Hi everyone,
I'm really glad I found this site- I'm not the only one out there dealing with this awful syndrome with a very benign sounding name!
I'm 37, and married mother of two. I was diagnosed with DES 9/2011 with a STT(2) of 3mm (yikes!) OU, and mild to moderate mybomian gland dysfunction with "sludgy" mybomian gland secretions. This diagnosis followed many months of frequent red looking eyes that I pretty much ignored (big mistake) because I wasn't in any discomfort. By September however, I was having discomfort and finally went to see an ophthamologist. From that point things seemed to move quickly downhill- I found that pretty much any and all drops are totally intolerable to my very sensitive eyes. I seem to have stabilized and improved somewhat however after getting punctal plugs in both my upper and lower puncta. Yes, I have the occasional spillover, but I will take that ANY DAY over what I was dealing with a month ago. This has also allowed me to tolerate medications much better. MY bloodwork so far has been negative for any systemic autoimmune disease, but a hormonal profile revealed low testosterone (low to low normal). I've been very aggressive and experimental with my treatment, so here's my little regimen so far. . .
Punctal plugs- upper and lower
Restasis 4X/day
Autologous Serum drops- used when I get that "burning tears" sensation
Castor oil drops
4000mg Fish Oil daily (for Omega 3)
100mg Doxycycline/day
Hot compresses and mybomian gland "massage"
5mg of Androgel daily (subcutaneously absorbed testosterone) to hopefully improve mybomian gland function
Humidifying goggles courtesy of this site which I would recommend to ANYONE needing extra relief
By far I am finding the toughest battle so far however to be with my emotions following this diagnosis. I am worried, angry, depressed, and really struggling with my diagnosis and a feeling of isolation. I hate my "new eyes" and am really mourning the loss of my old ones. Add to my above regimen 10mg of Paxil a day and 0.5mg Klonopin twice daily for these reasons. So far I'm not feeling much benefit of the Paxil (which has worked for me at that dose in the past) and would love to up the dose- but given its dry eye side effect am scared to do so- aaaah, the catch 22! Thoughts anyone?
In any case, I thought I'd finally post instead of just "lurking". This site has given me some good ideas for treatment and has helped me see that I'm not alone.
Thanks,
MLE
I'm really glad I found this site- I'm not the only one out there dealing with this awful syndrome with a very benign sounding name!
I'm 37, and married mother of two. I was diagnosed with DES 9/2011 with a STT(2) of 3mm (yikes!) OU, and mild to moderate mybomian gland dysfunction with "sludgy" mybomian gland secretions. This diagnosis followed many months of frequent red looking eyes that I pretty much ignored (big mistake) because I wasn't in any discomfort. By September however, I was having discomfort and finally went to see an ophthamologist. From that point things seemed to move quickly downhill- I found that pretty much any and all drops are totally intolerable to my very sensitive eyes. I seem to have stabilized and improved somewhat however after getting punctal plugs in both my upper and lower puncta. Yes, I have the occasional spillover, but I will take that ANY DAY over what I was dealing with a month ago. This has also allowed me to tolerate medications much better. MY bloodwork so far has been negative for any systemic autoimmune disease, but a hormonal profile revealed low testosterone (low to low normal). I've been very aggressive and experimental with my treatment, so here's my little regimen so far. . .
Punctal plugs- upper and lower
Restasis 4X/day
Autologous Serum drops- used when I get that "burning tears" sensation
Castor oil drops
4000mg Fish Oil daily (for Omega 3)
100mg Doxycycline/day
Hot compresses and mybomian gland "massage"
5mg of Androgel daily (subcutaneously absorbed testosterone) to hopefully improve mybomian gland function
Humidifying goggles courtesy of this site which I would recommend to ANYONE needing extra relief
By far I am finding the toughest battle so far however to be with my emotions following this diagnosis. I am worried, angry, depressed, and really struggling with my diagnosis and a feeling of isolation. I hate my "new eyes" and am really mourning the loss of my old ones. Add to my above regimen 10mg of Paxil a day and 0.5mg Klonopin twice daily for these reasons. So far I'm not feeling much benefit of the Paxil (which has worked for me at that dose in the past) and would love to up the dose- but given its dry eye side effect am scared to do so- aaaah, the catch 22! Thoughts anyone?
In any case, I thought I'd finally post instead of just "lurking". This site has given me some good ideas for treatment and has helped me see that I'm not alone.
Thanks,
MLE
Comment