Small update from me
Posted: Tue 12 Jun 2007 3:43 pm
Only a few people in here know me as I only remember about this group ater appointments.....stupid really I should hang around more often.
Anyway, had a small lens check today, no further progression in my right eye which has been static now for 2 years. However, I am on the verge of losing these beautifully comfortable kerasofts for a gas permeable in my left eye which would be a shame, but probably a necessary step.
Asides from that I have had a good few months, I probably should confess to being a hyperchondriat and fearing I had moto neuron disease from searching what a flutter sound in the ear could be. Went to the doctors paranoid and she assured me that a muscle twitching in the ear, or anywhere in the body for that matter (even the tongue) would have to be accompanied by upper motor neuron damage and severe weakness and atrophy (wasting of muscles) before they even send you to a neuro to confirm diagnosis. so that wasa relief. It got me thinking though about info on KC on the net and there isnt enough if you dont know where to look. Wikipedias page sums it up really well, but not too many people know how resourceful wikipedia can be and even then...it is authors opinins.
anyway hope everyone is well, ill hang about and reply to posts more often! How are the rest of you guys
Anyway, had a small lens check today, no further progression in my right eye which has been static now for 2 years. However, I am on the verge of losing these beautifully comfortable kerasofts for a gas permeable in my left eye which would be a shame, but probably a necessary step.
Asides from that I have had a good few months, I probably should confess to being a hyperchondriat and fearing I had moto neuron disease from searching what a flutter sound in the ear could be. Went to the doctors paranoid and she assured me that a muscle twitching in the ear, or anywhere in the body for that matter (even the tongue) would have to be accompanied by upper motor neuron damage and severe weakness and atrophy (wasting of muscles) before they even send you to a neuro to confirm diagnosis. so that wasa relief. It got me thinking though about info on KC on the net and there isnt enough if you dont know where to look. Wikipedias page sums it up really well, but not too many people know how resourceful wikipedia can be and even then...it is authors opinins.
anyway hope everyone is well, ill hang about and reply to posts more often! How are the rest of you guys