Unpaid carers play an essential role in our healthcare system, especially for those dealing with mental ill health or long-term cancer care. Matthew McKenzie’s lecture brings much-needed attention to the critical role unpaid carers play and offers insights for both healthcare professionals and family members on how to better support these individuals. Let’s delve into key aspects highlighted in the lecture aimed at care awareness and support.
To watch a more indepth version please see the video below.
The Importance of Acknowledging and Valuing Carers
Unpaid carers are often the closest relatives or friends of the patient and have substantial insights about the patient’s history, symptoms, and what has worked best in their care journey.
Understanding Unpaid Carers and the Vital Role of Carer Centers
This blog is by carer activist Matthew McKenzie. In the UK, millions of people, often unnoticed and unappreciated, dedicate their lives to caring for family members with long-term physical or mental health conditions. These unpaid carers are the backbone of the caregiving system, yet they face numerous challenges daily. Here, we delve into the crucial role of carer centers, the obstacles they encounter, and potential solutions to sustain and enhance their vital services.
Why Unpaid Carers Should Connect with Other Carers
Unpaid carers play an essential role in society, often providing support to loved ones with long-term illnesses, both physical and mental. However, the journey of caregiving can be challenging and isolating, making it crucial for carers to connect with others in similar roles. Establishing these connections can provide numerous benefits, including emotional support, practical advice, and a sense of community. In this blog by Matthew McKenzie, we will explore the reasons why unpaid carers should connect with other carers, structured around several key areas: emotional support, reducing isolation, accessing resources, practical advice, and mutual support for self-care.
If you want to watch the 20 minute in depth lecture, the click the video below.
In this blog by Carer activist Matthew McKenzie, you can learn how to establish and manage a carer peer support group effectively, from defining its purpose to recruiting members and creating a supportive environment. Gain insights on structuring meetings, engaging members, and overcoming challenges for long-term success.
The blog is fairly brief and short, but you can watch the video lecture below for a more detailed explanation. (32 mins organised as an index). Sorry for the picture in section 4 overlapping the example
Welcome to another blog post by Carer Activist Matthew McKenzie. This blog and video is from my lived experience caring for a close relative and also supporting my brothers.
To watch the video lecture, please click below.
The holiday season is a time filled with joy, celebration, and connection. However, for unpaid carers, it can also be a period laden with stress, isolation, and heightened responsibilities.
Welcome to another blog post by carer activist and ambassador Matthew McKenzie. I raise awareness of unpaid carers who support those with long term ill health. This time my blog focus is on the inclusion of carer only groups at mental health service development.
Here is another blog by Matthew McKenzie author of “Experiences of Mental Health unpaid caring”. This time I am covering a difficult and compex topic. Caring for someone and trying to maintain the family connection.
If you want to watch the detailed version of this blog, you can watch the video below.
Blog by Matthew McKenzie aimed at unpaid carers whose cared for will soon be discharged from hospital. Here are some tips to take note of to help in smooth transistion back into the community.
To watch the video lecture nearly 30 mins, see below.
Grief affects us all at some point in our lives, but for unpaid carers who have dedicated their energy and resources to looking after someone with a long-term illness, the passing of their loved one carries a unique weight. This article by carer activist Matthew McKenzie delves into the ways unpaid carers can cope with this profound sense of loss, exploring the emotional depths of grief and offering practical advice on navigating these difficult waters.
Hello all. Especially those who support someone with mental ill health. Treat someone with mental ill health or those who are interested in Carer’s Trust Triangle of Care. As an expert by experience regarding mental health unpaid care. I am delighted to be given the chance to chair these meetings, which I have been doing for around 2 years.
The meeting I chair is the national community group, which I try to run every 2 months and usually, I do not have the capacity to chair, organise and minute them, but now I have decided to attempt to update via my carers website. The main reason is to let carers know of the important themes that will affect them if caring for someone with mental ill health.
Topics covered for the ToC community meeting November 2024
The meeting covered various aspects of carer involvement in mental health care, including the Triangle of Care approach, challenges faced by carers, and the development of tools to improve communication between patients, clinicians, and carers. Discussions also focused on the Making Carers Count program presented by Carers Trust “Making Carers Count” programme lead Ben O’Hanlon, which aimed to support underrepresented carer groups.
Lastly we discussed the potential impacts of the new Mental Health Bill on carers. Concerns were raised about the implementation of the Mental Health Act reforms and their implications for carers, highlighting the need for better support and representation in the decision-making process.
Triangle of Care Update Meeting The meeting discussed promoting the Triangle of Care approach to involve families and unpaid carers in mental health care settings. Mary Patel, the new co-lead for Triangle of Care at Carers Trust, introduced herself and her background. A carer raised concerns that mental health services seem less willing now to genuinely listen to carers compared to when Triangle of Care was first launched.
We then had Marta, a researcher, who requested help from carers in London to complete a survey on shared decision-making in mental health that includes a carer version. The group then heard presentations from Alan Worthington on engaging carers in primary care and Karen on the Mental Health Act reform’s impact on carers.
Developing Patient-Clinician Carer Questionnaires In the meeting, Marta discussed the development of questionnaires for patients, clinicians, and carers to evaluate the effectiveness of conversations and identify discrepancies. She emphasized the importance of involving patients in treatment decisions and the need to make the questionnaires as succinct as possible while still capturing valuable information. A Carer raised concerns about the cultural aspects of the questionnaires and the need to address diversity issues. Another carer shared her experience as a carer lead at a mental health trust, highlighting the importance of co-producing carers questionnaires to gather valuable feedback.
Engagement and Support in Medical Practices Alan Worthington discussed the importance of engagement, involvement, and support in medical practices, particularly for carers. He emphasized the need for professionals to be prepared to talk to carers, share information, and break confidentiality. Alan also highlighted the significance of patient public involvement and feedback in improving the system. He shared his experience with a complaints book in his surgery, which became a valuable resource for patients to express their experiences. Alan also touched on the issue of support from medical staff, particularly doctors, and the need for special time with them. He concluded by discussing the impact of Covid-19 on carers and the need for self-help and monitoring.
Regular Health Monitoring With Alan Alan also discussed the importance of regularly checking weight and blood pressure, using a digital thermometer and blood pressure meter. He emphasized the significance of monitoring blood pressure, as it can be a lifesaver and help identify potential health issues. Alan also highlighted the importance of using a digital thermometer, as it provides quick and accurate readings. He further discussed the use of urine testing strips, which can help detect urinary tract infections. Alan concluded by emphasizing the importance of having a blood pressure meter, oximeter, and urine testing strips in one’s medical kit.
Covid-19 Risks and Carer Support Alan discussed the ongoing risks of Covid-19 and the importance of being vigilant. He also highlighted the potential benefits of certain painkillers and promoted their use by carers. Alan emphasized the need for carers to take charge of their situations and seek help when necessary. He also shared a personal experience caring regarding stroke and the importance of quick action. Alan suggested that the Carers Trust could share this information with unrecognized and unheard carers.
Making Carers Count Program Outcomes Ben discussed the Making Carers Count program, a three-year initiative aimed at supporting carers from underrepresented groups. A lot of the presentation was aimed at carer centre representatives, especially those involved in the “Making Carers Count” programme.
The program, which concluded earlier this year, focused on improving access to digital, online, and peer support. Ben highlighted the program’s positive outcomes, including improved reach, support, registration, and engagement for carers from these groups.
He also mentioned the publication of a final evaluation and five practical good practice guides based on the program’s key themes. These guides are intended to be accessible resources for organizations looking to improve their services for carers. Ben also mentioned the program’s legacy projects and the appointment of a new EDI lead at Carers Trust. Matthew McKenzie raised concerns about the program’s sustainability and the risk of losing the momentum and funding. Ben responded by emphasizing the importance of embedding the program’s work across the network and the potential for organic changes in practices.
Mental Health Bill Key Reforms Karen Machin discussed her passion for the Mental Health Bill, which has been in the works for a while. She highlighted the bill’s key reforms, including a higher bar for detention, stricter criteria for community treatment orders, and the establishment of a mental disorder within 28 days for detention. Karen also expressed concern about the support for family and friend carers in the bill, as well as the potential for a public discourse around risk. She encouraged everyone to read the full document of her presentation for more information.
Mental Health Act Changes Impact Carers Karen Machin presented on the changes to the Mental Health Act, focusing on the impact on carers. She expressed concerns about the potential decrease in the number of people detained, which could lead to increased responsibility for carers. Karen also highlighted the importance of considering the impact on carers’ mental health and the need for their voices to be heard in the decision-making process. She suggested that carers should contact their MPs to raise their queries or concerns and ensure their voices are represented. The group agreed that the changes of the Mental Health Act are welcomed, there will be significant implications for family carers and it is important that their input is crucial in shaping the future of mental health care.
UK Mental Health Act Reforms In this meeting segment, the key points discussed were concerns around the new Mental Health Act reforms in the UK. A carer shared her worrying experiences where her relative, who lacks insight into their mental illness, could potentially nominate an inappropriate person to make decisions on his behalf instead of his family carer. The group discussed how this law, while well-intentioned, fails to account for complex family situations and resource constraints in mental health services. There were also concerns about lack of funding for proper implementation of the reforms, and the need for better training and preparation for families and carers to understand their rights under the new law. The discussion highlighted the importance of mental health trusts and carer organizations being proactive in addressing these issues and advocating for the voices of carers to be heard.