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FM or another additional condition?
I am a brand new member and would love to get your thoughts on some of my symptoms. I do suffer from FM diagnosed in Dec 2009 after I started suffering completely numb feet and shin splints during my usual long runs I had long standing problems in my neck/shoulders and right elbow, shoulder blade and
I am a brand new member and would love to get your thoughts on some of my symptoms. I do suffer from FM diagnosed in Dec 2009 after I started suffering completely numb feet and shin splints during my usual long runs I had long standing problems in my neck/shoulders and right elbow, shoulder blade and
suzy1
in
Fibromyalgia Action UK
11 years ago
Help
What can I do to ease my constant back pain? I've tried paracetamol, ibuprofen, co-codamol. I've been prescribed naproxen by the gp but not willing to take that often as it keeps me awake throughout the night which I cannot be doing with as I already have an almost 2yr old who wakes throughout the night
What can I do to ease my constant back pain? I've tried paracetamol, ibuprofen, co-codamol. I've been prescribed naproxen by the gp but not willing to take that often as it keeps me awake throughout the night which I cannot be doing with as I already have an almost 2yr old who wakes throughout the night
sam_naylor
in
Endometriosis UK
11 years ago
Can anyone Help with nerve pain?
Nerve pain in my leg. It only affects my right leg and only at night. After three hours sleep it starts. It is like a shooting intense pain going right down the buttock and into my foot. Only relief is to sit on a chair with my foot raised. Desperate for some quality sleep! I am on co codamol 30/500mg
Nerve pain in my leg. It only affects my right leg and only at night. After three hours sleep it starts. It is like a shooting intense pain going right down the buttock and into my foot. Only relief is to sit on a chair with my foot raised. Desperate for some quality sleep! I am on co codamol 30/500mg
superannie
in
Pain Concern
11 years ago
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Azathioprine
i was just wondering if anyone else was put on azathioprine besides the hydroxi and prednislone. I also have to have steriod injections has a top up and always take co codamol. My rummi says they are struggling to get my lupus under control this i know is true because i am still in constant pain and
i was just wondering if anyone else was put on azathioprine besides the hydroxi and prednislone. I also have to have steriod injections has a top up and always take co codamol. My rummi says they are struggling to get my lupus under control this i know is true because i am still in constant pain and
Donnygirl
in
LUPUS UK
11 years ago
Rheumy nurse
Had a call yesterday from nurse to tell me what the consultant has advised regarding the pain and swelling in hands and feet. He said to try one of these:- 1. Butrans Patch 2. Tramadol 3. Co-codamol I have tried all these over the years for Fibromyalgia and had very bad adverse reactions
Had a call yesterday from nurse to tell me what the consultant has advised regarding the pain and swelling in hands and feet. He said to try one of these:- 1. Butrans Patch 2. Tramadol 3. Co-codamol I have tried all these over the years for Fibromyalgia and had very bad adverse reactions
Titchyj
in
NRAS
11 years ago
Hi, is it safe to take Co-Codamol, Butrans patches and Amitriptyline? I worry doing the pain relief, but I'm always still in pain.
Linda54
in
Fibromyalgia Action UK
11 years ago
Pain killer advice please! - At the moment taking Meveberine, Diclofenac, Co-codamol and still get pain.
My pain goes like this: Period pain (actually not too bad, paracetamol or naproxen will work) Ovulation pain last for a few days to a week. Stabbing pain on left side or right side depending on which month. none on the painkiller works. The pain goes from tummy where ovary is to bottom. Feels
My pain goes like this: Period pain (actually not too bad, paracetamol or naproxen will work) Ovulation pain last for a few days to a week. Stabbing pain on left side or right side depending on which month. none on the painkiller works. The pain goes from tummy where ovary is to bottom. Feels
shukudai
in
Endometriosis UK
11 years ago
Please can you advise me what I should do, or how I should move forward? See below.
I have taken Escitalopram 20mg a day for nearly two years now. Two months ago I tried to get out of moving car (60 mph!) and last month I sat on the loo and calmly swallowed at least 12 co-codamol + as much paracetamol and escitalopram as I could get my hands on! Getting an appointment with my doctor
I have taken Escitalopram 20mg a day for nearly two years now. Two months ago I tried to get out of moving car (60 mph!) and last month I sat on the loo and calmly swallowed at least 12 co-codamol + as much paracetamol and escitalopram as I could get my hands on! Getting an appointment with my doctor
Isabeau
in
Anxiety Support
11 years ago
At a crossroad with treatment
Hi, Like many of the stories I have read on here mine has been an on-going battle with pain, hospital visits, scans and operations. I was diagnosed in 2009 with endometriosis and had my first laparoscopy in 2010. At the time my main concern was having a baby (I already have one child who is now
Hi, Like many of the stories I have read on here mine has been an on-going battle with pain, hospital visits, scans and operations. I was diagnosed in 2009 with endometriosis and had my first laparoscopy in 2010. At the time my main concern was having a baby (I already have one child who is now
cutienosy
in
Endometriosis UK
11 years ago
I have fibromyalgia, chronic pain, RLS and take tramadol, pregavalin, co-codamol. Can HRT, Prozac, cause not sleeping in the night again?
Some days I sleep and I'm fine. I started reducing Prozac
Some days I sleep and I'm fine. I started reducing Prozac
Mispiernas
in
Restless Legs Syndrome
11 years ago
Systemic lupus. HELP
Hey guy's. I got diagnosed with lupus nearly 3 weeks ago now. Took them long enough as I've been in joint pain for 5-6 years. I am still finding out information about it. I am currently taking hydroxychloroquine but ain't seen any side effects as yet. Also are you guys taking any pain relief I am on
Hey guy's. I got diagnosed with lupus nearly 3 weeks ago now. Took them long enough as I've been in joint pain for 5-6 years. I am still finding out information about it. I am currently taking hydroxychloroquine but ain't seen any side effects as yet. Also are you guys taking any pain relief I am on
blondie22
in
LUPUS UK
11 years ago
could i have fibro cant spelll it lol
name is claire im 40 yrs of age and since last october i have been constantly exausthed and in chronic pain in my legs and back mainly.. it has started to get worse just recently. went to see my doc on tuesday who is checking me for arthritis and muscle waste.. i have an eating disorder and dont actually
name is claire im 40 yrs of age and since last october i have been constantly exausthed and in chronic pain in my legs and back mainly.. it has started to get worse just recently. went to see my doc on tuesday who is checking me for arthritis and muscle waste.. i have an eating disorder and dont actually
purpleclaire
in
Fibromyalgia Action UK
11 years ago
Just popped in.
Hi everyone. I thought I'd just pop in and see if there's anyone else out there either walking endlessly or looking for someone to chat to on here. It's 2.50 and there's not a lot on the TV at the moment. Just been for a walk round the garden. Hoping the Co-Codamol are going to cut in soon. They
Hi everyone. I thought I'd just pop in and see if there's anyone else out there either walking endlessly or looking for someone to chat to on here. It's 2.50 and there's not a lot on the TV at the moment. Just been for a walk round the garden. Hoping the Co-Codamol are going to cut in soon. They
arjay
in
Restless Legs Syndrome
11 years ago
Is methotrexate better option in the long term than increasing steroids?
Hi everyone! Just found this site which is so helpful. Finding that lots of my symptoms and feelings are shared by so many others. After diagnosis I got down from 20mg to 3mg prednisolne. Could not reduce any further but then pain etc returned so increased and am now on 5mg and hydroxy. for last
Hi everyone! Just found this site which is so helpful. Finding that lots of my symptoms and feelings are shared by so many others. After diagnosis I got down from 20mg to 3mg prednisolne. Could not reduce any further but then pain etc returned so increased and am now on 5mg and hydroxy. for last
saranne
in
LUPUS UK
11 years ago
Need help please
Hello, I have recently been diagnosed with PBC and Fibromyalgia and suffer with severe joint pain. I don't go to see a Gastro-enterologist until mid June and was wondering if anyone takes cod liver oil to help with joints or any other supplements/vitamins that may help for that matter? I am taking
Hello, I have recently been diagnosed with PBC and Fibromyalgia and suffer with severe joint pain. I don't go to see a Gastro-enterologist until mid June and was wondering if anyone takes cod liver oil to help with joints or any other supplements/vitamins that may help for that matter? I am taking
Lily-May
in
PBC Foundation
11 years ago
My first post ....looking for general advice?
Hi all, First I'd like to say thank you to all those who use this board - I've read countless blogs and the advice you guys give has been of great help to me. So I thought I'd write about my own situation to see if you could reply with advice, your views and if anyone is in a similar boat (I know
Hi all, First I'd like to say thank you to all those who use this board - I've read countless blogs and the advice you guys give has been of great help to me. So I thought I'd write about my own situation to see if you could reply with advice, your views and if anyone is in a similar boat (I know
meandmyfufu
in
Endometriosis UK
11 years ago
Fed up with pain!!!!!!!!!!!!!!!!!!!& desperately need to vent my feelings!!!!!!!!!!!!!!!!!!!!
It's driving me insane, wake up PAIN, sit down PAIN, lay down PAIN!!!!!!!!!!!!! Oh my God when will this stop??? I'm feeling really aggressive and think that i'm going to crack, can't handle another course of steroids they turn me into a looney tune! My feet and ankles hurt constantly. Do you ever get
It's driving me insane, wake up PAIN, sit down PAIN, lay down PAIN!!!!!!!!!!!!! Oh my God when will this stop??? I'm feeling really aggressive and think that i'm going to crack, can't handle another course of steroids they turn me into a looney tune! My feet and ankles hurt constantly. Do you ever get
beckybooboo
in
LUPUS UK
11 years ago
Do you have ET and siginificant bone pain? My lower back, legs & feet seem the worse
Hi All, Hope you are well! I have ET have had for 5 years, I suffer along with the other dibilitating side effects (severe fatigue, itch, headaches, dizziness etc) very significant bone pain, the worse pain seems to be in my lower back and legs but has now travelled to my feet and sometimes my hands
Hi All, Hope you are well! I have ET have had for 5 years, I suffer along with the other dibilitating side effects (severe fatigue, itch, headaches, dizziness etc) very significant bone pain, the worse pain seems to be in my lower back and legs but has now travelled to my feet and sometimes my hands
Rinty
in
MPN Voice
11 years ago
Do you have ET and siginificant bone pain? My lower back and legs & feet seem the worse
Hi All, Hope you are well! I have ET have had for 5 years, I suffer along with the other dibilitating side effects (severe fatigue, itch, headaches, dizziness etc) very significant bone pain, the worse pain seems to be in my lower back and legs but has now travelled to my feet and sometimes my hands
Hi All, Hope you are well! I have ET have had for 5 years, I suffer along with the other dibilitating side effects (severe fatigue, itch, headaches, dizziness etc) very significant bone pain, the worse pain seems to be in my lower back and legs but has now travelled to my feet and sometimes my hands
Rinty
in
MPN Voice
11 years ago
Where I am at the moment
I've been having a really hard time with the rls...my feet,legs,pelvis and lower back. I'm taking co codamol at night to get a little bit of sleep but it wakes me up when the pills wear off. I still won't take the dopamine drugs. I know my ssri has probably made things worse but I've been on them for
I've been having a really hard time with the rls...my feet,legs,pelvis and lower back. I'm taking co codamol at night to get a little bit of sleep but it wakes me up when the pills wear off. I still won't take the dopamine drugs. I know my ssri has probably made things worse but I've been on them for
thedragon
in
Restless Legs Syndrome
11 years ago
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