Causes of dry eye
Posted , 3 users are following.
I have been taking methotrexate for over 8 years for the treatment of rheumatoid arthritis, which I have had for most of my adult life, and then about 4 months ago my consultant suggested I started taking Hydroxycholoroquine as well as he thought that might further reduce morning stiffness and associated symptoms.
After several months of taking the extra mediation I did notice an improvement in my condition although towards the end of that period I started to get sore and a gritty feeling in my eyes in the evening only eased by closing them. I then happened to go to an optician with a view to trying contact lenses but he told me I had a significant case of dry eyes that he said was caused by the use of immunosupressants and suggested it damaged the cells that produce the tears and corneal lubricant.
When I did some online research I discovered that Sjogrine’s syndrome is when an autoimmune condition affects the tear and other similar glands and that Hydroxycholoroquine has been used for the treatment of dry eye rather than causing it. So I am now rather confused and unsure whether to stop the additional drug and get back to the state it was a few months back when I was only taking methotrexate, or to push on through it.
It does seem strange that the dry eye condition has only arisen since I started the additional drug rather than just creep up on me anyway in my late fifties.
Can anyone relate to this or give me some ideas? Thanks, Jules
0 likes, 5 replies
Poemsgalore
Posted
but the Sjogren's began a few years before I started them. I was still on NSAIDS then. It didn''t get any worse on Methotrexate, so any immunosuppressants should help the condition, not make it worse. I have never used Hydroxychloroquine, so don't know how it affects it. I have stopped using Methotrexate now, I had to stop in February as I was due to have chemotherapy. But I still take 10mg of Leflunomide.
I use preservative free Hypromellose eye drops, Beconase nasal spray and either Glandosane Oral spray, or Biotene oral gel, as my Sjogren's affects my eyes, nose, mouth, and through my digestive system, giving me symptoms similar to IBS.
If your GP is treating your disease, ask for a referral to the rheumatology department of your local hospital, the doctors there are more expert with these auto-immune diseases.
A good website to visit, is the Arthritis Care website: This link will take you to a page which contains a pdf file about Sjogren's:
http://www.arthritiscare.org.uk/Search/search_results_page_view?SearchableText=sjogrens%20syndrome&origSearchableText=sjogren's%20syndrome
All the best, Poemsgalore
kevin132
Posted
I get dry eyes and also have a lack of saliva and a dry mouth.
This can also cause dental problems.
rose77485
Posted
Poemsgalore
Posted
The link above will take you to a pdf file about Sjogren's, one quote from it says:
"and you may also experience stomach or bowel discomfort. Less common symptoms include dry skin and kidney problems."
poemsgalore
rose77485
Posted