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Proper grown up flare!?
Hello everyone, I've been hijacking Tilda's blog ( thank you ;) so thought I would write my own for some advice? I was diagnosed earlier in the year after two years of constant stiffness and pain, i was diagnosed as Sero-negative and the RA was mainly affecting my hands but also my knees, ankles, shoulder
Hello everyone, I've been hijacking Tilda's blog ( thank you ;) so thought I would write my own for some advice? I was diagnosed earlier in the year after two years of constant stiffness and pain, i was diagnosed as Sero-negative and the RA was mainly affecting my hands but also my knees, ankles, shoulder
Hidden
in
NRAS
11 years ago
Knee pain
Hi all, Pretty much unable to walk without an aid since Saturday, in unbearable pain, been put on co-codamol by GP but they are having no effect, been signed off of work for a week, awaiting blood test results to see if its a lupus flare. Any suggestions on what could help would be very much appreciated
Hi all, Pretty much unable to walk without an aid since Saturday, in unbearable pain, been put on co-codamol by GP but they are having no effect, been signed off of work for a week, awaiting blood test results to see if its a lupus flare. Any suggestions on what could help would be very much appreciated
March2012
in
LUPUS UK
11 years ago
Urgent advise. Can Pregavalin be the cause suddenly with painful, swollen knees Aquiles tendonitis, and other tendons. Also put on weight.
I am really worried about loosing a lot of movement and increased pain. Restless Legs are not too bad. But since I have to hide at work that I have RL, fibromyalgia , pain it has become impossible to pretend that all is well. Having no support makes it more difficult. I had a more understanding boss
I am really worried about loosing a lot of movement and increased pain. Restless Legs are not too bad. But since I have to hide at work that I have RL, fibromyalgia , pain it has become impossible to pretend that all is well. Having no support makes it more difficult. I had a more understanding boss
Mispiernas
in
Restless Legs Syndrome
11 years ago
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Feeling left high and dry to suffer alone...
So sorry, I only seem to post when I am feeling down! Am having the worst flare I have ever experienced, 5 days so far and no sign of a reprieve. My lower back pain is immense, as is my neck pain and tingling hands and feet. Bad arthritis is causing havoc in my hands and elbows, and Raynauds is bad
So sorry, I only seem to post when I am feeling down! Am having the worst flare I have ever experienced, 5 days so far and no sign of a reprieve. My lower back pain is immense, as is my neck pain and tingling hands and feet. Bad arthritis is causing havoc in my hands and elbows, and Raynauds is bad
sparkle247
in
LUPUS UK
11 years ago
anti-inflammatory meds with anti-tnf injections?
Can anyone advise if it is ok to take both medications. I have RA and a disc prolapse which I had a epidural yesterday. The specialist agreed that anti-inflammatory meds would be better than co-codamol. I have been trying to contact my rheumy clinic to ask the question.
Can anyone advise if it is ok to take both medications. I have RA and a disc prolapse which I had a epidural yesterday. The specialist agreed that anti-inflammatory meds would be better than co-codamol. I have been trying to contact my rheumy clinic to ask the question.
angel-delight
in
NRAS
11 years ago
COPD and general anaesthetics
Hi I have osteoarthritis (in addition to moderate copd), the arthritis in my hips is now getting bad enough to interfere with my ability to work, where I should be on my feet on and off for five plus hours.... (I love my job, and don't want to give it up). My GP, who I saw yesterday, has offered to
Hi I have osteoarthritis (in addition to moderate copd), the arthritis in my hips is now getting bad enough to interfere with my ability to work, where I should be on my feet on and off for five plus hours.... (I love my job, and don't want to give it up). My GP, who I saw yesterday, has offered to
postscript
in
Lung Conditions Community Forum
11 years ago
For how long after FCR are you supposed to take Aciclovir and Cotrimoxazole tablets on a daily basis ?
keepfit123
in
CLL Support
11 years ago
My partner suffers from Ovarian Fibroma ( possible cause of her chronic pelvic pain) and hypothyroidism....
...the Gynaecological surgeon we saw won't perform a laparoscopy until my partner (who has unstable Hypothyroidism) gets her levels in check. Meanwhile she can't get her levels in check because we can't find a decent Endocrinologist who could do that. We have seen quite a few endocrinologists already
...the Gynaecological surgeon we saw won't perform a laparoscopy until my partner (who has unstable Hypothyroidism) gets her levels in check. Meanwhile she can't get her levels in check because we can't find a decent Endocrinologist who could do that. We have seen quite a few endocrinologists already
Tony63
in
Pelvic Pain Support Network
11 years ago
Restless Legs And Surgery, I have Experienced something I would like to share with all. I recently had a minor gynaecology op and had a
spinal anaesthetic leaving my legs dead from the waist down. The op went well but in the recovery room I had a severe attack of RLS in both legs !! my legs were dead but felt the need to move them but just couldn't it was awful. How about that? It lasted for about half an hour and when back on the
spinal anaesthetic leaving my legs dead from the waist down. The op went well but in the recovery room I had a severe attack of RLS in both legs !! my legs were dead but felt the need to move them but just couldn't it was awful. How about that? It lasted for about half an hour and when back on the
jubilee
in
Restless Legs Syndrome
11 years ago
Osteo pain
I have osteo arthritis in hands, feet and knees, I am unable to tolerate strong pain killers, even co codamol 15/500 make me ill. I am unable to take anti inflammatories because of acid reflux and asthma and high blood pressure. I have a telephone consultation with my GP today and I am not sure what
I have osteo arthritis in hands, feet and knees, I am unable to tolerate strong pain killers, even co codamol 15/500 make me ill. I am unable to take anti inflammatories because of acid reflux and asthma and high blood pressure. I have a telephone consultation with my GP today and I am not sure what
Titchyj
in
Pain Concern
11 years ago
To lap or not to lap?
Hello, I am new to the forum but old to the world of Endo. (GO TO THE END FOR A MORE CONCISE VERSION) Here's a brief history of my case. I started with 'obvious' signs of Endo 13 years ago. After a battling 5 years I was finally given a laparoscopy and was diagnosed with Endometriosis. By that
Hello, I am new to the forum but old to the world of Endo. (GO TO THE END FOR A MORE CONCISE VERSION) Here's a brief history of my case. I started with 'obvious' signs of Endo 13 years ago. After a battling 5 years I was finally given a laparoscopy and was diagnosed with Endometriosis. By that
moodee
in
Endometriosis UK
11 years ago
Anyone had Amitriptyline and Co-Codamol for neuropathic pain? If so, what is your experience....side-effects, degree of success etc?
I have SLE, Hughes Sydrome and Sjogrens Syndrome and now have nerve damage where my C6 & C7 vertebrae are compressing the nerves, causing severe pain across one shoulder and down the arm into my hand Today, my rheumatologist decided to put me on Amitriptylene with Co-Codamol for this pain and discontinue
I have SLE, Hughes Sydrome and Sjogrens Syndrome and now have nerve damage where my C6 & C7 vertebrae are compressing the nerves, causing severe pain across one shoulder and down the arm into my hand Today, my rheumatologist decided to put me on Amitriptylene with Co-Codamol for this pain and discontinue
Rockhopper
in
LUPUS UK
11 years ago
Hi, I have SLE and Hyghes syndrome and am having difficulty managing pain. Im currently taking tramadol & co-codamol. Any ideas?
I was diagnosed with SLE, Hughes/Anti-Phospholipid Syndrome and Sjogrens Syndrome, 14 years ago. After a shaky start (2 strokes, PEs and a DVT) things seemed to have settled down. However since the menopause my joints snd muscles are extremely painful and sensitive. What do the rest of you take for pain
I was diagnosed with SLE, Hughes/Anti-Phospholipid Syndrome and Sjogrens Syndrome, 14 years ago. After a shaky start (2 strokes, PEs and a DVT) things seemed to have settled down. However since the menopause my joints snd muscles are extremely painful and sensitive. What do the rest of you take for pain
Rockhopper
in
Hughes Syndrome APS Forum
11 years ago
Day 5 after lap, still unable to go to the loo
Hi Sorry if u r eating when reading this. Had a diagnostic lap Monday morning. Have not been able to have a bowel movement since. Have been on co codamol which I know makes you constipated. So taken sodium discosate last night and this morning. Had quite a bit of fruit and veg but still nothing. Feels
Hi Sorry if u r eating when reading this. Had a diagnostic lap Monday morning. Have not been able to have a bowel movement since. Have been on co codamol which I know makes you constipated. So taken sodium discosate last night and this morning. Had quite a bit of fruit and veg but still nothing. Feels
malred8
in
Endometriosis UK
11 years ago
Enbrel
Enbrel and Mtx combo any one else on this ! Not having a good time of it ! Had to stop for the last couple of months because of an acute atipical attack of gout caused by chronic kidney disease and pyrosis ! Is there any one out there with any tips on pain relief, Not aloud anti inflammatory ! Only
Enbrel and Mtx combo any one else on this ! Not having a good time of it ! Had to stop for the last couple of months because of an acute atipical attack of gout caused by chronic kidney disease and pyrosis ! Is there any one out there with any tips on pain relief, Not aloud anti inflammatory ! Only
joanne5
in
NRAS
11 years ago
Pain medication
I know you can take Tramadol & paracetamol does anyone know if you can take Tramadol & co-codamol for breakthrough pain?
I know you can take Tramadol & paracetamol does anyone know if you can take Tramadol & co-codamol for breakthrough pain?
glochessum
in
Fibromyalgia Action UK
11 years ago
RA any connection with liver problems
yesterday I was told I have a problem with my liver. I don't drink, well only at Christmas and New Year. Tomorrow I am having a ultrasound as my blood test result is 203, I was told normal reading is 4-50. I am on anti-tnf injections. Can I ask if anyone has had the same problem. Rhuemy said it is very
yesterday I was told I have a problem with my liver. I don't drink, well only at Christmas and New Year. Tomorrow I am having a ultrasound as my blood test result is 203, I was told normal reading is 4-50. I am on anti-tnf injections. Can I ask if anyone has had the same problem. Rhuemy said it is very
angel-delight
in
NRAS
11 years ago
ibs stress and pain
I have had a pretty good few weeks up until recently occasional nausea and stomach discomfort but have now had stomach pain for about 24 hours. Could it be if not caused by at least exacerbated by the fact that I have a friend staying who I have known for years but find quite difficult to cope with My
I have had a pretty good few weeks up until recently occasional nausea and stomach discomfort but have now had stomach pain for about 24 hours. Could it be if not caused by at least exacerbated by the fact that I have a friend staying who I have known for years but find quite difficult to cope with My
annie-w
in
IBS Network
11 years ago
Does anyone have any experience with Pregabalina (Lyrica)?
I was on Amytriptyline for some time for neuropathetic pain even though I was on 50mgs it wasn't really working. I tried a Bustrans patch to which I reacted so the GP suggested Pregabalina, I've been on it for a month or so however it makes me feel rather whoozy & I'm nor sure it's helping with pain
I was on Amytriptyline for some time for neuropathetic pain even though I was on 50mgs it wasn't really working. I tried a Bustrans patch to which I reacted so the GP suggested Pregabalina, I've been on it for a month or so however it makes me feel rather whoozy & I'm nor sure it's helping with pain
Hidden
in
NRAS
11 years ago
Mini Pill Problems?
I've been on the mini pill (cerazette) for precisely a year now, and it has worked wonders! No periods = no pain (or only rarely at least), basically instead of taking the pill for 21 days and having a 7 day break, you take it every day and have no break, therefore I do not have the pain that comes with
I've been on the mini pill (cerazette) for precisely a year now, and it has worked wonders! No periods = no pain (or only rarely at least), basically instead of taking the pill for 21 days and having a 7 day break, you take it every day and have no break, therefore I do not have the pain that comes with
Hidden
in
Endometriosis UK
11 years ago
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