Hello friends (since that is what i consider you all even though ive never met you). My sister helensy has been kindly posting on my behalf

. My name is Becky, 31, if you want the statistics. I got diagnosed with Keratoconus in 2001 and had hydrops then to. I have been stable for 6 years without any type of lenses. The excellent vision in my left eye does a wonderful job at compensating for very blurry in the right. Got told couldn't wear any types of lenses as my eyes are very dry and extremely sensitive. The last two weeks have been a whirlwind of emotions before being told it was acute hydrops in my right eye which has the KC.I was sent to emergency opthalmology department on the 30th may and told to put saline drops and mydrilate drops in. I then saw the consultant on the 7th june who confirmed acute hydrops.Got very gd pair of sunglasses, getting better at light tolerance, feeling in major pain a lot of the time and nauseaus.Also on homeopathic tincture which tastes vile but hoping it helps

I have been off work for 12 days. Does anyone have any ideas/suggestions on anything else that would help please. Im really trying to sit and ride this out dont remember how long it lasted last time. feeling exhausted and frightened. Thanks to gareth and andrew. Becky [/list]