Online Charity & Non Profit Fundraising Services

loffa.ie

Laois Offaly Families For Autism (LOFFA) is a parent-led support group for families of children and young adults with an autism diagnosis in the Laois and Offaly area. The registered charity organises social events and outings for families, provides workshops, information sessions, and training, and liaises with schools to raise awareness of autism. Membership is open to families living in Laois and Offaly, and the organisation relies on fundraising as it receives no public funding.

Down Syndrome Ireland

dsilmb.ie

Down Syndrome Ireland Louth/Meath Branch provides support and information to families with a member who has Down syndrome in counties Louth and Meath. The branch is run voluntarily by parents and offers services such as early intervention, home teacher support, employment support, parent and toddler groups, and a regional resource officer. It also organises events and a funding scheme for members.

Northwest Regional Drug & Alcohol Task Force

nwdrugtaskforce.ie

The North West Regional Drug & Alcohol Task Force can help with family support, treatment, recovery & education and also prevention of alcohol and drug misuse in Sligo, Leitrim and Donegal.

EYP Ireland

eyp.ie

EYP Ireland is the Irish national committee of the European Youth Parliament, a non-profit, non-partisan, non-governmental organisation. It organises conferences for secondary school students across Ireland, including regional sessions in Leinster, Connacht-Ulster, Munster, and Dublin, as well as a national session. The organisation aims to develop interest in European issues among young people through team-building, committee work, and debate.

Roscommon PPN

roscommonppn.ie

Roscommon PPN is the main link connecting Roscommon County Council with the community, voluntary, social inclusion, and environmental sectors in the county. It serves as a network for these groups to engage with the council and each other.

HHT Ireland

hhtireland.org

HHT Ireland is a charity supporting people affected by Hereditary Hemorrhagic Telangiectasia (HHT), a rare genetic vascular disorder. The organisation provides information on symptoms, diagnosis, treatment, and care pathways, and offers support through resources, patient stories, and events. It also runs awareness campaigns and fundraising activities.