I add my support to this group of amendments, particularly Amendment No. 238KG, on, "““supporting members of local involvement networks to obtain””,"
their experiences. I wish to add to my noble friend Lord Howe’s search for clarity on the purpose of LINks.
Perhaps I may use an example from my local authority in Kent. Three years ago it wanted to support the patient forums by establishing an independent focal point to allow patients and residents to report their experiences of the NHS. We have, like many local authorities, a 200-seat, 24-hour-a-day call centre. We were simply suggesting that people could phone in, because one of the problems of patient forums is—and one of the problems of LINks will be—the large amount of anecdotal evidence. What they need is a professional organisation to take widespread opinion, to analyse that and produce hard evidence of patient experiences. This seemed a good idea. We called it Kent Health Watch, but at the time it was opposed by the NHS health authority. However, such an idea would be immensely valuable. Amendment No. 238KG and the clause bring that out. Will the Minister support the establishment of that kind of patient information base, which is very important both for information and choice?
Local Government and Public Involvement in Health Bill
Proceeding contribution from
Lord Bruce-Lockhart
(Conservative)
in the House of Lords on Monday, 23 July 2007.
It occurred during Committee of the Whole House (HL)
and
Debate on bills on Local Government and Public Involvement in Health Bill.
About this proceeding contribution
Reference
694 c603 Session
2006-07Chamber / Committee
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