Bloody Hell. Thanks for that advice - very useful and important for those of us who live in the UK.
I sometimes wish I could transfer or share how it feels to live with DES to the Doctor for a day/week - I think you'd get a lot more understanding then!
In fairness to the NHS, after a poor initial start ("migraines" my arse), I've seen some people who are at least trying. I might not get anywhere, and I reserve the right to change my opinion if the NHS becomes distinctively unhelpful though.
It's frustrating when your eyes look OK (my anterior margins and the white of my eyes are OK), and professionals can't see what you are moaing about, but you know it's severely affecting your life. Many people on here have thoughts relating to exiting this existence, and whilst I have no immediate plans, let me say that the idea of 40 approx years of DES suffering does not appeal. This is _not_ a minor issue for many DES sufferers.
Have you considered escalating to your PCT?
I sometimes wish I could transfer or share how it feels to live with DES to the Doctor for a day/week - I think you'd get a lot more understanding then!
In fairness to the NHS, after a poor initial start ("migraines" my arse), I've seen some people who are at least trying. I might not get anywhere, and I reserve the right to change my opinion if the NHS becomes distinctively unhelpful though.
It's frustrating when your eyes look OK (my anterior margins and the white of my eyes are OK), and professionals can't see what you are moaing about, but you know it's severely affecting your life. Many people on here have thoughts relating to exiting this existence, and whilst I have no immediate plans, let me say that the idea of 40 approx years of DES suffering does not appeal. This is _not_ a minor issue for many DES sufferers.
Have you considered escalating to your PCT?
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