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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
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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
Diabetic 1 can be managed in limit to enjoy yr life with family
I am diabetic since 2004 and today 64 yrs age is running having 6.0 ft + height & 68 kgswt. I am taking Glizid -M after lunch & dinner and fasting is 125. my fooding habits are - 01) Neem flower juice in morning / Methi powder with green tea. 02) sprouted channa & mung with Badam 2 pcs small qty +
I am diabetic since 2004 and today 64 yrs age is running having 6.0 ft + height & 68 kgswt. I am taking Glizid -M after lunch & dinner and fasting is 125. my fooding habits are - 01) Neem flower juice in morning / Methi powder with green tea. 02) sprouted channa & mung with Badam 2 pcs small qty +
vks7749
in
Diabetes India
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
A question about cod liver oil.
I have for many years taken one cod liver oil capsule per day hoping that it may help keep my joints working better. The doctors I have seen are all happy with this, even though some may not be convinced that there is much benefit. As it is a fatty acid I wonder whether it may increase the very long
I have for many years taken one cod liver oil capsule per day hoping that it may help keep my joints working better. The doctors I have seen are all happy with this, even though some may not be convinced that there is much benefit. As it is a fatty acid I wonder whether it may increase the very long
GeoffMahy
Volunteer
in
AMN EASIER
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 anyone under 40 using Nippy night time non invasive ventilation with oxygen and constant oxygen during the day
my daughter is trying to cope with severe lung damage caused by Sarcoidosis and day to day living on oxygen and night time ventilation - I think it would be helpful if she could communicate with someone nearer her age who is experiencing similar health problems.
my daughter is trying to cope with severe lung damage caused by Sarcoidosis and day to day living on oxygen and night time ventilation - I think it would be helpful if she could communicate with someone nearer her age who is experiencing similar health problems.
LynLouisa
in
Lung Conditions Community Forum
11 years ago
Time Off for good behaviour [taking meds and not overdoing things] - I know I am extremely lucky. Not bragging, just saying its possible.
I have had troubles since February 2011 when my hips suddenly felt like bone was rubbing on bone. Took a few months to diagnose and since then I have had good days and bad. Looking back, I think I can see a pattern. When I was good I would start to doubt the diagnosis and push myself, forgetting
I have had troubles since February 2011 when my hips suddenly felt like bone was rubbing on bone. Took a few months to diagnose and since then I have had good days and bad. Looking back, I think I can see a pattern. When I was good I would start to doubt the diagnosis and push myself, forgetting
Sarah-Jane
in
Fibromyalgia Action UK
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
RHEUMATIOD DISEASE......
Hello all, there was a bit of a rant yesterday about a subject that we all know about and have experienced. How many times have you been asked what you have only to be told "I have that too". Or what about "yes my granny has sore knees too". My favourite is "sure we all have a bit of that somewhere
Hello all, there was a bit of a rant yesterday about a subject that we all know about and have experienced. How many times have you been asked what you have only to be told "I have that too". Or what about "yes my granny has sore knees too". My favourite is "sure we all have a bit of that somewhere
jeanabelle
in
NRAS
11 years ago
Still smiling :-)
So I had to change my rheumy appointment as I had to have an operation. It turns out I have breast cancer, and with my huge family history of breast cancer plus the type of cancer they've found in me, the surgeon is recommending a preventative bilateral mastectomy. I hope I look as good as Angelina Jolie
So I had to change my rheumy appointment as I had to have an operation. It turns out I have breast cancer, and with my huge family history of breast cancer plus the type of cancer they've found in me, the surgeon is recommending a preventative bilateral mastectomy. I hope I look as good as Angelina Jolie
Chicklette
in
LUPUS UK
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
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