Search
Search
About
Log in
Join
Experiences with
Neuritis
Posts
Communities
156 public posts
Filter results
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
3 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
4 months ago
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
2 months ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
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
13 days 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
10 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
5 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
9 months 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
10 months 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
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
1 month 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
11 months 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
1 year ago
Could a previous diagnosis of brachial neuritis be a warning sign of PMR?
Dx at the time was brachial
neuritis
. It eventually calmed down and now I'm wondering if this could have been the beginnings of PMR which evolved into GCA /LVV. Has anyone else had previous episodes of one-sided pain from neck to arm before dx?
Dx at the time was brachial
neuritis
. It eventually calmed down and now I'm wondering if this could have been the beginnings of PMR which evolved into GCA /LVV. Has anyone else had previous episodes of one-sided pain from neck to arm before dx?
Dochaz
in
PMRGCAuk
1 year ago
Dr appt updates
She says I have only had one incident which was optic
neuritis
in my L eye so it’s only CIS (Clinically Isolated Syndrome. ) In 2014 I went from blurry one Friday to totally blind in that eye the next Friday. I end up having a lumbar puncture and more lab work.
She says I have only had one incident which was optic
neuritis
in my L eye so it’s only CIS (Clinically Isolated Syndrome. ) In 2014 I went from blurry one Friday to totally blind in that eye the next Friday. I end up having a lumbar puncture and more lab work.
PWilli
in
My MSAA Community
1 year ago
My Last (IFN) Dose, my Fateful Decision One Year Ago
A neurologist Dx Brachial
neuritis
, a known rare vax risk. Most neuro vax events improve over months or years, but can precede other things. By new year ’23 neuro was less severe. But on Sunday Jan 15 I was at parents’ new retirement home helping assemble furniture.
A neurologist Dx Brachial
neuritis
, a known rare vax risk. Most neuro vax events improve over months or years, but can precede other things. By new year ’23 neuro was less severe. But on Sunday Jan 15 I was at parents’ new retirement home helping assemble furniture.
EPguy
in
MPN Voice
4 months ago
B & B (NOT bed & breakfast)
Instead of telling me then that if you’ve had optic
neuritis
twice within seven years, you pretty much have MS, he asked me if I was having any bladder or bowel problems. To which in my embarrassment I answered “No!”. Then he sent me for an MRI. At least my diagnosis was easy! 🤣
Instead of telling me then that if you’ve had optic
neuritis
twice within seven years, you pretty much have MS, he asked me if I was having any bladder or bowel problems. To which in my embarrassment I answered “No!”. Then he sent me for an MRI. At least my diagnosis was easy! 🤣
Boudreaux2016
in
My MSAA Community
2 years ago
Effects of heat on vision....Optic neuritis
It is usually applied to optic
neuritis
and other visual symptoms but can also refer to fatigue, pain, balance, weakness, bladder issues, cognitive or sensory symptoms. (Web.MD) I've typed on and off since the '50s....I find I type more accurately and faster if I shut my eyes.
It is usually applied to optic
neuritis
and other visual symptoms but can also refer to fatigue, pain, balance, weakness, bladder issues, cognitive or sensory symptoms. (Web.MD) I've typed on and off since the '50s....I find I type more accurately and faster if I shut my eyes.
Grammy80
in
PMRGCAuk
2 years ago
How would it be
pulling out your chair How’s it going to be Not falling and meeting the floor again and again Raising fear and being picked up How would it be Without a wheelchair Without a walker Without a cane How would it be with no PT, OT and physiologist needed How would it be With clear vision and no optic
neuritis
pulling out your chair How’s it going to be Not falling and meeting the floor again and again Raising fear and being picked up How would it be Without a wheelchair Without a walker Without a cane How would it be with no PT, OT and physiologist needed How would it be With clear vision and no optic
neuritis
positiveness
in
My MSAA Community
2 years ago
1
2
...
8
Next page
Filter results
Clear filters
Posted in
All communities
My MSAA Community
52 results
Hughes Syndrome APS Forum
11 results
Pernicious Anaemia Society
10 results
View top 10 communities
Sort by
Most Relevant
Newest