The following are websites I have found useful...
The Patients
Association is an independent charity that highlights the concerns and needs of
patients. The Association advocates for greater and more equitable access to
high-quality, accurate and independent information for patients; to reduce
health inequalities by helping patients to be better informed and by
campaigning for patients to have the right to be involved in decision-making.
NAPP has over 30
years experience and expertise in promoting, supporting and developing Patient
Participation Groups (PPGs) and has developed a full range of resources
that can support practices and PCT's in implementing this contractual
Patient Participation requirement.
National Voices is
the coalition of national health and social care organisations that ensures a
strong voice for all those who come into contact with the NHS and care
services, and for the voluntary organisations that work for them.
In each of the nine
English regions there is a network which champions the engagement of the
voluntary and community sector (VCS) in regional policy and strategy. They
develop and support the contribution of the sector to regional progress and
raise awareness and understanding of the sector’s roles. This is a separate
organisation to National Voices.
The Healthcare
Quality Improvement Partnership (HQIP) was established in April 2008 to promote
quality in healthcare, and in particular to increase the impact that clinical
audit has on healthcare quality in England and Wales
The National PALS
Network is a membership organisation for people who work in the Patient Advice
and Liaison Services of the NHS in England. On this page you can find out about
the members' newsletter and link to a page from which you can download copies.
CQC regulates care
provided by the NHS, local authorities, private companies and voluntary
organisations. We aim to make sure better care is provided for everyone - in
hospitals, care homes and people's own homes. It is interested in hearing
people’s views of their care.
Healthwatch
HealthWatch
England is being proposed as a new “independent consumer champion for health
and social care. Its aim will be to achieve the systems described in the
Government’s NHS white paper where: patients are at the heart of everything the
NHS does.
The LINks exchange
(LX) is a web resource to help support Local Involvement Networks (LINks) talk
to one another and share best practice. Funded by the Department of Health, the
LX enables members to access LINks programme information and guidance, share
knowledge and experience.
Patient
UK was first launched in 1997 by PiP (Patient Information Publications). It
started as a directory of UK websites which provided information of health,
disease and related issues.
PatientView is an
independent, global, research-and-publishing organisation that works closely
with patients and health and social campaigning groups worldwide.
This is a Shared
Learning Group for people who work in national voluntary organisations who have
lead responsibility for service user and carer involvement.
OTHER NATIONS
Community Health
Council (CHC) work to enhance and improve the quality of local health services.
These are the statutory and independent voice in health services provided
throughout Wales.
The Scottish Health
Council was established in April 2005 to promote Patient Focus and Public
Involvement in the NHS in Scotland. By ensuring that NHS Boards listen and take
account of people's views, we can achieve a "mutual NHS" - where the
NHS works in partnership with patients, carers and the public.
The
overarching objective of the PCC is to provide a powerful, independent voice
for patients, clients, carers, and communities on health and social care issues
INTERNATIONAL
The "European Patients' Academy on Therapeutic Innovation" (EUPATI) will provide scientifically reliable, objective, comprehensive information to patients on pharmaceutical R&D. It will increase the capacity of well-informed patients to be effective advocates and advisors, e.g. in clinical trials, with regulatory authorities and in ethics committees.
EPF is the umbrella
organisation of pan-European patient organisations active in the field of
European public health and health advocacy.
IAPO is a unique global
alliance representing patients of all nationalities across all disease areas
and promoting patient-centred healthcare around the world.
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