/snip.
Castiel with all respect I am not sure you actually know what you've put there.
This is why sometimes it's best not to argue from Wikipedia and google searches. Knowledge and information are only pertinent of they are applied appropriately and in context. You've actually substantiated the points I made without realising it.
You are also assuming I would not argue for restricting access for at risk groups. I would strongly enforce that if possible in this country.
I feel very strongly that people like Tefal should not be detailing their woeful experience due to lack of provision and money in our system (on these forums) when people come into this country and have kids with their second cousin, come in with known expensive illnesses, and strong predisposition towards potential illness etc. We all fund (well most) The National Health Service - not The International Health service like half of Asia and Africa seems to think.
[TW]Fox;24676921 said:I think the understandable issue is why did they wait for 6 years of annual reviews to say get lost? Why didn't they reject his first application when he was even bigger?
That would require actual knowledge rather than a quick google. They've recently had a big reorganisation and focus on 'renal replacement therapy' due to low rates of live-related transplant and a lack of practitioners who are capable of facilitating peritoneal dialysis. Therefore, there has been a national drive to address risk factors for renal failure across the board.
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