Haven’t you and others (like Gelhead) posted numerous times that the foundation will pay for it? Is that wrong?
Oh, well, now I’ll definitely go on!
And they know the numbers effected by PFS how?
Whatever the reason; this process is too slow. I would prefer a ‘brute force’ approach. Get a few guys together that are 100% certain to have PFS and bombard them with tests. (I would like tests for demylination, antibodies to DHT, 5a-reductase, etc).
I think we are all agreed that the tests are important and we need to get participants for them asap.
Can anyone clarify about the offer of payment? And has anyone spoken to the Foundation, or people connected to the study, about how we can help get participants? For example, I’m happy to help contribute towards people’s costs if this is an issue.
Very wooly. ‘A few guys’? Come on. A definite number needs to be picked.
‘100% certain to have PFS’? Yes, and presumably you will be appointed as the person who identifies who does or does not have PFS.
‘bombard them with tests’? Right, let’s speculatively spend loads of money on an unknown quantity of men with tests selected without particular reason, so that results can be obtained by ‘brute force’.
This is why the studies are in the hands of paid researchers rather than armchair chancers posting waffle on a forum.