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Back and hips - is this a Flare??
Hi wonderful people, When I first had PMR and at each previous flare, the pain has been across my shoulders and down the backs of my legs. I am currently feeling it badly in my lower back and pelvic girdle and am not sure if it is a flare or summat else. I am somewhat stressed and know that this
Hi wonderful people, When I first had PMR and at each previous flare, the pain has been across my shoulders and down the backs of my legs. I am currently feeling it badly in my lower back and pelvic girdle and am not sure if it is a flare or summat else. I am somewhat stressed and know that this
MDT1
in
PMRGCAuk
6 months ago
Edinburgh Endo Clinic
Hello! Just wondering if anyone has been on a loooong waiting list to be seen by an Endo specialist for the first time since diagnosis? Currently, it's an 80-week waiting time in Edinburgh. I know there is an option to go privately but I am just totally shocked that someone has to suffer from pain etc
Hello! Just wondering if anyone has been on a loooong waiting list to be seen by an Endo specialist for the first time since diagnosis? Currently, it's an 80-week waiting time in Edinburgh. I know there is an option to go privately but I am just totally shocked that someone has to suffer from pain etc
Axolotl23
in
Endometriosis UK
6 months ago
Anticoagulant users
G'day, Just after some input from NOAC and Warfarin users. I use Warfarin and have done so for nearly 14 years. No sweat ! Never had bleed problems but have had an assortment of bruising problems in that time usually from DIY mishaps. All sorts of pretty colours of blues, greens, yellows and purples
G'day, Just after some input from NOAC and Warfarin users. I use Warfarin and have done so for nearly 14 years. No sweat ! Never had bleed problems but have had an assortment of bruising problems in that time usually from DIY mishaps. All sorts of pretty colours of blues, greens, yellows and purples
BenHall1
in
Atrial Fibrillation Support
6 months ago
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Laparoscopy found nothing - symptoms all point to endometriosis
I don’t suppose anyone has been in the same situation as me and can help? I have suffered from a range of issues from 15 with periods; bleeding and pain with intercourse, severe leg pain, always bleeding/spotting outside of periods, bad period pains, UTI like symptoms and odd bowel movements around
I don’t suppose anyone has been in the same situation as me and can help? I have suffered from a range of issues from 15 with periods; bleeding and pain with intercourse, severe leg pain, always bleeding/spotting outside of periods, bad period pains, UTI like symptoms and odd bowel movements around
puddl0503
in
Endometriosis UK
7 months ago
Endo on the bladder
Anyone else have the bladder and bowel endo? Willing to try anything, for any kind of relief. I have endo on and going into my bladder and now also effecting my bowel. It's triggered normally about day 3 of my period and last for a good 3 weeks. The first few days I just have to be near a toilet, when
Anyone else have the bladder and bowel endo? Willing to try anything, for any kind of relief. I have endo on and going into my bladder and now also effecting my bowel. It's triggered normally about day 3 of my period and last for a good 3 weeks. The first few days I just have to be near a toilet, when
Country-Girl100
in
Endometriosis UK
7 months ago
arthritis
having cervicogenic headaches from arthritis in neck. Any painkillers better than paracetamol that we can safely take? Thanks again.
having cervicogenic headaches from arthritis in neck. Any painkillers better than paracetamol that we can safely take? Thanks again.
Lindaj754
in
AF Association
7 months ago
How to deal with side effect of hot flashes and feeling hot all the time from pain meds?
How do you deal with the side effect of hot flashes and feeling hot all the time that is being caused from your pain medicine or antidepressants used for pain? I take Tramadol at the highest dosage everyday for my severe nerve pain from CRPS because it's the only thing that works for me. However it makes
How do you deal with the side effect of hot flashes and feeling hot all the time that is being caused from your pain medicine or antidepressants used for pain? I take Tramadol at the highest dosage everyday for my severe nerve pain from CRPS because it's the only thing that works for me. However it makes
Hidden
in
Neuro Support
7 months ago
How to deal with side effects of feeling hot from pain meds and antidepressants for pain?
How do you deal with the side effect of feeling hot all the time and having hot flashes that are caused from your pain medicine or your antidepressant used for pain? I take Tramadol at the highest dosage for my severe nerve pain from CRPS because it's the only thing that works for me however I find that
How do you deal with the side effect of feeling hot all the time and having hot flashes that are caused from your pain medicine or your antidepressant used for pain? I take Tramadol at the highest dosage for my severe nerve pain from CRPS because it's the only thing that works for me however I find that
Hidden
in
Neuropathy Support
7 months ago
RSV and Flare
hi everyone, I seem to be in the wars a bit at the moment and need some advice: - diagnosed PMR and RA April 23 - dosage of 30mg pred and 20 mg methotrexate - gradually reduced pred to 10.5 as per Rhumetologist instructions - had a flare in calf muscles, increased pred to 12.5 - travelled to NYC
hi everyone, I seem to be in the wars a bit at the moment and need some advice: - diagnosed PMR and RA April 23 - dosage of 30mg pred and 20 mg methotrexate - gradually reduced pred to 10.5 as per Rhumetologist instructions - had a flare in calf muscles, increased pred to 12.5 - travelled to NYC
MegfromOz
in
PMRGCAuk
7 months ago
Eugenol
I just happened to come across some information relating to cirrhosis. It is called eugenol and it comes from cloves. The NIH as recently as 2021 has done studies and as far as I can tell it is helping the liver to heal. I am not a scientist so the big scientific words are beyond me so I am not sure
I just happened to come across some information relating to cirrhosis. It is called eugenol and it comes from cloves. The NIH as recently as 2021 has done studies and as far as I can tell it is helping the liver to heal. I am not a scientist so the big scientific words are beyond me so I am not sure
leanne5000
in
British Liver Trust
9 months ago
compressed vertebrae, i asked dr about stronger pain medication and they said no -- i wonder why?
Mum's got probably vertebral pain, is on an otc pain tablet, plus a step up from that, the prescription version. a dr friend of mine said she should be on something stronger like oxycodone. i asked specialist if Mum could have a stronger pain medication, and was told no. why's that? maybe cause elderly
Mum's got probably vertebral pain, is on an otc pain tablet, plus a step up from that, the prescription version. a dr friend of mine said she should be on something stronger like oxycodone. i asked specialist if Mum could have a stronger pain medication, and was told no. why's that? maybe cause elderly
MayGodBlessYou
in
Bone Health and Osteoporosis UK
7 months ago
Adenomyosis/Endometriosis Pain Management
Hi All, Just looking for a bit of advice. I was diagnosed with Adenomyosis and Fibroids at 38. Its only been a year and a half but Im struggling hugely. I am very depressed and cant motivate myself day to day. I have constant pain in my lower abdomen, tailbone and Left bum. My pain has progressed
Hi All, Just looking for a bit of advice. I was diagnosed with Adenomyosis and Fibroids at 38. Its only been a year and a half but Im struggling hugely. I am very depressed and cant motivate myself day to day. I have constant pain in my lower abdomen, tailbone and Left bum. My pain has progressed
ABFr23
in
Endometriosis UK
7 months ago
Airing Pain 140: Out now!
[i]
Airing Pain
[/i] edition 140: Childhood Pain - Adverse Experiences and Parental Relationships is now available to listen to here: https://painconcern.org.uk/airing-pain-140-childhood-experiences/ Full transcript is available online and to download, as well as a captioned video on YouTube.
[i]
Airing Pain
[/i] edition 140: Childhood Pain - Adverse Experiences and Parental Relationships is now available to listen to here: https://painconcern.org.uk/airing-pain-140-childhood-experiences/ Full transcript is available online and to download, as well as a captioned video on YouTube.
PainConcernHelpline
Pain Concern
in
Pain Concern
7 months ago
constipation from panadeine, or vertebra nerves, or both?
so docs have said constipation can be caused by pain medication and by the nerves of the vertebra, what's your experience, thanks any pain medication comments welcomed, i think. a dr friend of mine has used patches.
so docs have said constipation can be caused by pain medication and by the nerves of the vertebra, what's your experience, thanks any pain medication comments welcomed, i think. a dr friend of mine has used patches.
MayGodBlessYou
in
Bone Health and Osteoporosis UK
7 months ago
Pelvic Pain Worse at Night
Hi all. Currently undiagnosed/suspected endo. Trying to document when I get flare ups of pelvic pain/cramping and notice any links/triggers. I don’t have periods due to having the coil (used to have incredibly painful periods/heavy periods) but still suffering from pelvic pain. If I get any spotting
Hi all. Currently undiagnosed/suspected endo. Trying to document when I get flare ups of pelvic pain/cramping and notice any links/triggers. I don’t have periods due to having the coil (used to have incredibly painful periods/heavy periods) but still suffering from pelvic pain. If I get any spotting
PBGV24
in
Endometriosis UK
7 months ago
Painkillers
I have been on Gabapentin and Tramadol for 5 years to help with pain. I have now been told GP will no longer prescribe as they are shown to have no effect on chronic pain and are addictive. Anyone else had the same?
I have been on Gabapentin and Tramadol for 5 years to help with pain. I have now been told GP will no longer prescribe as they are shown to have no effect on chronic pain and are addictive. Anyone else had the same?
Chardonnaylady
in
Fibromyalgia Action UK
7 months ago
back spasm, can anything be done?
what do you do to get comfy or relieve pain? e.g take magnesium? something topical? thanks question 2, what pain medication have you used? i guess it'll be up to the prescribing doctor, but people here often have extra knowledge and tips
what do you do to get comfy or relieve pain? e.g take magnesium? something topical? thanks question 2, what pain medication have you used? i guess it'll be up to the prescribing doctor, but people here often have extra knowledge and tips
MayGodBlessYou
in
Bone Health and Osteoporosis UK
7 months ago
Does this sound like endo?
I have had chronic pelvic/ lower back pain for the past 12 years, it flares up to the point where I can't do anything, but lay in bed and then after a few days to weeks it calms down to just the "usual pain/ache" and the cycle continues. I have been to see so many doctors and trips to A&E over the years
I have had chronic pelvic/ lower back pain for the past 12 years, it flares up to the point where I can't do anything, but lay in bed and then after a few days to weeks it calms down to just the "usual pain/ache" and the cycle continues. I have been to see so many doctors and trips to A&E over the years
Shellbell2023
in
Endometriosis UK
7 months ago
Seeking advice on burning feet symptom and an endocronoligist recommendation in London
Hi everyone. Over the last two years I’ve learnt so much from this site and I’m very grateful. I’m looking for some advice relating to my hypothyroid symptoms. I was diagnosed nearly three years ago and am taking 50mg of Teva. My symptoms arrived suddenly, and I still have bouts of anxiety and depression
Hi everyone. Over the last two years I’ve learnt so much from this site and I’m very grateful. I’m looking for some advice relating to my hypothyroid symptoms. I was diagnosed nearly three years ago and am taking 50mg of Teva. My symptoms arrived suddenly, and I still have bouts of anxiety and depression
FW23
in
Thyroid UK
7 months ago
Negative SVT Ablation experience
Good Morning All, So I had my SVT Ablation on Thursday at St Thomas’. Not a great experience. Procedure took 3 and half hours. I was awake the whole time and conscious of everything! Four puncture wounds on groin. Two either side. I could feel the catheters going up into my veins and tweaking around
Good Morning All, So I had my SVT Ablation on Thursday at St Thomas’. Not a great experience. Procedure took 3 and half hours. I was awake the whole time and conscious of everything! Four puncture wounds on groin. Two either side. I could feel the catheters going up into my veins and tweaking around
Carolx
in
AF Association
7 months ago
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