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CLL and oral cancer
has anyone here experienced oral cancers? I know we are 5 times more likely to get secondary cancers having CLL, I had a speckled Leukoplakia and have just two days ago had two lesions surgically removed both sides of my tongue, one is a very large wound both underneath my tongue, I’m in a lot of pain
has anyone here experienced oral cancers? I know we are 5 times more likely to get secondary cancers having CLL, I had a speckled Leukoplakia and have just two days ago had two lesions surgically removed both sides of my tongue, one is a very large wound both underneath my tongue, I’m in a lot of pain
Heidiypi1
in
CLL Support
2 years ago
Nervous wreck
don't know where to turn ,. I am worrying myself silly can't relax ,and as a result I am getting more migrain aura's. It's a vicious circle. The more migraines I get ,the more I worry. Would it be worth going private to see a nuero? Its going tobe over a year on NHS. The GP seems dismissive now
don't know where to turn ,. I am worrying myself silly can't relax ,and as a result I am getting more migrain aura's. It's a vicious circle. The more migraines I get ,the more I worry. Would it be worth going private to see a nuero? Its going tobe over a year on NHS. The GP seems dismissive now
Lancashirelass07
in
National Migraine Centre
2 years ago
In the words of Columbo - "just one more thing…”
Although battling chronic fatigue, muscle spasms, painful joints, sporadic
pain
from
head
to toe (comes & goes), constant nausea, lack of concentration, brain fog, etc.
Although battling chronic fatigue, muscle spasms, painful joints, sporadic
pain
from
head
to toe (comes & goes), constant nausea, lack of concentration, brain fog, etc.
Gulfstream_Maggie
in
Fibromyalgia Action UK
1 year ago
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swapped
Had a gp phone appointment this morning, and I swapped one of my painkillers for a muscle relaxant. Hopefully that will be more beneficial.
Had a gp phone appointment this morning, and I swapped one of my painkillers for a muscle relaxant. Hopefully that will be more beneficial.
Fibrofog
in
Fibromyalgia Action UK
2 years ago
Chronic Fatigue in Pelvic Pain Disease - Endometriosis/IBD/Bladder Pain
Hi everyone, I am new to this group, and am hoping for some help and support from seasoned pelvic pain sufferers. I will give a bit of background of my medical history, and wonder if there is anyone who can relate with any aspects with confirmed diagnosis of IBD or Endometriosis who could give advice
Hi everyone, I am new to this group, and am hoping for some help and support from seasoned pelvic pain sufferers. I will give a bit of background of my medical history, and wonder if there is anyone who can relate with any aspects with confirmed diagnosis of IBD or Endometriosis who could give advice
Hidden
in
Crohn's and Colitis Support
2 years ago
Chronic Fatigue in Pelvic Pain Disease - Endometriosis/IBD/Bladder Pain
Hi everyone, I am new to this group, and am hoping for some help and support from seasoned pelvic pain sufferers. I will give a bit of background of my medical history, and wonder if there is anyone who can relate with any aspects with confirmed diagnosis of IBD or Endometriosis who could give advice
Hi everyone, I am new to this group, and am hoping for some help and support from seasoned pelvic pain sufferers. I will give a bit of background of my medical history, and wonder if there is anyone who can relate with any aspects with confirmed diagnosis of IBD or Endometriosis who could give advice
Hidden
in
Endometriosis UK
2 years ago
Chronic Fatigue in Pelvic Pain Diseases - Endometriosis/IBD/Bladder Pain
Hi everyone, I am new to this group, and am hoping for some help and support from seasoned pelvic pain sufferers. I will give a bit of background of my medical history, and wonder if there is anyone who can relate with any aspects with confirmed diagnosis of IBD or Endometriosis who could give advice
Hi everyone, I am new to this group, and am hoping for some help and support from seasoned pelvic pain sufferers. I will give a bit of background of my medical history, and wonder if there is anyone who can relate with any aspects with confirmed diagnosis of IBD or Endometriosis who could give advice
Hidden
in
Pelvic Pain Support Network
2 years ago
Mental health issues?
I am also at the moment feeling a little better (it comes and goes) which has left me wondering if its all in my
head
. Can this be possible? The
pain
and nausea feel very real, but if there's no physical cause maybe it is psychological after all?
I am also at the moment feeling a little better (it comes and goes) which has left me wondering if its all in my
head
. Can this be possible? The
pain
and nausea feel very real, but if there's no physical cause maybe it is psychological after all?
Thirstycamel
in
IBS Network
1 year ago
Would like your advice please, ?increase Pred
This morning I woke with a severe headache particularly across the back of my
head
, bilateral temple
pain
and slight visual disturbance just on the edge of my vision on left side. It only lasted for a few minutes and the headache has subsided a bit with paracetamol.
This morning I woke with a severe headache particularly across the back of my
head
, bilateral temple
pain
and slight visual disturbance just on the edge of my vision on left side. It only lasted for a few minutes and the headache has subsided a bit with paracetamol.
Hidden
in
PMRGCAuk
2 years ago
Nitrates and me
After my HA I was put on nitrates the tablets that go straight in your system and my how I suffered My life came to a full stop Couldn’t go to shops or cook spent all day taking
pain
relief a old wet flannel on my
head
Phoned doc he said put up with them it will go away but after 6 months I’d suffered
After my HA I was put on nitrates the tablets that go straight in your system and my how I suffered My life came to a full stop Couldn’t go to shops or cook spent all day taking
pain
relief a old wet flannel on my
head
Phoned doc he said put up with them it will go away but after 6 months I’d suffered
Shoefairy
in
British Heart Foundation
1 year ago
functional abdominal pain
Now I'm thinking maybe i have tried to make my symptoms fit endo and maybe it is in my
head
.
Now I'm thinking maybe i have tried to make my symptoms fit endo and maybe it is in my
head
.
bee109
in
Endometriosis UK
1 year ago
constantly in pain..
I don’t even know where to begin its top to bottom
pain
from my fee to my
head
.. my hips hurt so bad I can barely walk. I have carpal tunnel in both wrists and both are so painful. I have endometriosis pains. I have anxiety depression I have polycystic ovaries I feel sick all the time.
I don’t even know where to begin its top to bottom
pain
from my fee to my
head
.. my hips hurt so bad I can barely walk. I have carpal tunnel in both wrists and both are so painful. I have endometriosis pains. I have anxiety depression I have polycystic ovaries I feel sick all the time.
Littleone88
in
Pain Concern
1 year ago
Looking for People With Palindrome Arthritis
Hi, I'm new here. I have a complex lot of health issues, and unfortunately, a dreadful GP, who referred me finally (I've been suffering "officially" since I was 6 yrs old, and I'm now 47), they sent me to an equally dreadfully Rheumatologist who discharge me in just 6 minutes without further examination
Hi, I'm new here. I have a complex lot of health issues, and unfortunately, a dreadful GP, who referred me finally (I've been suffering "officially" since I was 6 yrs old, and I'm now 47), they sent me to an equally dreadfully Rheumatologist who discharge me in just 6 minutes without further examination
ImSonia
in
NRAS
2 years ago
Active Surveillance Still a Good Option?
Hello, I (70 y/o active white male) was diagnosed with PC last October and I recently had my 3rd prostate MRI within 2 years. The results of the latest one was similar to the other 2: IMPRESSION: Benign prostatic hyperplasia with peripheral zone scarring. PI-RADS2. Elevated PSA density, increased from
Hello, I (70 y/o active white male) was diagnosed with PC last October and I recently had my 3rd prostate MRI within 2 years. The results of the latest one was similar to the other 2: IMPRESSION: Benign prostatic hyperplasia with peripheral zone scarring. PI-RADS2. Elevated PSA density, increased from
ironmanburg
in
Prostate Cancer Network
2 years ago
Views on my test results
Sore dry eyes and
pain
behind eyes, pressure feeling in my
head
. (Checked out, no pressure in eyes or issue with optic nerve). Given eye drops. GP kept saying I am in normal range and the NHS Endo refuses to see me.
Sore dry eyes and
pain
behind eyes, pressure feeling in my
head
. (Checked out, no pressure in eyes or issue with optic nerve). Given eye drops. GP kept saying I am in normal range and the NHS Endo refuses to see me.
Norash
in
Thyroid UK
10 months ago
Passing out from period pain
Hi, I am new to this group! I have always struggled with bad period pains and last year after many years of being told to 'grin and bear it' had keyhole surgery to investigate for endometriosis. I was told there was no evidence of it, although from previous internal camera investigations, I was told
Hi, I am new to this group! I have always struggled with bad period pains and last year after many years of being told to 'grin and bear it' had keyhole surgery to investigate for endometriosis. I was told there was no evidence of it, although from previous internal camera investigations, I was told
Hidden
in
Pelvic Pain Support Network
2 years ago
how long will the pain last
Asher the bone removal yesterday it felt so good. But towards bedtime it started to feel a little different and I tried to ignore it. But once again I had to wake up for painkillers. This must be pain after the removal of the the bone yeh? How long should I expect this for? Anybody any idea
Asher the bone removal yesterday it felt so good. But towards bedtime it started to feel a little different and I tried to ignore it. But once again I had to wake up for painkillers. This must be pain after the removal of the the bone yeh? How long should I expect this for? Anybody any idea
Junny123
in
Pain Concern
2 years ago
Pain after menopause
Hi all, I haven't been around for a few years. A brief back story. I had always suffered from painful heavy periods, since 16 years old. Numerous visits to the doctors over the years, being told it was normal or later on as I got into my 40s being told it was to do with the menopause, I finally got
Hi all, I haven't been around for a few years. A brief back story. I had always suffered from painful heavy periods, since 16 years old. Numerous visits to the doctors over the years, being told it was normal or later on as I got into my 40s being told it was to do with the menopause, I finally got
foosey
in
Endometriosis UK
2 years ago
Hello
I’ve had a really bad flare up the past few days, the worse one I’ve experienced to be honest the
pain
I my left side of my
head
neck and shoulders have brought me to tears a few times, does anyone else suffer like this? Any tips or other pain medications I could try?
I’ve had a really bad flare up the past few days, the worse one I’ve experienced to be honest the
pain
I my left side of my
head
neck and shoulders have brought me to tears a few times, does anyone else suffer like this? Any tips or other pain medications I could try?
Dash01
in
Fibromyalgia Action UK
1 year ago
Thanks gang
Just a big thank you for all the good wishes. I had at least five hours sleep last night and since 8 am have been easing off on the painkillers. Now down to gently niggle with occasional stabs so hoping another good night should see us over the worst. Still no idea what I did but time seems to be
Just a big thank you for all the good wishes. I had at least five hours sleep last night and since 8 am have been easing off on the painkillers. Now down to gently niggle with occasional stabs so hoping another good night should see us over the worst. Still no idea what I did but time seems to be
BobD
Volunteer
in
AF Association
2 years ago
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