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Medication for what?
After years of complex issues and knowing we can send satellites into space finding millions a miles away pictures are continuing send answers back. Continue multi-millions a year are sent up from more countries than ever before. Yet we live in a world full of undiscovered medications to cure such devastation
After years of complex issues and knowing we can send satellites into space finding millions a miles away pictures are continuing send answers back. Continue multi-millions a year are sent up from more countries than ever before. Yet we live in a world full of undiscovered medications to cure such devastation
123geoff
in
Dystonia Society
4 years ago
Still in pain and waiting for MDT, any advice about pain relief?!?
Hi all, I've been diagnosed with stage 4 endo (bowel, uterus, ovaries ect all stuck together and may have gone into my bowel) and I'm waiting for the endo specialist to have an MDT meeting (happening 2nd march) in the mean time I've been trying different pain relief, so I'm now on the depo injection
Hi all, I've been diagnosed with stage 4 endo (bowel, uterus, ovaries ect all stuck together and may have gone into my bowel) and I'm waiting for the endo specialist to have an MDT meeting (happening 2nd march) in the mean time I've been trying different pain relief, so I'm now on the depo injection
Pureunicorn
in
Endometriosis UK
4 years ago
Has anyone been on Tramadol long term?
Im taking 50mg Tramadol and it is helping not totally but enough that I can get a few hours of sleep. I try to go without it some nights thinking magnesium, potassium and iron will do the trick but inevitably resort back to the tramadol. With it being an opiod, Im worried about the addiction factor.
Im taking 50mg Tramadol and it is helping not totally but enough that I can get a few hours of sleep. I try to go without it some nights thinking magnesium, potassium and iron will do the trick but inevitably resort back to the tramadol. With it being an opiod, Im worried about the addiction factor.
mmb8083
in
Restless Legs Syndrome
4 years ago
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Constipation
I have always suffered with constipation due to having spinal dysraphim (which is a form of spina bifida) , I take tramadol and been on them 10 years now but it the only thing that kills the pain I suffer in my back , I asked to come off them but due to trying different meds sadly they don't work ,over
I have always suffered with constipation due to having spinal dysraphim (which is a form of spina bifida) , I take tramadol and been on them 10 years now but it the only thing that kills the pain I suffer in my back , I asked to come off them but due to trying different meds sadly they don't work ,over
Julz78
in
Healthy Eating
4 years ago
Help and advice
Can docs refer you to pain management if no other meds r touching the pain, am currently on tramadol, naproxen and gabapentin and nothing is touching it, been on diff meds, now there telling me there ain't anything else they can do 4 me apart frm wait to hear frm hydrotherapy ppl???
Can docs refer you to pain management if no other meds r touching the pain, am currently on tramadol, naproxen and gabapentin and nothing is touching it, been on diff meds, now there telling me there ain't anything else they can do 4 me apart frm wait to hear frm hydrotherapy ppl???
Tiny09
in
Andover Fibromyalgia & ME Community Group
4 years ago
Opinions on instant release tramadol compared to slow release tramadol
Hi guys doctor has changed me from instant to slow release tramadol has anyone benefitted from this. I was on 400mg a day instant tramadol along with oramorph plus a range of other meds but the doctor has given me only 200mg of slow release ? Are the slow release actually stronger than the usual ones
Hi guys doctor has changed me from instant to slow release tramadol has anyone benefitted from this. I was on 400mg a day instant tramadol along with oramorph plus a range of other meds but the doctor has given me only 200mg of slow release ? Are the slow release actually stronger than the usual ones
Lanadc88
in
Pain Concern
4 years ago
Levator muscle syndrome; Levator ani syndrome
Twelve years ago I was diagnosed with levator ani syndrome with excruciating pain. After seeing 19 doctors over 2 years, and trying botox injections, caudal epidural, acupuncture treatments, cold laser treatment, electric galvanic stimulation, cortisone shots, many kinds of pain medication and nerve
Twelve years ago I was diagnosed with levator ani syndrome with excruciating pain. After seeing 19 doctors over 2 years, and trying botox injections, caudal epidural, acupuncture treatments, cold laser treatment, electric galvanic stimulation, cortisone shots, many kinds of pain medication and nerve
nosagraft
in
Pelvic Pain Support Network
4 years ago
Post circumcision Story
Hey! No question here, I just wanted to share my story. 24 years old. Phimosis all my life so penis tip never exposed. Got circumcised 6 weeks ago. For the first week it was agony if my penis brushed against anything and occasional bleeding. The sensitivity was insane. Stories about pain lasting for
Hey! No question here, I just wanted to share my story. 24 years old. Phimosis all my life so penis tip never exposed. Got circumcised 6 weeks ago. For the first week it was agony if my penis brushed against anything and occasional bleeding. The sensitivity was insane. Stories about pain lasting for
BrianGlavey
in
Men's Health Forum (Penis Health)
4 years ago
Where do I go from here ?
Hi guys, back here posting after quite some time. So I had been doing reasonably well on the 0.125mg dose of Pramipex until early Nov when I started feeling signs of augmentation as my Rls began earlier in the afternoon at times. Since I already knew what it was, I decided to cut down the dosage and
Hi guys, back here posting after quite some time. So I had been doing reasonably well on the 0.125mg dose of Pramipex until early Nov when I started feeling signs of augmentation as my Rls began earlier in the afternoon at times. Since I already knew what it was, I decided to cut down the dosage and
Heatherlss
in
Restless Legs Syndrome
4 years ago
Catheter pain
Anyone have any catheter experience?? I’ve had an indwelling in since last April, nurse came to change this afternoon as planned four weekly. Took her an hour to get it in as I have bad scar tissue. But now, I’m in real bad pain. I know catheters are uncomfortable but never been this bad before? Any
Anyone have any catheter experience?? I’ve had an indwelling in since last April, nurse came to change this afternoon as planned four weekly. Took her an hour to get it in as I have bad scar tissue. But now, I’m in real bad pain. I know catheters are uncomfortable but never been this bad before? Any
Nikkilouisex
in
Endometriosis UK
4 years ago
Pain management
For my pain control I'm on gabapentin x4 daily and tramadol. I feel I am now addicted to tramadol as I am on the max dose but not feeling the benefits. I'm still in chronic pain and wondered if anyone has advice on pain control?
For my pain control I'm on gabapentin x4 daily and tramadol. I feel I am now addicted to tramadol as I am on the max dose but not feeling the benefits. I'm still in chronic pain and wondered if anyone has advice on pain control?
sssglsjhs
in
Fibromyalgia Action UK
4 years ago
Stage 4 Osteoarthritis in both knees
My double knee replacements have been cancelled for a few months due to having an unexpected Heart Attack which I have recovered well from. I have had two stents fitted. I am in terrible pain with my knees and the effects on my mobility is not good. As a last resort fur pain management my doc is going
My double knee replacements have been cancelled for a few months due to having an unexpected Heart Attack which I have recovered well from. I have had two stents fitted. I am in terrible pain with my knees and the effects on my mobility is not good. As a last resort fur pain management my doc is going
Moags
in
Osteoarthritis Action
4 years ago
Please help! They can’t operate because of high blood pressure
Hi all, I desperately need some wise words. I’m a long term endo sufferer and had 4 ops previously. I’ve been in the chemical menopause for the last 6 months and suffer pretty horrendous side effects. I was hospitalised over the weekend due to a flare up (I’ve got severe stage with bowel endo etc) and
Hi all, I desperately need some wise words. I’m a long term endo sufferer and had 4 ops previously. I’ve been in the chemical menopause for the last 6 months and suffer pretty horrendous side effects. I was hospitalised over the weekend due to a flare up (I’ve got severe stage with bowel endo etc) and
SunflowerGarden
in
Endometriosis UK
4 years ago
PMR Shingles and tapering pred
Hello all. Just emerging from the fog of shingles and wondering when I should start tapering the pred again. I had an aborted attempt, I'm on 10mg. I reduced to 8, too much I know, on 3rd January and by 13th was in awful pain which I assumed was a PMR flare. l put the pred up to 13. But by 20th Jan
Hello all. Just emerging from the fog of shingles and wondering when I should start tapering the pred again. I had an aborted attempt, I'm on 10mg. I reduced to 8, too much I know, on 3rd January and by 13th was in awful pain which I assumed was a PMR flare. l put the pred up to 13. But by 20th Jan
Seraphina56
in
PMRGCAuk
4 years ago
Struggling to cope
I've reached a bit of breaking point today where I burst into tears at work! I've been seeing doctors about heavy, painful periods and pelvic pain for 12 years and finally had a laparoscopy last year which discovered endometriosis and adhesions. Most of it was removed but some was left behind. I was
I've reached a bit of breaking point today where I burst into tears at work! I've been seeing doctors about heavy, painful periods and pelvic pain for 12 years and finally had a laparoscopy last year which discovered endometriosis and adhesions. Most of it was removed but some was left behind. I was
Fliss666
in
Endometriosis UK
4 years ago
Stopping lansoprazole or PPI's
As I have been on it for 18 years or so because of a non steroidal anti inflammatory. But was never taken off it. So I take meds for my heart . Ramipril , ranolazine apixaban diltiazem. Tramadol . As we know PPI's they stop production of stomach acid but also stops up take of vital nutrients mag cal
As I have been on it for 18 years or so because of a non steroidal anti inflammatory. But was never taken off it. So I take meds for my heart . Ramipril , ranolazine apixaban diltiazem. Tramadol . As we know PPI's they stop production of stomach acid but also stops up take of vital nutrients mag cal
Pippy23
in
British Heart Foundation
4 years ago
Pain Relief
Does anyone know of any alternative pain relief options for endometriosis / adenomyosis? I’ve struggled with endometriosis for the last 14 years but I’m currently in the middle of a big flare up and have been off work since October. I had a laparoscopy 2 weeks ago but unfortunately the endometriosis
Does anyone know of any alternative pain relief options for endometriosis / adenomyosis? I’ve struggled with endometriosis for the last 14 years but I’m currently in the middle of a big flare up and have been off work since October. I had a laparoscopy 2 weeks ago but unfortunately the endometriosis
Lauramcg1
in
Adenomyosis Advice Association
4 years ago
Pain Relief
Does anyone know of any alternative pain relief options for endometriosis? I’ve struggled with endometriosis for the last 14 years but I’m currently in the middle of a big flare up and have been off work since October. I had a laparoscopy 2 weeks ago but unfortunately the endometriosis tissue has now
Does anyone know of any alternative pain relief options for endometriosis? I’ve struggled with endometriosis for the last 14 years but I’m currently in the middle of a big flare up and have been off work since October. I had a laparoscopy 2 weeks ago but unfortunately the endometriosis tissue has now
Lauramcg1
in
Endometriosis UK
4 years ago
Returning to work
Just wondering if anyone can offer any advice on returning to work after a RA diagnosis. I’m at the point of making a decision about returning to work and am so conflicted about what is best I was diagnosed with RA in November and prior to this I had a hip replacement in September, so I have been off
Just wondering if anyone can offer any advice on returning to work after a RA diagnosis. I’m at the point of making a decision about returning to work and am so conflicted about what is best I was diagnosed with RA in November and prior to this I had a hip replacement in September, so I have been off
Eden1
in
NRAS
4 years ago
24, London, Living with M.E & Fibromyalgia
I’m prescribed pregabalin for my fibromyalgia and it helps my brain fog so much. My brain fog usually used to happen when my body would shake with my M.E & Fibromyalgia would kick in, then the pain would hit me and my brain would get brain fog due to the confusion in my body/brain. The pregabalin really
I’m prescribed pregabalin for my fibromyalgia and it helps my brain fog so much. My brain fog usually used to happen when my body would shake with my M.E & Fibromyalgia would kick in, then the pain would hit me and my brain would get brain fog due to the confusion in my body/brain. The pregabalin really
Jamesmac100
in
Foggy's "Invisible Illness" Support
4 years ago
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