Search
Search
About
Log in
Join
Experiences with
Co-tenidone
Posts
Communities
1,551 public posts
Filter results
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
Want to take advantage of all our features? Just log in!
Log in
or
Join
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
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
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
Pain after Dental Appointment
Last Thursday, I went to the dentist, originally it was because I was in need of 2 fillings on the bottom teeth (5th one on both sides) and because of pressure building between the teeth (due to overcrowding) it was decided after one of the teeth shattered that it would be better to remove them completely
Last Thursday, I went to the dentist, originally it was because I was in need of 2 fillings on the bottom teeth (5th one on both sides) and because of pressure building between the teeth (due to overcrowding) it was decided after one of the teeth shattered that it would be better to remove them completely
Hidden
in
Asthma Community Forum
11 years ago
My story so far........
In July 2011, I was expeiriencing bad period pains as usual. When I went through to get some painkillers, I suddenly felt hot, dizzy and weak, and got the most excruciating pain throughout my whole abdomen. Thinking I was going to pass out, I lay on the floor and asked my 13yr old (then aged 11yrs) to
In July 2011, I was expeiriencing bad period pains as usual. When I went through to get some painkillers, I suddenly felt hot, dizzy and weak, and got the most excruciating pain throughout my whole abdomen. Thinking I was going to pass out, I lay on the floor and asked my 13yr old (then aged 11yrs) to
Nicci9904
in
Endometriosis UK
11 years ago
Please help me!!
Hi everyone, Firstly I'm new to this website so wanna say how helpful reading things on here has been and also wanna apologise if I'm repeating anything anyone has written previously but I'm struggling at the mo and cud do with some advice/suggestions from anyone who can help. I'm 26 and 16 months ago
Hi everyone, Firstly I'm new to this website so wanna say how helpful reading things on here has been and also wanna apologise if I'm repeating anything anyone has written previously but I'm struggling at the mo and cud do with some advice/suggestions from anyone who can help. I'm 26 and 16 months ago
Danni1608
in
Endometriosis UK
11 years ago
Abatacept = the risks / the rewards
ive got severe rheumatoid arthritis, ive tried numerous drugs over the last 10 years. now im on infusions. I started with Retuximab = no change, then was put on Toxcillimab infusions = no change EXCEPT I put on 3 STONES in weight in 6 months while having them, then went to see my consultant only to be
ive got severe rheumatoid arthritis, ive tried numerous drugs over the last 10 years. now im on infusions. I started with Retuximab = no change, then was put on Toxcillimab infusions = no change EXCEPT I put on 3 STONES in weight in 6 months while having them, then went to see my consultant only to be
mumoftwokids
in
NRAS
11 years ago
Can anybody define a flare up !!
Good morning Luppies. Can anybody define a flare up for me please. Every day i am in constant pain and some days cant even move I feel like every bone is broke. With the help of co codamol this eases it for me. I have shocking memory loss even were i can be doing something and forget what im doing.
Good morning Luppies. Can anybody define a flare up for me please. Every day i am in constant pain and some days cant even move I feel like every bone is broke. With the help of co codamol this eases it for me. I have shocking memory loss even were i can be doing something and forget what im doing.
Donnygirl
in
LUPUS UK
11 years ago
Too much sleep?
My husband has been sleeping a lot in the day lately. Besides COPD and oxygen 24/7 he has been taking co-dydramol for his rheumatism. The doctor has now suggested that he now takes co-codamol which will not make him so sleepy I am waiting to see if it works. As I type this he has been asleep for
My husband has been sleeping a lot in the day lately. Besides COPD and oxygen 24/7 he has been taking co-dydramol for his rheumatism. The doctor has now suggested that he now takes co-codamol which will not make him so sleepy I am waiting to see if it works. As I type this he has been asleep for
jeanghost
in
Lung Conditions Community Forum
11 years ago
iv had migrains since puperty but i had a bad one lasting 5 days and now it has seemed to leave a lingering ache
iv had migrains since puperty but i had a bad one lasting 5 days and now it has seemed to leave a lingering ache and i have a sever migrain at least once a week that is so croppling i feel like banging my head on the wall. the doctor has prescribed triptans and co-dydramol for the pain but its at a point
iv had migrains since puperty but i had a bad one lasting 5 days and now it has seemed to leave a lingering ache and i have a sever migrain at least once a week that is so croppling i feel like banging my head on the wall. the doctor has prescribed triptans and co-dydramol for the pain but its at a point
ladyflower
in
National Migraine Centre
11 years ago
At the end of my tether...
Hi everyone, I've been reading bits on this website since september, when I was diagnosed with endo, and it's been a massive help to me but this week I'm actually about at the end of my tether and decided it might help me to actually get involved rather than just read! So, last year I was in a
Hi everyone, I've been reading bits on this website since september, when I was diagnosed with endo, and it's been a massive help to me but this week I'm actually about at the end of my tether and decided it might help me to actually get involved rather than just read! So, last year I was in a
leanne1982
in
Endometriosis UK
11 years ago
1
...
66
67
68
...
78
Next page
20
30
40
50
60
70
Filter results
Clear filters
Posted in
All communities
Endometriosis UK
261 results
Fibromyalgia Action UK
233 results
NRAS
181 results
View top 10 communities
Sort by
Most Relevant
Newest