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Minutes of the Present: Jonathan
Ellis – Vice-Chair (Help the Aged); Sara Apps (Which?);
Peter Walsh (AvMA); Brian McGinnis (L’Arche); Gerda
Loosemore-Reppen (Sign); Eileen Neilson (RPSGB); Geraldine
Amos (Home from Hospital Care); Barbara
Wood (BMA and RCR); Christine Hogg; Sally Brearley (Healthlink);
Judith Wardle (Continence Foundation);
In attendance: Diana
Basterfield (Patients Forum) Apologies: Carol
Myer ( Speaker:
Farkhanda Maqbool (GMC)
Good Medical Practice Review
(Consultation) (See appendix for Powerpoint presentation) Minutes
of last meeting The minutes of the last general meeting, held on July 13th were agreed. Minutes
of the last Management Committee The Minutes of the last Management Committee held on 1st September were noted. Chair’s
Report Follow-up
from the Patients Forum Awayday – potential new role for PF around
health inequalities It was reported that this was to be followed up by a consultation of members and expressions of interest bids were being sought from people interested to help with this project. The Management Committee would be making a decision soon on the consultants and the timescales. Members would be kept up-to-date and it was hoped to be able to report back to the full membership by April 2006. The Patients Forum would still have 12 months of Department of Health funding to either implement or consider other options if people did not feel that was an appropriate way for the Forum to go. Peter Walsh (Action against Medical Accidents) It was reported that with the help of Which? they would be hosting a meeting directly following this Patients Forum meeting about the NHS Redress Bill. This would have huge implications for the way that the NHS dealt with clinical negligence. They were running a conference about the reforms to redress and also the NHS complaints procedure on 1st December. Brian
McGinnis (L’Arche UK)
It was reported that for those who had not seen
the Bulletin of the Royal College of Psychiatrists, there was a very
interesting review of the Maudsley Group Practice in relation to
implementing the NICE guidelines on involving patients in decisions on
psychotropic medicine. The
gist of the findings are that it is not happening. Gerda Loosemore-Reppen (Sign) It was reported that they were issuing and launching in the following weeks the “Basic Rights Pack” on mental health and deafness together with the Mental Health Foundation. This included a briefing on everything about mental health and deafness, a poster in more visual format (so that it would be accessible for deaf people), a fact sheet on specialist services for deaf people with psychiatric problems and the Charter itself. This would be on the website of both organisations as it was a partnership project. It was also reported that there would be a course on communication tactics which was accredited to healthcare professionals in particular. Barbara
Wood (BMA Patients Liaison Group)
It was reported that they were constantly being asked to
feedback into the development of BMA responses but they were also trying
to keep their own independent voice and their own independent projects
going. A major project for
them at the moment, and they would
appreciate help on this, was a “Who’s Who” project – a glossary
of descriptions of health professionals accessible to patients and the
public. When visiting
someone described as a ‘Specialist Registrar’ or a ‘Consultant
Podiatrist’ or a ‘Surgical Practitioner’ the person might have
some idea about what that title meant.
They were also trying to gather information in order to do a best
practice guidance on how patients should be informed of the role of the
health professional that they are meeting – labeling, photographs,
handouts, form of introduction, what people want to know and how they
could be informed of that. They
would be sending out questionnaires for a number of groups that are
members of the Patients Forum to try and get some patient feedback on
what they would like to know and what their actual experience is so that
they could work from there. Judith Wardle (Continence Foundation) It was reported that, almost by default, Judith had become the Chair of the Patients Involved in NICE group (PIN). She observed that quite a number of new people were becoming involved in the group and it would, therefore, again, be providing training to people who needed it. If anyone knew of people involved in any of the aspects of NICE who might like some training provided through the PIN group (most of this training is provided by their Patient Involvement Unit), do let them know that the group is there. It was also reported, and this follows on from the talk at the Patients Forum AGM, at the Continence Foundation AGM about two weeks’ later, Judith was asked to write to Nigel Crisp and Patricia Hewitt expressing very serious concerns about the impact on services that are largely primary care based – as continence services are led from primary care – of the latest merry go round of PCTs and practice-based commission and people not knowing whether they were coming or going, whether they would have a job etc. If anybody else has put in a similar kind of comment to the Department or to the Health Committee, which was meeting the previous week and this week, to look at that, she would be very interested to know what people have said. Jonathan Ellis (Help the Aged) It
was reported at the last meeting that a major programme of work for them
in the coming period was issues related to the end of life.
Their were currently holding a series of workshops – an
opportunity for people to come together to talk about end of life
related issues around the
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| Last updated 21/11/2005 | © The Patients Forum 2005 |