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59 and finally diagnosed
I had given up complaining so regularly about constipation, painful sex, side
pain
, hip
pain
etc as constantly told - menopausal symptoms and my
arthritis
(which I do have).
I had given up complaining so regularly about constipation, painful sex, side
pain
, hip
pain
etc as constantly told - menopausal symptoms and my
arthritis
(which I do have).
Hidden
in
Endometriosis 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
Newly diagnosed
Had xrays bloods checked for
arthritis
long covid MRI for back neck and shoulder
pain
skin conditions boils nerve conductivity test neurology appointment pain in knees hands fingers ribs Brian fog fatigue random aches and pains in muscles and bones .
Had xrays bloods checked for
arthritis
long covid MRI for back neck and shoulder
pain
skin conditions boils nerve conductivity test neurology appointment pain in knees hands fingers ribs Brian fog fatigue random aches and pains in muscles and bones .
Aka-Ice
in
Fibromyalgia Action UK
1 year ago
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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
dreading camera
I have rheumatoid and osteoarthritis, but lately had trouble swallowing even drinks won’t go down sometimes, so I’ve now got an appointment on Monday for a Gastroscopy, Ive had them before and really can’t stand them, I’m getting more stressed and worried about it any tips to calm myself please .
I have rheumatoid and osteoarthritis, but lately had trouble swallowing even drinks won’t go down sometimes, so I’ve now got an appointment on Monday for a Gastroscopy, Ive had them before and really can’t stand them, I’m getting more stressed and worried about it any tips to calm myself please .
jools34
in
NRAS
2 years ago
osteoarthritis alongside rheumatoid….
I’ve had RA and Fibromyalgia for a long time now, on meds and see rheumatologist regularly. I also, increasingly seem to have osteoarthritis- I’ve got real problems with my knees at the moment. My question is…… will both conditions be looked at by rheumatology or is the osteoarthritis another specialism
I’ve had RA and Fibromyalgia for a long time now, on meds and see rheumatologist regularly. I also, increasingly seem to have osteoarthritis- I’ve got real problems with my knees at the moment. My question is…… will both conditions be looked at by rheumatology or is the osteoarthritis another specialism
girli1111
in
NRAS
2 years ago
sulfasalazine & wrong med issued - Another update
hi everyone just a quickie in relation to the cockup boots made with my medication giving (me sulfadiazine instead of sulfasalazine) I arrive back from hols later tonight & have sulfasalazine at home,my question is,I'd only been on it 4 weeks before coming away & had to take 1 tablet a day
hi everyone just a quickie in relation to the cockup boots made with my medication giving (me sulfadiazine instead of sulfasalazine) I arrive back from hols later tonight & have sulfasalazine at home,my question is,I'd only been on it 4 weeks before coming away & had to take 1 tablet a day
Garnacha
in
NRAS
2 years ago
Turmeric??
I started taking it for inflammation and
pain
from
arthritis
. My RLS has flared up again and it seems like too much of a coincidence. Any help would be greatly appreciated!
I started taking it for inflammation and
pain
from
arthritis
. My RLS has flared up again and it seems like too much of a coincidence. Any help would be greatly appreciated!
chihuahualuver
in
Restless Legs Syndrome
2 years ago
Went from Psoriatic arthritis to fibromyalgia to osteoarthritis
Hello everyone. It’s been awhile since I’ve used this account. I was previously diagnosed with endometriosis. After two surgeries I’m mostly symptom free. Then found out I also have hemochromatosis. Psoriasis runs in the family as well as arthritis but no one I know of has gone to a specialist.
Hello everyone. It’s been awhile since I’ve used this account. I was previously diagnosed with endometriosis. After two surgeries I’m mostly symptom free. Then found out I also have hemochromatosis. Psoriasis runs in the family as well as arthritis but no one I know of has gone to a specialist.
Sunshine23
in
Arthritis Action
2 years ago
Leflunomide - has anyone had success on this?
Hi I’ve just started Leflunomide I really hope it works for me as I’ve failed methotrexate and Sulfasalazine due to bad side effects. Has Leflunomide been successful for anyone else? 🙂
Hi I’ve just started Leflunomide I really hope it works for me as I’ve failed methotrexate and Sulfasalazine due to bad side effects. Has Leflunomide been successful for anyone else? 🙂
mistygrey
in
NRAS
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
very sore heels at the end of the day, up on a foot rest. They burn and ache and the skin is tight and dry.
my New Poiatrist did a fungal test and told me that she believed that my “ Psoriasis “ was actually Athlete’s foot that had spread to my soles, heels sides of the feet and toenails. I have been treating it as Psoriasis for years. After” Lamisil once “ my feet look better and my nails are clearly going
my New Poiatrist did a fungal test and told me that she believed that my “ Psoriasis “ was actually Athlete’s foot that had spread to my soles, heels sides of the feet and toenails. I have been treating it as Psoriasis for years. After” Lamisil once “ my feet look better and my nails are clearly going
SheffieldJane
in
PMRGCAuk
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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