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Pain everywhere.
Migraines and seizures, vision loss, diplopia, vomiting and peeing blood and
pain
everywhere. Confusion, paranoia and always lost. Nothing. I was worked up numerous times for psychogenic seizures. I was told I was malingering or had a somataform disorder.
Migraines and seizures, vision loss, diplopia, vomiting and peeing blood and
pain
everywhere. Confusion, paranoia and always lost. Nothing. I was worked up numerous times for psychogenic seizures. I was told I was malingering or had a somataform disorder.
CountryGirl9636
in
Partners for Behcet's
10 months ago
Negative SVT Ablation experience
I feel quite let down that I had to suffer, when they should have realised I was in
pain
, discomfort and obviously wide awake! The nurse actually said “Carol you’re hardcore, it’s not having any affect on you” I counted 10 people in there with me.
I feel quite let down that I had to suffer, when they should have realised I was in
pain
, discomfort and obviously wide awake! The nurse actually said “Carol you’re hardcore, it’s not having any affect on you” I counted 10 people in there with me.
Carolx
in
AF Association
11 months ago
Hi I'm Tawnie 🤗
The
pain
of the lesions is getting very bad can't even touch them I was just wondering how are you all handling or do you have
pain
in your lesions 😑 really confused and scared if could please help me 🙏 God bless each and every one of you 💖🙏😇🪄
The
pain
of the lesions is getting very bad can't even touch them I was just wondering how are you all handling or do you have
pain
in your lesions 😑 really confused and scared if could please help me 🙏 God bless each and every one of you 💖🙏😇🪄
Tawnie123
in
MY SKIN
3 months ago
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surgery update: 5am, and after the clouds, the Sun!
Medical staff were also slightly surprised that no
pain
killers were needed…. Oh well. Ive saved the health service 32p in medication and probably cost them £100k in staff and theatre time. The procedure was more serious than expected. 8 theatre staff and 5 hours, but went well.
Medical staff were also slightly surprised that no
pain
killers were needed…. Oh well. Ive saved the health service 32p in medication and probably cost them £100k in staff and theatre time. The procedure was more serious than expected. 8 theatre staff and 5 hours, but went well.
Hidden
Community Ambassador
in
Changing Faces
11 months ago
Urethra pain -Sorry its a long post!
Hi everyone.I am new to this community, I usually post in kidney/dialysis one. Healthunlocked has been a valuable support to me regarding my kidney journey. However I am absolutely demented about my current situation. I am 53 years old. I had my last period about 6 years ago. I have had a relatively
Hi everyone.I am new to this community, I usually post in kidney/dialysis one. Healthunlocked has been a valuable support to me regarding my kidney journey. However I am absolutely demented about my current situation. I am 53 years old. I had my last period about 6 years ago. I have had a relatively
Ziggydoodah
in
Menopause and Perimenopause Support
4 months ago
Dexa Scan and my Pain - Hello :)
I have been in
pain
all over for weeks now and whatever I do it won't go away. I do the Parrotsatethemall and Ibuprofen thing but still in
pain
. I did a 2500 step walk the other day and it was awful with my legs, calves, hands and hips really giving me some grief.
I have been in
pain
all over for weeks now and whatever I do it won't go away. I do the Parrotsatethemall and Ibuprofen thing but still in
pain
. I did a 2500 step walk the other day and it was awful with my legs, calves, hands and hips really giving me some grief.
Hidden
in
PMRGCAuk
5 months ago
Update Myocarditis
Hi everyone, just to update after one month and half diagnosed with Myocarditis, I still feel chest
pain
and sometimes at my neck. However, I can control my anxious but sometimes I will felt anxiety due to my chest
pain
.
Hi everyone, just to update after one month and half diagnosed with Myocarditis, I still feel chest
pain
and sometimes at my neck. However, I can control my anxious but sometimes I will felt anxiety due to my chest
pain
.
Khal1
in
British Heart Foundation
3 months ago
SIGN Chronic Pain guidelines survey
The Scottish Intercollegiate Guidelines Network (SIGN) is looking for your views on how they should present the recommendations in their upcoming Management of Chronic
Pain
guideline to patients and the public.
The Scottish Intercollegiate Guidelines Network (SIGN) is looking for your views on how they should present the recommendations in their upcoming Management of Chronic
Pain
guideline to patients and the public.
Aribah-NRAS
NRAS
in
NRAS
7 months ago
shoulder pain on tapering after GCA flare
Hi everyone, well after flare of GCA and going back up to 40 mgs pred daily I felt really well and no symptoms but now down to 30 mgs I have shoulder and biceps
pain
. My GP thinks that because these have not responded to the pred at such a high dose they are a separate issue.
Hi everyone, well after flare of GCA and going back up to 40 mgs pred daily I felt really well and no symptoms but now down to 30 mgs I have shoulder and biceps
pain
. My GP thinks that because these have not responded to the pred at such a high dose they are a separate issue.
Golfers1
in
PMRGCAuk
4 months ago
Does anyone have s3vere hip and leg pain?
I was diagnosed with PMR in March of this year. The Prednisone is worse than the affliction.
I was diagnosed with PMR in March of this year. The Prednisone is worse than the affliction.
Beetoven
in
PMRGCAuk
1 month ago
Symptoms of a Hashimoto flare
- low grade fever; swollen lymph nodes; extreme fatigue; muscle
pain
(burning
pain
); join
pain
; photosensitivity; muscle weakness; noise intolerance; neuropathic issues; mild rashes. My next appointment with my immunologist is soon, and I would like to be informed before meeting him.
- low grade fever; swollen lymph nodes; extreme fatigue; muscle
pain
(burning
pain
); join
pain
; photosensitivity; muscle weakness; noise intolerance; neuropathic issues; mild rashes. My next appointment with my immunologist is soon, and I would like to be informed before meeting him.
Itsme_thebeaver
in
Thyroid UK
2 months ago
Flare Help
I also don’t think it’s helping as I am coping with joint
pain
too. Thank you for reading and as I said any advice would be appreciated. I actually feel a bit better for writing this down!
I also don’t think it’s helping as I am coping with joint
pain
too. Thank you for reading and as I said any advice would be appreciated. I actually feel a bit better for writing this down!
Primrose2
in
IBS Network
26 days ago
Knee pain
I’m findinding the 6 minute walking test awful because about half way through my knees begin to give me much more
pain
. I know my left is bone on bone but with the waiting just to get advice I’m not quite sure how much
pain
I should endure.
I’m findinding the 6 minute walking test awful because about half way through my knees begin to give me much more
pain
. I know my left is bone on bone but with the waiting just to get advice I’m not quite sure how much
pain
I should endure.
Marmite55
in
My EXI Community
10 months ago
endometrioma pain
Since then I seen to have developed sharp back
pain
. Not sure if its the cysts or the endometriosis. Anyway wondered if anyone also suffered and had any effective
pain
relief tips as I'm struggling to find anything to dull the
pain
.
Since then I seen to have developed sharp back
pain
. Not sure if its the cysts or the endometriosis. Anyway wondered if anyone also suffered and had any effective
pain
relief tips as I'm struggling to find anything to dull the
pain
.
Eeyorecasb
in
Endometriosis UK
10 months ago
GLA:D program, arthritis and PMR
- the arthritic
pain
reduced somewhat again and so did the PMR symptoms.
- the arthritic
pain
reduced somewhat again and so did the PMR symptoms.
redruth123
in
PMRGCAuk
20 days ago
You're NOT alone
That would help ease the
pain
and it's a good way to meet people and just chat. Just remember talking does help. Lots of gentle hugs coming your way.🤗💕
That would help ease the
pain
and it's a good way to meet people and just chat. Just remember talking does help. Lots of gentle hugs coming your way.🤗💕
Shooby
in
Pain Concern
1 month ago
How did you feel after excision?
Before the op I suffered with pretty much daily
pain
(pelvic, lower back and tops of legs mainly). I haven’t really felt much of an improvement to the
pain
so far. I still get
pain
most days, and some days very severe flare ups like I did before the excision.
Before the op I suffered with pretty much daily
pain
(pelvic, lower back and tops of legs mainly). I haven’t really felt much of an improvement to the
pain
so far. I still get
pain
most days, and some days very severe flare ups like I did before the excision.
Banders93
in
Endometriosis UK
6 months ago
stomach acid
happy new year everyone I was diagnosed with PA approx 9yrs ago with some atrophic gastritis and metaplasia (I think) I also have arthritis in my knees/hips I SI every 7 to 10 days Im 56 and I’m fairly fit and active so I know I’m lucky compared to some what I’m confused about is stomach acid.
happy new year everyone I was diagnosed with PA approx 9yrs ago with some atrophic gastritis and metaplasia (I think) I also have arthritis in my knees/hips I SI every 7 to 10 days Im 56 and I’m fairly fit and active so I know I’m lucky compared to some what I’m confused about is stomach acid.
lifegems
in
Pernicious Anaemia Society
9 months ago
Beyond enraged atm.
So I spoke to the pharmacist who had expressed concern about my
pain
management... Amitriptyline + pregabalin are now thefirst line treatments for neuropathic
pain
. Apparently, they both work synergistically and: voila !
PaIn
AlL gOnE !
So I spoke to the pharmacist who had expressed concern about my
pain
management... Amitriptyline + pregabalin are now thefirst line treatments for neuropathic
pain
. Apparently, they both work synergistically and: voila !
PaIn
AlL gOnE !
Oscarcat63
in
Restless Legs Syndrome
4 months ago
Symptoms worse after internal exam
Anyway I have essentially lived with the return of my endometriosis- I have a High
pain
threshold for the most part for 10 years.
Anyway I have essentially lived with the return of my endometriosis- I have a High
pain
threshold for the most part for 10 years.
Bumblebee11
in
Endometriosis UK
2 months ago
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