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Experiences with
Facial pain
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face pain
has anyone ever dealt with
facial
pain
? They at one point said I had Ms and mg, then said no to mg, but I have
facial
, jaw
pain
. Went to dentist he said teeth looked good. Hummm
has anyone ever dealt with
facial
pain
? They at one point said I had Ms and mg, then said no to mg, but I have
facial
, jaw
pain
. Went to dentist he said teeth looked good. Hummm
Hjgarden
in
My MSAA Community
4 days ago
mid segment facial pain
anyone else got this ??
anyone else got this ??
Kimbad1990
in
National Migraine Centre
7 months ago
Facial pain
I am gradually learning how to walk again The stroke has affected the nerves in the left side of my face and eye Is there anything I can do or treatment I can seek to reduce this
facial
pain
? Many thanks Andykilburn
I am gradually learning how to walk again The stroke has affected the nerves in the left side of my face and eye Is there anything I can do or treatment I can seek to reduce this
facial
pain
? Many thanks Andykilburn
Andykilburn
in
Different Strokes
10 months ago
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Headaches and facial pain
Although I have experienced
facial
pain
, headaches and slurred speech as this is how my condition presents itself. However, this year, I have had four episodes with my slurred speech going on from 1 week to 2 or 3 weeks.
Although I have experienced
facial
pain
, headaches and slurred speech as this is how my condition presents itself. However, this year, I have had four episodes with my slurred speech going on from 1 week to 2 or 3 weeks.
AngieB68
in
Functional Neurological Disorder - FND Hope
9 months ago
facial pain after suro
Since the brain surgery I have been getting really bad
facial
pain
on and off but they said it shouldn’t be happening because they have removed the trigeminal nerve in my head. Has anyone else had these symptoms ?
Since the brain surgery I have been getting really bad
facial
pain
on and off but they said it shouldn’t be happening because they have removed the trigeminal nerve in my head. Has anyone else had these symptoms ?
Elephant0
in
Acoustic Neuroma Support
9 months ago
Trigeminal Neuralgia pain
For me this means constant
facial
pain
(migraine earache and toothache all at the same time ) I am told this is a very rare health condition . Are there any other members on the forum that have this condition ?
For me this means constant
facial
pain
(migraine earache and toothache all at the same time ) I am told this is a very rare health condition . Are there any other members on the forum that have this condition ?
moyramm
in
Pain Concern
4 months ago
Multiple unexplained pains!
I've had daily chest
pain
since 2020, unexplained (excruciating) atypical
facial
pain
since 2021 and now unexplained throat pain since June 2023. I've had multiple MRIs, cameras, x-rays and no explanation for any of it.
I've had daily chest
pain
since 2020, unexplained (excruciating) atypical
facial
pain
since 2021 and now unexplained throat pain since June 2023. I've had multiple MRIs, cameras, x-rays and no explanation for any of it.
Adora12
in
Pain Concern
6 months ago
struggling 6 weeks after diagnosis
phone update with GP early December suggested I taper to 12.5 which I did on 11th dec About 4 days after started to feel fatigued and headaches now constant , 20th December shoulder
pain
, feeling of
facial
pain
more like sinus pain earache/tooth pain (no jaw pain) fatigue worse Struggles on with
phone update with GP early December suggested I taper to 12.5 which I did on 11th dec About 4 days after started to feel fatigued and headaches now constant , 20th December shoulder
pain
, feeling of
facial
pain
more like sinus pain earache/tooth pain (no jaw pain) fatigue worse Struggles on with
Emilydarby
in
PMRGCAuk
8 months ago
Quieten app
it got bad after a very stressful emotional period of a year or so - constant fight or flight status, bad sleep etc - and
facial
pain
.
it got bad after a very stressful emotional period of a year or so - constant fight or flight status, bad sleep etc - and
facial
pain
.
Londonia2073
in
Tinnitus UK
3 months ago
gluten ataxia and cluster headaches
Hello friends, has anyone with a diagnosis of GA or another type of ataxia been diagnosed with cluster headaches or a
facial
pain
type headache if so how do you get on with it while having typical ataxia symptoms. Thank you NO SURRENDER
Hello friends, has anyone with a diagnosis of GA or another type of ataxia been diagnosed with cluster headaches or a
facial
pain
type headache if so how do you get on with it while having typical ataxia symptoms. Thank you NO SURRENDER
Guardsman68
in
Ataxia UK
10 months ago
shocking price of glasses
I have GPA and have
facial
pain
across bridge of nose managed by medication daily. Some days after work (computer based) I can’t wait to take them off (I only work two days due to GPA).
I have GPA and have
facial
pain
across bridge of nose managed by medication daily. Some days after work (computer based) I can’t wait to take them off (I only work two days due to GPA).
Red-head44
in
Vasculitis UK
9 months ago
Pneumonia vaccines
hello all My question is about the Pneumovax-23 and Prevnar 13. I got the Prevnar 13 in 2015 The Pneumovax-23 in 2015 as well. Is it time to get these again? I live in the US. On W/W for over 20 years. Having immune globulin infusions for the last 5 years or so. Thank you for any insight.
hello all My question is about the Pneumovax-23 and Prevnar 13. I got the Prevnar 13 in 2015 The Pneumovax-23 in 2015 as well. Is it time to get these again? I live in the US. On W/W for over 20 years. Having immune globulin infusions for the last 5 years or so. Thank you for any insight.
Mother1943
in
CLL Support
1 month ago
vimpat / lacosamide stopped fully working
the Vimpat stopped working to completely resolve my RLS. Recent MRIs showed multiple Tarlov cysts on my spine, which is possibly causing the left leg pain and movement. It is positional and separate from the RLS in both legs in my arms and body. I see a new neurosurgeon next week. I’ve had multiple
the Vimpat stopped working to completely resolve my RLS. Recent MRIs showed multiple Tarlov cysts on my spine, which is possibly causing the left leg pain and movement. It is positional and separate from the RLS in both legs in my arms and body. I see a new neurosurgeon next week. I’ve had multiple
SleeplessinNC
in
Restless Legs Syndrome
2 months ago
Dulcolax
I took one dulcolax last night at about 10pm. I had 3 bowel movements in the space of an hour, 11am-12pm today. No pain or discomfort. I felt amazing after but it’s now 3:30pm and i feel like i’m constipated again and that there is still more to be released. Shall I take another one tonight to clear
I took one dulcolax last night at about 10pm. I had 3 bowel movements in the space of an hour, 11am-12pm today. No pain or discomfort. I felt amazing after but it’s now 3:30pm and i feel like i’m constipated again and that there is still more to be released. Shall I take another one tonight to clear
HI1237
in
IBS Network
2 months ago
Littlejoy
I had pelvic prolapse, cystocele and rectocele. Had pelvic prolapse repair 1 year ago, they took out uterus and tightened vagina to hold bladder & bowel. When I came too after op, they said I had a cyst one my left ovary so would need another op yo remove this. I have been in pain since op, it depends
I had pelvic prolapse, cystocele and rectocele. Had pelvic prolapse repair 1 year ago, they took out uterus and tightened vagina to hold bladder & bowel. When I came too after op, they said I had a cyst one my left ovary so would need another op yo remove this. I have been in pain since op, it depends
Operation
in
Pelvic Pain Support Network
4 months ago
Walking Speed
I know our bodies are different, but we all have something in common. Has anyone done or tried something besides ampyra that increased the speed that you walk? I've tried ampyra, dysport and I'm still moving like a turtle. My legs still feel very heavy! I'm still hoping to be walking normal again!
I know our bodies are different, but we all have something in common. Has anyone done or tried something besides ampyra that increased the speed that you walk? I've tried ampyra, dysport and I'm still moving like a turtle. My legs still feel very heavy! I'm still hoping to be walking normal again!
Diva1976
in
My MSAA Community
5 months ago
crazy or not?
I am in chronic pain in spine painkillers not helping. What I need help with is the way it all makes me feel I have no ffamily or friends . Isolated. I get panicky when pain is out of control, I feel freaked out and alone and am devoid of positive feelings everything everyday feels bleak no respite
I am in chronic pain in spine painkillers not helping. What I need help with is the way it all makes me feel I have no ffamily or friends . Isolated. I get panicky when pain is out of control, I feel freaked out and alone and am devoid of positive feelings everything everyday feels bleak no respite
faith12
in
Pain Concern
2 months ago
heel pain
I have an agonizing pain in the back right and under part of my Left heel, often occurs in bed and for no memorable reason, also on my right thigh/hip area is a patch that feels quite numb to touch But inside it feels like a firework is burning. Are these pains due to the back stenosis?. I was referred
I have an agonizing pain in the back right and under part of my Left heel, often occurs in bed and for no memorable reason, also on my right thigh/hip area is a patch that feels quite numb to touch But inside it feels like a firework is burning. Are these pains due to the back stenosis?. I was referred
lubarr
in
Pain Concern
2 months ago
I know Nitrous Oxide can cause b12 deficiency, but could Nitrogen Dioxide do it too?
I had low b12, took ppi and h2 before Mt body crashed. But I also realised that we did an experiment in the labs I was working in, when my body began to feel awful, around the time I started PPIs (before my body totally crashed months later) I know Nitrous Oxide messes with b12... Does anyone know
I had low b12, took ppi and h2 before Mt body crashed. But I also realised that we did an experiment in the labs I was working in, when my body began to feel awful, around the time I started PPIs (before my body totally crashed months later) I know Nitrous Oxide messes with b12... Does anyone know
Suffering_sunny
in
Pernicious Anaemia Society
6 months ago
Cladribine
I have recently been diagnosed as having RRMS. I have only had 2 relapses in the past year, both of which involved temporary loss of eyesight. On both occasions, my vision returned to normal by itself, without any need or medication to be prescribed. However, my most recent MRI contrast scan shows that
I have recently been diagnosed as having RRMS. I have only had 2 relapses in the past year, both of which involved temporary loss of eyesight. On both occasions, my vision returned to normal by itself, without any need or medication to be prescribed. However, my most recent MRI contrast scan shows that
max011
in
My MSAA Community
6 months ago
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