Hi All
For the past week I keep having episodes of burning in my eyes, like smoke or some other noxious irritant. Just wondered whether it could be to do with hydroxy. I have not seen my ophthalmologist in almost 2 years Should I be concerneded, or (like I am prone to do, ignore).
Thank you lovely people.
Babs xx
Could be dry eye - and you need to see at least a really good optician at least every 2 years.
Eye tests are recommended every year on hydroxchloroquine.i had mine done in sept
Didn't notice that, oops. But surely THAT should be up to the rheumy to emphasise?
Yes it should and mine does but once I had my first eye test on hydroxchloroquine my optician sends me a reminder x
Do you not get a baseline assessment?
I get a full eye test and have the amsler scale chart at home on my fridge.i think it's the colour spectrum test they dont do I think the hospital do that one but I'm not sure 🤔
Sorry it's the cambridge colour test x
Hi I would definitely not ignore , I ended up at eye hospital as I was on hydroxychloroquine and it really messed with my eyes so had to come off it - you should be seen at least yearly whilst on hydroxychloroquine x
Your eyes should be tested every year whilst taking hydroxchloroquine as it can cause retinal toxicity. You could try some hypomellose eye drops.i have sjorgens which causes dry eyes and that's what I use xx
Hi
I have lupus and sjogrens which is common to have more than one autoimmune condition and I suffer with dry eyes, burning sensation as well. I have ointment for nighttime and use drops during the day which helps alleviate the symptoms. Also, like everyone has said, make sure you have your eyes checked. My rheumatologist sorted that out for me.
Some local opticians are emergency eye clinics for your local health authority .Find out yours and have an appointment you don’t need to pay as it is NHS.
Hi Babssara,
I recommend that you get your eyes checked to monitor if any changes have been made to your eyes since your last appointment.
A burning sensation of the eyes can be associated with Sjögren’s syndrome. Sjögren’s syndrome can cause dryness of the eyes, mouth, nose and vagina.
We published a blog article on coping with dry eyes and mouth, the article contains some general tips for preventing dry eyes which you may find helpful - lupusuk.org.uk/dry-eyes-and...
The NHS Choices’ website provides information on various types of treatments to help relieve the symptoms associated with Sjögren’s syndrome which I hope will be of help to you: nhs.uk/Conditions/Sjogrens-...
Best wishes,
Chanpreet
Hi Thanks. I have been diagnosed with Sjogrens, Hughes and a couple of other SLE little pathways. But my eyes (and skin) are causing my sleepless nights.
Babs x
As many have written already, it sounds like Sjogrens. I have both SLE and Sjogrens. My eyes are slowly getting worse. I see an ophthalmologist every 6 months and currently am getting fitted for scleral lenses (PROSE device) to help with the dryness and irritation. I’m also on blood serum tears (eye drops made from my blood serum) which are really great.
If I were you I’d go see an eye specialist to see what’s going on.
Please go to your optician. I had mine tested every six months on Hydroxychloroquine 400 mg so when they upped the dose to 600 mg the Optician spotted the problems immediately and sent me to the Macular Unit. Good luck xx
When taking hydroxychlorquine I have to see the eye doctor every 6 months and I also have dry eyes and use xiidra eyedrops
Dry eyes question and cancelled appointment :(
Dry eyes
Red and painful eyes
problems with my leg
