Thank you for posting this. I am particularly interested as my disabled brother did not have his testicular cancer found in time because it took so long for the crazy system in place for vulnerable people like this amazing man to even access tests. His gp twice put him on antibiotics and because of his severe mental disability he had to be referred for a best interests meeting at the hospital which was pretty much mostly a waste of time due to the total lack of understanding from the person we originally met with, he (my brother) was not able to attend hospital like other people so could not come to the meeting or appointments, they did attempt an ultrasound under some sedation but as we had predicted, he still could not cope with it and a month later they had to bring him back under more sedation and a general anaesthetic to remove the testicle and diagnose the cancer (which we then found out another month later had spread (he again had to be sedated and have a general anaesthetic to have the ct scan and blood tests) so from when the large swelling was noticed in March 2014 by carers to diagnosis of it being cancer and having spread in February 2015, I would like to know what if anything will be changed for people like my brother