Service Checker

A charity that provides assistance dogs for children and adults living with physical disabilities free of charge

Drop Call service for dating adverts, i.e.fixed price call for placing dating advert on service. Not currently advertised but it is live.

The Irish Motor Neurone Disease Association (IMNDA) is the only organisation of its kind providing care and support to people with Motor Neurone Disease, their families, friends and carers. We provide support services to help people living with the disease - these services include access to 6 MND Nurses, provision of specialised equipment, counselling sessions, funding towards research, funding towards homecare and operation of a helpline. Our National Drink Tea for MND campaign happens for the month of March and enables us to continue providing these services.

The Hope Foundation is a registered charity working with street-connected and slum-dwelling children in Kolkata (formerly Calcutta), India. We work to free children and poor families from lives of pain, abuse, poverty and darkness. Living on the streets, children are exposed to horrendous physical and sexual abuse. Those who survive are left to fend for themselves, with no promise of a safe future. They are forced to work from as young as five years of age to earn money for food and so cannot go to school. HOPE works to free them from child labour. HOPE funds and operates 58 projects.

The Alzheimer Society of Ireland works across the country in the heart of local communities providing dementia specific services and supports and advocating for the rights and needs of all people living with dementia and their carers.Our vision is an Ireland where no one goes through dementia alone and where policies and services respond appropriately to the person with dementia and their carers, at the times they need support. A national non-profit organisation, The Alzheimer Society of Ireland is person centred, rights-based and grassroots led with the voice of the person with dementia and their carer at its core.

The Alzheimer Society of Ireland works across the country in the heart of local communities providing dementia specific services and supports and advocating for the rights and needs of all people living with dementia and their carers.Our vision is an Ireland where no one goes through dementia alone and where policies and services respond appropriately to the person with dementia and their carers, at the times they need support.A national non-profit organisation, The Alzheimer Society of Ireland is person centred, rights-based and grassroots led with the voice of the person with dementia and their carer at its core.

The Hope Foundation is a registered charity working with street-connected and slum-dwelling children in Kolkata (formerly Calcutta), India. We work to free children and poor families from lives of pain, abuse, poverty and darkness. Living on the streets, children are exposed to horrendous physical and sexual abuse. Those who survive are left to fend for themselves, with no promise of a safe future. They are forced to work from as young as five years of age to earn money for food and so cannot go to school. HOPE works to free them from child labour. HOPE funds and operates 58 projects.

The Irish Motor Neurone Disease Association (IMNDA) is the only organisation of its kind providing care and support to people with Motor Neurone Disease, their families, friends and carers. We provide support services to help people living with the disease - these services include access to 6 MND Nurses, provision of specialised equipment, counselling sessions, funding towards research, funding towards homecare and operation of a helpline. Our National Drink Tea for MND campaign happens for the month of June and enables us to continue providing these services.

To provide access to free Clinical Assessment and Management to all families of a young person who are living with an Inherited Cardiac Condition or have suffered, or are at risk of, a sudden cardiac death. To provide a Family Support Programme, offering free access to Listening Volunteers, Mentors and bereavement specialists. To organize events, and provide access to information and networks. To support research into the causes and prevention of sudden cardiac death, in collaboration with other likeminded bodies.

To provide access to free Clinical Assessment and Management to all families of a young person who are living with an Inherited Cardiac Condition or have suffered, or are at risk of, a sudden cardiac death. To provide a Family Support Programme, offering free access to Listening Volunteers, Mentors and bereavement specialists. To organize events, and provide access to information and networks. To support research into the causes and prevention of sudden cardiac death, in collaboration with other likeminded bodies.

To provide access to free Clinical Assessment and Management to all families of a young person who are living with an Inherited Cardiac Condition or have suffered, or are at risk of, a sudden cardiac death. To provide a Family Support Programme, offering free access to Listening Volunteers, Mentors and bereavement specialists. To organize events, and provide access to information and networks. To support research into the causes and prevention of sudden cardiac death, in collaboration with other likeminded bodies.

To provide access to free Clinical Assessment and Management to all families of a young person who are living with an Inherited Cardiac Condition or have suffered, or are at risk of, a sudden cardiac death. To provide a Family Support Programme, offering free access to Listening Volunteers, Mentors and bereavement specialists. To organize events, and provide access to information and networks. To support research into the causes and prevention of sudden cardiac death, in collaboration with other likeminded bodies.

To provide access to free Clinical Assessment and Management to all families of a young person who are living with an Inherited Cardiac Condition or have suffered, or are at risk of, a sudden cardiac death. To provide a Family Support Programme, offering free access to Listening Volunteers, Mentors and bereavement specialists. To organize events, and provide access to information and networks. To support research into the causes and prevention of sudden cardiac death, in collaboration with other likeminded bodies.

Over the years, our purpose has evolved: our main focus is on creating the social change needed to end domestic violence. We continue to work closely with 37 frontline services, throughout Ireland, to achieve this. Together, we support the development and provision of critical lifelines to women and children. We also provide direct specialist domestic violence services for women and children including refuge. These services are primarily provided for women and children living in Mayo and surrounding counties.

To provide access to free Clinical Assessment and Management to all families of a young person who are living with an Inherited Cardiac Condition or have suffered, or are at risk of, a sudden cardiac death. To provide a Family Support Programme, offering free access to Listening Volunteers, Mentors and bereavement specialists. To organize events, and provide access to information and networks. To support research into the causes and prevention of sudden cardiac death, in collaboration with other likeminded bodies.

We are making the 10th anniversary of the ICE Bucket Challenge and we are hoping to raise funds to support those living with MND. The Irish Motor Neurone Disease Association (IMNDA) is the only organisation of its kind in this country. It was set up in May 1985 to provide care and support to people with Motor Neurone Disease, their carers, families, and friends. There are currently over 450 people living with MND in Ireland. MND is often referred to as the 1,000 day disease as most people die within 1,000 days of being diagnosed. Our key services include: o Home visiting by our six MND Nurse Specialists o Financial assistance towards home care o Providing specialist medical equipment free of charge to our clients o Assistance towards counselling, travel to and from medical appointments, recharge grant and voice banking grant (these new additional services are a result of Charlie Bird Development fund) o Supporting research into the causes and treatments of MND o Freefone Information support line for clients and families The Association relies heavily on fundraising activities from our members and supporters. We need to raise over 85% of our overall income. It costs approx. 2.4 million to run the Association each year.

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