Links to other websites
These links are for information only and are not an endorsement of any group.We have no control over the nature, content and availability of those sites. S.O.F.T. Ireland does not necessarily imply a recommendation or endorse the content of these sites.
SOFT UK provides information and support to families affected by Trisomy 13 (
Your Unborn Baby was written by SOFT UK to provide a basis for discussions between you and your medical advisers
SOFT inspires hope and respects all on theirTrisomy journey
The birth of a healthy baby is one of the most exciting and eagerly anticipated events a family can experience
Trisomy Online is a free email based support group that was formed in 1997 for families and professionals
Chromosome 18’s mission is to help individuals with chromosome 18 abnormalities
Carmichael is the leading specialist training and support body for nonprofits in Ireland
A place where parents of children who were diagnosed with a terminal condition can share….
Stillbirth and Neonatal Death Association of Ireland aims to offer support to anyone affected by the death of a baby during pregnancy…
Provides support services for bereaved parents. Anam Cara Parent Bereavement understands we don’t live in an ideal world, we live in a world after our precious children have died before their time.
A Little Lifetime Foundation is the voice for bereaved parents and their families across Ireland…
The Irish Childhood Bereavement Network (ICBN) is a hub for those working with bereaved children…
The Jack & Jill Children’s Foundation provides direct funding, to families for home respite care…
Laura Lynn is a hospice for children with life-limiting conditions that provides palliative care and support....
We aim to act as an international group, supporting, informing and networking with anyone affected by a rare chromosome disorder
Affiliated photographers in Ireland have been instrumental in providing this most precious service – the gift of professional portraits to grieving families.
Rare Diseases Ireland (RDI) is the National Alliance for Rare Diseases in Ireland and its objective is to represent the voice of those who have or are at risk of developing a rare disease.