Our Partners
As a charity dedicated to supporting families in times of need, we have recognised the unique challenges faced by those who have lost a twin, triplet, or multiples.
The loss of a multiple birth can be particularly devastating, as it involves not only the loss of a child but also the unique bond shared between siblings. In order to provide comprehensive and specialised support to these families, we have partnered with other charities who share our commitment, helping those in grief.
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By collaborating with other charities, we are able to gather our resources and expertise to offer a wider range of services and support to families who have experienced the loss of a twin, triplet, or multiples. Through these partnerships, we are able to provide support groups, educational resources and staff training. Together, we aim to create a network of support that can help families navigate the complex emotions and challenges that come with such a profound loss.
Our Partners
Footprints Baby Loss
Footprints Baby Loss is a bereavement charity that provides vital support to parents and families who experience the death of one or more of their twins or triplets before, during or after birth.
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‘We are a charity run by bereaved parents, for bereaved parents.’
Our support is provided by those who have had first hand experience of twin or triplet loss. We understand the value of having a safe space to be able to communicate with someone who has been through something similar, and provide a kind, caring and inclusive approach with our bereavement services.
We provide bereavement support in the form of befriending, online support groups and an online community private group. You can find out more details on our website.
Taps Support
The TAPS Support Foundation is a registered charity dedicated to changing the way monochorionic twin pregnancies are diagnosed, handled, and treated, as well as raising the profile of Twin Anemia Polycythemia Sequence (TAPS).
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​Our primary goal is to break down the barriers between research and patients. Patients should have access to research that can help them advocate for care, as well as easy access to resources that can help them get the treatment they need.