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Experiences with
Vision loss
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how far could dad be into the psp
my dad has the double vision blurry vision alot of the time in one eye, he is somedays not real steady, he gets the shaky hands I have noticed he does,not have the strength to hold his legs up to put shoes on for very long. he falls maybe 1or 2 times a month. he was falling more that seems to bebetter
my dad has the double vision blurry vision alot of the time in one eye, he is somedays not real steady, he gets the shaky hands I have noticed he does,not have the strength to hold his legs up to put shoes on for very long. he falls maybe 1or 2 times a month. he was falling more that seems to bebetter
rochestermn
in
PSP Association
12 years ago
Light at the end of the tunnel
Been diagnosed with Lupus for over 20 years, am in my 41st year now. Plodded on as best I could until 2002 as I had spondylilothesis, with was repaired with a spinal fusion in Sept 2002. Best thing I ever had done, gave me a new lease of life. 3 years after the operation I started running just
Been diagnosed with Lupus for over 20 years, am in my 41st year now. Plodded on as best I could until 2002 as I had spondylilothesis, with was repaired with a spinal fusion in Sept 2002. Best thing I ever had done, gave me a new lease of life. 3 years after the operation I started running just
poole_odyssey
in
LUPUS UK
12 years ago
ON OXYGEN - CAUSING MORE DRY SKIN
On the good advice of the Nurse, I have stopped the dryness in my nose with KY jelly. However, I have dry cracking on my lips but I don't know what to use as I was told lip balms have petroleum jelly in them. Does anyone have any ideas please? MERRY CHRISTMAS TO EVERYONE.
On the good advice of the Nurse, I have stopped the dryness in my nose with KY jelly. However, I have dry cracking on my lips but I don't know what to use as I was told lip balms have petroleum jelly in them. Does anyone have any ideas please? MERRY CHRISTMAS TO EVERYONE.
Gucci
in
Lung Conditions Community Forum
12 years ago
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What is happening am I developing treatment resistance ?
Recently I have been diagnosed with optical neuritis with peripheral
vision
loss
and colour
vision
loss
and I have been experiencing TIA'S on a weekly basis .
Recently I have been diagnosed with optical neuritis with peripheral
vision
loss
and colour
vision
loss
and I have been experiencing TIA'S on a weekly basis .
Dann
in
Hughes Syndrome APS Forum
12 years ago
ho ho boo hoo
Hate to put all this to you as I may spoil everyones xmas cheer. I am sick fed up, and got the blues. I had my discs removed, spinal fusion and spinal cage 3 weeks ago and it has been quite hard. I am not allowed to drive, wash up, iron or lean down. Now I can hear lots of you saying you lucky so
Hate to put all this to you as I may spoil everyones xmas cheer. I am sick fed up, and got the blues. I had my discs removed, spinal fusion and spinal cage 3 weeks ago and it has been quite hard. I am not allowed to drive, wash up, iron or lean down. Now I can hear lots of you saying you lucky so
allanah
in
NRAS
12 years ago
i have ca is headaches blurd double vision one of the symtoms
i have ca is headaches blurd double vision one of the symtoms
i have ca is headaches blurd double vision one of the symtoms
gazzal
in
Ataxia UK
12 years ago
Low Oxygen and Vision Loss ??
Hi there I have ben having problems with blurred and double
vision
and
loss
and also field
vision
problems, that the Eye department cannot diagnose and they seem to have lost interest after I had nerve tests on the eyes.
Hi there I have ben having problems with blurred and double
vision
and
loss
and also field
vision
problems, that the Eye department cannot diagnose and they seem to have lost interest after I had nerve tests on the eyes.
andreafm
in
Behçet's UK
12 years ago
Low oxygen levels and vision loss ??
Hi there I have ben having problems with blurred and double
vision
and
loss
and also field
vision
problems, that the Eye department cannot diagnose and they seem to have lost interest after I had nerve tests on the eyes.
Hi there I have ben having problems with blurred and double
vision
and
loss
and also field
vision
problems, that the Eye department cannot diagnose and they seem to have lost interest after I had nerve tests on the eyes.
andreafm
in
Lung Conditions Community Forum
12 years ago
Hello
Just a quick message to thank everyone for all your lovely comments when I had my op. Katy did well with coping with phone calls visitors and blogs I think, hubby didn't , but was good helping me lol! The op seems to have gone well, I had three discs removed, spinal fusion and metal cage done. The dressing
Just a quick message to thank everyone for all your lovely comments when I had my op. Katy did well with coping with phone calls visitors and blogs I think, hubby didn't , but was good helping me lol! The op seems to have gone well, I had three discs removed, spinal fusion and metal cage done. The dressing
allanah
in
NRAS
12 years ago
Spinal fusion????
HI i had a 70% L4/L5 discectomy 5 years ago and was told i would more than likely need a fusion in time, well that may be now as MRI shows problem with remaining disc and a trapped nerve that is causing constant pain any way i'm enquiring if any one else has gone through this and how the fibro is affected
HI i had a 70% L4/L5 discectomy 5 years ago and was told i would more than likely need a fusion in time, well that may be now as MRI shows problem with remaining disc and a trapped nerve that is causing constant pain any way i'm enquiring if any one else has gone through this and how the fibro is affected
Hidden
in
Fibromyalgia Action UK
12 years ago
VIRAL MENINGITIS - A COUPLE'S STORY - DAVE & PAMELA PART 1
The after-effects have been very strong, ranging from bad head and neck spasms, blurred
vision
and degradation in eyesight, lack of concentration and memory
loss
and severe fatigue amongst others.
The after-effects have been very strong, ranging from bad head and neck spasms, blurred
vision
and degradation in eyesight, lack of concentration and memory
loss
and severe fatigue amongst others.
davehancock1
in
Meningitis Now
12 years ago
Is Fibromyalgia just an alternative name for ME?
I am a type 1 diabetic with cardiac problems and fibromyalgia as well as retinopathy, neuropathy, severe back damage and circulation problems and PCOS. What is the best weight loss diet to follow for someone who finds exercise both painful and exhausting?
I am a type 1 diabetic with cardiac problems and fibromyalgia as well as retinopathy, neuropathy, severe back damage and circulation problems and PCOS. What is the best weight loss diet to follow for someone who finds exercise both painful and exhausting?
janedyson
in
Fibromyalgia Action UK
12 years ago
Has anyone had a spinal fusion - with good results? And how do you get a 2nd opinion?
Hi I was rushed to A&E on the 1st of September - after the weekend had an MRI and discovered I had a large central prolapsed disc (L4/L5 - no exciting war story!). Had been chasing my GP for months with stiffness and sciatica pain but had been brushed off then bam - pure agony. After 3 days the
Hi I was rushed to A&E on the 1st of September - after the weekend had an MRI and discovered I had a large central prolapsed disc (L4/L5 - no exciting war story!). Had been chasing my GP for months with stiffness and sciatica pain but had been brushed off then bam - pure agony. After 3 days the
SillyYak
in
Pain Concern
12 years ago
A Thank You
My practice nurse told me that the neurologist I had seen had written to my GP expressing that my peripheral
vision
loss
was most probably part of a mental health condition. To say I am upset is an understatement and in no way help me with my current blindness.
My practice nurse told me that the neurologist I had seen had written to my GP expressing that my peripheral
vision
loss
was most probably part of a mental health condition. To say I am upset is an understatement and in no way help me with my current blindness.
Jazzy21
in
Behçet's UK
12 years ago
Should I have a blocked tear duct repaired under general anaesthetic?
I was diagnosed with Cerebral Vasculitis 12 months ago and also suffered a stroke behind my left eye causing 30%
loss
of
vision
. It also caused a blocked tear duct in my left eye so it now constantly waters.
I was diagnosed with Cerebral Vasculitis 12 months ago and also suffered a stroke behind my left eye causing 30%
loss
of
vision
. It also caused a blocked tear duct in my left eye so it now constantly waters.
LMB2
in
Vasculitis UK
12 years ago
Peripheral vision loss and feeling down
Thank so very much for all the help I received I truly owe my life and well being to you all on this forum. Thank God for it.
Thank so very much for all the help I received I truly owe my life and well being to you all on this forum. Thank God for it.
Jazzy21
in
Behçet's UK
12 years ago
Depressed After Losing Peripheral Vision Loss
I am feeling so low after 10 days and no ideas as to why i have lost my peripheral vision and my normal vision is reduced. All MRIs, CT scans and angiograms proved to be normal. I am now trying to get to see my rheumy to ask what is happening to me. My question is this how do you stay positive with
I am feeling so low after 10 days and no ideas as to why i have lost my peripheral vision and my normal vision is reduced. All MRIs, CT scans and angiograms proved to be normal. I am now trying to get to see my rheumy to ask what is happening to me. My question is this how do you stay positive with
Jazzy21
in
Behçet's UK
12 years ago
Hello :)
I've spent ages reading the forums - didnt realise they existed until recently! I've been looking for experiences with Xolair, as I have my outpatient appointment at Papworth tomorrow and want to ask them if they will consider it for me. I have severe asthma, with allergies - which I may cope with
I've spent ages reading the forums - didnt realise they existed until recently! I've been looking for experiences with Xolair, as I have my outpatient appointment at Papworth tomorrow and want to ask them if they will consider it for me. I have severe asthma, with allergies - which I may cope with
Hidden
in
Asthma Community Forum
12 years ago
i developed menigitis after a neck spinal fusion surery. i have a very bad ammune system and was told the donor bone/blood/chemial that was
implanted caused a life threatening non viral memingitus. has anyone else had this experience. i have not been right since, two months ago, and want advice throgh experience, thanks fusion
implanted caused a life threatening non viral memingitus. has anyone else had this experience. i have not been right since, two months ago, and want advice throgh experience, thanks fusion
fushion
in
Meningitis Now
12 years ago
Does anybody get these symptoms even when anticoagulated?
I really thought warfarin would help, and it has to some degree but the days of pain seem to be getting more frequent, the episodes are just like strokes without the
loss
of
vision
. Nothing still shows up in blood tests and a ct scan showed 'no acute change'.
I really thought warfarin would help, and it has to some degree but the days of pain seem to be getting more frequent, the episodes are just like strokes without the
loss
of
vision
. Nothing still shows up in blood tests and a ct scan showed 'no acute change'.
emmaj
in
Hughes Syndrome APS Forum
12 years ago
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