episcleritis- painful inflammation of the eye

New Topic Post Reply Printable Version
[ << Previous Thread | Next Thread >> ]

jla
Regular Member


Date Joined May 2005
Total Posts : 75
   Posted 7/8/2008 8:32 PM (GMT -7)   
does anyone have episcleritis with their crohns ? I have a reoccurance of this on a weekly basis as soon as I taper off of the eye drops. It hurts very bad also. I have been on humira weekly dosing and low dose of pred. with minimal benefits now. (initial response was great but have lost response).
thanks,
jamie

Shoshanna
Regular Member


Date Joined Feb 2008
Total Posts : 91
   Posted 7/8/2008 9:05 PM (GMT -7)   
Jamie,

I am sorry to hear you are having problems with your eyes. I have Uveitis and I know that I have to do a slow tappering of prednisone eye drops or it just comes back quickly. As for the humira I can't help you I can't take it due to having problems with Remicade to include a cranial bleed.

Shoshanna
CD diagnosed 34 years ago
Stem Cell Transplant may be back on
Lap-assisted Ileocolic Resection- February 2008
Ankylosing Spondylitis
Uveitis
Back on Prednisone - I hate it
Methotrexate
Ranitidine HCL 
Prednisone 1% (eye drops)
Maxidex  (eye ointment)
Homatropine 5% (eye drops)
B12, Folic Acid, Vitaman D, Calcium


bentwistle
Regular Member


Date Joined Jul 2006
Total Posts : 330
   Posted 7/10/2008 4:34 PM (GMT -7)   
I've also had eye issues - uveitis and episcleritis have both been diagnosed on occasion - I'm just tapering from another round of eye drops for uveitis that was particularly painful. I really sympathize with you. I'm on remicade and this is the first time my eye has bothered me since I started it (6 infusions ago). I always think of my eye problems as a window to my crohn's inflammation (when the eye flares - usually bad things are happening within too). I hope this isn't a sign that the remicade is not working properly anymore. (Although I had other indications that I might be developing antibodies and the effectiveness is reducing).

Thanks for starting this post.

Bev

Writer
Regular Member


Date Joined Aug 2006
Total Posts : 443
   Posted 7/11/2008 7:06 AM (GMT -7)   
Those of you with inflammatory eye disease who may be losing response to biologics
 
I've mentioned this case report before, but I think it worth repeating for those of you who have particular concerns about eye disease. It describes a patient with Crohn's and scleritis, as well as psoriasis that developed while on Remicade. (She'd already tried the other standard Crohn's medications.). Her scleritis originally responded to Remicade, but returned as she lost response to the drug. Remicade was withdrawn and she was started on total enteral nutrition (special liquid diet use for people with Crohn's) instead. Her psoriasis started to improve in four days, and she regained her vision in the eye affected by scleritis within three weeks. After reaching remission, she was able to maintain full remission on a maintenance regimen of two regular meals per day plus two meals of enteral nutrition per day. Granted, sticking with a liquid diet is not the easiest treatment for a disease, but it's good to know there is another treatment possibility out there if you run out of medications to try.

indigosunrise
Regular Member


Date Joined Nov 2007
Total Posts : 497
   Posted 7/11/2008 7:53 AM (GMT -7)   

Hi Jla,

I have had both Episcleritis and Scleritis.  Mine started a little over a year ago, with Episcleritis in both eyes.  I tried several drops--Tobradex, Fluromethalone, Prednisolone--and they would help, but then a few months ago, my left eye got really bad and the doctor said it was now Scleritis. 

I am currently on Prednisone and Methotrexate, to help with the inflammation.  I also am using Acular eye drops for the pain, as needed.

My heart goes out to you because both conditions are very painful and even when mine seemed to be going away, it always came back.  In fact, after having Episcleritis for about 6 months, I went to see my Internist and she immediately suspected Crohn's.  I was just diagnosed a few weeks ago (long story). 

I have noticed a link now to my eyes and my stomach issues.  Before I had even heard of Crohn's, I remember last summer, when both my eyes were bad, having bad stomach problems, but I always thought it was something I ate or a nerves, etc.

Please keep us posted and please feel free to ask me anything.

Take care,

Indigo

 

 

 


justarose4him
Veteran Member


Date Joined Feb 2004
Total Posts : 730
   Posted 7/11/2008 9:59 AM (GMT -7)   

Now this is all making sense to me !

Can you tell me who dx your eye issues...

I only had an optomitrist give me some kind of dx ; but he didn't know much about it because what he told me to do was making me worse ..then I saw a cataract specialist that is in the area where I work - he said it is strojens disease - but would not say it in writing or be definite about it ...but got me started on a steroid drop and lacerites. ( I finished with them about a month to 6 weeks ago )

Meanwhile I have had 3 infusions of remicade - and I didn't think it was working ..but my eyes have gotten better ...I still have to put the drops in each night and day or they will get bad again ...but I am not needing the $150 per month med ( thats with ins! ) that he prescribed as a forever drop !  

So...maybe they have really gotten better because of the Remicade ??? !

Well, I see a NEW GI next week ...hopefully he will know more of this disease then the other ?@$% that I was / am seeing ... I have been so patient with him and his office but just can't do it anymore ...they are simply incompetent .. and trust me I don't curse !! At all ! But this was easy to use those symbols to express my feelings tongue


Dx with Crohns 25 years ago
1 surgery ; 16 years ago ... 
Cervical DDD and restless leg syndrome
Currently on ;  Requip ,  cymbalta, dIovan HCT, tramazone,
Remicade, FML (eyes ; steroid ) , Restasis (eyes)   
 


Dave D
Regular Member


Date Joined Aug 2005
Total Posts : 404
   Posted 7/11/2008 10:57 AM (GMT -7)   

After 10 Remicade infusions, I'm finally on top of mine for now. I had to have a top specialist from Baskin Palmer Eye Institute in Miami lead me through the treatment after having my local Opthamologist plus a Retina Specialist give up. She said for treating the eye, Remicade should be given every 4 weeks for best results. After two retina detachments and going down to 20/400, mine is much better. But all the Prednisone I took this last 1 1/2 years really advanced a cataract I was growing. The cataract was removed June 5, and now my eyesight is 20/30 in the bad eye. I still watch my eyes like a hawk. If I get a "sinis" headache, like I thought the original pain was, I take a single dose of 50 mg of Pred instead of any pain killer. It works. I don't want it to get ahead of me again.

This was the worst 1 1/2 years of my life anticipating blindness.

Dave D


Retired male in late 60's. Perforated Colon in 92. Diagnosed as Ulcerative Colitis in 93. Uncontrolled flareup in 97 dictated J-pouch surgery. 04 Capsule endoscopy diagnosed as Crohns not UC. Emergency surgery in 05 to remove lodged camera capsule. Biopsies positively diagnosed Crohns at that time. 12/06 Unsucessfully tried Naltrexone(LDN). 2/07 developed scleritis of the eye, tearing and detaching the retina. Treated with high doses of Prednisone. 6/07 Thought eye was healing and started taking Entocort counting on the residual (non-systemic portion) as treating the eye. Wrong. In October eye was not stabilized. 11/07 Started Remicade to try and reduce the ocular inflamation of the Scleritis since I had been requiring more and more Prednisone to keep the eye quiet. 12/07, retina tares and detaches again. Started Remicade every 4 weeks plus 20mg of Prednisone per day. Six months and seven infusions later, good eye is back to 20/14. Bad eye is 20/70. Had cataract surgery on June 05 on bad eye. Eye returned to a correctable visionary level of 20/40. Life looks good (literally) today.
Married with 4 grandkids.


indigosunrise
Regular Member


Date Joined Nov 2007
Total Posts : 497
   Posted 7/11/2008 3:20 PM (GMT -7)   
My Optometrist first diagnosed the Episcleritis and when it was not going away, I went to see an Opthalomologist who diagnosed it as the same thing. 
 
When it got really bad, my Opthalmologist said it was Scleritis--he also said you can have both Episcleritis and Scleritis together, and he thinks that may have been my case in the one eye. 
 
Anyhow, he said that eye drops work for Episcleritis but do not work for Scleritis because it is a deeper inflammation. 
 
I really hope your new GI helps you!  My situation might be somewhat the same, in that my first GI did not diagnose me with Crohn's--I think she was looking for a biopsy that comfirmed Crohn's.  I saw the second GI maybe about a month ago, and he believes it is Crohn's and I had the small capsule done about two weeks ago.  My follow up with him isn't till August--ugh!  But I am thankful he is going to be willing to treat it!  He also believes that once I am on the appropriate medicine, my eye inflammation and arthritis will go away as well, and I hope they do! 
 
Take care and be sure to let us know how you are doing!
 

jla
Regular Member


Date Joined May 2005
Total Posts : 75
   Posted 7/11/2008 9:26 PM (GMT -7)   
the opthamologist diagnosed me with this. I see an opth. for my eyes bc he is a medical doc. and familiar with this condition in people with crohns. My GI doc. recognized what it was right away and referrred me to the eye doctor.

My doc. wants me to keep taking the humira and pointed out that I have almost completely weaned off prednisone since starting the humira. I agree that it is helpimg me somewhat. joint pains are significantly better. I am having a big increase in running to the bathroom, pain and bleeding. The inflammation is very painful in the bum !How much is the question ? He is very well known in my area for doing research in crohns.I trust him and think he knows whats best but I just want to feel better and do not think I am feeling as well as I could be. He is unsure about cimzia helping me anymore than humira. Tysabri is to risky for me. He wants to hold off on the stem cell treatment study for now. I feel like I am not sure what to do.
thank you all for your support ! This disease is very hard to struggle with alone !
jamie
New Topic Post Reply Printable Version
Forum Information
Currently it is Friday, December 02, 2016 9:48 PM (GMT -7)
There are a total of 2,731,950 posts in 300,977 threads.
View Active Threads


Who's Online
This forum has 151137 registered members. Please welcome our newest member, Country girl2.
271 Guest(s), 2 Registered Member(s) are currently online.  Details
NewspaperLover, cilly


Follow HealingWell.com on Facebook  Follow HealingWell.com on Twitter  Follow HealingWell.com on Pinterest
Advertisement
Advertisement

©1996-2016 HealingWell.com LLC  All rights reserved.

Advertise | Privacy Policy & Disclaimer