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Woke up middle of last night in absolute agony
And still have all the pain now, from my neck right down to my feet, and have mild numbness in my right arm/hand. I am still unable to get a docs appointment and no pharmacy will let me buy anything stronger than paracetamol without a prescription =( ( that includes over the counter co-codamol & ibuprofen
And still have all the pain now, from my neck right down to my feet, and have mild numbness in my right arm/hand. I am still unable to get a docs appointment and no pharmacy will let me buy anything stronger than paracetamol without a prescription =( ( that includes over the counter co-codamol & ibuprofen
E-bunny
in
Restless Legs Syndrome
11 years ago
Medication is making me ill
A few weeks ago I was advised to increase my amitryptyline from 10mgs to 50mgs. For the last week my legs have been numb and walking almost impossible. It takes so much effort just to move my legs, it was like they were no longer part of my body. I couldn't even turn over in bed. I forgot to take
A few weeks ago I was advised to increase my amitryptyline from 10mgs to 50mgs. For the last week my legs have been numb and walking almost impossible. It takes so much effort just to move my legs, it was like they were no longer part of my body. I couldn't even turn over in bed. I forgot to take
hollykarma
in
Fibromyalgia Action UK
11 years ago
Hi! I've had a failed hysterectomy. Had chocolate cysts (largest 12cm with which they removed the ovary), fibroid's etc.
Been told I have a frozen pelvis (risk of having a bag for life if they did the job I was told). I was on Prostap 3. I have sought a second opinion but they won't touch me after my op record's. Now on Noresthisterone, for how ever long. I am nearly 40. Swollen joints, especially in the right hand, cold
Been told I have a frozen pelvis (risk of having a bag for life if they did the job I was told). I was on Prostap 3. I have sought a second opinion but they won't touch me after my op record's. Now on Noresthisterone, for how ever long. I am nearly 40. Swollen joints, especially in the right hand, cold
rainey6373
in
Endometriosis UK
11 years ago
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New Year ... New Me?
I've been off air for a while (and all of your eyes were no doubt grateful), due to a very busy time at work, and hectic homelife, but I thought I should pop back and say 'hello' to my fibrofriends! It's been an odd one, really. I sat down with my boss before Christmas, and admitted that I was
I've been off air for a while (and all of your eyes were no doubt grateful), due to a very busy time at work, and hectic homelife, but I thought I should pop back and say 'hello' to my fibrofriends! It's been an odd one, really. I sat down with my boss before Christmas, and admitted that I was
SootyB
in
Fibromyalgia Action UK
11 years ago
Taking Co- codamol with underactive Thyroid
I've been taking Levothyroxine for many years and my Dr. has just given me Co-codamol as I suffer real bad headaches, these are stronger than 'over the counter' ones you can buy. The paperwork that comes with them says not to be taken if you have an underactive thyroid problem. Just wondered what
I've been taking Levothyroxine for many years and my Dr. has just given me Co-codamol as I suffer real bad headaches, these are stronger than 'over the counter' ones you can buy. The paperwork that comes with them says not to be taken if you have an underactive thyroid problem. Just wondered what
maryct
in
Thyroid UK
11 years ago
Advice and ideas needed, please! What should I do about constantt pain, sickness and piles of medication?
I take gabapentin, tramadol and sertraline on a daily basis. With co-codamol 30/500 thrown in occasionally! I am still in pain and have started having problems with keeping food down and headaches (twice weekly). It is suspected I have damaged nerves or adhesions but no one has given me a definate
I take gabapentin, tramadol and sertraline on a daily basis. With co-codamol 30/500 thrown in occasionally! I am still in pain and have started having problems with keeping food down and headaches (twice weekly). It is suspected I have damaged nerves or adhesions but no one has given me a definate
purpledragonfly
in
Pelvic Pain Support Network
11 years ago
Help relieve period pain?
They get worse as I get older, I'm nearly doubled up. Anyone found a pain killer for this? Co codamol is not touching me.
They get worse as I get older, I'm nearly doubled up. Anyone found a pain killer for this? Co codamol is not touching me.
Tray
in
Fibromyalgia Action UK
11 years ago
endo/adhesions in lower back?
Wondering if anyone has ever developed endo or adhesions in the lower back? My back pain started a few months before my first lap but my GP said it was just my joints and to take some cod-liver oil. Ever since my lap the pain in my back can get really bad sometimes. It's my lower back, right in the middle
Wondering if anyone has ever developed endo or adhesions in the lower back? My back pain started a few months before my first lap but my GP said it was just my joints and to take some cod-liver oil. Ever since my lap the pain in my back can get really bad sometimes. It's my lower back, right in the middle
zara19
in
Endometriosis UK
12 years ago
New to Forum...not sure if I have RLS and advice would be great.
I am wondering if anyone on this forum can help as I am not sure whether I have RLS. I initially thought it was something like Benign Fasiculation Syndrome but am not sure. I've had pains in my right leg that have come and gone since I was a child (am now mid-forties) and was told they were growing
I am wondering if anyone on this forum can help as I am not sure whether I have RLS. I initially thought it was something like Benign Fasiculation Syndrome but am not sure. I've had pains in my right leg that have come and gone since I was a child (am now mid-forties) and was told they were growing
pumpkinmum
in
Restless Legs Syndrome
12 years ago
Urgent recommendation needed please for hypo allergenic post surgery pain relief (coeliac with hypochlorydia)
Before you even say it, no the NHS is not on the case. They have only said they will give intraveinous pain relief while i am there, but i will be discharged on the day and dont know what i wall take after? The surgery is known to be painful. I get nausea and diarrhoea from paracetamol, codeine, etc
Before you even say it, no the NHS is not on the case. They have only said they will give intraveinous pain relief while i am there, but i will be discharged on the day and dont know what i wall take after? The surgery is known to be painful. I get nausea and diarrhoea from paracetamol, codeine, etc
Hidden
in
Thyroid UK
12 years ago
Appointment tomorrow
I've got an appointment tomorrow with my Rheumy, it's to get the results of my recent xrays of hand & feet Plus blood results. It's 3 years since I last had xrays & he wants to see if there is any change and if it's inflammotory or wear. I am really hoping that he is going to up my meds as sulpha &
I've got an appointment tomorrow with my Rheumy, it's to get the results of my recent xrays of hand & feet Plus blood results. It's 3 years since I last had xrays & he wants to see if there is any change and if it's inflammotory or wear. I am really hoping that he is going to up my meds as sulpha &
Hidden
in
NRAS
12 years ago
More meds!!!
I am still in pain with no definate reason - lots of "thinking" and "could be". On a positive note have made it to the half way point of my final year of degree course. Today went to see Dr as pain is increasing and abdomen is very tender...he has prescribed Gabapentin - I now take that tramadol,
I am still in pain with no definate reason - lots of "thinking" and "could be". On a positive note have made it to the half way point of my final year of degree course. Today went to see Dr as pain is increasing and abdomen is very tender...he has prescribed Gabapentin - I now take that tramadol,
purpledragonfly
in
Pelvic Pain Support Network
12 years ago
Have had a really bad week
Morning all I have had an extremely hard week with depression severe anxiety & panic attacks. I have'nt been able to leave home since Tuesday. I have thought to myself I can handle the pain Fibro throws at me but cannot handle my Mental Health. Does anyone else feel like this? I had such
Morning all I have had an extremely hard week with depression severe anxiety & panic attacks. I have'nt been able to leave home since Tuesday. I have thought to myself I can handle the pain Fibro throws at me but cannot handle my Mental Health. Does anyone else feel like this? I had such
Hidden
in
Fibromyalgia Action UK
12 years ago
Does anyone else feel like this?
Hi all, this may sound a little strange coming from someone who's been ill for 2 years, but to be honest I was sure back in November 2010 that I'd be better in a few weeks, and as time has gone on it's taken me a while to accept that this is as good as it gets for now at least. I know all the usual
Hi all, this may sound a little strange coming from someone who's been ill for 2 years, but to be honest I was sure back in November 2010 that I'd be better in a few weeks, and as time has gone on it's taken me a while to accept that this is as good as it gets for now at least. I know all the usual
SickAndTired35
in
EDMESH
12 years ago
Apparently runnng out of options for pain relief???
I saw a gp today to say that the co-codamol I was prescribed last week was not touching the pain. My gp said to me 'well theres not a lot left to try now, you are running out of options'. This is the second time a gp has said this to me in the last few weeks! The medication I have tried so far for
I saw a gp today to say that the co-codamol I was prescribed last week was not touching the pain. My gp said to me 'well theres not a lot left to try now, you are running out of options'. This is the second time a gp has said this to me in the last few weeks! The medication I have tried so far for
megs_tom
in
LUPUS UK
12 years ago
wk2 r1
well i did it but it was hard at first. the podcasts dont tell you to warm up and its seems opinion is divided on the benefits of warming up. so im now not sure if the 5min brisk walk is enough to warm my muscles up? the first run was a bit like my knees where locked slightly and i did think i wouldnt
well i did it but it was hard at first. the podcasts dont tell you to warm up and its seems opinion is divided on the benefits of warming up. so im now not sure if the 5min brisk walk is enough to warm my muscles up? the first run was a bit like my knees where locked slightly and i did think i wouldnt
Flart
in
Couch to 5K
12 years ago
Pain management
I am new to this site and have had IBS for nearly 5 years. I suffer from excruciating lower left side pain, dizziness, loss of consciousness, vary constantly between constipation and diarrhoea. I have tried the following medicines (plus CBT) without success: mebeverine, colpernin, buscopan, paracetamol
I am new to this site and have had IBS for nearly 5 years. I suffer from excruciating lower left side pain, dizziness, loss of consciousness, vary constantly between constipation and diarrhoea. I have tried the following medicines (plus CBT) without success: mebeverine, colpernin, buscopan, paracetamol
whiteladder42
in
IBS Network
12 years ago
Really can't cope no more
I have had this blog for some time now but I normally just read everyone's blogs but today I just ha enough , I found out I had endo at 17 am now 34 I have had lots off operations which have helped but not for long , I found out at 19 I couldn't get pregnant which just crumbled my whole world I've been
I have had this blog for some time now but I normally just read everyone's blogs but today I just ha enough , I found out I had endo at 17 am now 34 I have had lots off operations which have helped but not for long , I found out at 19 I couldn't get pregnant which just crumbled my whole world I've been
jusweelou
in
Endometriosis UK
12 years ago
hi im new to this so here gose.dose anyone know if its safe to use the ibuleve gel while taking the painkiller co-codamol .
starr
in
NRAS
12 years ago
DLA unsuccessfull RANT!! :-(
I applied for DLA in March 2011, I had a 'no' reply in June 2011, it finally went to a tribunal hearing at end of October 2012!!! Which has been unsuccesful and have been informed I'm not emtitled on any level for care or mobility. I have arthritis, lupus, raynauds, fibromyalgia etc to name but a few
I applied for DLA in March 2011, I had a 'no' reply in June 2011, it finally went to a tribunal hearing at end of October 2012!!! Which has been unsuccesful and have been informed I'm not emtitled on any level for care or mobility. I have arthritis, lupus, raynauds, fibromyalgia etc to name but a few
heatherx
in
LUPUS UK
12 years ago
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