This is to let you know that we have launched a new website for people with birdshot. We are base in the UK but all are welcome. it is a patient information website linked to Uveitis Information Group, a scottish charity, but specifically with information for people with birdshot chorioretinopathy.
As it is a new site we know it is not perfect and we would welcome comments and feed back so that we can change it to make it more user friendly. We are not IT specialists so forgive us if it we have a few hiccups.
However please do give it a visit and register if you would like to receive further information in the future.
We are to help and we would love it if you visited the site.
Rea and I were inspired to get this up and running after Dr Foster's conference for doctors and people with birdshot in October last year.
He is an inspiration to us for helping patients get better treatment.
if you google us we are are lsited under birdshot uveitis society, but we come up under birdshot uveitis or birdshot socieity.
No good on AOL at the moment, but it takes a little time for search engines to pick us up.
Please keep trying - sometimes it takes a couple of goes for the server to connect. I have not idea why. All coomments gratefully received. Annie and Rea
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