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Severe headaches
The doctor has put me on
Zapain
they are not helping trying to get back to the doctor can anyone recommend what tablets I can ask for.?
The doctor has put me on
Zapain
they are not helping trying to get back to the doctor can anyone recommend what tablets I can ask for.?
Tula1276
in
Headway
3 years ago
Appointment with Rheumatologist and my falling!
Well, yesterday was my visit to the rheumatologist. But let’s go back to Friday when I rang the GP after seeing the pharmacist on Thursday. My right shin and left ankle, which were both badly bruised after a second fall in three weeks, had become swollen and yellow/white inside with what looked like
Well, yesterday was my visit to the rheumatologist. But let’s go back to Friday when I rang the GP after seeing the pharmacist on Thursday. My right shin and left ankle, which were both badly bruised after a second fall in three weeks, had become swollen and yellow/white inside with what looked like
Bowenlady
in
LUPUS UK
3 years ago
Period pains but no pains at other times
Hi everyone I get agonising period pains and always have done, but they have got worse in recent years. I usually have period pains for the first 3 days and they vary from mild cramps to an excruciating pain that cannot be controlled with painkillers. The excruciating pain feels like a heaviness and
Hi everyone I get agonising period pains and always have done, but they have got worse in recent years. I usually have period pains for the first 3 days and they vary from mild cramps to an excruciating pain that cannot be controlled with painkillers. The excruciating pain feels like a heaviness and
Curlygirl13
in
Endometriosis UK
3 years ago
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Question for all
Have or any of your on pain pills? Do you all feel like it helps or that it makes you worse? My doctor has me on 5 and I don't feel like it's strong enough I want something for a long something for long term pain any suggestions you suggestions I was thinking about about Asking her about methadone
Have or any of your on pain pills? Do you all feel like it helps or that it makes you worse? My doctor has me on 5 and I don't feel like it's strong enough I want something for a long something for long term pain any suggestions you suggestions I was thinking about about Asking her about methadone
Jackjosh
in
My MSAA Community
3 years ago
After hysterectomy and surgical menopause
Having had a full hysterectomy and coming of hrt and having injections every three months postrap I think endo is back nearly 20 years later(has been going on for at least ten years) So after seeing a colorectal surgeon and a cat scan she said she can see some diverticular,I am not medically
Having had a full hysterectomy and coming of hrt and having injections every three months postrap I think endo is back nearly 20 years later(has been going on for at least ten years) So after seeing a colorectal surgeon and a cat scan she said she can see some diverticular,I am not medically
Shazmo
in
Endometriosis UK
3 years ago
Metastatic prostate cancer chronic lower back and pelvic pain which gets much, much worse at night.
Hi everyone! I have metastatic prostate cancer which has got into my bones. I’m currently on Zoladex long term hormone therapy following a 10 month course of chemotherapy which was not that successful so we’re looking at other options. FYI I have noted quite a lot of muscle wastage as a result of long
Hi everyone! I have metastatic prostate cancer which has got into my bones. I’m currently on Zoladex long term hormone therapy following a 10 month course of chemotherapy which was not that successful so we’re looking at other options. FYI I have noted quite a lot of muscle wastage as a result of long
RobbieSELDN
in
Advanced Prostate Cancer
3 years ago
Update
Hello all! I have read everyone’s wonderful messages - it’s been hard to get back. Ryan is okay. He started ipilimumab on November 23rd, 2021. Onco said we will not see fast results like some other drugs like Keytruda and Taf/Mek. A little nerve racking because of course time isn’t on our side. He has
Hello all! I have read everyone’s wonderful messages - it’s been hard to get back. Ryan is okay. He started ipilimumab on November 23rd, 2021. Onco said we will not see fast results like some other drugs like Keytruda and Taf/Mek. A little nerve racking because of course time isn’t on our side. He has
kellyOd
in
Melanoma Caregivers
3 years ago
Any ideas to help with pain ??
Hi I’m 2 weeks into a really nasty painful relapse ! Steroids 30 mg not doing much and painkillers seem to be doing less. Any suggestions gratefully received . Thank you 😊
Hi I’m 2 weeks into a really nasty painful relapse ! Steroids 30 mg not doing much and painkillers seem to be doing less. Any suggestions gratefully received . Thank you 😊
Sidneydog1
in
PMRGCAuk
3 years ago
My partner's story
Hello to everyone, I've been a silent member of this group for a few weeks and I have found your posts really helpful. I have decided that now is the time to share with you the story so far with my partner and his diagnosis of alcohol related liver disease. He's 43 years old and he's been a daily drinker
Hello to everyone, I've been a silent member of this group for a few weeks and I have found your posts really helpful. I have decided that now is the time to share with you the story so far with my partner and his diagnosis of alcohol related liver disease. He's 43 years old and he's been a daily drinker
Bibbs
in
British Liver Trust
3 years ago
Cannot stomach this pain
Hi all, I'm hoping someone will be able to help/explain and any advice will be gratefully received. I have A.I.H. P.B.C and antiphospholipid syndrome and for two years I have been experiencing severe pain either soon after eating or three hours later. My gastro consultant put it down to reflux. I have
Hi all, I'm hoping someone will be able to help/explain and any advice will be gratefully received. I have A.I.H. P.B.C and antiphospholipid syndrome and for two years I have been experiencing severe pain either soon after eating or three hours later. My gastro consultant put it down to reflux. I have
Wonderfullife68
in
British Liver Trust
3 years ago
TMJ and migraine
Does anyone know anything about TMJ/TMD temporo-mandibular disorder and migraine. I have had migraine for many years but after a big filling 4 weeks ago developed an intermittent roving stabbing pain in the upper and lower jaw on the side that had the filling. My dentist has checked the filling and
Does anyone know anything about TMJ/TMD temporo-mandibular disorder and migraine. I have had migraine for many years but after a big filling 4 weeks ago developed an intermittent roving stabbing pain in the upper and lower jaw on the side that had the filling. My dentist has checked the filling and
Katya3
in
National Migraine Centre
3 years ago
Worried
Hi So I found out on Thursday that my retina is detaching and I’ll go blind if they don’t operate as soon as possible. I’ve obviously said no because I was in shock and not able to process it all plus because I’m scared that I will react to painkillers as I usually do I also only have one adrenal gland
Hi So I found out on Thursday that my retina is detaching and I’ll go blind if they don’t operate as soon as possible. I’ve obviously said no because I was in shock and not able to process it all plus because I’m scared that I will react to painkillers as I usually do I also only have one adrenal gland
Natz36
in
Anxiety and Depression Support
3 years ago
How did people get there Endometriosis diagnosis?
I have been struggling with endo like symptoms for years with only a recent gynaecology referral. This pain has resulted in daily pain killers. I don't understand how a doctor can prescribe an opiod pain killer regularly and not refer to gynaecology without a struggle. Im looking for advise on how to
I have been struggling with endo like symptoms for years with only a recent gynaecology referral. This pain has resulted in daily pain killers. I don't understand how a doctor can prescribe an opiod pain killer regularly and not refer to gynaecology without a struggle. Im looking for advise on how to
Nicolepat48
in
Endometriosis UK
3 years ago
Hi guys!
Hi guys, just like clockwork, I’m back again. Apparently my OCD likes to come and go, whenever it pleases. *trigger warning for drug use* This time, it’s on drug use. I was in the hospital last week, and was given quite a few doses of morphine for chest pain I was having (I have extensive health
Hi guys, just like clockwork, I’m back again. Apparently my OCD likes to come and go, whenever it pleases. *trigger warning for drug use* This time, it’s on drug use. I was in the hospital last week, and was given quite a few doses of morphine for chest pain I was having (I have extensive health
AlexisKY
in
My OCD Community
3 years ago
Painkillers and Apixaban
Hi all, Those of you on Apixaban what pain killers do you use. Particulary interested in anyone who also has osteoarthrits as only one offered to me was Naproxen which is listed on Drugs sites as a no no as could increase risk of bleeding. Thanks.
Hi all, Those of you on Apixaban what pain killers do you use. Particulary interested in anyone who also has osteoarthrits as only one offered to me was Naproxen which is listed on Drugs sites as a no no as could increase risk of bleeding. Thanks.
cmjoyce
in
AF Association
3 years ago
Shoulder injury & pain killers with HD
I have what doc and physio think might be a shoulder injury (although I don’t remember injuring it) or possibly rotator cuff problem or impingement.. they can’t decide. I’m know I’m not supposed to take anti inflammatory painkillers, so what can I take? The doc is next to useless and tried to prescribe
I have what doc and physio think might be a shoulder injury (although I don’t remember injuring it) or possibly rotator cuff problem or impingement.. they can’t decide. I’m know I’m not supposed to take anti inflammatory painkillers, so what can I take? The doc is next to useless and tried to prescribe
Forestdweller
in
British Heart Foundation
3 years ago
An Update and Thank You
I had a lot of useful information and advice in my previous two posts which gave me a lot to think about and discuss with my GP, as a consquence of all your advice and suggetions I asked my GP for blood tests and urine test to rule out any secondary causes. I had a barrage of blood tests, one of the
I had a lot of useful information and advice in my previous two posts which gave me a lot to think about and discuss with my GP, as a consquence of all your advice and suggetions I asked my GP for blood tests and urine test to rule out any secondary causes. I had a barrage of blood tests, one of the
Daisi124
in
Osteoporosis Support
3 years ago
Struggling with flare up
I was diagnosed with PMR in May. Started on 15mgs of pred and successfully tapered to 8mgs by Oct. Now experiencing a massive flare and have gone up to 12.5mgs with no relief on the pain and stiffness. Painkillers don’t help. I have a GP review later this week. How long can flares last? I am 69 years
I was diagnosed with PMR in May. Started on 15mgs of pred and successfully tapered to 8mgs by Oct. Now experiencing a massive flare and have gone up to 12.5mgs with no relief on the pain and stiffness. Painkillers don’t help. I have a GP review later this week. How long can flares last? I am 69 years
Paul76
in
PMRGCAuk
3 years ago
Pain in the morning and endo concerns
Hi everyone, I suffer from endometriosis and always find myself with constant pelvic pain which is always worse in the morning and often wakes me from sleep in the middle of the night. Does this happen to anyone else and what do you do to help it? On another note, The pain and fatigue is always so
Hi everyone, I suffer from endometriosis and always find myself with constant pelvic pain which is always worse in the morning and often wakes me from sleep in the middle of the night. Does this happen to anyone else and what do you do to help it? On another note, The pain and fatigue is always so
Pusheen96
in
Endometriosis UK
3 years ago
Golf ball in rib cage left side post covid. Any ideas?
I am recovering from having covid and was quite poorly with it. It has played havoc with my asthma. My self isolating ended on Monday and yesterday I did a flow test which was negative. I still have the occasional cough and my sense of smell is still not back. Last night when I went to bed and lay
I am recovering from having covid and was quite poorly with it. It has played havoc with my asthma. My self isolating ended on Monday and yesterday I did a flow test which was negative. I still have the occasional cough and my sense of smell is still not back. Last night when I went to bed and lay
Pinkcat24
in
Thyroid UK
3 years ago
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