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Dry eyes
Hi I have RA for years on lefluminide celebrex thyroxine b12 ,I have suffered terrible head and face sweating for a few years getting worse,just had cataracts done sight is fine but my dry eyes are causing me so much discomfort,I have hi lo tears and ikervis at night it's 5 weeks since cataracts done
Hi I have RA for years on lefluminide celebrex thyroxine b12 ,I have suffered terrible head and face sweating for a few years getting worse,just had cataracts done sight is fine but my dry eyes are causing me so much discomfort,I have hi lo tears and ikervis at night it's 5 weeks since cataracts done
Pansy78
in
NRAS
1 year ago
Sore slightly red eye lids - Cosopt
Hello all, I currently have COVID and it’s not very nice! I have noticed over the last couple of days that my eye lids are a little, red, sore and a tiny bit puffy could just be the redness though. I am currently only on Cosopt twice a day and have been for a few months. This is the first time my
Hello all, I currently have COVID and it’s not very nice! I have noticed over the last couple of days that my eye lids are a little, red, sore and a tiny bit puffy could just be the redness though. I am currently only on Cosopt twice a day and have been for a few months. This is the first time my
KBIOW
in
Glaucoma UK
1 year ago
UPDATE: Eyes Irritated, Itching, Etc.
The saga contines. Still mostly in bed 9 weeks now. No date for vertebral plasties or Zolendronic acid infusion...yet, inspite of many calls. My eyes are extremely irritated but now I know why. Made appointment (referred myself) to the Ophthalmology Clinic at the VG here in Halifax. Had to convince Resident
The saga contines. Still mostly in bed 9 weeks now. No date for vertebral plasties or Zolendronic acid infusion...yet, inspite of many calls. My eyes are extremely irritated but now I know why. Made appointment (referred myself) to the Ophthalmology Clinic at the VG here in Halifax. Had to convince Resident
Missus835
in
PMRGCAuk
1 year ago
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FND SUCKS
Hi I'm Debby and I'm in the USA in Utah. I have been dealing with constant pain all over, abdominal pain, constipation that lasted sometimes 17 days with no help from anything, slirred speech, loss of the ability to walk flat( I walk on my tipsy toes) and need a cane, walker or scooter to get around
Hi I'm Debby and I'm in the USA in Utah. I have been dealing with constant pain all over, abdominal pain, constipation that lasted sometimes 17 days with no help from anything, slirred speech, loss of the ability to walk flat( I walk on my tipsy toes) and need a cane, walker or scooter to get around
Luv2teezeu
in
Functional Neurological Disorder - FND Hope
4 months ago
I was diagnosed 4 years ago with relapsing remitting. In the MS community no one ever talks about lesions black holes or myelin. Why!
After my initial diagnosis on my next visit I asked my neurologist how many lesions I had. He said “ I don’t really know. This guy is one of the most renowned neurologists in the world. I said, how long have you been doing this? X years. Then what does your gut say? He said in between 50 and 75 but
After my initial diagnosis on my next visit I asked my neurologist how many lesions I had. He said “ I don’t really know. This guy is one of the most renowned neurologists in the world. I said, how long have you been doing this? X years. Then what does your gut say? He said in between 50 and 75 but
Mark1499
in
My MSAA Community
1 year ago
sjogrens
Hi Everyone, Diagnosed last Nov with PBC. 2 weeks ago I started getting a really bad taste in mouth and some dry mouth. The taste is terrible ! How do you treat this to get rid of taste? Does anyone have Sjogrens w/ PBC? What are the symptoms? How is this treated? I see my doc in Oct. Thanks
Hi Everyone, Diagnosed last Nov with PBC. 2 weeks ago I started getting a really bad taste in mouth and some dry mouth. The taste is terrible ! How do you treat this to get rid of taste? Does anyone have Sjogrens w/ PBC? What are the symptoms? How is this treated? I see my doc in Oct. Thanks
Samanthaann
in
PBC Foundation
1 year ago
visual disturbances and eye problems
Hi everyone, If have moth FND & FM and have had some strange things going on , does anyone have strange vision. I see eye floaters all day when my eyes are open and when I close my eyes but this has also developed into what I can only describe as black and white static vision. I’ve have issues with
Hi everyone, If have moth FND & FM and have had some strange things going on , does anyone have strange vision. I see eye floaters all day when my eyes are open and when I close my eyes but this has also developed into what I can only describe as black and white static vision. I’ve have issues with
Loobyloo1966
in
Functional Neurological Disorder - FND Hope
1 year ago
Hopelessness
I've been diagnosed officially with PTSD this week which is not a shock. I begin EMDR sessions next week so hope those are able to help. I have these bouts of feeling hopeless. I'm trying not to go too hard on myself but just feel that things will never get easier. Cry myself to sleep most nights with
I've been diagnosed officially with PTSD this week which is not a shock. I begin EMDR sessions next week so hope those are able to help. I have these bouts of feeling hopeless. I'm trying not to go too hard on myself but just feel that things will never get easier. Cry myself to sleep most nights with
Hidden
in
ICUsteps
5 months ago
visual snow and fibromyalgia
does anyone have strange vision. I see eye floaters all day and when I close my eyes but this has also developed into what I can only describe as black and white static vision. I’ve have issues with my eyelids not automatically opening too. Migraines are most likely linked but not the reason. It’s bizarre
does anyone have strange vision. I see eye floaters all day and when I close my eyes but this has also developed into what I can only describe as black and white static vision. I’ve have issues with my eyelids not automatically opening too. Migraines are most likely linked but not the reason. It’s bizarre
Loobyloo1966
in
Fibromyalgia Action UK
1 year ago
Tapering - have I got it wrong?
Hi. I am a new member and this is my first post. Diagnosed with PMR in March 2023, started on 15mg of pred on 31st March. It worked like a dream and within 48 hrs, my pain was down 70% and my energy was up 70%. I felt fantastic and within a month started slowly to increase my level of exercise and activity
Hi. I am a new member and this is my first post. Diagnosed with PMR in March 2023, started on 15mg of pred on 31st March. It worked like a dream and within 48 hrs, my pain was down 70% and my energy was up 70%. I felt fantastic and within a month started slowly to increase my level of exercise and activity
EnyaBlue
in
PMRGCAuk
1 year ago
What's your experience of coming of steroids
So I have my rheumatology appointment next week so hopefully will get a better understanding of what's going on. In the meantime I am on mycophenalate and a weaning dose of prednisolone for eye inflammation, started with 800mg in December and am now on 2.5mg before stopping in 2 months time. However
So I have my rheumatology appointment next week so hopefully will get a better understanding of what's going on. In the meantime I am on mycophenalate and a weaning dose of prednisolone for eye inflammation, started with 800mg in December and am now on 2.5mg before stopping in 2 months time. However
Autolupus
in
LUPUS UK
1 year ago
brain fog!
hi there, last year I had a closed angle glaucoma. I had little warning, thr blood pressure in my right eye suddenly shot up to 80 and I was temporarily blind in that eye. I had a week’s stay in hospital and an operation to bring the pressure down. It is amazing that I have retained quite a bit of
hi there, last year I had a closed angle glaucoma. I had little warning, thr blood pressure in my right eye suddenly shot up to 80 and I was temporarily blind in that eye. I had a week’s stay in hospital and an operation to bring the pressure down. It is amazing that I have retained quite a bit of
Belladoodle
in
Glaucoma UK
1 year ago
Good Morning Monday People
Good morning all, I haven't posted in a while since getting my ESA and starting EMDR. I've experienced a lot of improvement and have adjusted well to the Citalopram which leaves me feeling more alive than the Sertraline I was on. I've been feeling contemplative lately about motivation. What are some
Good morning all, I haven't posted in a while since getting my ESA and starting EMDR. I've experienced a lot of improvement and have adjusted well to the Citalopram which leaves me feeling more alive than the Sertraline I was on. I've been feeling contemplative lately about motivation. What are some
ClassicalBlueKitty
in
Anxiety and Depression Support
5 months ago
New Diagnosis: Right Eye Normal Pressure Glaucoma.
Apparently two yrs ago at my previous eye test with photos of the back of my eye, a note was made that there seemed to be something going on with the optic nerve. I wasn't informed. At my last eye test the new optician reported the same and told me of the previous photo. She referred me to the hospital
Apparently two yrs ago at my previous eye test with photos of the back of my eye, a note was made that there seemed to be something going on with the optic nerve. I wasn't informed. At my last eye test the new optician reported the same and told me of the previous photo. She referred me to the hospital
Timesarrow
in
Glaucoma UK
1 year ago
Ectropion eye
Has anyone any advice on ectropion eye? I have glaucoma and diplopia and have been advised to have an operation to tighten the bottom eyelid. This is on my good eye, so I am rather nervous about it.
Has anyone any advice on ectropion eye? I have glaucoma and diplopia and have been advised to have an operation to tighten the bottom eyelid. This is on my good eye, so I am rather nervous about it.
Tequilasunrise
in
Glaucoma UK
1 year ago
EYES DRY, ITCHY, BURNING, TEARING
My eyes have changed over the last few weeks. They are so dry, but I use eye gel. Tearing at random, blurry when reading. Feels scratchy and like there's somethinf in them. Eye drops help for less than an hour. When reading I find myself inadvertently closing my right eye, left eye is better. Yesterday
My eyes have changed over the last few weeks. They are so dry, but I use eye gel. Tearing at random, blurry when reading. Feels scratchy and like there's somethinf in them. Eye drops help for less than an hour. When reading I find myself inadvertently closing my right eye, left eye is better. Yesterday
Missus835
in
PMRGCAuk
1 year ago
Update
hi l have had a consultation this morning following up on me after surgeries and brachytherapy. The outcome is they can offer me no more radio, and am to carry on with my normal day to day life! To anyone out there who is thinking shall l or shall l not get professional guidance with my symptoms my
hi l have had a consultation this morning following up on me after surgeries and brachytherapy. The outcome is they can offer me no more radio, and am to carry on with my normal day to day life! To anyone out there who is thinking shall l or shall l not get professional guidance with my symptoms my
AlexaMac
in
Endometriosis UK
1 year ago
Pegasys --> Besremi and HCT
Hi, What a great forum - thanks to you all for contributing. I'm a 37 year old male - diagnosed with PV 3 years ago. I recently made the jump from Pegasys to Besremi. I was on 135ug every 9 days without need of supporting venesection (at least for the last 8 months or so). Since switching medication
Hi, What a great forum - thanks to you all for contributing. I'm a 37 year old male - diagnosed with PV 3 years ago. I recently made the jump from Pegasys to Besremi. I was on 135ug every 9 days without need of supporting venesection (at least for the last 8 months or so). Since switching medication
Swede99
in
MPN Voice
1 year ago
Supplements to reduce glutamate
I was inspired by Widebody's comments on taurine and glycine to look into supplements that reduce glutamate. I found the following on an autism website that I cannot vouch for, but here is the list: (those of us taking gabapentin, pregabalin, horizont are taking medicine that is reducing brain glutamate
I was inspired by Widebody's comments on taurine and glycine to look into supplements that reduce glutamate. I found the following on an autism website that I cannot vouch for, but here is the list: (those of us taking gabapentin, pregabalin, horizont are taking medicine that is reducing brain glutamate
wantokporo
in
Restless Legs Syndrome
11 months ago
Longtime glaucoma patient
Hi. I just wanted to say that my experience with Glaucoma has been over many, many years. I’ve been very fortunate to have had treatment, isoptocarpine which was horrible. I have Myopia and these drops made it almost impossible to see for any length of time. They were to reduce the eye pressure quickly
Hi. I just wanted to say that my experience with Glaucoma has been over many, many years. I’ve been very fortunate to have had treatment, isoptocarpine which was horrible. I have Myopia and these drops made it almost impossible to see for any length of time. They were to reduce the eye pressure quickly
Dougalldoo
in
Glaucoma UK
1 year ago
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