I have been taking increasing amounts of Levodopa in the form of Madopar and Stalevo since diagnosis 8 years ago. I am now experiencing end dose dyskinesia which is becoming extremely uncomfortable. At a recent consultation with my Parkinson's Specialist Nurse it was put to me that I would benefit from Apomorphine therapy. I would like to find out more about Apomorphine before I decide whether to have this form of treatment or not, preferably from someone who is presently on Apomorphine and has a pump fitted. Can you manage the pump yourself? Does the pump make a noise? How often do you have to change the site of the needle/tube and can you manage this yourself? Has the dyskinesia disappeared? Any practical advice would be greatly appreciated.