Let's make Mullingar accessible to everyone, bring the bus!

Both my parents are hard of hearing, they had three children with full hearing. We grew up with sign language, with subtitles on the telly and with an appreciation for how hard things are for deaf people. There's 103,000 deaf or hard of hearing people in Ireland. They deserve a decent subtitling service, regardless of the T.V station, show or type of programme. Unfortunately subtitling is patchy, sometimes out of sync or sometimes not provided at all. Please support this by adding your name.

Children in Balbriggan and surrounding areas do not have the abillity to swim. Only 6/23 schools surveyed in north county Dublin have swimming on the curriculum. Balbriggan was promised a swimming pool in partnership with the rugby club in a plan scrapped in 2016. Skerries was promised a swimming pool years previously. People have to spend time and money to access a pool outside the area. Swimming is a basic life skill and contributes to sport and health of our community.

Disabled people want to live full and equal lives. We want to work in secure, adequately paid employment with the necessary education, skills, qualifications, access, opportunities, and services i.e. Personal supports and transport. Forcing people into discriminatory and degrading assessments and being categorised based on impairments for the purpose of social protection is degrading, inhumane, and tramples over our human rights as per UN Convention on Rights of People with Disabilities and the Employment Equality Act.

Join this campaign to emphasise a logical solution to the housing crisis.

Who is affected? Deafblind children, their families, and the broader community are concretely affected by the existing barriers to inclusive education. The current lack of specialized services and resources denies these children the opportunity to fully participate in educational settings. As a result, they are often isolated, unable to communicate effectively, and face significant challenges in acquiring the necessary skills to thrive academically, socially, and emotionally. What is at stake? The consequences of maintaining the status quo are far-reaching and deeply impactful. Without inclusive education and tailored support, deafblind children risk being left behind, depriving them of a quality education and limiting their future opportunities. By neglecting their needs, we deny them the chance to develop their talents, contribute to society, and lead independent and fulfilling lives. Additionally, the lack of equal access to education perpetuates social inequality and discrimination, further marginalizing an already vulnerable group. Why is now the time to act? Immediate action is imperative as every passing day without intervention exacerbates the challenges faced by deafblind children. The critical developmental stages during early childhood necessitate early intervention services that foster communication skills, sensory development, and social interaction. By addressing these needs promptly, we can enable deafblind children to reach their full potential, unlocking a brighter future for them and empowering them to become active, engaged members of society. We firmly believe that every child, regardless of their abilities, has the right to an inclusive education and equal access to educational resources and services. Therefore, we respectfully request that you consider the following measures: Develop comprehensive guidelines and policies that ensure inclusive education for deafblind children at all levels of the education system. Allocate sufficient resources to provide specialized training for teachers and educational professionals to effectively support deafblind children. Establish early intervention programs that focus on the unique needs of deafblind children, providing appropriate services and support from an early age. Collaborate with relevant stakeholders, including organizations specializing in deafblind education, to develop and implement best practices for inclusive education and support services. Raise awareness among the broader public about the rights and needs of deafblind children, fostering a more inclusive and accepting society. We urge you to take immediate action to address the pressing issue of inclusive education and equal access for deafblind children. By doing so, you will contribute to a more inclusive society where every child can thrive and fulfil their potential. We kindly request a meeting with you to discuss our concerns in more detail and explore collaborative solutions. We are confident that by working together, we can bring about meaningful change and ensure a brighter future for deafblind children.

Encourage & facilitate use of public transport. Currently women, girls, people in wheelchairs, with bikes & buggies are either afraid or cannot access station.

An equal society is a better society for everyone.

This petition is asking the Spike Island Development Company Limited wholly owned by Cork County Council to provide a wheelchair-accessible bus on the island to ensure all visitors including disabled visitors can safely reach the exhibition area, Until this happens, an exhibition celebrating the life of Kay McShane, who grew up on Spike island and won acclaim as a medal-winning Paralympian cannot go ahead.

Endometriosis affects 200 million people worldwide and yet there's only 200 specialists globally to perform effective excision surgery. Every single day patients are suffering debilitating chronic pain, extreme fatigue and a variety of horrific symptoms which leaves us with zero quality of life. Our economy suffers because we are unable to work. In the UK endometriosis costs the economy £8.2bn a year in treatment, loss of work and healthcare costs. A note from the organiser below. A chara, We invite you to join us for the Irish EndoMarch 2023 on Sunday 26th March. This event is part of the global EndoMarch movement, aimed at raising awareness about endometriosis, its associated issues, and creating a supportive community for those affected. Endometriosis has a significant impact on the lives of women in Ireland, and more needs to be done to improve diagnosis, treatment, and support for those affected by the condition. A dedicated multidisciplinary centre is required to improve care for those living with endometriosis in Ireland. Improved Diagnosis: A multidisciplinary centre would assemble an expert group from diverse backgrounds, encompassing gynaecologists, radiologists, pain management specialists, pelvic physiotherapists, and surgeons. This collaboration would result in a precise identification of endometriosis, leading to a prompt and accurate diagnosis for patients and reducing the requirement for multiple surgeries and procedures. In Ireland, the delay to diagnosis is an average of 9 years. Coordinated Care: A multidisciplinary centre would allow for seamless coordination of care, with all members of the team working together to develop and implement a comprehensive treatment plan. This would minimise the current issues faced by those with endometriosis and reduce the risk of miscommunication, ensuring that patients receive the best possible care. At present, women are left to source individual care providers with no standardised model of care. Access to Expertise: A multidisciplinary centre would bring together a team of specialists with a wealth of experience and expertise in endometriosis. Patients would have access to the latest treatments and technologies, as well as the expertise of specialists who are up-to-date on the latest research and developments in the field. It would also allow for Irish research teams to recruit participants and generate new research potential. Improved Quality of Life: A multidisciplinary centre would provide a comprehensive approach to care, including pain management and support for emotional and psychological well-being. This would help to improve the quality of life for patients with endometriosis, reducing the impact of the condition on their daily lives. It would reduce the delay to diagnosis, reduce the need for women to travel outside of Ireland for treatment and improve not only the health outcomes, but also the fertility outcomes of those availing of the services. It is imperative for both the medical community and society as a whole to give endometriosis the attention it deserves. It is crucial to listen to the experiences of individuals living with endometriosis in Ireland and to have faith in women's accounts. Whether you have personal experience with endometriosis or simply want to support the cause, this event is open to everyone who is passionate about improving endometriosis health and awareness outcomes. To register for the event and for more information, please visit the EndoMarch 2023 event page on Eventbrite: https://EndoMarch2023.eventbrite.ie We hope to see you there to join us in the campaign to raise awareness about endometriosis. Sincerely, Kathleen King Team Ireland EndoMarch 2023

We call on the Minister to implement the UNCRPD and UN resolution on disability and for those living with rare disease and chronic illness, to ensure they survive in this cost of living crisis.

The phrase ‘conversion therapy,’ brings to mind harmful efforts to ‘cure’ gay, trans and other queer people… Now imagine similar coercion and trauma were inflicted on Neurodivergent people - Autistics, People with Down Syndrome, People with Intellectual Disabilities and others… You don’t need to imagine. (1) It’s real, it’s been going on for 60 years, and it is happening right now across Ireland in schools, in adult and child services, and in peoples’ homes. How could this be? Is this legal? Yes, it’s legal… It is the go-to ‘therapy’ for many Neurodivergent people of all ages to make us appear ‘normal,’ taught to psychologists and psychiatrists, social care workers, SNAs, and special ed. teachers. That is why we need your support. Behaviourist conversion methods hide behind a plethora of credible-sounding names - Applied Behavioural Analysis (ABA), Positive Behavioural Support (PBS), Early Intensive Behavioural Intervention (EIBI), Social Skills Training, PECS, ‘behavioural plans,’ and others. They are so ingrained into the practice of Irish professionals that many are oblivious to the harm. It’s just ‘what you do’ for ‘those people.’ We are ‘those people,’ and we’re telling you: this is doing us real lasting harm. Almost half (46%) of those subjected to ABA display PTSD symptoms.(2) This is why our communities oppose all such ‘therapies,’ including the so-called ‘gentle ABA.’ All variants assume we are defective humans who must be shamed and bribed to mimic ‘normal.’ All it really does is teach us to silently suffer the trauma of living a lie. The UN agrees: “Autistic persons are particularly exposed to professional approaches and medical practices which are unacceptable from a human rights point of view. Such practices … violate their basic rights, undermine their dignity, and go against scientific evidence.”(3) Behaviourist conversion methods ignore our human rights. They do us terrible harm. They don’t work. We do not consent. This has to stop. Now. And yet it continues. Ireland is even hosting an international ABA conference in September,(4) possible only because this kind of conversion ‘therapy’ remains legal here. Prioritising a diversity of Neurodivergent voices in the upcoming Autism Innovation Strategy as per UNCRPD(5) may help, but will not secure our safety in law. Therefore, we call on Minister Rabbitte to ensure Neurodivergent citizens are protected from further harm by banning all behavioural interventions in this state. To find out more about behaviourist conversion, the harm it causes, and further steps you can take to help, follow the links below Facebook: https://www.facebook.com/profile.php?id=100084052330540 Twitter: tbc Follow similar campaigns internationally: [links]: https://twitter.com/A4AOntario/status/1548669666066833408?s=20&t=lDtix0HmixgWn3sY0v72yw https://autcollab.org/aba https://twitter.com/ekverstania/status/1532818556693389312?s=20&t=2xKe2Lr09vMYcBrfw0mHHw https://www.facebook.com/BetterWaysThanABA/ https://www.facebook.com/endseclusion/ #BanABA #SayNoToABA #BetterWaysThanABA #StopTheShock ______________________________________________________ 1. Ole Ivar Løvaas: Originator of ABA & Gay Conversion methods https://www.lgbtqnation.com/2021/03/man-behind-ex-gay-conversion-therapy-started-trying-make-autistic-children-normal/ 2. Kupferstein, H. (2018), "Evidence of increased PTSD symptoms in autistics exposed to applied behavior analysis", Advances in Autism, Vol. 4 No. 1, pp. 19-29. https://doi.org/10.1108/AIA-08-2017-0016 or https://www.emerald.com/insight/content/doi/10.1108/AIA-08-2017-0016/full/html 3. UN Office of the High Commissioner for Human Rights, 2015 Special Report: https://www.ohchr.org/en/press-releases/2015/04/discrimination-against-autistic-persons-rule-rather-exception-un-rights 4. Applied Behavioral Analysis International, ABAI Conference 2022: https://www.abainternational.org/events/international/dublin-2022/conference-home.aspx 5. UN Convention on the Rights of People with Disabilities, 2006: https://www.un.org/disabilities/documents/convention/convention_accessible_pdf.pdf