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Help change Health Professionals' attitudes to FM and FM diagnosis - your experiences, please... Sorry, a bit of a long read...
Background to my question.
Just had my second total knee replacement and my lovely Physio Salma at my hospital is particularly interested in trying to change attitudes toward FM in certain health sector groups and has made this a major part of her Senior Physio Thesis for which she is presenting
Background to my question.
Just had my second total knee replacement and my lovely Physio Salma at my hospital is particularly interested in trying to change attitudes toward FM in certain health sector groups and has made this a major part of her Senior Physio Thesis for which she is presenting
denny_the_wench
in
Fibromyalgia Action UK
2 years ago
Peripheral Neuropathy PN Activist
PN at Mayo Clinic offers better care and definition - see Peripheral Neuropathy. John Hopkins Medicine https://www.hopkinsmedicine.org/health/conditions-and-diseases/peripheral-neuropathy Peripheral Neuropathy | Johns Hopkins Medicinereports “Usually a peripheral neuropathy can’t be cured, but you
PN at Mayo Clinic offers better care and definition - see Peripheral Neuropathy. John Hopkins Medicine https://www.hopkinsmedicine.org/health/conditions-and-diseases/peripheral-neuropathy Peripheral Neuropathy | Johns Hopkins Medicinereports “Usually a peripheral neuropathy can’t be cured, but you
CIPN
in
Neuropathy Support
2 years ago
help what painkillers best for flares and fibro
spent yesterday with the world going on and me out of it tramadol seems to be losing effect started antidepressant not sure if its doing anything any ideas
spent yesterday with the world going on and me out of it tramadol seems to be losing effect started antidepressant not sure if its doing anything any ideas
pauluk60
in
NRAS
2 years ago
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Is this a flare
Hi all thought I’d update you on my post is this a flare!!!! As no painkillers helped just wondered if I was having a flare but thank goodness no I’m not. I’ve had an MRI and found a disc pressing on a nerve but requires no surgery at the moment. however my ESR was raised as was my CRP. Have been
Hi all thought I’d update you on my post is this a flare!!!! As no painkillers helped just wondered if I was having a flare but thank goodness no I’m not. I’ve had an MRI and found a disc pressing on a nerve but requires no surgery at the moment. however my ESR was raised as was my CRP. Have been
Reddev
in
PMRGCAuk
2 years ago
Sunday’s Poem is Tarantella
Do you remember an Inn, Miranda? Do you remember an Inn? And the tedding and the spreading Of the straw for a bedding, And the fleas that tease in the High Pyrenees, And the wine that tasted of the tar? And the cheers and the jeers of the young muleteers (Under the vine of the dark verandah)
Do you remember an Inn, Miranda? Do you remember an Inn? And the tedding and the spreading Of the straw for a bedding, And the fleas that tease in the High Pyrenees, And the wine that tasted of the tar? And the cheers and the jeers of the young muleteers (Under the vine of the dark verandah)
Lyd12
in
Lung Conditions Community Forum
2 years ago
I had the worst pain of my life last night. I couldn’t get out of bed for 1.5 hrs!
I come on here sometimes to have a good moan. I’ve had RA since i was 21. (30 yrs). Plus Iritis & Glaucoma. I’ve had an awful time the last month. First i had a very painful flare of my Iritis. Deep throbbing, burning, aching in my right eye, very bad vision. Had to go to Moorfields a&e. Went at about
I come on here sometimes to have a good moan. I’ve had RA since i was 21. (30 yrs). Plus Iritis & Glaucoma. I’ve had an awful time the last month. First i had a very painful flare of my Iritis. Deep throbbing, burning, aching in my right eye, very bad vision. Had to go to Moorfields a&e. Went at about
Vixen2
in
NRAS
2 years ago
tooth extraction
yesterday I went to the emergency dentist-I was referred there by my city main emergency dentist. Anyway it was because of an away night and day off tooth pain I had I just could not Cope with. The dentist said what was wrong and told me the best thing was to take it out. I agreed and it was obviously
yesterday I went to the emergency dentist-I was referred there by my city main emergency dentist. Anyway it was because of an away night and day off tooth pain I had I just could not Cope with. The dentist said what was wrong and told me the best thing was to take it out. I agreed and it was obviously
Junny123
in
Pain Concern
2 years ago
RLS what works for me
After bilateral hip replacement in 2015, I developed RLS in both legs, seem to hit at once when it attacks. Mainly at night of course or during meetings or when I'm still too long. I take a plant product called kratom. It might not be legal in all states but is in mine (for now). I learned about it
After bilateral hip replacement in 2015, I developed RLS in both legs, seem to hit at once when it attacks. Mainly at night of course or during meetings or when I'm still too long. I take a plant product called kratom. It might not be legal in all states but is in mine (for now). I learned about it
restle
in
Restless Legs Syndrome
2 years ago
Medical cannabis
Hi everyone you might find interesting this article regarding the benefits of medical cannabis https://www.thecourier.co.uk/fp/lifestyle/health-wellbeing/3561418/angus-woman-benefits-of-medical-cannabis/ unfortunately it seems the article is now only for subscribers but basically talks about a woman
Hi everyone you might find interesting this article regarding the benefits of medical cannabis https://www.thecourier.co.uk/fp/lifestyle/health-wellbeing/3561418/angus-woman-benefits-of-medical-cannabis/ unfortunately it seems the article is now only for subscribers but basically talks about a woman
JoseT
in
Fibromyalgia Action UK
2 years ago
New to pmr, advice please
When I was first diagnosed with pmr, I was put on 15mg pred, I felt better so I tried to taper down to 10mg ….big mistake! The pmr came back with a vengeance and my doctor put me on 20mg pred. After 3 weeks, I am still suffering even worse, it feels like I’m having the inside of my body stretched and
When I was first diagnosed with pmr, I was put on 15mg pred, I felt better so I tried to taper down to 10mg ….big mistake! The pmr came back with a vengeance and my doctor put me on 20mg pred. After 3 weeks, I am still suffering even worse, it feels like I’m having the inside of my body stretched and
Sueloobyloo
in
PMRGCAuk
2 years ago
pain killers
what’s the best pain killers to take after, I’m having mine done Monday and want to get some ready.
what’s the best pain killers to take after, I’m having mine done Monday and want to get some ready.
Badboy321
in
Men's Health Forum (Penis Health)
2 years ago
restriction
I wanted to ask a question etc on the pain medication site re pregabalin and it seems I am restricted. Can you tell me why please ?
I wanted to ask a question etc on the pain medication site re pregabalin and it seems I am restricted. Can you tell me why please ?
Stoneferry8
in
Pain Concern
2 years ago
First Lap in the morning
Hi All, I’ve been reading all the posts on here for a while and tomorrow I’m going for my first Lap. I’ve had painful periods my entire life, but in recent years these have left me unable to move with severe D&V, on a few occasions as I’ve been unable to keep pain medication down I’ve been admitted
Hi All, I’ve been reading all the posts on here for a while and tomorrow I’m going for my first Lap. I’ve had painful periods my entire life, but in recent years these have left me unable to move with severe D&V, on a few occasions as I’ve been unable to keep pain medication down I’ve been admitted
eeh12
in
Endometriosis UK
2 years ago
should I go to A&E
dr will not give me any pain killers until I attend face to face appointment. I have just started a new job and I’m scared of missing work. I haven’t slept in 2 weeks the pain is numbing now I cry myself to sleep I vomit constantly I feel Dizzy and faint. My full pelvic area is in agony I feel so Dismissed
dr will not give me any pain killers until I attend face to face appointment. I have just started a new job and I’m scared of missing work. I haven’t slept in 2 weeks the pain is numbing now I cry myself to sleep I vomit constantly I feel Dizzy and faint. My full pelvic area is in agony I feel so Dismissed
Littlebug77
in
Endometriosis UK
2 years ago
Pelvic Physio in Manchester on the NHS?
Hello! After watching The Women's Health Programme on channel 5 last night and a woman on there saying Pelvic Physio has basically changed her life and reduced the amount of pain killers she needs to take I am going to ask my GP if I can be referred. However, is anyone aware of any places that offer
Hello! After watching The Women's Health Programme on channel 5 last night and a woman on there saying Pelvic Physio has basically changed her life and reduced the amount of pain killers she needs to take I am going to ask my GP if I can be referred. However, is anyone aware of any places that offer
JadeH92
in
Endometriosis UK
2 years ago
Pelvic Physio in Manchester on the NHS?
Hello! QgterAfter watching The Women's Health Programme on channel 5 last night and a woman on there saying Pelvic Physio has basically changed her life and reduced the amount of pain killers she needs to take I am going to ask my GP if I can be referred. However, is anyone aware of any places that
Hello! QgterAfter watching The Women's Health Programme on channel 5 last night and a woman on there saying Pelvic Physio has basically changed her life and reduced the amount of pain killers she needs to take I am going to ask my GP if I can be referred. However, is anyone aware of any places that
JadeH92
in
Pelvic Pain Support Network
2 years ago
No Period after Zoladex?
Hi all. I hope you’re enjoying the UK heatwave! ☀️ I (22F) have just completed my 2nd course of Zoladex treatment for my Adenomyosis & Endometriosis. I had my last Injection 17th March 2022. A bit of back story… I was diagnosed with Stage 1 Endo and Pelvic Congestion Syndrome via Laparoscopy in
Hi all. I hope you’re enjoying the UK heatwave! ☀️ I (22F) have just completed my 2nd course of Zoladex treatment for my Adenomyosis & Endometriosis. I had my last Injection 17th March 2022. A bit of back story… I was diagnosed with Stage 1 Endo and Pelvic Congestion Syndrome via Laparoscopy in
LuceRM
in
Endometriosis UK
2 years ago
Clear ultrasound- feeling deflated
Hello, I had an ultrasound last week and as expected they said they couldn’t see any obvious signs to suggest endometriosis, and said everything looked normal. However, the lady was very nice and told me to keep pushing my doctor for further tests and a referral to a gynaecologist as an ultrasound isn
Hello, I had an ultrasound last week and as expected they said they couldn’t see any obvious signs to suggest endometriosis, and said everything looked normal. However, the lady was very nice and told me to keep pushing my doctor for further tests and a referral to a gynaecologist as an ultrasound isn
Lotus95x
in
Endometriosis UK
2 years ago
Update on referral post
Hi everyone, Just an update on my last post.i have got my gynaecology appointment next Sunday. I've been trying to forget about it but now I'm feeling really anxious about it and what they might want to do. I tried to go back on the pill a couple of months ago but the side effects are worse than
Hi everyone, Just an update on my last post.i have got my gynaecology appointment next Sunday. I've been trying to forget about it but now I'm feeling really anxious about it and what they might want to do. I tried to go back on the pill a couple of months ago but the side effects are worse than
Sheep2
in
Endometriosis UK
2 years ago
we are waiting for diagnosis. And I am so scared…
My husband had very strange sensation about 2 months ago. He describes it “electric ants marching from his temple to the end of the arms” and felt nauseous. If I think back, it might have been seizures. It went away after 2 weeks, then he started suffering from daily headache. He always had migraine
My husband had very strange sensation about 2 months ago. He describes it “electric ants marching from his temple to the end of the arms” and felt nauseous. If I think back, it might have been seizures. It went away after 2 weeks, then he started suffering from daily headache. He always had migraine
Springbunny
in
Meningioma Support
2 years ago
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