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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.
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.
GCN (Gay Community News) is Ireland's longest-running national LGBT+ publication and a not-for-profit registered charity. GCN is owned and published by the National Lesbian and Gay Federation (NLGF Ltd). This will be an ONGOING CAMPAIGN for GCN.
Competition: “Win a trip for two to Oasis in Croke Park” competition run by Wireless Radio (ROI) Ltd which runs from May 6th to May 16th, when a guaranteed winner will win the overall prize of a VIP trip for 2 to see Oasis in Dublin on August 16th 2025 including overnight accommodation and transfers to and from the hotel to the concert. There will be just one entry period across the length of the promotion - Monday 12th at 7am to Friday May 23rd at 4pm In order to win the overall prize the entrant must be selected from our random overall prize draw and be available to take our call on Friday May 23rd between 4.15pm and 4.45pm. The call must be answered within 5 rings. If the selected entrant does not answer the call then we will continue to randomly select from the draw until we have a successful entrant who answers a test of skill question correctly and is therefore deemed the overall winner. The winning call will be broadcast on all the participating FM stations on Friday May 23rd before 6.00pm.
reland’s 1st Community based Cancer Support Centre, founded in 1990 – Registered charity in Ireland, number 12589, Charity Regulator No: 20037178 – We provide professional Cancer Support & Psycho-Oncology services to people affected by Cancer – Supporting families affected by Cancer Nationwide in Ireland – We provide all of our services free of charge – We accept donations where possible to cover the costs of our services – We cater for patients, survivors, carers, families, friends and healthcare workers – We provide services to people of all ages, children and adults – We help over 1,500 families each year in Ireland
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.