There are thousands of people affected by this issue and yet it is ignored by planning/councils and government.  People with medical conditions needing urgent toilet access experience pain, accidents and humilation when refused access to toilets when out in publuc spaces. Shops/businesses have a right to refusal, legalising the "No wait card" would stop this.  It would bring a better quality of life, take away anxiety and stress when going out in society and bring dignity to people affected. #Nowaitcard  #invisible disabilities 

This heartfelt appeal from parents, educators, and SNAs across Ireland highlights the urgent need to reconsider new Special Needs Assistant (SNA) guidelines. The proposed changes—rigid staffing limits, narrow definitions of need, and rushed implementation—risk dismantling inclusive education and jeopardizing the well-being of children with Autism and complex needs. Without adequate SNA support, vulnerable children face emotional distress, medical risks, and exclusion from mainstream classrooms. Families are pushed to crisis, teachers are overwhelmed, and the entire school community suffers. The call is clear: listen to lived experiences, and build a fair, responsive, and properly funded system that protects every child’s right to feel safe, supported, and included.

Why This Matters — To Everyone Huntington’s disease families in Ireland have been promised and then denied basic care and support. We are a small, relatively rich country and our healthcare system is failing those who need it as well as those who work in it.  Huntingtons Disease has NO specialist teams in Ireland. ONE Nurse for 800 people and their families with 3000 more living at risk. No coordinated services. And now, with a groundbreaking gene therapy on the way, our health service isn’t prepared to deliver it. If the system can continue to ignore a disease as devastating as this, when there are things that can be done...what does that tell us? Time to speak as a group, as a country as citizens who care about one another.  Sign this petition to support families : • Proper Huntingtons Disease care through specialist multi-disciplinary teams (like Scotland has - same population but a specialist team in all 7 major cities) • A health system ready for advanced therapies like the Uniqure trial making the news • Leadership that keeps its promises Because a health service that fails us today will fail our tomorrows.

The Clonlara residing along the R463 would like to request the support of all residents of Clonlara for the following reasons: • Improved accessibility for those of us at these addresses means more economic activity in Clonlara village.   • It would allow us to access bars and restaurants. It would also create a higher footfall for the village shop which has now closed twice previously due to this challenge. It would increase bus service user numbers thus ensuring the service is not cancelled and more bus services may be added. • It would reduce traffic at Clonlara bridge as many would choose to walk and cycle such a short distance rather than sit on the bridge in traffic. • It would bring members from your community who are currently not spending time in the village due to a lack of accessibility across the bridge and create a more unified community.   We would also like to request the support of those who have  accessibility concerns for relatives living in the area. We thank you all for your support on this matter.

Why is it important? Because none of us are safe under a mental health system that’s stuck in 2001. The Mental Health Act 2001 still allows forced treatment, restraint, and seclusion—even though these practices are now widely recognised as harmful, especially to neurodivergent people (like those with autism, ADHD, or trauma-related conditions). It treats emotional overwhelm as illness. It punishes difference as danger. This law was written before most people had smartphones. Before we had language for sensory overload, neurodivergence, or digital expression. It’s outdated, invasive, and not trauma-informed—and it puts thousands of people at risk every year. Why should others join? Because you don’t have to be in crisis to care. This campaign is about protecting our freedom, dignity, and human rights. It’s about making sure no one is silenced, secluded, or forcibly medicated for being misunderstood. If you’ve ever: • Had your feelings dismissed as “too much” • Been misdiagnosed • Been afraid to seek help because the system might punish you Then this campaign is for you. We need to audit the Mental Health Act 2001—and bring Ireland in line with modern science and EU human rights law. Join us. Share. Demand better. ACTIVATE. AGITATE. AMPLIFY!

Make my village safer – install bollards in Ballina, Co Tipperary.

Please sign this petition so our children with Autim/ Autistic Children can continue to enjoy these classes.

Special Needs Assistants (SNAs) play a vital part in the lives of pupils with Special Educational Needs and Disabilities (SEND). The current lack of centralised Garda Vetting makes it very hard for SNAs to work in schools, as at the minute they have to vetted for every single school they might want to work in. This means that schools can often struggle to get a substitute SNA since the SNA is not vetted for their school (even if they are vetted for the exact same role in other schools), resulting in pupils missing out on important educational supports. If other professionals can have centralised vetting, like how teachers have universal vetting through The Teaching Council, why can SNAs not have the same option? Centralised vetting would also help to reduce the amount of time and resources that school management members would have to spend preparing SNA vetting paperwork for SNA staff. Even if a nationwide organisation was set up to manage the centralised vetting of SNAs, most SNAs would appreciate being part of a group where they can connect with other likeminded SNAs and peers. The role of an SNA is often misunderstood and overly simplified by people, so it would be a nice acknowledgement of the importance of their everyday work with SEND pupils. Thank you for taking the time to read this, hopefully it will result in the introduction of centralised Garda Vetting for SNAs in the near future! Amy Reynolds *I am a qualified Special Needs Assistant (SNA), Teaching Assistant (TA) and Teaching English as a Foreign Language (TEFL) teacher. I am passionate about education, particularly inclusive education, and the benefits it brings, especially for pupils with SEND. I myself have struggled to get opportunities to work as an SNA (even as a substitute) as my vetting for other settings would not cover me for that particular school. I now work in pharmacy and am completing an apprenticeship pharmacy technician style course. I would like my future work to combine education and pharmacy / healthcare*

  No child should be left without the care they need to grow, learn, and thrive — yet across Donegal and Ireland, children with disabilities have been forgotten. Families have waited years, sometimes a decade, for essential services like occupational therapy, speech therapy, and early intervention. My own child has gone without occupational therapy for the past two years, with only 4–5 appointments in the last ten years. This is not an isolated case — it’s a nationwide crisis. By joining this campaign, you are standing up for every child who has been denied the opportunity to reach their full potential. You are giving a voice to parents who have been fighting, unheard, for the care their children deserve. And you are demanding accountability and immediate action from the government to fix this failing system. Together, we can push for real change — increased funding, reduced waiting lists, and a future where no child is left behind. Your support can make the difference between years of neglect and a system that truly serves the most vulnerable in our communities. Let’s fight for their future — because every child matters.

Here’s why you should sign: ✅ Hold Politicians Accountable – If an elected official ignores their campaign promises or fails to take action on critical issues, voters should have the power to respond before the next election. ✅ Strengthen Democracy – Other democracies like the US, Canada, and parts of Europe already allow citizens to recall politicians. Ireland should modernise its system to give people a stronger voice. ✅ Ensure Promises Are Kept – Campaigns should not be built on empty promises. If politicians know they can be recalled for inaction, they will have a stronger incentive to follow through on their commitments. ✅ Empower Citizens – Democracy doesn’t stop at the ballot box. Irish voters deserve a mechanism to ensure they are truly represented throughout a politician’s term. Signing this petition is a step toward real accountability in Irish politics. Let’s make sure our leaders work for the people—not just for re-election. Sign now to demand change!

This is a human rights issue:   A recent ERSI report highlighted the basic inequalities in the provision of Personal Assistants across the country. Ranging from differences of approach to completely inadequate resource allocation depending on on where people live. Most damming of all is that if you are over 65 you will not be considered for a PA ; a clear case of discrimination. We are asking you to sign this petition to get the government to take immediate action. 

The Late Late Toy Show is more than just a TV program—it’s a beloved Irish tradition that brings families together to celebrate the magic of childhood. For many children, it’s the most anticipated night of the year, a chance to see toys, hear stories, and experience the joy of Christmas kicking off. However, the current 9:30 PM start time is simply too late for most young children. By then, many are too tired to fully enjoy the show or can’t stay up at all. This leaves parents torn between letting kids miss out on the excitement or allowing them to stay up and face the consequences of a late night. Moving the Toy Show to 7 PM would: • Allow children to fully participate in this iconic event without sacrificing their sleep. • Create magical family moments for parents and kids to share together. • Honor the tradition of the Toy Show as a celebration for all ages, ensuring that no one feels excluded. This is about making a small but meaningful change that aligns with the Toy Show’s mission of joy, connection, and inclusivity for all Irish families. Let’s make it happen!