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IOptic neuritis
I just wanted to share a little bit about my experience with optic
neuritis
, and the aftermath.
I just wanted to share a little bit about my experience with optic
neuritis
, and the aftermath.
Hidden
in
My MSAA Community
8 months ago
Vestibular Neuritis
Diagnosed as vestibular
neuritis
. My question is, I usually self inject weekly which I have continued to do. I don't know if I'm imagining it but the vertigo symptoms seem to greatly improve for a couple of days after my B12 injection and then come back again.
Diagnosed as vestibular
neuritis
. My question is, I usually self inject weekly which I have continued to do. I don't know if I'm imagining it but the vertigo symptoms seem to greatly improve for a couple of days after my B12 injection and then come back again.
Ipsofacto01
in
Pernicious Anaemia Society
8 months ago
Ischemic optic neuropathy?
Eye Hospital A and E tentively suggester optic
neuritis
but the Consultant says ischemic optic neuropathy, ' a circulation problem', basically a mini stroke behind the eye. I am very keen to contact anyone who has experienced this as I am extremely anxious and feel isolated.
Eye Hospital A and E tentively suggester optic
neuritis
but the Consultant says ischemic optic neuropathy, ' a circulation problem', basically a mini stroke behind the eye. I am very keen to contact anyone who has experienced this as I am extremely anxious and feel isolated.
HedgeHogHome
in
Glaucoma UK
4 months ago
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PMR and brachial neuritis
It looks like I have developed a fairly rare condition called Parsonage-Turner syndrome (PTS), also called brachial
neuritis
. It started with terrible pain in the shoulder, so initially I thought it would appear in the other shoulder and be the beginning of a PMR relapse.
It looks like I have developed a fairly rare condition called Parsonage-Turner syndrome (PTS), also called brachial
neuritis
. It started with terrible pain in the shoulder, so initially I thought it would appear in the other shoulder and be the beginning of a PMR relapse.
dmart7
in
PMRGCAuk
7 months ago
Coping with sudden vision loss
Eye A and E said optic
neuritis
, private specialist consultant, a ciculatory problem, a mini stroke behind the eye damaging the optic nerve. I have had no support whatsoever from the hospital . I have periods of great upset and distress.
Eye A and E said optic
neuritis
, private specialist consultant, a ciculatory problem, a mini stroke behind the eye damaging the optic nerve. I have had no support whatsoever from the hospital . I have periods of great upset and distress.
HedgeHogHome
in
Glaucoma UK
3 months ago
New to the community
I was diagnosed in the early 2000's after having optic
neuritis
twice. My neurologist thinks I had MS since at least 1995 when I had my son since I had classic post-partum MS symptoms that my OBGYN ignored. (I thought I had a stroke.)
I was diagnosed in the early 2000's after having optic
neuritis
twice. My neurologist thinks I had MS since at least 1995 when I had my son since I had classic post-partum MS symptoms that my OBGYN ignored. (I thought I had a stroke.)
jezebellydancer
in
My MSAA Community
5 months ago
Liver symptoms appeared after treatment
After end of hepatitis treatment I had one treatment for optic
neuritis
with high dose corticosteroids. After I finish with the treatment from this
neuritis
all was good till the middle of June. Just to mention that for 5 years I have several times drinking wine..
After end of hepatitis treatment I had one treatment for optic
neuritis
with high dose corticosteroids. After I finish with the treatment from this
neuritis
all was good till the middle of June. Just to mention that for 5 years I have several times drinking wine..
Motik
in
British Liver Trust
2 months ago
Tb meds that don't effect eyes
It appears all the tb first line meds and moxifloxacin can cause optic
neuritis
except pyrazinamide. Just need alternative - delamanid safe instead?
It appears all the tb first line meds and moxifloxacin can cause optic
neuritis
except pyrazinamide. Just need alternative - delamanid safe instead?
gurms31
in
TB Alert
1 year ago
Terrified Before Appointment
The optometrist said that my eyes look great, but she also took a very close look at the optic nerves and found swelling (and signs of recovering) in my left optic nerve (optic
neuritis
). She mentioned Thyroid and then mentioned that it could be ‘other’ autoimmune diseases that attack nerves.
The optometrist said that my eyes look great, but she also took a very close look at the optic nerves and found swelling (and signs of recovering) in my left optic nerve (optic
neuritis
). She mentioned Thyroid and then mentioned that it could be ‘other’ autoimmune diseases that attack nerves.
Totmama
in
My MSAA Community
3 months ago
Some issues with color differentiation~~
At the onset of GCA, my right optic nerve was left a bit pale and with some white spots on it, plus I have optic
neuritis
. Now, it does not concern me and I thought I'd share it in case anyone is experiencing this intermittently. I'm all set and pleased it doesn't indicate an issue.
At the onset of GCA, my right optic nerve was left a bit pale and with some white spots on it, plus I have optic
neuritis
. Now, it does not concern me and I thought I'd share it in case anyone is experiencing this intermittently. I'm all set and pleased it doesn't indicate an issue.
Grammy80
in
PMRGCAuk
10 months ago
GCA and what I learned today.....
I believe the target was my optic
neuritis
and neuralgia. Now the only pain I have is in my blind eye...it is strange. My forehead hurts over my eyebrow; then, the pain goes through the eyeball and into my nose, then numbness.
I believe the target was my optic
neuritis
and neuralgia. Now the only pain I have is in my blind eye...it is strange. My forehead hurts over my eyebrow; then, the pain goes through the eyeball and into my nose, then numbness.
Grammy80
in
PMRGCAuk
13 days ago
Generic Teriflunomide
Prior to this past summer, my symptoms were on my right side and had been since my initial optic
neuritis
and walking troubles at the time of my diagnosis in 1995.
Prior to this past summer, my symptoms were on my right side and had been since my initial optic
neuritis
and walking troubles at the time of my diagnosis in 1995.
GeorgiaJunebug
in
My MSAA Community
6 months ago
Treating PVCS on a virtual ward
I was admitted for 1 night, querying a stroke, but diagnosed with acute vestibular
neuritis
. I was sent home on the virtual ward which is a brilliant concept and is working very well. My palpitations have been very bad.
I was admitted for 1 night, querying a stroke, but diagnosed with acute vestibular
neuritis
. I was sent home on the virtual ward which is a brilliant concept and is working very well. My palpitations have been very bad.
Norfolk_spaniel
in
AF Association
1 year ago
New Member and PPPD/ Vestibular Migraine
PPPD usually follows on from either a vestibular condition like labrynthitis or vestibular
neuritis
, neither of which I had. Neither was I anxious or depressed before hand, another risk factor. I've done a heck of alot of reading these past two years to tryand figure out what's happening.
PPPD usually follows on from either a vestibular condition like labrynthitis or vestibular
neuritis
, neither of which I had. Neither was I anxious or depressed before hand, another risk factor. I've done a heck of alot of reading these past two years to tryand figure out what's happening.
Sparklingsunshine
in
Functional Neurological Disorder - FND Hope
7 days ago
Inflammatory Pain and T
I have had T for over two years now following an attack of vertigo with varying diagnoses of labyrinthitis, bppv or vestibular
neuritis
, none of which have ever been confirmed.. and after all this time I feel stuck with no sign of reaching habituation..
I have had T for over two years now following an attack of vertigo with varying diagnoses of labyrinthitis, bppv or vestibular
neuritis
, none of which have ever been confirmed.. and after all this time I feel stuck with no sign of reaching habituation..
Shozza1
in
Tinnitus UK
1 year ago
Pregabalin
I have just been diagnosed with progressive Multiple Sclerosis, I have lots of terrible symptoms such as ¬ Pins and needles throughout my body, especially the head Vision problems which has caused optical
Neuritis
and loss of Peripheral vision, now unable to drive.
I have just been diagnosed with progressive Multiple Sclerosis, I have lots of terrible symptoms such as ¬ Pins and needles throughout my body, especially the head Vision problems which has caused optical
Neuritis
and loss of Peripheral vision, now unable to drive.
bubbatetley
in
Restless Legs Syndrome
1 year ago
Advice on RLS as a reaction to medication?
Hello, I currently have long covid and vestibular
neuritis
, and have had these conditions for around six months. The vestibular
neuritis
is causing considerable vertigo symptoms. Just over a month ago, my GP gave me Betahistine to try and ease the vertigo.
Hello, I currently have long covid and vestibular
neuritis
, and have had these conditions for around six months. The vestibular
neuritis
is causing considerable vertigo symptoms. Just over a month ago, my GP gave me Betahistine to try and ease the vertigo.
RiversofLondon
in
Restless Legs Syndrome
1 year ago
MS or Lupus
I was diagnosed with Optic
Neuritis
in February and was put on short intensive steroids in March sleep deprivation the worst! but sight hasn’t fully and won’t fully return. Ophthalmology thought MS. MRI showed lesions on brain Neurologist thinks lupus not MS.
I was diagnosed with Optic
Neuritis
in February and was put on short intensive steroids in March sleep deprivation the worst! but sight hasn’t fully and won’t fully return. Ophthalmology thought MS. MRI showed lesions on brain Neurologist thinks lupus not MS.
Gossygirl76
in
LUPUS UK
1 year ago
Blue Horizon blood results
Around 20 years ago I had optical
neuritis
, for which I was prescribed corticosteroids - wondering if there could be a link between this and some of my current symptoms. *I am due to see an endocrinologist in September (GP reffered me to weight management clinic). Thanks in advance
Around 20 years ago I had optical
neuritis
, for which I was prescribed corticosteroids - wondering if there could be a link between this and some of my current symptoms. *I am due to see an endocrinologist in September (GP reffered me to weight management clinic). Thanks in advance
ZM1980
in
Thyroid UK
1 year ago
Just told I need a partial Nephrectomy
Also, as a side note, I developed Optic
Neuritis
after being very sick in my mid-20's. I have suffered significant migraines for 15 years following the birth of my daughter. I also had massive uterine clots which resulted in a need for ablation surgery back then.
Also, as a side note, I developed Optic
Neuritis
after being very sick in my mid-20's. I have suffered significant migraines for 15 years following the birth of my daughter. I also had massive uterine clots which resulted in a need for ablation surgery back then.
myarabella
in
Hughes Syndrome APS Forum
2 years ago
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