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Stepping my game up
Alright so I have one last appointment with the GP before I change and I am going to get referred to a pain clinic because I think I need someone to look at me and give me guidance. I think I'd prefer the opium clinic even though I don't want to be "off" them, I just need some guidance with how to
Alright so I have one last appointment with the GP before I change and I am going to get referred to a pain clinic because I think I need someone to look at me and give me guidance. I think I'd prefer the opium clinic even though I don't want to be "off" them, I just need some guidance with how to
Sleepybear987
in
British Heart Foundation
1 year ago
Switching from Methadone to buprenorphine
I’ve been taking Methadone for a little over 2 years after I augmented on Tramadol. I absolutely love how well the Methadone works. I rarely have symptoms and when I do get them a quick hot bath and I’m good again. The part I don’t like is the 20 pounds I’ve gained. It makes me feel hungry all the
I’ve been taking Methadone for a little over 2 years after I augmented on Tramadol. I absolutely love how well the Methadone works. I rarely have symptoms and when I do get them a quick hot bath and I’m good again. The part I don’t like is the 20 pounds I’ve gained. It makes me feel hungry all the
Poe7
in
Restless Legs Syndrome
1 year ago
Ropinirole
Hi Guys, I'm in the process of reducing my dosage of Ropinirole. I was taking 4mg a night but after a few months Im down to 2mg. My Doctor has prescribed Gabapentin and told me while Im reducing the Ropinirole to introduce the Gabapentin. Im now taking 2mg of Ropinirole and 1200mg of Gabapentin. Does
Hi Guys, I'm in the process of reducing my dosage of Ropinirole. I was taking 4mg a night but after a few months Im down to 2mg. My Doctor has prescribed Gabapentin and told me while Im reducing the Ropinirole to introduce the Gabapentin. Im now taking 2mg of Ropinirole and 1200mg of Gabapentin. Does
Kjh100
in
Restless Legs Syndrome
1 year ago
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It has been my longest and toughest journey of my life.
My fibromyalgia started in a writer way. In 2019, I became very ill with several bloody UTIS, which then affected my skin, my body was producing what was similar to small fish scales, they would ping out of my skin all over my body. Come out my tear ducks. When I was on the loo I could hear them hitting
My fibromyalgia started in a writer way. In 2019, I became very ill with several bloody UTIS, which then affected my skin, my body was producing what was similar to small fish scales, they would ping out of my skin all over my body. Come out my tear ducks. When I was on the loo I could hear them hitting
Mazymoo
in
Fibromyalgia Action UK
1 year ago
I just don’t know what to do anymore
Hey everyone, I just need to rant to people that get it… I’ve been pretty much bed ridden since I had surgery in March, this was to remove part of my uterus(I had an extra bit that hadn’t developed correctly), a fallopian tube & endometriosis on my right side as well as a womb ablation but I feel
Hey everyone, I just need to rant to people that get it… I’ve been pretty much bed ridden since I had surgery in March, this was to remove part of my uterus(I had an extra bit that hadn’t developed correctly), a fallopian tube & endometriosis on my right side as well as a womb ablation but I feel
SCords
in
Endometriosis UK
1 year ago
Gabapentin side effects
I have been prescribed Gabapentin for RLS. I just increased the dose from 600mg to 900 mg. I am experiencing a mixture of chronic fatigue, nausea and depression. I haven't been able to eat anything for days and I am almost comatose with the depression. Does anyone else have any of these issues
I have been prescribed Gabapentin for RLS. I just increased the dose from 600mg to 900 mg. I am experiencing a mixture of chronic fatigue, nausea and depression. I haven't been able to eat anything for days and I am almost comatose with the depression. Does anyone else have any of these issues
welschrispy
in
Restless Legs Syndrome
1 year ago
Newbie to the group.
Hi all, I’m new to the group although 6 months in on a PMR diagnosis. My symptoms started in April 2020 2 months after as knee injury, both my shoulders at first, I couldn’t even get a cup off the side, couldn’t lay on my side or touch my shoulders. I thought that it was over use. My GP prescribed
Hi all, I’m new to the group although 6 months in on a PMR diagnosis. My symptoms started in April 2020 2 months after as knee injury, both my shoulders at first, I couldn’t even get a cup off the side, couldn’t lay on my side or touch my shoulders. I thought that it was over use. My GP prescribed
Binnie49
in
PMRGCAuk
1 year ago
Costochronditis and Fibromyalgia
Does anyone suffer from the above? I had a stroke in Nov 2020 and despite some complications from this, recovery has been slow. In 2021 I started experencing severe and sharp chest pain and pain under my breast and radiating through to my shoulder blades. Having attended A&E on advice of the NHS doctor's
Does anyone suffer from the above? I had a stroke in Nov 2020 and despite some complications from this, recovery has been slow. In 2021 I started experencing severe and sharp chest pain and pain under my breast and radiating through to my shoulder blades. Having attended A&E on advice of the NHS doctor's
Hidden
in
Fibromyalgia Action UK
1 year ago
Question about reducing Pred
The last six weeks I have been reducing very slowly by .5mg from 4mg to 3.5mg. I have done this a few times without success ending in a flare. This time I am at the moment totally free in the upper half of my body from pain or stiffness, but have been getting what I think is withdrawal symptoms around
The last six weeks I have been reducing very slowly by .5mg from 4mg to 3.5mg. I have done this a few times without success ending in a flare. This time I am at the moment totally free in the upper half of my body from pain or stiffness, but have been getting what I think is withdrawal symptoms around
Purplegloss
in
PMRGCAuk
1 year ago
Why Do I pain in my left ribs?
I would like to thank the BHF Nurse that actually took the bother to call me after I emailed for help and advice, she was very empathetic and gave me good advice about keeping a record of my blood pressure’s and taking it in the morning when I get up after I’ve pottered about but before any medication
I would like to thank the BHF Nurse that actually took the bother to call me after I emailed for help and advice, she was very empathetic and gave me good advice about keeping a record of my blood pressure’s and taking it in the morning when I get up after I’ve pottered about but before any medication
Ls1958
in
British Heart Foundation
1 year ago
Tappering off Oxy and help with Insomnia
I am trying to wean myself off percocet and just stay on Horizant 1200 mg and also use medical marihuana as needed for RLS. Percocet is being used for augmentation from being on Pramipexole for 10 years and for some back pain. I have been on Percocet 10 mg nightly for 8 months and want to start weaning
I am trying to wean myself off percocet and just stay on Horizant 1200 mg and also use medical marihuana as needed for RLS. Percocet is being used for augmentation from being on Pramipexole for 10 years and for some back pain. I have been on Percocet 10 mg nightly for 8 months and want to start weaning
kturenne
in
Restless Legs Syndrome
1 year ago
Tramadol & buprenorphine & RLS
I feel that I might be augmenting on Tramadol having recently increased my intake to 150mg from 100mgHowever I notice buprenorphine mentioned and wondered what the difference is between Tramadol & buprenorphine
I feel that I might be augmenting on Tramadol having recently increased my intake to 150mg from 100mgHowever I notice buprenorphine mentioned and wondered what the difference is between Tramadol & buprenorphine
m1946
in
Restless Legs Syndrome
1 year ago
Mauimags
I've lived with chronic lower back pain and gone from 10yrs of high dose buprenorphine then 5yrs of tramadol then taken off it completely. Now on paracetamol and naproxen which do nothing for pain. I can't walk very well or domy physio now.
I've lived with chronic lower back pain and gone from 10yrs of high dose buprenorphine then 5yrs of tramadol then taken off it completely. Now on paracetamol and naproxen which do nothing for pain. I can't walk very well or domy physio now.
Mauimags
in
Arthritis Action
1 year ago
Just a quick one about little things that can affect us
I had my follow up on Wednesday as I mentioned I’m still not 100%. My heart failure is going to be checked out next month with an echo. The doctor wants at least a month to give the pacemaker a chance to do some magic. My EP does not just treat the heart as if the person does not exist. After our
I had my follow up on Wednesday as I mentioned I’m still not 100%. My heart failure is going to be checked out next month with an echo. The doctor wants at least a month to give the pacemaker a chance to do some magic. My EP does not just treat the heart as if the person does not exist. After our
DawnTX
in
AF Association
1 year ago
Maggie
Due to arthritis I've been living with chronic back pain for 15yrs, had a knee replacement and also hip bursitis. I had an operation on one hip last year but I find I can't get very far with the physio because of my back pain.I've also been taken off buprenorphine then more recently tramadol.my pain
Due to arthritis I've been living with chronic back pain for 15yrs, had a knee replacement and also hip bursitis. I had an operation on one hip last year but I find I can't get very far with the physio because of my back pain.I've also been taken off buprenorphine then more recently tramadol.my pain
Mauimags
in
Pain Concern
1 year ago
Half Sineset
Have been asked to try Half Sineset for RLS Anybody used this ,it is for Parkinson but also used for RLS told to come off Gabapentin and Tramadol ,the Consultant say these make RLS worse bit confused .
Have been asked to try Half Sineset for RLS Anybody used this ,it is for Parkinson but also used for RLS told to come off Gabapentin and Tramadol ,the Consultant say these make RLS worse bit confused .
auldreekie18
in
Restless Legs Syndrome
1 year ago
Post Pred motivation?
Hi all, I'm finally off Pred after starting at 50mg back in Aug '21 for a crippling PMR attack. I took my final (hopefully) 0.5 mg about three weeks ago. However, I'm now often feeling very slow and lacking in motivation to do much at all. "Brain dead" would be a good way to express it. This is not
Hi all, I'm finally off Pred after starting at 50mg back in Aug '21 for a crippling PMR attack. I took my final (hopefully) 0.5 mg about three weeks ago. However, I'm now often feeling very slow and lacking in motivation to do much at all. "Brain dead" would be a good way to express it. This is not
Hidden
in
PMRGCAuk
1 year ago
Pre diagnosis and lost in the weeds
Hi everybody, I hope I'm doing this correctly. I'm feeling very lost at the moment. What did any of you do for pain relief while waiting for your rhuem appt and diagnosis? I'll happilly accept recommendations if that is allowed here or maybe I missed a pinned post? I'm pre diagnosis, so no 'good drugs
Hi everybody, I hope I'm doing this correctly. I'm feeling very lost at the moment. What did any of you do for pain relief while waiting for your rhuem appt and diagnosis? I'll happilly accept recommendations if that is allowed here or maybe I missed a pinned post? I'm pre diagnosis, so no 'good drugs
Quinni
in
NRAS
1 year ago
Stopping Cerazette
First time poster, but I’ve taken many tips from this board so thank you all in advance. 2 years ago I doubled over in agony, eventually got sent to A&E via my GP with suspected appendicitis. Wasn’t appendicitis, it was a haemorrhaging ovarian cyst. Sent home with painkillers, had a couple of scans and
First time poster, but I’ve taken many tips from this board so thank you all in advance. 2 years ago I doubled over in agony, eventually got sent to A&E via my GP with suspected appendicitis. Wasn’t appendicitis, it was a haemorrhaging ovarian cyst. Sent home with painkillers, had a couple of scans and
Bookworm3371
in
Endometriosis UK
1 year ago
Cyst on ovary
I recently posted here about pain on my left side after an ulcerative colitis flare. I’ve been having this pain since October and was given antibiotics for diverticulitis. All my other UC symptoms are now gone and a colonoscopy and CT scan have ruled out any further bowel issues but the pain is still
I recently posted here about pain on my left side after an ulcerative colitis flare. I’ve been having this pain since October and was given antibiotics for diverticulitis. All my other UC symptoms are now gone and a colonoscopy and CT scan have ruled out any further bowel issues but the pain is still
Jooniper
in
Endometriosis UK
1 year ago
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