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Antiphospholipid Antibodies Overlapping in Isolated Neurological Syndrome and Multiple Sclerosis: Neurobiological Insights & Diagnostic . .
Thus, typical demyelinating lesions of MS, transverse myelitis and optic
neuritis
, may also be present in the pathological spectrum of APS (Cikes et al., 2008).
Thus, typical demyelinating lesions of MS, transverse myelitis and optic
neuritis
, may also be present in the pathological spectrum of APS (Cikes et al., 2008).
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
5 years ago
What the Heck do those codes Mean?
Human Stem Cell Therapy LP – Lumbar Puncture (Spinal Tap) MRI –Magnetic Resonance Imaging NAC N-Acetylcysteine NMO – Neuromyelitis optica PHSYCO-ME - “Mental Me” PBA - Pseudobulbar Affect RRMS – Relapsing Remitting MS SPMS – Secondary Progressive MS PRMS – Progressive Relapsing MS PPMS - ON – Optic
Neuritis
Human Stem Cell Therapy LP – Lumbar Puncture (Spinal Tap) MRI –Magnetic Resonance Imaging NAC N-Acetylcysteine NMO – Neuromyelitis optica PHSYCO-ME - “Mental Me” PBA - Pseudobulbar Affect RRMS – Relapsing Remitting MS SPMS – Secondary Progressive MS PRMS – Progressive Relapsing MS PPMS - ON – Optic
Neuritis
CalfeeChick
CommunityAmbassador
in
My MSAA Community
5 years ago
My most recent hypothesis
It finally occurs to me that this is residual damage from optic
neuritis
so many years ago. It's obviously (now that I think about it, duh) something to do with light/glare/my eyes. I may have to become a bat, live in a cave and come out only at dusk.
It finally occurs to me that this is residual damage from optic
neuritis
so many years ago. It's obviously (now that I think about it, duh) something to do with light/glare/my eyes. I may have to become a bat, live in a cave and come out only at dusk.
goatgal
in
My MSAA Community
5 years ago
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Exactly what I was worried about!
After looking over all of my MRIs, and giving me a thorough exam AND having me "tell my story" from the last 10 yrs of symptoms, specialist visits and tests, he seemed confused as to how I was diagnosed (even tho I also had a relapse, optic
neuritis
last yr too).
After looking over all of my MRIs, and giving me a thorough exam AND having me "tell my story" from the last 10 yrs of symptoms, specialist visits and tests, he seemed confused as to how I was diagnosed (even tho I also had a relapse, optic
neuritis
last yr too).
cassielynn71
in
My MSAA Community
5 years ago
Neuritis
I have been diagnosed with neuropathy both motor and peripheral there is constant pain to all areas of my body. Can anyone offer any advice on pain relief please. Thank you
I have been diagnosed with neuropathy both motor and peripheral there is constant pain to all areas of my body. Can anyone offer any advice on pain relief please. Thank you
ceedy
in
Fibromyalgia Action UK
5 years ago
Is it possible for APS to be reversed?
In my 20's I developed Optic
Neuritis
following an extremely high fever. I later read that Optic
Neuritis
is common with MS and APS patients. I am not looking for problems that aren't there, however, I do want to prepare for what may be to come down the road. Any thoughts?
In my 20's I developed Optic
Neuritis
following an extremely high fever. I later read that Optic
Neuritis
is common with MS and APS patients. I am not looking for problems that aren't there, however, I do want to prepare for what may be to come down the road. Any thoughts?
myarabella
in
Hughes Syndrome APS Forum
5 years ago
APS AND EYESIGHT PROBLEMS
I was diagnosed with optic
neuritis
in 1990 and apart from Prof D’Cruz who is a lovely doctor I’ve been treated like dirt by every single neuro since my diagnosis back in 1996. I take 75mg Clopidogrel daily and have noticed no difference in any symptoms.
I was diagnosed with optic
neuritis
in 1990 and apart from Prof D’Cruz who is a lovely doctor I’ve been treated like dirt by every single neuro since my diagnosis back in 1996. I take 75mg Clopidogrel daily and have noticed no difference in any symptoms.
Stereolover
in
Hughes Syndrome APS Forum
5 years ago
Lupus and Celiac?
When I was first having symptoms of Autoimmune disease (prior to diagnosis) - I had severe optic
neuritis
and tingling/numbness in my toes, i gave up gluten and dairy. I have slipped and eat gluten again and I'm wondering if this is part of the reason I am getting symptoms again.
When I was first having symptoms of Autoimmune disease (prior to diagnosis) - I had severe optic
neuritis
and tingling/numbness in my toes, i gave up gluten and dairy. I have slipped and eat gluten again and I'm wondering if this is part of the reason I am getting symptoms again.
claretech
in
LUpus Patients Understanding and Support
5 years ago
RE: Opinion on Thyroid/Hormone results
Thanks Male, 23 Other medical issues: Vestibular
neuritis
/vertigo
Thanks Male, 23 Other medical issues: Vestibular
neuritis
/vertigo
AJ-AJ
in
Thyroid UK
5 years ago
deaf
) I have felt dizzy & disoriented with nausea ( now stable )... i was led to believe it might be Labrynthitis or Vestibular
neuritis
which bothers the inner ear by the cochlea ...
) I have felt dizzy & disoriented with nausea ( now stable )... i was led to believe it might be Labrynthitis or Vestibular
neuritis
which bothers the inner ear by the cochlea ...
dizzyfairy
in
Lung Conditions Community Forum
5 years ago
More questions!
There is a suspicion by the neurologist that I have had Optic
Neuritis
as the Visual Evoked Potential test in September was abnormal. Does APS cause problems with dry eyes and sight? Additionally, I was wondering if the GP can do any other blood tests to check for 'sticky blood'?
There is a suspicion by the neurologist that I have had Optic
Neuritis
as the Visual Evoked Potential test in September was abnormal. Does APS cause problems with dry eyes and sight? Additionally, I was wondering if the GP can do any other blood tests to check for 'sticky blood'?
Mand25
in
Hughes Syndrome APS Forum
6 years ago
Hello! MS newbie here.
I was just diagnosed with MS in Jan after a bout of severe optic
neuritis
. I lost a bunch of vision in my left eye. Starting on Ocrevus soon, even though it seems kinda scary because it's so new. But I'm going through with it anyway because it might work!
I was just diagnosed with MS in Jan after a bout of severe optic
neuritis
. I lost a bunch of vision in my left eye. Starting on Ocrevus soon, even though it seems kinda scary because it's so new. But I'm going through with it anyway because it might work!
sski1
in
My MSAA Community
6 years ago
Feeling Frustrated
As a result of the immunosuppressants I’ve also gotten a virus that affected my inner ear , called vestibular
neuritis
, and it’s caused vertigo and nausea and a boatload if other things. Just feeling pretty beat down and sad about things, and thought I’d just vent here.
As a result of the immunosuppressants I’ve also gotten a virus that affected my inner ear , called vestibular
neuritis
, and it’s caused vertigo and nausea and a boatload if other things. Just feeling pretty beat down and sad about things, and thought I’d just vent here.
RedFlamingo27
in
Crohn's and Colitis Support
6 years ago
Severe eye pain
I’ve never been dx with optic
neuritis
so I’m wondering if anyone has ever experienced the same symptoms?
I’ve never been dx with optic
neuritis
so I’m wondering if anyone has ever experienced the same symptoms?
Eveliz
in
My MSAA Community
6 years ago
Looking for some help please - not diagnosed
As well as the above symptoms I developed a problem with blurred vision and sight deterioration in one eye, pain in the eye and worsening headaches and scalp pain, worsening of pins and needles in legs, feet and arms and pain and weakness in my legs - VEP was positive suggesting optic
neuritis
, MRI shows
As well as the above symptoms I developed a problem with blurred vision and sight deterioration in one eye, pain in the eye and worsening headaches and scalp pain, worsening of pins and needles in legs, feet and arms and pain and weakness in my legs - VEP was positive suggesting optic
neuritis
, MRI shows
Mand25
in
Hughes Syndrome APS Forum
6 years ago
Opinion on Thyroid/Hormone results
Thanks Male, 23 Other medical issues: Vestibular
neuritis
Thanks Male, 23 Other medical issues: Vestibular
neuritis
AJ-AJ
in
Thyroid UK
6 years ago
New to site and wondering if I'm going slightly nutty 🙄
My doctors and neurologist keeps sending me for tests for MS all so far negative thankfully or vestibular
neuritis
( been doing some very weird balance exercises for 7months lol) which has helped a little bit.
My doctors and neurologist keeps sending me for tests for MS all so far negative thankfully or vestibular
neuritis
( been doing some very weird balance exercises for 7months lol) which has helped a little bit.
IOWJO
in
Pernicious Anaemia Society
6 years ago
Cognitive issues? Can MS cause it?
It was ongoing for 6 years and I never knew why nor bothered to look into it until I had optic
neuritis
. I didn't act my normal self for many years (remission?) and I knew something was wrong.
It was ongoing for 6 years and I never knew why nor bothered to look into it until I had optic
neuritis
. I didn't act my normal self for many years (remission?) and I knew something was wrong.
Hidden
in
My MSAA Community
6 years ago
HELP MRI RESULTS
No evidence of optical
neuritis
or orbital pathology. Anyone im out my mind with worry.
No evidence of optical
neuritis
or orbital pathology. Anyone im out my mind with worry.
SpiritualT
in
Multiple System Atrophy Trust
6 years ago
MRI HELP NEEDED
No evidence of optical
neuritis
or orbital pathology. Anyone im out my mind with worry.
No evidence of optical
neuritis
or orbital pathology. Anyone im out my mind with worry.
SpiritualT
in
My MSAA Community
6 years ago
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