British experience shared by Alex Fox, with the impacts of the use of “lowest bidder” on client community based care.
… This was not what was envisaged by disabled people and their families who developed personalisation, which was the idea that people would plan the most effective care and support when they were in control of an individual planning process which started with what a good life looked like, not with a list of low-cost services. Planning creatively in this way enables people to make best use of their own capacity and of the family and community resources available to them. That also usually results in the most independence and lowest overall cost to the state, whereas narrow price-focused processes bring missed opportunities for independence, or lead to family care breaking down. But instead of people planning a life, and then choosing the support they need to live it, care providers now compete for the individual, and an algorithm makes the choice. …
see the article here: https://alexfoxblog.wordpress.com/2017/11/14/reverse-auctions/
From the Community Workspace on Homelessness – “an interactive space for communities and by communities!”
If you are a professional whose work relates to homelessness, please consider completing this anonymous 3-minute survey titled, “Hospital Discharge for Patients Experiencing Homelessness.” This research is being conducted by Dr. Kristy Buccieri, Assistant Professor at Trent University, to better understand professional opinions on discharge planning for patients experiencing homelessness. For further information, please contact email@example.com.
From the Change Foundation
“Our health care system is dependent on unpaid caregivers. And the reality is that these caregivers are often not recognized or respected for the role they play. At best, there is an inconsistent approach to family caregivers. In many cases, they are not even considered as key members of the care team.”
The Change Foundation
Out of the Shadows and Into the Circle
The Change Foundation’s new strategic plan, Out of the Shadows and Into the Circle, builds on past work focused on improving experiences for patients and family caregivers as they move across Ontario’s healthcare system. Although many ideas and trends were evident during our previous work, there was one consistent theme: the vital, yet often unrecognized, role of informal or family caregivers in the system. We are committing to shining a light on this area. Based on what we know already, we believe that valuing and recognizing family caregivers as integral members of the health care team should be an urgent focus for our health system.
Our strategic goal: to improve the experience of family caregivers as they help their family members transition through and interact with Ontario’s health and community care systems.
Research tells us that most Ontarians have been or will be a family caregiver at some point. Twenty-nine percent of the provincial population – or 3.3 million people – provide some form of support, assistance, care or enrichment to a family member or friend. Both women (53%) and men (47%) in Ontario take on caregiving roles.
We believe, that by recognizing, facilitating and supporting the role of the family caregivers, we can improve patient experience, coordinate care more effectively and create an environment in which the highest quality health care can be delivered. This plan was developed with input, insight, and ideas from over 100 people, including our Strategic Plan Renewal Working Group, our Sounding Board and TCF’s citizen’s panel, PANORAMA.
Our agenda will evolve and flesh out in the first year, The Change Foundation will focus on listening and learning to better understand the family caregiver experience as part of the patient experience and to identify promising models or initiatives for effective and collaborative engagement between family caregivers and providers. This exploratory work will help us scope out and identify our specific projects and policy work that will be the focus in the remaining years of the strategic plan.
15 % of the population is elderly29 % of Ontarians provide some form of caregiving support48 % of family caregivers are looking after parents or in-laws30 % of caregivers are part of the “sandwich generation” of Ontarians provide some form of caregiving support
DEVELOP A FRAMEWORK FOR UNDERSTANDING A FOCUS ON FAMILY CAREGIVERS AS PART OF THE PATIENT EXPERIENCE.
We will use the framework to illustrate how the focus of the Foundation fits within the big picture and the important work of other organizations. This will help us identify where our focused contribution will have the biggest impact.
LEARN MORE ABOUT FAMILY CAREGIVERS IN ONTARIO.
We will ask: who they are, what they need, who is helping them and how they are helped, what are common challenges for all family caregivers, what are unique challenges for sub-groups of family caregivers.
ENGAGE WITH FAMILY CAREGIVERS, PATIENTS AND PROVIDERS.
We want to learn more about the challenges that family caregivers encounter when they interact with providers and the health and community care systems and in particular, we want to learn more about the issues facing diverse and multicultural families. We will also engage with providers to understand their frustrations with the status quo.
DEVELOP AN ENGAGEMENT PLAN FOR MOVING FORWARD.
We will develop an engagement plan to best listen and learn family caregivers, patients, providers and system representatives as we further define and implement our strategic plan.
LEARN ABOUT INNOVATIVE PROVIDER AND FAMILY CAREGIVER PARTNERSHIPS AND INITIATIVES.
We will undertake a systematic review of the literature and informally published reports and documents to learn more about innovative initiatives within Ontario and in other jurisdictions where providers and organizations are collaborating with family caregivers and patients for mutual benefits. We will use this reconnaissance to shape and identify our priority initiatives.
LEARN ABOUT EFFORTS TO INTEGRATE HEALTH AND COMMUNITY CARE.
We will also monitor efforts in other jurisdictions to join-up and better integrate health and community care given how this integration can help to improve the experience of family caregivers and patients.
Read our new strategic plan.
This … dare I say pithy focus through articles on our health system attempts to bridge academic writing to the worlds of both patients and the front line. The search for better practices continues!
Why We Need More Canadian Health Policy in the Media is our fourth in a series of eBooks, bringing together opinion-based commentaries on pressing Canadian health policy issues from Evidence Network’s more than 80 Canadian and international academic experts. Why do we do this? To make sure the evidence matters.
(BTW, you have to dig a bit to find the pdf rather than links to the other sites where you can download)
British paper “exploring the views of mental services users/survivors and disabled people about how they felt mental health issues were understood in society and how they themselves understood them”
From Mental Illness to a Social Model of Madness and Distress.
… While divided about the social model of disability, most service users who took part in the project feel that social approaches to mental health, which take account of the whole person and wider societal issues affecting them, are the most helpful. Some feel that such social approaches need to be incorporated more widely in medical practice. Service users value an holistic or combined approach which takes account of both the individual and their social circumstances. Findings highlighted the complexity of service users’ views, their reluctance to impose monolithic interpretations on their feelings and experience and desire to take account of both personal and social issues. While some service users value some medical interventions, they draw a distinction between that and a narrow medical model and overreliance on medication.
While seeing benefits to be gained from social approaches to mental health, particularly for members of black and minority ethnic communities, they also see practical obstacles in their way. Most service users involved in the project strongly support the idea of developing discussion about social approaches to mental health issues, particularly among service users/survivors. Some feel that progress is already beginning to be made and that there is more preparedness to think in such ways among some mental health professionals. …
The Ottawa Social Planning Council’s The Ottawa Neighbourhoods Social Capital Forum (ONSCF) http://www.spcottawa.on.ca/research-voluntary-sector/building-vibrant-communities demonstrates various examples of their efforts. It would be useful in talking about community development for social workers to hear more directly how we work to link our individual practice to community action and “advocacy,” policy and dare I say Macro approaches to practice with the people we serve.
In the videos found on the site, you can hear participants/clients link their own individual challenges to social action.
This post helps to describe some of the process’ involved bridging individual support to “macro” actions. https://socialhealthpracticeottawa.wordpress.com/2014/11/26/exploring-empowerment-in-our-daily-practice/
Dr. Ameneh Mirzaei, psychiatrist, Mood and Anxiety program, The Royal outlines the relevance health professionals have in helping women to address potential partner violence. Local Ottawa Resources and literature are shared.
Because healthcare practitioners are often the first and sometimes only professional point of contact for victims of violence, they are in a unique position to identify and address the issue head on. According to studies, however, only 12-20% of women report ever being asked by their doctors about intimate partner violence, and when they do disclose that violence exists, support from healthcare providers has been lacking.