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Medication interactions
Hi all, I'm getting into a muddle about taking my meds with what I can and can't take at the same time. Could anyone help and assist?? With food/without food / avoid certain foods etc I have also been told to take iron with vitamin c so I have a satsuma but 3 times a day - never have an empty stomach
Hi all, I'm getting into a muddle about taking my meds with what I can and can't take at the same time. Could anyone help and assist?? With food/without food / avoid certain foods etc I have also been told to take iron with vitamin c so I have a satsuma but 3 times a day - never have an empty stomach
lmoran1969
in
Thyroid UK
7 years ago
Hello I am new here.
I have been suffering with Fibromyalgia for three years and only now have been properly diagnosed a few months ago after changing my doctor. I get shooting pains in a lot of areas of my body, numbness in my toes and hands and my joints are painful especially in the morning when I get out of bed. When
I have been suffering with Fibromyalgia for three years and only now have been properly diagnosed a few months ago after changing my doctor. I get shooting pains in a lot of areas of my body, numbness in my toes and hands and my joints are painful especially in the morning when I get out of bed. When
Kacky69
in
Fibromyalgia Action UK
7 years ago
Right leg extreme pain
Hi all hope your all as well as can be ,I was finally diagnosed with Fybromyalgia after 15 of back and forth to the doctors ...firstly oh it's muscular,then it's wear and tear physio will help .It didn't ..kept going back then pain all down my left leg sciatica pain killers given co codamol 30/500 ..
Hi all hope your all as well as can be ,I was finally diagnosed with Fybromyalgia after 15 of back and forth to the doctors ...firstly oh it's muscular,then it's wear and tear physio will help .It didn't ..kept going back then pain all down my left leg sciatica pain killers given co codamol 30/500 ..
Andreab60
in
Fibromyalgia Action UK
7 years ago
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Recently diagnosed with FM & Osteoarthritis.
Hi all, new to the site. I have recently been diagnosed with FM. Taken 18 months to get an answer from Dr's. Also have Osteoarthritis. I am finding it so so difficult to adjust and accept that the things that I used to do, I can no longer do. My mind still wants to but my body can't. Does anyone know
Hi all, new to the site. I have recently been diagnosed with FM. Taken 18 months to get an answer from Dr's. Also have Osteoarthritis. I am finding it so so difficult to adjust and accept that the things that I used to do, I can no longer do. My mind still wants to but my body can't. Does anyone know
Amyhan
in
Fibromyalgia Action UK
7 years ago
CFS Pain
Can I take Co-dydramol with BuTans 5micros
Can I take Co-dydramol with BuTans 5micros
Hidden
in
Pain Concern
7 years ago
Sinus getting me down
Hi All Anyone else having sonus probs? For past six months ive had blocked nose constant blood streaked nasal discharge. And i upped my pred to 25mg from 12.5 for dental work which didnt occur. However the bleeding stopped for a couple of weeks now im down to 17.5mg pred and slight blood again. It
Hi All Anyone else having sonus probs? For past six months ive had blocked nose constant blood streaked nasal discharge. And i upped my pred to 25mg from 12.5 for dental work which didnt occur. However the bleeding stopped for a couple of weeks now im down to 17.5mg pred and slight blood again. It
sorefeetsoldier
in
Vasculitis UK
7 years ago
Letter to GP from Connective Tissue Clinic
I spoke on the phone to my GP about whether he had a report following my 30 March appt. I'll see him to get a copy of the letter but this is what he's told me as "good news". ANA down "a little". Diagnosis is query mild lupus/scleroderma, with definite secondary Raynaud's, plus OA lower spine, hips,
I spoke on the phone to my GP about whether he had a report following my 30 March appt. I'll see him to get a copy of the letter but this is what he's told me as "good news". ANA down "a little". Diagnosis is query mild lupus/scleroderma, with definite secondary Raynaud's, plus OA lower spine, hips,
Lupiknits
in
LUPUS UK
7 years ago
Prednisolone 'come down' vs flare?
Hi everyone, Just before Christmas, I experienced a bad bout of costochondritis, which ended up with me being off sick from work for a few weeks. My regular rheumy refused to give me steroids, saying that because I'd never had them before there was no evidence they would work for me (?!?!?), so I had
Hi everyone, Just before Christmas, I experienced a bad bout of costochondritis, which ended up with me being off sick from work for a few weeks. My regular rheumy refused to give me steroids, saying that because I'd never had them before there was no evidence they would work for me (?!?!?), so I had
Nurseladybird
in
LUPUS UK
7 years ago
Worrying Article
Hi Everyone Was just having a quick look at The Guardian website (like you do) and came across an article: https://www.theguardian.com/science/2017/may/05/unnecessary-opioid-painkiller-prescriptions-thousands-addicted-nhs-doctors-warn?CMP=Share_iOSApp_Other hope the link works never done one before!
Hi Everyone Was just having a quick look at The Guardian website (like you do) and came across an article: https://www.theguardian.com/science/2017/may/05/unnecessary-opioid-painkiller-prescriptions-thousands-addicted-nhs-doctors-warn?CMP=Share_iOSApp_Other hope the link works never done one before!
ginger31
in
Pain Concern
7 years ago
Back pain
Good morning everyone and I wish you all a pain free and peaceful positive day! I haven't posted in a while, I have been busy with family, counselling sessions and a new addition to the family, a Puppy 🐶 I am not so sure it was the wisest decision, she is gorgeous and cute, but, high energy, mischievous
Good morning everyone and I wish you all a pain free and peaceful positive day! I haven't posted in a while, I have been busy with family, counselling sessions and a new addition to the family, a Puppy 🐶 I am not so sure it was the wisest decision, she is gorgeous and cute, but, high energy, mischievous
Wingz26
in
Fibromyalgia Action UK
7 years ago
Pregabalin
Does anybody know if I can take co-codamol with 25mg pregabalin if so how much? I have been advised to reduce the neupro patch. I am now on 1mg from 3mg but suffering badly with rls especially at night. The pregabalin doesnt seem to make any difference. Thank you
Does anybody know if I can take co-codamol with 25mg pregabalin if so how much? I have been advised to reduce the neupro patch. I am now on 1mg from 3mg but suffering badly with rls especially at night. The pregabalin doesnt seem to make any difference. Thank you
antelope99
in
Restless Legs Syndrome
7 years ago
Still in pain
I'm on co codamol and extended release 20mg morphine for my severe pain and I have been in this for a while and I'm still in so much pain it helped at first but it seems to be getting worse or my body has got used to these medications. I feel so bad as I have a little boy who's two and a half and I
I'm on co codamol and extended release 20mg morphine for my severe pain and I have been in this for a while and I'm still in so much pain it helped at first but it seems to be getting worse or my body has got used to these medications. I feel so bad as I have a little boy who's two and a half and I
Yummymummy31
in
Pelvic Pain Support Network
7 years ago
a rant..because i have to..
So a few days ago I was sat on a train,staring blankly out of the window trying to read the graffiti on the walls and bridges anything really to take my mind off the pain and block out the constant chattering of the many on their mobiles. I sank into my seat and attempted to close my eyes,perhaps I thought
So a few days ago I was sat on a train,staring blankly out of the window trying to read the graffiti on the walls and bridges anything really to take my mind off the pain and block out the constant chattering of the many on their mobiles. I sank into my seat and attempted to close my eyes,perhaps I thought
underscorehashtag
in
Fibromyalgia Action UK
7 years ago
Varraces banded
Hi everyone, I am new here, and my question is, should I be in so much pain after having two varraces banded two days ago? It is agony to eat and drink and the pain also comes in spasams at other times. I am real very uncomfortable, but frightened to take much co-codamol. This was my first endoscapy
Hi everyone, I am new here, and my question is, should I be in so much pain after having two varraces banded two days ago? It is agony to eat and drink and the pain also comes in spasams at other times. I am real very uncomfortable, but frightened to take much co-codamol. This was my first endoscapy
donaldsgirl
in
British Liver Trust
7 years ago
I'm new.
I have been on zero prednisolone (to treat PMR) for 5 weeks. Over nearly 4 years this is my fourth attempt on a tapered reducing programme due to 3 flair ups. The rheumatologist specialist thinks the PMR has 'burnt itself out' and suggests I take anti inflammatories whilst my system
I have been on zero prednisolone (to treat PMR) for 5 weeks. Over nearly 4 years this is my fourth attempt on a tapered reducing programme due to 3 flair ups. The rheumatologist specialist thinks the PMR has 'burnt itself out' and suggests I take anti inflammatories whilst my system
ScorpioUK
in
Thyroid UK
7 years ago
VSL#3
Some time ago I bought some VSL#3 probiotics to see if it helped the gastric problems, and said I'd report back. First of all, a period of having difficulty getting anything down meant I didn't take it ( that stuff is too expensive to waste). Now, I've got through the best part of a month's worth. Please
Some time ago I bought some VSL#3 probiotics to see if it helped the gastric problems, and said I'd report back. First of all, a period of having difficulty getting anything down meant I didn't take it ( that stuff is too expensive to waste). Now, I've got through the best part of a month's worth. Please
Lupiknits
in
LUPUS UK
7 years ago
Feels like me life has come to a stop!!
Hi Ladies, I am waiting for the comfromation of diagones but I have suffered from crippling period pain since I was 14. Heavey bleeding and dizziness/ fainting. I have tried many treatments over the years from orale contracetives, hormone injections which seams to help. But due to developing a blood
Hi Ladies, I am waiting for the comfromation of diagones but I have suffered from crippling period pain since I was 14. Heavey bleeding and dizziness/ fainting. I have tried many treatments over the years from orale contracetives, hormone injections which seams to help. But due to developing a blood
Jenaust1985
in
Endometriosis UK
7 years ago
Antihistamines.
Hi all. :) Does anyone have any idea which hay fever remedies are ok to take when you have RLS? I am taking Gabapentin and Co-codamol which work for me quite well now but I am very cautious about buying anything that might tip me back into hellish nights and miserable days again. Any help greatly appreciated
Hi all. :) Does anyone have any idea which hay fever remedies are ok to take when you have RLS? I am taking Gabapentin and Co-codamol which work for me quite well now but I am very cautious about buying anything that might tip me back into hellish nights and miserable days again. Any help greatly appreciated
Twitch_1
in
Restless Legs Syndrome
7 years ago
Dosage far too high!
Hi all. On Thursday just gone, I had a phone consultation with a GP (not my usual GP), explained to him that i have Severe OA, & the prescribed meds (Gabapentin) are not kicking in anymore. Explained how i was feeling, losing my balance, continuous pains etc etc. Told me he could prescribe Co-Codamol
Hi all. On Thursday just gone, I had a phone consultation with a GP (not my usual GP), explained to him that i have Severe OA, & the prescribed meds (Gabapentin) are not kicking in anymore. Explained how i was feeling, losing my balance, continuous pains etc etc. Told me he could prescribe Co-Codamol
Hidden
in
NRAS
7 years ago
Co trimoxazole?
Hi everyone! My nephrologist has put me on co- trimoxazole as i am on Rituximab and will be every 6 months for 3 years. I have to take the tablets every other day to help stop infections. Any one ever had them? Any side effects? Im concerned as the side effects say you can hillucinate!
Hi everyone! My nephrologist has put me on co- trimoxazole as i am on Rituximab and will be every 6 months for 3 years. I have to take the tablets every other day to help stop infections. Any one ever had them? Any side effects? Im concerned as the side effects say you can hillucinate!
Rach459
in
LUPUS UK
7 years ago
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