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Really bad pelvic pain a week after manual internal examination
Hi I have a pelvic examination by my GP by hand where they press on ovaries and feel around for lumps nothing found which is great. I had swabs taken to rule anything out this was all precausitonary as I had no symptoms of infection during this time. She said my cervix had a lot of disahcarge which
Hi I have a pelvic examination by my GP by hand where they press on ovaries and feel around for lumps nothing found which is great. I had swabs taken to rule anything out this was all precausitonary as I had no symptoms of infection during this time. She said my cervix had a lot of disahcarge which
Nicjane
in
Endometriosis UK
8 months ago
info on parathyroid please
Hi. This post isn’t about me but looking for info to help my daughter. She has had low kidney function since she had a tummy bug aged 11. She is now mid 40s and at her latest kidney review was told her parathyroid blood level was high. She showed me the numbers but I can’t remember them - they were not
Hi. This post isn’t about me but looking for info to help my daughter. She has had low kidney function since she had a tummy bug aged 11. She is now mid 40s and at her latest kidney review was told her parathyroid blood level was high. She showed me the numbers but I can’t remember them - they were not
HighlandMo
in
Thyroid UK
2 months ago
Day 9 of head injuryness. It started off tediously and got boringer and boringer from there.
At least my grammar hasn't suffered though. Still here. Feet up on the injury couch, a bag of peas parcel-taped to my head, begging sympathy from the world. I know what you’re thinking. Always the good guys, right? This is day 9 and I’m still knocking back paracetamol like they’re smarties. I’ve
At least my grammar hasn't suffered though. Still here. Feet up on the injury couch, a bag of peas parcel-taped to my head, begging sympathy from the world. I know what you’re thinking. Always the good guys, right? This is day 9 and I’m still knocking back paracetamol like they’re smarties. I’ve
PaulS83
Ultramarathon
in
Fun Beyond 10K & Race Support
8 months ago
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endo help, don’t know what to do.
O have suffered with what I was told was ibs since my teens. I was diagnosed with endo a few years ago after they removed a 14cm cyst and found endo on my umbilical (not sure what the scientific term is) once it was removed, the pains were not as bad. They also had to remove one of my ovaries due to
O have suffered with what I was told was ibs since my teens. I was diagnosed with endo a few years ago after they removed a 14cm cyst and found endo on my umbilical (not sure what the scientific term is) once it was removed, the pains were not as bad. They also had to remove one of my ovaries due to
Saharnia
in
The Endometriosis Foundation
8 months ago
Lupus and PMR
Wife has PD and Polymyalgia rheumatica (PMR) seems that it's getting worse and she can't find any pain medication that she can take since she has PD and takes C/LAny suggestions would be greatly appreciated. Thanks
Wife has PD and Polymyalgia rheumatica (PMR) seems that it's getting worse and she can't find any pain medication that she can take since she has PD and takes C/LAny suggestions would be greatly appreciated. Thanks
Furch
in
Cure Parkinson's
8 months ago
Tips for explaining chronic pain to family?
Hello all, I’ve been taking painkillers longterm for my chronic pelvic pain while I’ve waited for and recovered from procedures, and now while I wait for laparoscopy for endometriosis. But completely unexpectedly, I found myself in an intervention with my whole family the other day. 😳 Apparently they
Hello all, I’ve been taking painkillers longterm for my chronic pelvic pain while I’ve waited for and recovered from procedures, and now while I wait for laparoscopy for endometriosis. But completely unexpectedly, I found myself in an intervention with my whole family the other day. 😳 Apparently they
Orange8
in
The Endometriosis Foundation
8 months ago
Tips on explaining chronic pain to family?
Hello all, I’ve been taking painkillers longterm for my chronic pelvic pain while I’ve waited for and recovered from procedures, and now while I wait for laparoscopy for endometriosis. But completely unexpectedly, I found myself in an intervention with my whole family the other day. 😳 Apparently they
Hello all, I’ve been taking painkillers longterm for my chronic pelvic pain while I’ve waited for and recovered from procedures, and now while I wait for laparoscopy for endometriosis. But completely unexpectedly, I found myself in an intervention with my whole family the other day. 😳 Apparently they
Orange8
in
Pelvic Pain Support Network
8 months ago
how long is a long time
hi everyone have been reading posts for a while and it seems to me that everyone's journey with PMR is different. so here is my story. I was diagnosed with PMR in march 2021 by my GP I have not got below 8mg of prednisolone every time I drop to 7.5mg much more discomfort. I have aches and a little
hi everyone have been reading posts for a while and it seems to me that everyone's journey with PMR is different. so here is my story. I was diagnosed with PMR in march 2021 by my GP I have not got below 8mg of prednisolone every time I drop to 7.5mg much more discomfort. I have aches and a little
bluenumbertwo
in
PMRGCAuk
8 months ago
Chronic pain medication review - help!
Hi all. I've been taking opioid medication for over 10 years for endometriosis/adenomyosis. I'm now finally on the waiting list for a total hysterectomy which should get rid of the bulk of my pain - and therefore i will stop the pain medication.However, I've now to have a meeting with a chronic pain
Hi all. I've been taking opioid medication for over 10 years for endometriosis/adenomyosis. I'm now finally on the waiting list for a total hysterectomy which should get rid of the bulk of my pain - and therefore i will stop the pain medication.However, I've now to have a meeting with a chronic pain
KM1986
in
Pain Concern
8 months ago
Bowel Symptoms, Post Surgery 10 weeks, started pre-chemo and continuing/evolving
Hello again lovely ladies. I had my first Carbo/Taxol infusion last Thursday. The day before I had to go to the dentist as I had bad jaw ache and thought it must be a tooth infection. It wasn't luckily. (I think I had had pre-chemo nerves-related nightmares the previous two nights and had been grinding
Hello again lovely ladies. I had my first Carbo/Taxol infusion last Thursday. The day before I had to go to the dentist as I had bad jaw ache and thought it must be a tooth infection. It wasn't luckily. (I think I had had pre-chemo nerves-related nightmares the previous two nights and had been grinding
Emcee71
in
My Ovacome
8 months ago
3 week period
Also have
rectal
bleeding but so much
pain
generally and not sleeping. Have just got transemix acid but can only take four days and so far not totally working. Any advice welcome.
Also have
rectal
bleeding but so much
pain
generally and not sleeping. Have just got transemix acid but can only take four days and so far not totally working. Any advice welcome.
asread
in
Endometriosis UK
7 months ago
lack of mobility
hi I have a number of health problems. I have high blood pressure, liver problems, insomnia and osteoarthritis . I cannot walk more than a few yards (using walking sticks) as both my knees have no cartlidge. I try to keep off painkillers as much as I can, as it affects my liver. My weight is just
hi I have a number of health problems. I have high blood pressure, liver problems, insomnia and osteoarthritis . I cannot walk more than a few yards (using walking sticks) as both my knees have no cartlidge. I try to keep off painkillers as much as I can, as it affects my liver. My weight is just
chirpy1
in
Weight Loss Support
8 months ago
PMR flare and Pred advice please
Hi Everyone thanks again for all the wonderful info out there . It is now just over 2 years since I was diagnosed with PMR . When I initially started on pred the reduction of pain in my shoulders and hips was remarkable . I was on 15mg daily , after a while the symptoms cam back and I went up to 20
Hi Everyone thanks again for all the wonderful info out there . It is now just over 2 years since I was diagnosed with PMR . When I initially started on pred the reduction of pain in my shoulders and hips was remarkable . I was on 15mg daily , after a while the symptoms cam back and I went up to 20
Marek1
in
PMRGCAuk
8 months ago
nausea and vomiting
I get nausea with bloating and pain regularly, but never vomited…. I often wonder if it will happen, occasionally getting that salivating sensation, or if the nausea is just a symptom of the endo or the pain killers (naproxen/amitriptyline). Do any of you ever actually vomit during a flare up?
I get nausea with bloating and pain regularly, but never vomited…. I often wonder if it will happen, occasionally getting that salivating sensation, or if the nausea is just a symptom of the endo or the pain killers (naproxen/amitriptyline). Do any of you ever actually vomit during a flare up?
JEWM
in
Endometriosis UK
8 months ago
marina
hi all I have had fibromyalgia for 2 years I have pain during day and night Don’t find any pain killers help Would be interested in what others find helpful Marina
hi all I have had fibromyalgia for 2 years I have pain during day and night Don’t find any pain killers help Would be interested in what others find helpful Marina
Speedway99
in
Fibromyalgia Action UK
8 months ago
CBD oil?
hi - has anyone taken CBD oil (20% x 2 drops under tongue) whilst on flecainide and bisoprolol ? I haven’t taken it since being on tablets but wanted to as a painkiller . Interested if anyone in community has tried it? thanks Update 25th Jan : just saw cardiologist and he said fine to take CBD
hi - has anyone taken CBD oil (20% x 2 drops under tongue) whilst on flecainide and bisoprolol ? I haven’t taken it since being on tablets but wanted to as a painkiller . Interested if anyone in community has tried it? thanks Update 25th Jan : just saw cardiologist and he said fine to take CBD
patience12
in
AF Association
8 months ago
Lanzaprozole and magnesium deficiency
Hi all, I was diagnosed with GCA in 2018. With the help and support of this group I came through some tough times, and will always be grateful for that. After a very gradual taper, I have now completed 13 months without prednisolone, and, fingers crossed, the GCA is still quiet. I am still having sub-cutaneous
Hi all, I was diagnosed with GCA in 2018. With the help and support of this group I came through some tough times, and will always be grateful for that. After a very gradual taper, I have now completed 13 months without prednisolone, and, fingers crossed, the GCA is still quiet. I am still having sub-cutaneous
Dontwannabesick
in
PMRGCAuk
11 months ago
fibro pain and pregnancy
Hi As I'm new here and new to the pregnancy thing and chronik pain I thouth I'll ask you guys, maybe someone was where I am right now. I live with pain all my life in one form or another. to be honest i don't remember day withiout pain anymore. It's over 30 years now. I'm 19 weeks pregnant at the
Hi As I'm new here and new to the pregnancy thing and chronik pain I thouth I'll ask you guys, maybe someone was where I am right now. I live with pain all my life in one form or another. to be honest i don't remember day withiout pain anymore. It's over 30 years now. I'm 19 weeks pregnant at the
momwithfibro
in
Pain Concern
8 months ago
Two Years On - What Treatment?
Hey all, So, I officially got a diagnosis for PNES - FND back in March 2023, after what we realised is 19 years of misdiagnosed, mistreated, and ignored symptoms. I'm coming up to a year with an official diagnosis, and I'm realising that this is it. This is just my life now. I'm consciously having
Hey all, So, I officially got a diagnosis for PNES - FND back in March 2023, after what we realised is 19 years of misdiagnosed, mistreated, and ignored symptoms. I'm coming up to a year with an official diagnosis, and I'm realising that this is it. This is just my life now. I'm consciously having
LilyMarshell
in
Functional Neurological Disorder - FND Hope
8 months ago
Periodontal Disease and CKD
I am CKD level 3 and now have gingivitis that is becoming chronic even with dental treatment . Please share your story.
I am CKD level 3 and now have gingivitis that is becoming chronic even with dental treatment . Please share your story.
orangecity41
NKF Ambassador
in
Kidney Disease
8 months ago
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