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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
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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
Me Again!!
Well I haven't been on here for a while and so have a few updates.... Firstly, anniversary holiday to Spain was lovely. The journey there was uncomfortable and my hips were agony when we arrived but then three days in the sun was just bliss, pain free and lovely to just be able to sit and read in
Well I haven't been on here for a while and so have a few updates.... Firstly, anniversary holiday to Spain was lovely. The journey there was uncomfortable and my hips were agony when we arrived but then three days in the sun was just bliss, pain free and lovely to just be able to sit and read in
ellybw
in
NRAS
11 years ago
Has anyone had good results with 15mg/500mg Co-codamol? For leg pains.
Rhapsody
in
Pain Concern
11 years ago
Does Amitriptyline cause bloating, swelling, increase in weight? And is there an alternative for someone who has epilepsy and reflux?
Hi, I recently increased Amitriptyline by 5mg and after 2 weeks found my feet were swelling worse and not going down after a nights rest with them raised. I have not been able to get back to my doctor about this but it has made me wonder whether my extra weight could also be down to this med? I am
Hi, I recently increased Amitriptyline by 5mg and after 2 weeks found my feet were swelling worse and not going down after a nights rest with them raised. I have not been able to get back to my doctor about this but it has made me wonder whether my extra weight could also be down to this med? I am
Sarah-Jane
in
Fibromyalgia Action UK
11 years ago
medications help
Hi i was just wondering what sort of medication people where being given there fibro. I am on alsorts i take pregabalin 300mg twice a day tramadol 50mg twice a day and also have fentanyl transdermal patch 12.5 every 3 days and now pain management are going to give me a tens machine as im still in agony
Hi i was just wondering what sort of medication people where being given there fibro. I am on alsorts i take pregabalin 300mg twice a day tramadol 50mg twice a day and also have fentanyl transdermal patch 12.5 every 3 days and now pain management are going to give me a tens machine as im still in agony
gillyb59
in
Fibromyalgia Action UK
11 years ago
Amitriptyline doesn't seem to be helping my headaches anymore !!! PLEASE HELP !!
I've been taking amitriptyline for about 3/4 months now and the first two months I was on 10mg and it did relieve the headaches, I felt like a new person ! But then they stopped being as effective so they put me up to 25mg and the same is happening again, If anything my headaches are back to how they
I've been taking amitriptyline for about 3/4 months now and the first two months I was on 10mg and it did relieve the headaches, I felt like a new person ! But then they stopped being as effective so they put me up to 25mg and the same is happening again, If anything my headaches are back to how they
NatashaBee
in
National Migraine Centre
11 years ago
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