I wanted to share this video from Steph Bailey and UNLIMITED on Access Riders and how useful they can be. They also have a few great guides that are so helpful when writing one, especially on things like how you want to be referred to and moving away from medicalisation - ie, having your needs framed by a medically described impairment. The definition of disability below is also super helpful. “The social model of disability is a way of viewing the world, developed by disabled people. The Social model of disability says that people are disabled by barriers in society, not by their impairment or difference. Barriers can be physical, like buildings not having accessible toilets. Or they can be caused by people's attitudes to difference, like assuming disabled people can't do certain things. The social model helps us recognise the barriers that make life harder for disabled people. Removing these barriers creates equality and offers disabled people more independence, choice and control. #AccessRider #AccessDocument #Inclusion #Diversity #Culture https://lnkd.in/dFvDZCaw
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To demonstrate how this plays out with a personal example: In the last year I've been wanting to get into a gym to build strength. Something that is great for fall prevention, pain management and joint stability. All vital for my physical conditions and also help mental health. I've been a victim of violence and while I know I can't run/defend myself if this happens again, 'feeling strong' is something that would help hugely with my confidence in getting out & about. What's stopped me from doing something that is clearly so beneficial? - Cost - Time/energy - As I use most of my pain/fatigue 'allowance' to work - Lack of informed PTs for my type of challenges - Stigma on how others will perceive me. - Fear of surveillance & losing what I need to support the additional costs of existing as a disabled person. In this time how many times have I fallen? Had a 'bad leg day' and had to crawl around my flat? Not go out for lack of confidence in my safety? I am missing out. I have had a PIP assessor "remind" me that they could review CCTV footage of me doing my groceries. They wanted me to know I was being observed, judged, and constantly under the threat of losing the minimal support this benefit offers if they decided I had misrepresented my experiences. That moment still stays with me every time I step outside my flat, even often when I'm inside and I worry what neighbours see through the windows when I'm doing my daily physio that helps me manage my wellness, stay in work and feel good. That is how deeply that message lands in the disabled community. I can't 'un-disable' myself (after all, the disablement is by society 😉) but the management of these conditions is made less of a load for me as a person in my work and in living a full life, if I can move during the times when I'm able to and have the resources. But if you were told that what you need to support your health in all the other ways you need, including and beyond physical, could be removed, for simply how you are observed doing your groceries.... would you go to gym? Take up a sport? Go for a walk? even if you were excited and motivated to do so? Never underestimate the oppressive force of the threat of or actual surveillance of disabled people and its lasting impacts on every element of our lives. Social, employment, health and more. I speak in this case from a (deeply) personal perspective because I know this often lands well with those of you following me here. However if you've followed my work for a while you'll know that I also regularly educate & advocate for individual & community access and inclusion for disabled folks, and the stories I hear are the same widely. I'm fortunate to have some other layers of privilege, but this issue is further compounded with layered intersectionality. Listen to experts like John Amaechi OBE 📢 Engage with this issue. Use your power to make change.
Leadership Transformation Expert @ APS Intelligence. Chartered Psychologist and Associate Fellow British Psychological Society. Professor of Leadership University of Exeter Business School.
50% of disabled people fear losing their benefits if they are seen as physically active. It's a difficult Catch-22. Many disabled individuals rely on benefits to afford activities that could improve their well-being, but if they are perceived as too active, they risk being accused of fraud and losing their support. Last week, Activity Alliance launched a new strategy aimed at ensuring disabled people feel they belong in sport. I’d like to take this opportunity to highlight the important work they are doing by sharing their latest strategy report below. Please take a moment to read it if you can.
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❤️ This week is #carersweek which is an annual campaign to raise awareness of caring, highlight the challenges carers face and recognise the contribution they make to families and communities throughout the UK. 💞 It also helps people who don't think of themselves as having caring responsibilities to identify as carers and access much-needed support. 🗺 This year the theme is 'Putting Carers on the Map' highlighting the invaluable contributions of carers across the UK and ensuring their voices are heard loud and clear. 🚸 Children as young as five can often find themselves in a role as young carer to a family member sometimes carrying out 50 hours of care each week on top of their normal school life. 🏫 Schools, colleges and universities can identify children, young people and adults with caring responsibilities. They can recognise the impact caring can have on their studies, as well as their personal lives. They can take action to ensure carers get the help they need to cope with what can be an intense additional pressure. 📈 Last week, we learnt that, for the second year in a row, schools in BCP were the most effective at identifying young carers across the UK 🏆 MYTIME Young Carers' Level Up Programme once again proving a vital resource and support to schools. 🧐 But there's still work to do as 72% of schools nationally say that they don't know of young carers! 📺 If you can spare a couple of minutes to watch Oritsé Williams talk of his experiences around being a young carer it really will be one of the most worthwhile break you have today.
Fantastic young carer awareness! Having someone speak to passionately about his own experiences as a young carer, as Oritsé Williams, is invaluable to raising the awareness that is so needed around young carers and the challenges they face. Well worth 2 minutes out of anyone's day! 🤩 #youngcarers #awareness #GMB
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Danny Josephs (COO/Client Lead at mFuse ) tackles the challenging realities of accessibility head-on in his latest campaign article. The piece is both honest and thought-provoking. While systemic change is crucial, there's one action you can take today: Ask "Do you have any accessibility requirements?" when organising meetings, just as you would dietary needs. Small changes, big impact. #accessibility #inclusion #meetings #mFuse
Our COO, Danny Josephs, challenges us to think beyond the screen and consider the real-world barriers faced by disabled people. His latest article for Campaign UK is a call to action for greater accessibility in all areas of life. Read it here:
Beyond the screen: why real-world accessibility for disabled people still falls short
campaignlive.co.uk
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Watch as two of our team members, Richard Blakeborough (interviewer) and Tony (interviewee and head of DIAS at Independent Living) talk about the EGL (Enabling Good Lives) Principle: ‘Ordinary life outcomes’. Tony discusses what Ordinary Life Outcomes look like for him personally as well as what that means in our Independent Living context. Whaikaha - Ministry of Disabled People #EGL #EnablingGoodLives #IndependentLiving
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💡Did you know?💡 Special Olympics BC’s Champions for Inclusive Health Stakeholder Coalition brings stakeholders of all backgrounds together to challenge the status quo and proactively contribute to achieving health equity for individuals with intellectual disabilities. This coalition aims to end the harm and unequal conditions experienced by individuals with intellectual disabilities in B.C., and establish impactful resources, expertise, and best practices that can encourage other jurisdictions to follow B.C.’s lead. 🍎 If you are active in health and passionate about helping people with intellectual disabilities, please join our newsletter to find ways on how you can make an impact: ➡️https://lnkd.in/gSBi-Nqw
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Today, the European Blind Union was invited to participate in the #NDAConference2024 of the National Disability Authority focused on promoting the participation of people with disabilities in cultural life, tourism and sports. In the event, we participated in a panel discussion about Article 30 of the UNCRPD at an international level. In the discussion, EBU underlined its main commitments in this area: - The evaluation and mid-term review of the Creative Europe programme by paying attention to its MEDIA Strand. - Ensuring the correct implementation of the European Accessibility Act as far e-books are concerned. - The review of the EU legal framework for the implementation of the #MarrakeshTreaty.
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Below is a link of me speaking on Clare FM https://lnkd.in/egDEEkyQ
Clare Disability Group Seeks Urgent NTA Meeting Over Public Transport Shortfalls - Clare FM
clare.fm
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Welcome disabled visitors this Purple Tuesday - and beyond - by sharing your disabled access information! Our blog post has some helpful suggestions on how you can quickly and simply welcome disabled visitors. #PurpleTuesday
Welcome disabled visitors this Purple Tuesday by sharing your disabled access information
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Today is Carers Rights Day and it feels like the perfect time to reflect on the work that Carers Trust and Carers UK have done to support carers, especially those who are traditionally underserved by carer support services. Over the past couple of years, I have been working with Sally Cupitt on an evaluation of their Making Carers Count programme. Based on data from this evaluation, together with Ben O'Hanlon and some brilliant carers services around the UK, we developed a series of good practice guides designed to help organisations and services better support carers. It was a rewarding process to pull together these guides as they were rooted in evidence and practical insights from the evaluation. The titles of the guides are: 📘 Developing an inclusive organisation 📘 Creating more inclusive spaces for carers 📘 A whole family approach to supporting carers 📘 Working in partnership to better identify and support carers 📘 Developing young adult carer services – a practical guide Carers play such important and often challenging roles. And it’s so important that support services meet their needs, particularly for those who often face barriers to accessing help. I’m hopeful these guides can contribute to making a difference in the lives of carers and their families. https://lnkd.in/ehHET7kJ #CarersRightsDay #Evaluation
Making Carers Count
carers.org
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