Community Advisory Committee

Nicole has been involved with Sands since her first child, son Nicholas, was stillborn in 2006. Nicole has held many roles including Chairperson of Sands Queensland. She has attended many events, overseen the running of others, and remains an active and supportive member of the organisation. In her professional life, Nicole provides strategic stakeholder engagement, government relations and communications advice through her company, Nicole Ireland Communications.

Nicole says, “As a long-time member of the Sands family and a passionate advocate for our grass roots activities, I am delighted the Board of Red Nose, including Sands, has endorsed the formation of the Community Advisory Committee. I feel honoured and privileged to chair this Committee as I truly value the collective support of bereaved parents and the community we have created, and will continue to grow, together. To me, this Committee provides a strong link between this community of bereaved parents from both Red Nose and Sands right across the country to the broader organisation and to our external stakeholders. I believe we have a fantastic opportunity to share best practice events, ideas and programs to support our community and ensure everyone remains connected, engaged and included – and to make sure that all bereaved parents, including those who will unfortunately join our community in the future, will be able to access the care and support they deserve.”

David Brown is a bereaved parent from Western Australia. David experienced the stillbirth of his daughter Edie Violet in 2017.

David speaks to an ongoing family commitment acknowledging Edie as a part of their family and would like to see a community where families feel comfortable sharing their experiences. 

David is a community engagement professional and has worked for government and community organisations in Western Australian regional centres and now Perth.

Megan Warren is a bereaved parent from Western Australia. Megan experienced the loss of four sons through miscarriage, stillbirth and newborn death in the late 90s and early 2000s.

Megan has been extensively engaged with Red Nose and Sands across support and community activities. Megan is a writer and is currently on the Esperance Readers and Writers’ Committee and has also held Workplace Health and Safety committee roles in her workplace.

Megan is currently taking a leave of absence from the committee while in a staff team role.

Ari Magalhaes is a bereaved parent from Tasmania. Ari experienced the 2019 and 2020 stillbirths of daughters Mia and Lily due to a genetic condition.

Originally from Brazil and educated in Europe, Ari is an economist with a Masters’ Degree in International Management. She has been highly engaged with local not for profits in Tasmania.

Ari has been engaged with Red Nose and Sands remotely and is thoughtful about way that we can be more engaged with people in communities like Tasmania where we don’t currently have any paid team members.

​Samantha Jager is a bereaved parent from Queensland. Samantha experienced the stillbirth of her son Gabriel in 2014 and has also experienced early pregnancy loss.

Samantha is a volunteer peer support group facilitator in Brisbane and has been highly engaged with a range of Sands community engagement events. She is a former lawyer who is now a teacher.

Emma Hain is a bereaved parent from NSW. Emma experienced the death of her infant son Eli at three months. Eli was born with a rare lung disease, Pulmonary Hyperplasia, a condition which was only diagnosed after he passed away. Emma received precious hand and foot casts from Red Nose and her family have become highly engaged members of the Red Nose community in the Hunter region.

Emma describes our community as important to her whole family, “my children have other children around them who understand, my husband has other men and supportive people around him, we have a tribe where we have a sense of belonging and understanding.”

Emma brings 12 years’ experience as director and manager of a children’s entertainment company.

Bonnie Carter (OAM) is a bereaved parent from the ACT. Bonnie tragically experienced the stillbirth of Grace in 2016 and then Matilda in 2017, and has also experienced early pregnancy loss.

Bonnie and her husband have been active in advocacy through the stillbirth inquiry and community events through Red Nose, local family led initiatives. Bonnie’s key interest is holding space for bereaved families in the community. Drawing on her experience as Assistant Director in DFAT’s Diversity and Inclusion space, Bonnie believes there are small, but meaningful steps to make our community activities more inclusive.