← Return to Map Dot Fingerprint Dystrophy
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Replies to "@bobr1040 hi, this is Rhoda @rckj. Sorry it took me a day to get back to..."
Rhoda
I also am sorry to here of your cornea troubles. All the best.
Hi Rhoda, this is Bob again. I'm almost 4 weeks from the debridement and very much improved. My vision has improved from 20/400 to 20/40 last week and I will be fitted for a new prescription next week. Your information was most helpful. I came to the realization that I too had to grin and bear it with the pain. However, if there is a next time I will demand pain pills for the peripheral pain. It helps some. I did get a few hydrocodone from a friend and while they did not reduce some of the direct pain it did help minimize the pain overall - eyelid, etc. I do have access to some corneal specialists in Dallas through several references. However if your specialist knows someone in Dallas he would recommend I would be glad to consider it. I will eventually have to have a cataract done in my left eye which also has the map dot dystrophy disease. I'm thinking I might want a specialist to do that if possible to avoid disturbing the disease. I would be interested if you could guide me in the direction of any books related to self-hypnosis. I have used alpha-genics and Sylvan mind control in the past but gotten away from it. I used my meditation to try to direct some healing with the eyes and would like to explore other possibilities if you recommend some. Thanks, Bob
Hi Rhonda this is janice and I live in Massachusetts. I have been diagnosed with this map dot fingerprint dystrophy and am being seen at mass eye and ear. My doctor is taking a conservative approach with the contact lens, drops, lubricants, antibiotics, etc. I am frustrated as I am self employed and have been dealing with recurrent erosions for several months. At what point does a doctor recommend surgery and is my ability to d Ed or know severely impaired. Should I see dr Raizman? Ty janice
Hi Rhoda! I'm Rachel and I found some of what you said very interesting. I have Fuch's dystrophy. I needed cataract surgery and cornea transplants when I was 43. Between the 2 procedures, my sensitivity to light was to have been dealt with. Unfortunately, it was not and grew worse. I know all about hiding out in the dark, living under hats and behind sunglasses. No more movie theaters, fireworks, concerts etc...Light sensitivity is normal during the healing time after surgeries but my healing apparently never ended. I used to drive home in the dark from work wearing dark sunglasses. Kept my cataract glasses for a long time. The snow and rain would make matters so much worse due to glare. It was very dangerous. Always worried about not seeing a pedestrian on the side of the road. My cornea specialist could never understand why this was and I was referred to a neuro-opthlemologist who blamed it on scar tissue from my past surgeries and oh yeah, I have blue eyes...what a crock! Last winter I finally threw in the towel. It's been 6 years now and each year has gotten worse driving at night. Sharp pains like daggers in my eyes on top of enducing migraines made me give up driving. Even as a passenger I need to wear hats and dark glasses and keep my eyes closed tight when car lights flash by. Often I may lay down in the back seat to avoid well lit areas, traffic lights and cars. This year I was diagnosed with small fiber peripheral neuropathy and can not help but wonder if the fact that there are a large amount nerve fibers in the corneas, it may be the contributing factor to my photophobia. Could neuropathy possibly do this? There is a cornea confocal microscope used for diagnosing SFPN so it only makes sense to me that there would be a connection.I have a message in to my neurologist to shed some light (no pun intended) and my cornea specialist has yet to weigh in. I'd appreciate your thoughts or anyones thoughts for that matter. Mayo Clinic in MN turned me down so why not ask here?Thanks a bunch and I hope you are having an uplifting day!!!
Rachel