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Pain is back
Hi all, So I have always suffered with painful periods, lower back pain and pelvic pain. About 2 years ago doctor said it is most likely Endometriosis and to try the combined pill. This had pretty much kept the pains at bay but recently I’ve got the lower stomach cramps, back pain, pubic pain into
Hi all, So I have always suffered with painful periods, lower back pain and pelvic pain. About 2 years ago doctor said it is most likely Endometriosis and to try the combined pill. This had pretty much kept the pains at bay but recently I’ve got the lower stomach cramps, back pain, pubic pain into
Kimbad1990
in
Endometriosis UK
7 months ago
Control endometriosis with diet?
Hi All, So I've been told I may have a cyst in my right ovary and suspected endometriosis as well as adenomyosis. This was only detected because I was in considerable amounts of pain last year and had to in emergency to the hospital At first I was dismissed and told it is 'only period pain' and I should
Hi All, So I've been told I may have a cyst in my right ovary and suspected endometriosis as well as adenomyosis. This was only detected because I was in considerable amounts of pain last year and had to in emergency to the hospital At first I was dismissed and told it is 'only period pain' and I should
Jenna111
in
Endometriosis UK
7 months ago
Gym 💪🏻
Heart rate stayed good whole time had some
leg
pain
as usual but that's a good thing I've been told by my Consultant 🙈. 35 mins was better then nothing! 💪🏻
Heart rate stayed good whole time had some
leg
pain
as usual but that's a good thing I've been told by my Consultant 🙈. 35 mins was better then nothing! 💪🏻
Yumz199725
in
British Heart Foundation
11 months ago
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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
7 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
7 months ago
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
7 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
7 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
7 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
7 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
7 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
7 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
7 months ago
Adalimubab and leg pains
Rheumatology has suggested a change of meds but I’m reluctant to give up taking something which has done so much good to control my RA if my
leg
pain
is unrelated.
Rheumatology has suggested a change of meds but I’m reluctant to give up taking something which has done so much good to control my RA if my
leg
pain
is unrelated.
Kestrelfriend
in
NRAS
11 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
7 months ago
Any suggestions ?
Hi I've been diagnosed with fnd I have tremmers in my right leg and hand and my speech is affected also, the neurologist has put me for a EEG scan and that's not until April any one have any advice on how to help with my speech stutter slurred and repeating words I just don't know how to make it any
Hi I've been diagnosed with fnd I have tremmers in my right leg and hand and my speech is affected also, the neurologist has put me for a EEG scan and that's not until April any one have any advice on how to help with my speech stutter slurred and repeating words I just don't know how to make it any
Nicnacs1
in
Functional Neurological Disorder - FND Hope
6 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
7 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
7 months ago
Gelastic seizures advice
hi I’m a foster carer to a 2yr old boy who we have had since birth,who has a lot of underlying health issues . He suffers from a lot of issues with his gut which gives him lots of loose stools and vomiting ,he’s also had absence like episodes and a lot of unusual and inappropriate laughing with no apparent
hi I’m a foster carer to a 2yr old boy who we have had since birth,who has a lot of underlying health issues . He suffers from a lot of issues with his gut which gives him lots of loose stools and vomiting ,he’s also had absence like episodes and a lot of unusual and inappropriate laughing with no apparent
Heather2010
in
Epilepsy Action
6 months ago
Collapsed vein -another thing to fret about?
I do have Peripheral Artery Disease in my left
leg
but no
pain
or restrictions in my arms. She did manage to take blood from my left arm. Is this something to worry about? oh, I’m taking Clopidogrel, Atorvastatin and Famotidine.
I do have Peripheral Artery Disease in my left
leg
but no
pain
or restrictions in my arms. She did manage to take blood from my left arm. Is this something to worry about? oh, I’m taking Clopidogrel, Atorvastatin and Famotidine.
Ladylovesmilktray
in
British Heart Foundation
4 months ago
Facet joints
(The disc bulge is still there but much smaller some residual
leg
pain
but joint.is the source). So 4 lots of injections in the facet joints. He also mentioned radio frequency nerve abalation. They won't consider joint fusion has to be as part of a research trial.
(The disc bulge is still there but much smaller some residual
leg
pain
but joint.is the source). So 4 lots of injections in the facet joints. He also mentioned radio frequency nerve abalation. They won't consider joint fusion has to be as part of a research trial.
AMS_1
in
Pain Concern
6 months ago
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