Landsdowne Valley park is mostly used by dog walkers and joggers currently. It has a disused pitch & putt section - that has become home to many birds. The lock-down showed how important local green spaces are. The climate crisis is showing the importance of biodiversity. Landsdowne Valley Park has a lot of untapped potential and we ask the council to take steps, to come up with an upgrade plan for Landsdowne Valley Park in partnership with the local community and stakeholders. The run down, polluted condition of the River Camac flowing through Landsdowne Valley Park, is of serious concern. We the undersigned look forward to partnering with Dublin City Council, in creating an upgrade plan for this park.

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

I am a woman living with Young Onset Parkinsons Disease and working as a Dietitian who provides a dietetic call back service for people living with Parkinson’s. I come off my calls depressed at the negligence of care of my fellow PD patients around the country. Tonight I cannot sleep after the awful stories I heard today. I cannot stand by and hear it happen again and again. It is negligent how the state is treating people with Parkinson’s. I cannot even put into words the awful ways people are suffering. The over 12,000 people battling the fastest growing neurological disease are being mistreated and forgotten. Many of those battling this condition do not have the voice (some literally due to the disease) and their care givers are too worn out to fight the system. Please lend your voice to raise the voices of the many who are suffering around the country. It has to stop. Imagine your mum, dad, sibling, son, daughter, friend or colleague being left to deteriorate slowly but surely and you have to watch helplessly. This is what is happening AROUND the country and it is negligent. People with Parkinson’s are meeting with TDS for an AV Room presentation on July 6th in the Dail campaigning for proper care for people with Parkinson’s Disease. We need 5000 signatures to raise the voices of those suffering. Please sign my petition and please share with your network and ask them to sign.

The local community in Inchicore have used the public library for generations since 1937. Now the Art Deco library needs refurbishment and a wheelchair access ramp built. The architects plan has been drawn up by DCC, but the tender has not been reissued after Covid. There may be alternative plans to convert the historic building into a tourist attraction - a possible social history museum, similar to EPIC. The library keys were handed over by the librarian to the DCC Dept of Property Development and Planning in January 2022. No one in the local community has been consulted about this. The local community are worried that they will lose access to this valuable community space. We are asking DCC to work with the local community on the future of the library, maintaining community access. The building has been empty for 3 years and is unheated. Refurbishment works are urgently needed due to the wet weather. The wheelchair access ramp has been fully designed - the tender just needs to be reissued by DCC.

If our Speech and Language Therapy teacher is withdrawn it means that out of 55 children receiving Speech and Language Therapy in the school only 5 will continue to receive it in St Mary's. Parents of special needs children have to fight tooth and nail for any services for their children and to think a service that is having a positive effect on all these children's progression is going to be withdrawn is absolutely disgraceful and unforgivable. We are calling on all our local Councillors and TD's particularly those in Government for support and to use their influence to have this decision reversed.

At the beginning of the year these students signed up to third level education and paid their student contribution fees with the understanding that they could safely and effectively complete their studies for this academic year. The change in accommodation mid-year is discriminatory towards students whos disabilities and illnesses mean they cannot risk in-person attendance while COVID-19 is still a factor.

I am a Masters Graduate. I am a Presenter, Podcaster, Producer and Filmmaker who happens to live with Cerebral Palsy as an electric wheelchair user. Without the support of a PA, I am facing the prospect of living in a care home, becoming institutionalised and invisible. This would be a living nightmare for me and my family and I'm not the only one. Here is an article about why this matters so much https://www.uplift.ie/wp-content/uploads/2022/01/2022.01.08-Irish-Times-.pdf

We are failing the women and children in the community. Currently we have a population of 218,018 and no domestic violence refuge. The shortage of emergency accommodation for people affected by domestic violence is an issue that is getting progressively worse. Domestic violence spikes significantly during the festive season which is exacerbated by the pressures brought about by Covid-19 and the housing crisis. The provision for domestic violence in our area is comprehensively under developed. There are 144 refuge spaces available nationwide yet Dublin alone needs 143 refuge spaces, and Ireland needs almost 500. There are only 31 spaces, in 4 refuges, to service the entire Dublin area. 68% of the calls Women's Aid made to refuges are being turned away due to there being no room left. The nearest refuge for Rathdown is in Bray, this means that many people may have to travel for over an hour on public transport to be turned away. This huge lack of essential support services results in: • Unmet requests for refuge everyday; • Accommodation problems and homelessness; • People trapped in abusive relationships; • Increasing likelihood of people returning to violent and abusive homes; • Fear of reporting the abuse due to the lack of emergency accommodation available; The government is failing women and children. The most vulnerable people in our society are being failed on every level and government inaction continues to silence them. This is a national issue - there are currently 9 counties without a refuge. Please sign this petition, and please support the work of Carlow Women's Refuge Campaign too: https://my.uplift.ie/petitions/carlow-needs-a-women-s-refuge

To promote inclusion and access to local beaches. I travel to many beaches with my family and friends and am usually restricted to the car park. Check out our campaign website for more information.