Just been diagnosed with an ulcer on ... - Hughes Syndrome A...

Hughes Syndrome APS Forum

10,484 members10,661 posts

Just been diagnosed with an ulcer on my cornea, is this common for APS sufferers or completly unrelated?

AllyB68 profile image
5 Replies
Written by
AllyB68 profile image
AllyB68
To view profiles and participate in discussions please or .
5 Replies
MaryF profile image
MaryFAdministrator

Hi there, they need to check you out for sjogrens syndrome! This is quite common with APS. Hope it heals up soon. Mary F x

AllyB68 profile image
AllyB68

Thank you Mary, I have got daily check ups with the eye doc so I will ask tomorrow.

Izzchick profile image
Izzchick

I've had this several times, it first occurred at the time when I tried wearing contact lenses as a teenager ,and at the time was thought to be related to the herpes/cold sore virus.

I now wonder if it was related to having dry eyes as a result of my autoimmuneness; my eyes were extremely dry on Schirmers testing last year, and i've never got on with contact lenses.

Hope this helps, AllyB68. :-)

siveinvan profile image
siveinvan

Hmmm, I had some oddball thing called Map-dot Dystrophy about 12 years ago. Had to have my corneas resurfaced with a laser. I wonder if there is a connection with Hughes. Wouldn't be surprised.

I just had one in April of this year. Not sure of the cause but two things specialist mentioned were the APS/Lupus as a cause and also herpes virus is known to cause it, but they didn't test for anything. I took drops for a few weeks and it went away. Felt like it was coming back so I used drops for a few days and it seems fine now.

I have noticed that my eyes are drier lately than they have in the past, and get irritated and sore, redness as well.

Not what you're looking for?

You may also like...

Just been diagnosed with Aps

Hello my name is Sally. And have just this week been diagnosed with Aps because of recurrent...
Sally27 profile image

Hi everyone I just wondering if anyone in my area has been diagnosed with APS.

Hi, my name is Stephanie L., though I go by Soul Rebel on line. I live in Roswell, NM. I was just...

Not sure if numbness is from the APS or from issues with my neck

Hi everyone I was diagnosed with APS in 2005. Prior to that they said I had 'probable' MS this was...
Juejue11 profile image

I am new to this site, six mos post broken ankle and resulting dvt, just diagnosed with APS

Six mos. ago I was post five IVF failures and had selected an egg donor, and was ready to start my...
Sandrapanda profile image

Is it true that with an APS diagnosis you can not have either and Ablation or a Hysterectomy.....???

Just back from Gynecology Appointment where I was told that because of my APS and Warfarin use that...
loppylou68 profile image

Moderation team

See all
MaryF profile image
MaryFAdministrator
KellyInTexas profile image
KellyInTexasAdministrator
HollyHeski profile image
HollyHeskiAdministrator

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.