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Labour pain
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Copper IUD Agony
I had the copper coil inserted over a year ago now. The pain has been unbearable. During the first few days of my period, I’m bed-bound with the severity of the cramps which I never got before. Painkillers don’t touch it. I feel mislead and lied to because when I got it fitted, I was reassured this would
I had the copper coil inserted over a year ago now. The pain has been unbearable. During the first few days of my period, I’m bed-bound with the severity of the cramps which I never got before. Painkillers don’t touch it. I feel mislead and lied to because when I got it fitted, I was reassured this would
millymoo1234
in
BASHH
3 years ago
Problems with a sore and poisonous tasting mouth.
Any advise for my mother who is U.K. based would be much appreciated. For more than 15 years she has complained about a sore tongue and mouth and in her words that most food tasted like poison. I took her to see an oral Consultant who was a locum, he diagnosed sore mouth syndrome very quickly claiming
Any advise for my mother who is U.K. based would be much appreciated. For more than 15 years she has complained about a sore tongue and mouth and in her words that most food tasted like poison. I took her to see an oral Consultant who was a locum, he diagnosed sore mouth syndrome very quickly claiming
Hidden
in
Pernicious Anaemia Society
3 years ago
Just a 3K Run, 40:30 Jeffing ☀️🥵
After an enforced break from running due to a painful tooth abscess I decided to make my comeback run this morning. Root canal treatment starting in 6 weeks, something to look forward to! 😬 The gremlins were out in full force this morning 😈. I had put everything on charge last night. Got up at 6 am
After an enforced break from running due to a painful tooth abscess I decided to make my comeback run this morning. Root canal treatment starting in 6 weeks, something to look forward to! 😬 The gremlins were out in full force this morning 😈. I had put everything on charge last night. Got up at 6 am
Jools2020
Graduate10
in
Bridge to 10K
3 years ago
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Hashimoto's Thyroiditis
Morning lovely people Saw my doctor yesterday and was told I have Hashimoto'sThyroiditis . I believe its linked with Fibro? I feel so drained and still in a lot of pain from my neck to below my shoulder blades and down to my wrists. I try and stretch but if I stretch just a bit over I cramp all over
Morning lovely people Saw my doctor yesterday and was told I have Hashimoto'sThyroiditis . I believe its linked with Fibro? I feel so drained and still in a lot of pain from my neck to below my shoulder blades and down to my wrists. I try and stretch but if I stretch just a bit over I cramp all over
Suffering21
in
Fibromyalgia Action UK
3 years ago
Continuous Headache
Has anyone had, what seems like, a never-ending headache/migraine with their tinnitus? I am new to this condition, both started within a couple of days, 3 months ago. No painkillers seem to work on the headache. Has anyone any tips for me, please. Thank you.
Has anyone had, what seems like, a never-ending headache/migraine with their tinnitus? I am new to this condition, both started within a couple of days, 3 months ago. No painkillers seem to work on the headache. Has anyone any tips for me, please. Thank you.
genorm
in
Tinnitus UK
3 years ago
A journey to come home
Around 3 weeks ago I put a post up asking for prayers. I want to thank you all for your thoughtful comments and keeping us in mind. I pray for you all daily. As an update, my dad is currently in palliative care at home. I wanted to provide a bit of back story on the situation - both the bad and good
Around 3 weeks ago I put a post up asking for prayers. I want to thank you all for your thoughtful comments and keeping us in mind. I pray for you all daily. As an update, my dad is currently in palliative care at home. I wanted to provide a bit of back story on the situation - both the bad and good
ArabianNights
in
Advanced Prostate Cancer
3 years ago
Waiting times
Hi this is my first post so please bare with me if I start rambling 😆. I have always suffered with bad periods but last year everything started getting worse. I was getting period type pain everyday, was badly constipated and had bad back pain. I rang the doctor in September last year and spoke to a
Hi this is my first post so please bare with me if I start rambling 😆. I have always suffered with bad periods but last year everything started getting worse. I was getting period type pain everyday, was badly constipated and had bad back pain. I rang the doctor in September last year and spoke to a
Funkonerd
in
Endometriosis UK
3 years ago
Period cramps at night from 3dpt. Did anyone else get these with a positive outcome?
I’m now 6dpt 5dt and still having period cramps at night and briefly on and off in the day. Not bad enough I need pain killers but bad enough I could imagine period starting? I know I won’t know till test day which is not till the 25th but just interested to see what other people experienced. Thanks
I’m now 6dpt 5dt and still having period cramps at night and briefly on and off in the day. Not bad enough I need pain killers but bad enough I could imagine period starting? I know I won’t know till test day which is not till the 25th but just interested to see what other people experienced. Thanks
Ey2020
in
Fertility Network UK
3 years ago
Should I accept it’s a failed cycle?
Hi all, I had an FET on the 5th. (6dt). OTD was on Wednesday for a home test. 3 negative urine home tests since - 3 different types. No period as yet. Clinic said it’s unlikely that it’s been a successful cycle due to the negative tests and it’s up to me if I want to stop meds or continue until period
Hi all, I had an FET on the 5th. (6dt). OTD was on Wednesday for a home test. 3 negative urine home tests since - 3 different types. No period as yet. Clinic said it’s unlikely that it’s been a successful cycle due to the negative tests and it’s up to me if I want to stop meds or continue until period
Wizzadora01
in
Fertility Network UK
3 years ago
What helps with the your pain
I've got a few illnesses on some medication and painkillers but try cut down on painkillers so was wondering what helps other people with pain x ? Hope you don't mind me asking this question x
I've got a few illnesses on some medication and painkillers but try cut down on painkillers so was wondering what helps other people with pain x ? Hope you don't mind me asking this question x
Zarabee
in
Pain Concern
3 years ago
help
I am not sleeping from so many days just of this pain had an appointment with gp for depression and anxiety and he had given me more strong painkiller i was on naproxen but it was not helpful so gp has prescribed me tramadol hydrochloride for pain and Sertraline for anxiety and low mood. does anyone
I am not sleeping from so many days just of this pain had an appointment with gp for depression and anxiety and he had given me more strong painkiller i was on naproxen but it was not helpful so gp has prescribed me tramadol hydrochloride for pain and Sertraline for anxiety and low mood. does anyone
Mylovepari1
in
Endometriosis UK
3 years ago
Arthritis
Does anyone know of a safe pain killer or herbal medicine that can be taken for osteoarthritis
Does anyone know of a safe pain killer or herbal medicine that can be taken for osteoarthritis
trixie100
in
AF Association
3 years ago
On going Pain after knee op
I had an op for total knee replacement last year, but still get a strange pain in the leg it feels like a bone moving under the knee , cracks and sends a pain through the leg. A bit like when you hit the funny bone in your arm but slightly more severe. Any ideas on what to do ?, other than persist
I had an op for total knee replacement last year, but still get a strange pain in the leg it feels like a bone moving under the knee , cracks and sends a pain through the leg. A bit like when you hit the funny bone in your arm but slightly more severe. Any ideas on what to do ?, other than persist
katieoxo60
in
Pain Concern
3 years ago
Doctors prescribe pain killer for RLS
I have been trying to take low dose ropinole with hydro ozone This worked for me several years Switched insurance took my pain killer away Now my RLS show up in vengeance
I have been trying to take low dose ropinole with hydro ozone This worked for me several years Switched insurance took my pain killer away Now my RLS show up in vengeance
help3
in
Restless Legs Syndrome
3 years ago
Thought it was under control after years of multiple serious surgeries and diet changes but now facing new battles - any advice welcome
Hello all, I was diagnosed with endometriosis aged 21 after 8 years of awful problems and symptoms. After my first laparoscopy I was initially told it was “just a few spots of endometriosis” and my options were chemically induced menopause (gnrh and add back HRT) or to get pregnant and they fitted
Hello all, I was diagnosed with endometriosis aged 21 after 8 years of awful problems and symptoms. After my first laparoscopy I was initially told it was “just a few spots of endometriosis” and my options were chemically induced menopause (gnrh and add back HRT) or to get pregnant and they fitted
Greys90
in
Endometriosis UK
3 years ago
New member and started on gabapentin .
Hi im new here, I've been prescribed gabapentin 100mgs x3 daily after refusing the 'only drug' the doctor said was available ..namely ropinorole. I refused that as first line, as I'm aware of augmentation , and other side effects like impulsive behaviours. I am aware of NICE guidelines. I pointed
Hi im new here, I've been prescribed gabapentin 100mgs x3 daily after refusing the 'only drug' the doctor said was available ..namely ropinorole. I refused that as first line, as I'm aware of augmentation , and other side effects like impulsive behaviours. I am aware of NICE guidelines. I pointed
Lizzybuz27
in
Restless Legs Syndrome
3 years ago
The END
The end:dne ehT That's the inevitable, when the meds no longer work no matter the dose.. when the body no longer moves no matter the therapy. when the brain barely functions no matter the supplements... when the pain never stops no matter the pain killers... When the comforting words of loved ones
The end:dne ehT That's the inevitable, when the meds no longer work no matter the dose.. when the body no longer moves no matter the therapy. when the brain barely functions no matter the supplements... when the pain never stops no matter the pain killers... When the comforting words of loved ones
Grumpy77
in
Cure Parkinson's
3 years ago
Who else has had Covid?
My family and I all got Covid, quarantine ends tomorrow. It felt very much like a hypo episode with some extras thrown in. Day 1, I felt lethargic, normal tasks felt like an effort. Day 2, my torso felt sweaty and sensitive, prickly. Day 3, dry cough and more lethargy. Day 4, my head feels stuffy,
My family and I all got Covid, quarantine ends tomorrow. It felt very much like a hypo episode with some extras thrown in. Day 1, I felt lethargic, normal tasks felt like an effort. Day 2, my torso felt sweaty and sensitive, prickly. Day 3, dry cough and more lethargy. Day 4, my head feels stuffy,
NWA6
in
Thyroid UK
3 years ago
Labour pain Vs period pain endometriosis: similarities?😱
I have read that very painful periods are a strong indicator of how bad your
labour
pain
will be. If that's the case I'm very worried !! Would you be so kind and let me know how bad your
labour
pains were compared to your period
pain
, and if you had a peridural ? First birth? Any complications?
I have read that very painful periods are a strong indicator of how bad your
labour
pain
will be. If that's the case I'm very worried !! Would you be so kind and let me know how bad your
labour
pains were compared to your period
pain
, and if you had a peridural ? First birth? Any complications?
Lapinblanc88
in
Endometriosis UK
3 years ago
concerned
know no one can really give medical advice here but hoping for a bit of perspective and hope..... I've been diagnosed since 2019 and experienced the following regular flare ups and multiple steroid injections sickness and dizziness due to medication not being able to due basic things around the
know no one can really give medical advice here but hoping for a bit of perspective and hope..... I've been diagnosed since 2019 and experienced the following regular flare ups and multiple steroid injections sickness and dizziness due to medication not being able to due basic things around the
cpr02
in
NRAS
3 years ago
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