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Patients Psoriatic arthritis
Does anyone struggle with eye problems?
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LizziB
Community managerGood advisor
LizziB
Community manager
Last activity on 02/04/2024 at 00:46
Joined in 2022
280 comments posted | 7 in the Psoriatic arthritis Forum
19 of their responses were helpful to members
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Hi @JennaRra
How are you doing today?
I am sorry to hear about your dry eyes. If after a few days, your eyes don't clear up, I would suggest going to see a physician for a check up, just to make sure it is not an infection. But let me tag a few other members - they may be able to share whether or not they have experienced something similar and what they did to make their eyes feel 'normal'
@Alim244 @Parranquet @HazelWilliams @FionaV @Jenfa69 @Torrie @Nuttree @Karen1965 @Trishb @AustinS @Lisam76 @Arthur1234 @Loneshania @DawnieB @ziggy7678 @Debz70 @Sonia1983 @Sam4095 @MellyFlay @Sarahbar @Debbie76 @Jan160261 @Ashley @FrustratedSufferer @ClaraJane2022 @LarnyG @Inès_ra_uk198 @lyndoneyles1 @kateheath @hela-am
Have you experienced any eye issues like dry or red eyes? Did you go to the doctor or did it eventually resolve itself? If OTC drops don't work, do you have any other suggestions?
Thanks in advance for sharing!
Take care,
Lizzi from the Carenity team
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Lizzi
DeenieBop
DeenieBop
Last activity on 27/11/2024 at 22:46
Joined in 2017
1 comment posted | 1 in the Psoriatic arthritis Forum
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Hi there, I’ve just been diagnosed with MGD which can be one of the symptoms of PsA.
I was going through a lot of drops and my eyes were very dry and sore.
As well as tear ducts we have oil glands on upper and lower lids, which get blocked meaning there is no oil to stop tear duct water from drying out.
a heat mask twice a day, cleaning eyelids after with tea tree oil wipes and then eye drops has been an absolute lifesaver.
if you google Meibomian Gland Dysfunction you’ll get more info, hope that helps x
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reikiboo64
@Courtney_J
Hi
Well where do I start!
I get frustrated by the constant exhaustion in my muscles. The slightest action feels like I have just done a work out to that part of my body whether it be an arm or a my legs for example.
I am aware that my disease isn't managed at all yet even though I have been diagnosed 18 months or so. It just feels like Russian Roulette with my medication as to whether I will be allowed to continue it from one blood test to the next as my liver rebells.
Everyday a new part of my body starts to creak and feel stiff and painful. To be honest it's scaring me just how quickly things are progressing. It is really getting me down. I can't walk far, self care is difficult . I'm determined to be independent so I'll struggle to succeed in the task.
I want to have the energy to get through my day as I work full time running a women's refuge which is mentally very demanding but fortunately not too physically. I'm so tired at the end of each day. It's an uncomfortable exhaustion. I also suffer from Narcolepsy diagnosed at a similar time to the arthritis, and this also gives me fatigue- I have a double whammy of fatigue.!
I am shielding at the moment so I have had a chance to rest. The first week off work I slept solidly and now I feel more rested. I confess I am anxious about becoming so exhausted again but I am determined this illness won't stop me from doing what I love.
Overall I feel distressed with it all and just want it to go away, My healing has gone to pot. I have put weight on as I can't exercise, I dread going upstairs and at times I just don't know how to deal with it.
Sorry to sound so down hearted, I just don't feel I can bring any positivity to this discussion.
x..
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reikiboo64
@Courtney_J
Hi
Well where do I start!
I get frustrated by the constant exhaustion in my muscles. The slightest action feels like I have just done a work out to that part of my body whether it be an arm or a my legs for example.
I am aware that my disease isn't managed at all yet even though I have been diagnosed 18 months or so. It just feels like Russian Roulette with my medication as to whether I will be allowed to continue it from one blood test to the next as my liver rebells.
Everyday a new part of my body starts to creak and feel stiff and painful. To be honest it's scaring me just how quickly things are progressing. It is really getting me down. I can't walk far, self care is difficult . I'm determined to be independent so I'll struggle to succeed in the task.
I want to have the energy to get through my day as I work full time running a women's refuge which is mentally very demanding but fortunately not too physically. I'm so tired at the end of each day. It's an uncomfortable exhaustion. I also suffer from Narcolepsy diagnosed at a similar time to the arthritis, and this also gives me fatigue- I have a double whammy of fatigue.!
I am shielding at the moment so I have had a chance to rest. The first week off work I slept solidly and now I feel more rested. I confess I am anxious about becoming so exhausted again but I am determined this illness won't stop me from doing what I love.
Overall I feel distressed with it all and just want it to go away, My healing has gone to pot. I have put weight on as I can't exercise, I dread going upstairs and at times I just don't know how to deal with it.
Sorry to sound so down hearted, I just don't feel I can bring any positivity to this discussion.
x..
See the best comment
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JennaRra
JennaRra
Last activity on 26/07/2023 at 15:24
Joined in 2023
2 comments posted | 1 in the Psoriatic arthritis Forum
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Well, my eyes have been giving me some trouble lately. My eyes hurt, get blurry, and are quite red. They don't itch the way allergies do. To keep my eyes moist, I've tried over-the-counter eye drops, but they don't last very long. What do you think about this?