Hi This is my first time on CWD, so feeling a lilttle nervous at what to put, but here goes. My son was diagnosed 1 August 2006, age 8. We have been asking for a pump through our PCT for the past 2-3 years but unfortunatley there isn't any funding. We were told in October that they were hopeful for January this year as it would be their 4th year of applying. We heard last week that it has been refused yet again and therefore no pumps are available for at least another year. I feel enough is enough so I am going to see George's consultant next week and I shall be challenging the PCT about this. Does anyone have any info that will help me with my cause or any guidance they can give. Thank you so much.