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headache, throbbing, eye pain & rolling
For the last 2 weeks of Jan I suddenly got really bad headaches (forehead, temple, back),
pain
above and around the eyes. I was nauseous, my eyes felt like they wouldn't focus, kept rolling. My head throbbed and felt incredibly 'full', heavy and hot.
For the last 2 weeks of Jan I suddenly got really bad headaches (forehead, temple, back),
pain
above and around the eyes. I was nauseous, my eyes felt like they wouldn't focus, kept rolling. My head throbbed and felt incredibly 'full', heavy and hot.
softekcom
in
Glaucoma UK
6 months ago
Recovering from debulking
I’m also wondering how long the intestinal
pain
tends to last? Everything is moving along, it’s just wind causing the
pain
I think.
I’m also wondering how long the intestinal
pain
tends to last? Everything is moving along, it’s just wind causing the
pain
I think.
DMP-H
in
My Ovacome
4 months ago
Problems with my GP
* Physiotherapy and GYM. * 1 year in the
pain
clinic. GP says that there is no test or examination that can determine that I have the disease and sends me home. I am physically and mentally exhausted with the issue of my
pain
.
* Physiotherapy and GYM. * 1 year in the
pain
clinic. GP says that there is no test or examination that can determine that I have the disease and sends me home. I am physically and mentally exhausted with the issue of my
pain
.
ftorres18
in
Fibromyalgia Action UK
22 days ago
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Glandular Thyroid Supplements
Have been on levothyroxine 150 mcg for 17 years and have been experiencing a bucket load of side effects(joint
pain
, back
pain
, eyebrows growing bushy, lack of labido, depression, weight gain around the waist, sharp pains in my toes, muscle weakness, dizzy spells when standing up, etc.
Have been on levothyroxine 150 mcg for 17 years and have been experiencing a bucket load of side effects(joint
pain
, back
pain
, eyebrows growing bushy, lack of labido, depression, weight gain around the waist, sharp pains in my toes, muscle weakness, dizzy spells when standing up, etc.
GROUNDHO
in
Thyroid UK
5 days ago
CRP elevated too high - why?
I had
pain
and increased my prednisone to 3mg. My
pain
stopped snd Ive been feeling great. Now my Labs todsu in August show a further increase in CRP to 19. My ESR is normal at 12. I dont understand why as Im feeling good and tnought my CRP should be down.
I had
pain
and increased my prednisone to 3mg. My
pain
stopped snd Ive been feeling great. Now my Labs todsu in August show a further increase in CRP to 19. My ESR is normal at 12. I dont understand why as Im feeling good and tnought my CRP should be down.
Dragonflys
in
PMRGCAuk
8 days ago
When do you use GTN spray
I'm confused as when I had chest
pain
and was admitted to hospital I thought it was indigestion ( only went in because of breathlessness).
I'm confused as when I had chest
pain
and was admitted to hospital I thought it was indigestion ( only went in because of breathlessness).
Alfiesmum6
in
British Heart Foundation
11 days ago
HELP Please
I explained that they will make my RLS worse and that if I could just get rid of the constant
pain
than my mood would lift. So she said she would give me something to help with
pain
and help sleep, and when I got them they are amitriptyline.
I explained that they will make my RLS worse and that if I could just get rid of the constant
pain
than my mood would lift. So she said she would give me something to help with
pain
and help sleep, and when I got them they are amitriptyline.
Marymill
in
Restless Legs Syndrome
2 months ago
Methotrexate and adalimumab
I have been using adalimumab for 3 years for my Ankylosing spondylitis and it has been great for my neck and lower back
pain
. I have now developed some finger
pain
, wear and tear in my knees and painful toes, as well as plantur fasciitis.
I have been using adalimumab for 3 years for my Ankylosing spondylitis and it has been great for my neck and lower back
pain
. I have now developed some finger
pain
, wear and tear in my knees and painful toes, as well as plantur fasciitis.
TraceyDevon
in
NRAS
15 days ago
Nortriptyline advice
I just wanted to ask if anyone has experience of it and has it helped with nerve
pain
. I’m worried about not having the amitriptyline as it really helps me sleep. Any comment welcome, thanks for reading 💛 xx
I just wanted to ask if anyone has experience of it and has it helped with nerve
pain
. I’m worried about not having the amitriptyline as it really helps me sleep. Any comment welcome, thanks for reading 💛 xx
endowarrior12
in
Endometriosis UK
1 month ago
advice?
Result non stop
pain
, lack of trust in my medical supposed support , living alone my AF has gone wild , I am used to dealing with it( long term mediication) now I have chest
pain
. Never had chest
pain
before . Probably stress , I know but , who to turn to.
Result non stop
pain
, lack of trust in my medical supposed support , living alone my AF has gone wild , I am used to dealing with it( long term mediication) now I have chest
pain
. Never had chest
pain
before . Probably stress , I know but , who to turn to.
Luludean
in
NRAS
3 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
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
29 days ago
What Now?
Pain
returned after a few months. In November I was put on Zoladex injections with Tibilone HRT tablets, this helped the
pain
a lot and reduced it to a few times within the 3 month period of being on it. Now the last 2 weeks the
pain
has returned with a vengeance.
Pain
returned after a few months. In November I was put on Zoladex injections with Tibilone HRT tablets, this helped the
pain
a lot and reduced it to a few times within the 3 month period of being on it. Now the last 2 weeks the
pain
has returned with a vengeance.
Mummaamber
in
Endometriosis UK
5 months ago
This is a long one
I’ve been in so much
pain
lately with my arthritis in desperation I booked an appointment at my GPs for a conversation about
pain
management and physiotherapy.
I’ve been in so much
pain
lately with my arthritis in desperation I booked an appointment at my GPs for a conversation about
pain
management and physiotherapy.
Maisie2014
in
British Heart Foundation
1 year ago
nausea after eating
I’m still waiting for scan results due to very heavy periods/large clots/extreme pelvic
pain
/ bleeding between periods/
pain
during sex plus I’m anemic due to blood loss. I’m 20 yrs old. Ever since my first bout of
pain
(before Xmas) I’ve just lost my appetite and feel sick after I’ve eaten.
I’m still waiting for scan results due to very heavy periods/large clots/extreme pelvic
pain
/ bleeding between periods/
pain
during sex plus I’m anemic due to blood loss. I’m 20 yrs old. Ever since my first bout of
pain
(before Xmas) I’ve just lost my appetite and feel sick after I’ve eaten.
Magsag
in
Endometriosis UK
5 months ago
help - anyone have this
hi I have an endometrioma in my right ovary and it causes
pain
- especially in my hip, any way today the pains so bad that everytime I put my foot down it’s all in my hip and pelvis and where my ovary is.
hi I have an endometrioma in my right ovary and it causes
pain
- especially in my hip, any way today the pains so bad that everytime I put my foot down it’s all in my hip and pelvis and where my ovary is.
Scoops22
in
Endometriosis UK
22 days ago
Pain in neck and back with AF
Bizarrely the
pain
in my back and neck is along the right side of my spine - not the left as I might have expected. Am I a freak, or does anyone else get this?
Bizarrely the
pain
in my back and neck is along the right side of my spine - not the left as I might have expected. Am I a freak, or does anyone else get this?
Singingforever
in
Atrial Fibrillation Support
3 months ago
is this RLS?
But lots of people mention
pain
and cramps, mine is more a sensation. More trembly and tingly. I’m 66 and this has only recently come on. It’s bloody awful but there’s definitely no
pain
. As it seems I think to have been triggered by taking nytol for longer than suggested I’m hopeful it might pass.
But lots of people mention
pain
and cramps, mine is more a sensation. More trembly and tingly. I’m 66 and this has only recently come on. It’s bloody awful but there’s definitely no
pain
. As it seems I think to have been triggered by taking nytol for longer than suggested I’m hopeful it might pass.
Denny3
in
Restless Legs Syndrome
23 days ago
Pain in Forehead
I get
pain
at both sides of the top part of my forehead. A lot of the time it seems to coincide with dizziness of fibro fog. Just wondering has anyone else suffered with this and what to recommend to do? Thanks
I get
pain
at both sides of the top part of my forehead. A lot of the time it seems to coincide with dizziness of fibro fog. Just wondering has anyone else suffered with this and what to recommend to do? Thanks
Redd_
in
Fibromyalgia Action UK
9 months ago
Back Pain/Tingling
Hi, 5 months diagnosed with Fibro. In the last few weeks I have been getting a tingling feeling in my back in between the lower part of my shoulder blades. Sometimes it can hurt but its more than tingling that is annoying. Just wondering has anyone else suffered with this and what to recommend to do?
Hi, 5 months diagnosed with Fibro. In the last few weeks I have been getting a tingling feeling in my back in between the lower part of my shoulder blades. Sometimes it can hurt but its more than tingling that is annoying. Just wondering has anyone else suffered with this and what to recommend to do?
Redd_
in
Fibromyalgia Action UK
9 months ago
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