HiThanks noblehead. All my ophthalmologists seem to have a different theory about what it is. Guess I'll just have to wait and see. Have had other side effects too (droopy eyelid now and enlarged cataracts doing in either eye ich may or may not sort themselves out.
I was hoping for everyone to say " don't worry that's normal and will all fix itself"oh well I can still hope. I can at least see out of the eye again which is an improvement.
Sorry to sound like a moaning Minnie. Am not really. Kinda just comes out that way sometimes when I get on a roll Doh!!!
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All my ophthalmologists seem to have a different theory about what it is. Guess I'll just have to wait and see. Have had other side effects too (droopy eyelid now and enlarged pupil) which may or may not sort themselves out.
I was hoping for everyone to say " don't worry that's normal and will all fix itself"oh well I can still hope. I can at least see out of the eye again which is an improvement.
Sorry to sound like a moaning Minnie. Am not really. Kinda just comes out that way sometimes when I get on a roll Doh!!!
Hi all, I haven't been on here for a while but really wanted to come back and let people know how things have gone for me since developing severe proliferative retinopathy in march 2012.
I have had many thousands laser shots in each eye and ended up needing a vitrectomy operation to remove the vitreous gel in each eye. There was a time that my vision wad sooooo bad becausefof the amount of blood in my eyes that I literally could not see things other than outlines and shapes. 1 year after my last and 18months after my first vitrectomy i have just been given my 3 year licence from the dvla. Something that I thought would never happen.
I finally found an amazing consultant, after having two others that seemed to just want to laser away. It was my now consultant that said I needed the op as there was part of my retina that was being pulled thus causing the constant bleeds. I do have a partial detachment in both eyes but fortunately these are far enough in my periferol vision not to affect my driving.
I know how scary it can be when you are first diagnosed with this awful condition and I wanted to give you hope that no matter how bad things might seem there is always a chance it could be stabilised. I know im one if the very very lucky ones and not everyone will have the same outcome but there is a possibility. Sometimes a little bit of hope goes a long way
if anyone gas any questions regarding my situation I am more thsn happy to share my journey. I'm no pro im just someone who's been there.
Wishing everyone the best outcome possible. Best wishes to you all xx
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