 5' phosphate Does anyone rate Igennus Super B Complex? All suggestions welcome 🤗
Back to the search for the best B complex (Thorne being elusive at the moment and didn't do particularly well at keeping my B12 up)... one which contains pyridoxal 5' phosphate Does anyone rate Igennus Super B Complex? All suggestions welcome 🤗
TiggerMe
in
Thyroid UK
1 year ago
LDH high
Looking back, my specialist tested my LDH at diagnosis and it was in fact elevated. He told me that it’s very common for MPN’s to cause elevated LDH levels and said with treatment we can correct them.. is that true? I was worried for a second about any organ or tissue damage, but he reassured and said
Looking back, my specialist tested my LDH at diagnosis and it was in fact elevated. He told me that it’s very common for MPN’s to cause elevated LDH levels and said with treatment we can correct them.. is that true? I was worried for a second about any organ or tissue damage, but he reassured and said
JAKboy
in
MPN Voice
1 year ago
Moving forward
Before my diagnosis, I had various symptoms that I could not control, and afterward would lose parts of my memories, it was people's names and events later I had a seizure but sometimes in my sleep. It was either when I was fully awake and alert and I could see my surroundings but then if I did have
Before my diagnosis, I had various symptoms that I could not control, and afterward would lose parts of my memories, it was people's names and events later I had a seizure but sometimes in my sleep. It was either when I was fully awake and alert and I could see my surroundings but then if I did have
mavem100
in
Functional Neurological Disorder - FND Hope
3 months ago
Best natural anti anxiety remedy
Hi, I was wondering what natural treatments people are taking to help with the anxiety that a lot of us with T have to deal with every day ? Does 5-htp work ? How about St Johns wort and L Theanine ? Which seems to work best for you ?
Hi, I was wondering what natural treatments people are taking to help with the anxiety that a lot of us with T have to deal with every day ? Does 5-htp work ? How about St Johns wort and L Theanine ? Which seems to work best for you ?
woodman72
in
Tinnitus UK
1 year ago
The "other" symptoms of PMR?
I was diagnosed with PMR in July 2022 after 2 months of sudden onset of symptoms. I was very fit & healthy at time of first symptoms. I am using DSNS weaning regime & down to 7mg & had 2 flares during this time. Currently stuck on 7mg for a month due to slight hip discomfort. My question is less
I was diagnosed with PMR in July 2022 after 2 months of sudden onset of symptoms. I was very fit & healthy at time of first symptoms. I am using DSNS weaning regime & down to 7mg & had 2 flares during this time. Currently stuck on 7mg for a month due to slight hip discomfort. My question is less
Flinders61
in
PMRGCAuk
1 year ago
Inflammatory Pain and T
I have had T for over two years now following an attack of vertigo with varying diagnoses of labyrinthitis, bppv or vestibular neuritis, none of which have ever been confirmed.. and after all this time I feel stuck with no sign of reaching habituation.. I had months of complaining of a dullness in my
I have had T for over two years now following an attack of vertigo with varying diagnoses of labyrinthitis, bppv or vestibular neuritis, none of which have ever been confirmed.. and after all this time I feel stuck with no sign of reaching habituation.. I had months of complaining of a dullness in my
Shozza1
in
Tinnitus UK
1 year ago
Spontaneous remission of some blood counts after Dx
This just is a question of curiosity I've discussed briefly before. If any members have seen something like this it would be interesting to know. I've asked two MPN Drs about it and all I hear is "it's complicated" and/or "things fluctuate". -- These plots show some counts and when I started aspirin
This just is a question of curiosity I've discussed briefly before. If any members have seen something like this it would be interesting to know. I've asked two MPN Drs about it and all I hear is "it's complicated" and/or "things fluctuate". -- These plots show some counts and when I started aspirin
EPguy
in
MPN Voice
1 year ago
Excessive Sleeping
My husband was diagnosed in early 2020 with MSA. The decline was rapid - he is now on PEG for feeds, intermittent urine catheter, flatus tube for bowel movement, and a tracheotomy with ventilator on at night He has speech therapy, physiotherapy, occupational therapy that fills up his days However
My husband was diagnosed in early 2020 with MSA. The decline was rapid - he is now on PEG for feeds, intermittent urine catheter, flatus tube for bowel movement, and a tracheotomy with ventilator on at night He has speech therapy, physiotherapy, occupational therapy that fills up his days However
binnyrox
in
Multiple System Atrophy Trust
4 months ago
Occupational Therapy
Hi everyone, my 11 year old was diagnosed with ADHD six years ago. I am just wondering for those who are having occupational therapy as part of an accommodation - it what ways has it been helpful or if it has been helpful? Just trying to get a sense of how occupational therapy might fit in.
Hi everyone, my 11 year old was diagnosed with ADHD six years ago. I am just wondering for those who are having occupational therapy as part of an accommodation - it what ways has it been helpful or if it has been helpful? Just trying to get a sense of how occupational therapy might fit in.
Uptowngirl12121
in
CHADD's ADHD Parents Together
5 months ago
Pulsatile tinnitus
Hi there. Does anyone else have pulsatile T. Mostly it comes and goes, always one-sided as the T is that side. I can make it go away by turning my head to the opposite side. But when i turn it back the T comes back. Shrugging my shoulders helps as well as stretching my neck. Have spoken to the doctor
Hi there. Does anyone else have pulsatile T. Mostly it comes and goes, always one-sided as the T is that side. I can make it go away by turning my head to the opposite side. But when i turn it back the T comes back. Shrugging my shoulders helps as well as stretching my neck. Have spoken to the doctor
penelope2
in
Tinnitus UK
9 months ago
colonoscope
Just wondering if anybody had deep sedation with this procedure and how was it thanks Sue. Just anxious about it all with Emphysema.
Just wondering if anybody had deep sedation with this procedure and how was it thanks Sue. Just anxious about it all with Emphysema.
soul-123
in
Lung Conditions Community Forum
9 months ago
Asbestos
Hi, everybody I had breathing problems last year. Went to my doctor & had a blood test that night I got a call to go straight to local hospital. Was there for14 hours but excellent service. Found build up of liquid in lungs & my ankles & lower legs were bigger. I had been cutting my socks as I thought
Hi, everybody I had breathing problems last year. Went to my doctor & had a blood test that night I got a call to go straight to local hospital. Was there for14 hours but excellent service. Found build up of liquid in lungs & my ankles & lower legs were bigger. I had been cutting my socks as I thought
wimbledon
in
Lung Conditions Community Forum
9 months ago
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