- Animal Rights
- Corporate accountability
- Disability rights
- Food and Sustainable Production
- Gender Equality
- Governance and Transparency
- LGBT rights
- Mental health
- Privacy and Data Protection
- Rural Inequality
- Social Justice
- Transport and Infrastructure
- Workers' Rights
Make Irish politicians use the public health services only. No private care.Our health service is in crisis. I heard a lady on the radio say "you would never believe the conditions unless you see it". I firmly believe that to be true. Our health service will never improve until Irish politicians (and preferably their families) have to rely solely on the public health system. Do we not have the right to prompt and effective healthcare. It shouldn't become a matter of your ability to pay. It might stop them trying to fix the public health services by pumping unending money into private hospitals. Please sign and share.
Demand full rights for people with disabilities in Ireland - add your voiceAfter an 11-year delay, the Government recently took the final steps towards ratifying the United Nations Convention on the Rights of People with Disabilities. However, it turns out that the government has for now abandoned its pledge to at the same time ratify a key protocol that goes along with the Convention. The protocol gives people with disabilities a real chance to achieve their rights in cases where the government is failing them. The protocol allows groups or individuals to make complaints to the UN to ensure the government does what it says it will do. This government has effectively turned its back on 640,000 people with disabilities in this State by failing to ratify this protocol.
We demand our Right2Water Referendum.We want the people's voice to be heard respecting water and sanitation services in Ireland, and a referendum be held. Across the globe ordinary people have undergone tremendous hardship and suffering when water services are privatised. Water is a human right and must never be under the control of 'for profit' companies. Publicly owned, funded and managed water and sanitation services, free at the point of use, is the only way to guarantee access for all.
Fixed charged fines for parking illegally in all disabled parking spaces.While the current €80 fixed charge fine ensures that some people don’t misuse disabled parking spaces, it’s clearly not enough of a deterrent. We need to root out this practice which causes real inconvenience for people who actually rely on disabled parking spots.
"'Shame'rock for Trump - Not in our name"An Taoiseach is our representative abroad. When he accepts prejudice, racism and bigotry, it shames the people of our country. We feel that such an alliance is not good for our country's reputation and undermines our relationship with other countries. Trump is a despicable human being. A point must be reached where falling at the foot of a powerful man, at the expense of our values and morals and international reputation is not acceptable! "'Shame'rock for Trump: Not in our Name"
Appoint a qualified Consultant for C.S.F leaks in IrelandA cerebrospinal fluid (CSF) leak is a potentially incapacitating condition where a hole, year or defect forms in the dura matter . The dura matter is a membrane which holds in the CSF, a clear and colourless fluid that supports bathes and protects the brain and spinal cord. When CSF leaks out, the volume of fluid around the brain reduces. This can cause the brain to sag, impacting upon nerves brain stem and spinal cord. And that is only the beginning of the catalogue of symptoms that inflict us; some, life threatening. Early diagnosis and intervention is fundamental for long term prognosis and care, but unfortunately Ireland does not have one, qualified, appointed specialist in the whole country. This has lead to people with CSF leaks and SIH becoming so de-conditioned, with years of no medical intervention, that they cannot work, function and sometimes cannot walk. I was only diagnosed in my late 30's, with these said conditions and still awaiting an outcome regards help From consultants doctors hospital etc , And unfortunately the time between this condition taken hold of me and nothing being done for me regards a solution or medical intervention taking place has now passed two and a half years .. My story isn't special, or unique -it's a very similar story for most Irish patients. This cannot continue. We cannot let another generation of CSF patients go undiagnosed and untreated. Please support our campaign -Sign the petition and share on social media
Social Hubs instead of rural post officesWe seem to be allowing a continuous stripping of services from rural Ireland, this would be a start of a serious opportunity to reverse this trend and offer a genuine service to elderly people who want to remain in their homes. We could customise these hubs to suit each village or location, eg combine this service with the local community centre, a cafe a local business or a stand alone unit. This hub could be staffed by locals and would offer all the services of a post office, plus access for the elderly to a government services help desk, environmental help, grants, tourist info etc, it could also be a start of decentralisation from Dublin.
Gain Irish exemption for 14 year old daughter with DyslexiaIt is important because 1. Irish being a compulsory subject in this country is of little importance to my daughter who struggles with reading and writing in English because of her dyslexia. 2. Because of an outdated educational psychology system in Ireland my daughter can drop 2 other subjects to give her time for learning support.
Ratify the Convention on the Rights of Persons with DisabilitiesWe have to end the inconceivable injustices and degrading treatment of disabled people here in Ireland. Too many disabled children and adults are living in forced institutions, separated from our families and communities, with no control over our lives, bodily integrity, often afraid, abused and unheard. Ireland is the last country in the European Union to ratify the convention. Ratifying the Convention will mean formal recognition of our rights and enable independent living and freedom from discrimination. 11 years after the UN adopted the Convention, Ireland is the only county in the EU that has failed to ratify it. We are asking all of you, to help us to shine a spotlight on our government’s inaction. It is NOT okay that disabled people have no control over our lives. We, disabled people, need your support and cannot do it alone. We need everyone to please support the legal protection of Disabled people's rights. By signing this important petition to ratify the United Nations Convention on the Rights of Disabled People, your support will help to positively change our country and the lives of many for the better. Thank you very much!
Stop Nursing Homes Charging Extra FeesNursing homes need to be up front with an 'additional charges'. Many elderly people are too infirm to participate in 'additional extra’s and services! whatever they turn out to be. A reported example is of some being charged €20 for Mass is disgraceful. All private nursing homes should publish their list of what they are charging for over and above the fee for care. The list of ‘services’ should have the cost next to each item listed as well.
Appoint a qualified consultant for Ehlers-Danlos syndrome in IrelandEhlers-Danlos is a complex genetic condition resulting in faulty collagen. Because of this fault, patients' joints can dislocate on a daily basis, leaving us in agony. And that is only the beginning of the catalogue of symptoms that inflict us; some, life threatening. Early diagnosis and intervention is fundamental for long term prognosis and care, but unfortunately Ireland does not have one, qualified, appointed specialist in the whole country. This has lead to people with EDS becoming so de-conditioned, with years of no medical intervention, that they cannot work, function and sometimes cannot walk. I was only diagnosed in my early 30's, after a life in pain -at times, extreme agony. I saw numerous specialists in various areas, spent my 20's on waiting lists. By the time of my diagnoses I had deteriorated so much that I found it very difficult to find even a physiotherapist or occupational therapist to keep me on as a patient. I am slowly clawing back parts of my life, but must pay out of my own pocket for treatment in the UK. My story isn't special, or unique -it's a very similar story for most Irish patients. This cannot continue. People are literally being left to rot. We cannot let another generation of EDS patients go undiagnosed and untreated. Please support our campaign -Sign the petition and share on social media.