Where do caregivers turn after their loved one passes on? What support is there when the caregiving team disbands? These are the difficult questions caregivers face at the start of the bereavement process. To address these overlooked issues, Zelda Freitas, a social worker from Caregiver Grief Connexion and member of the 51³Ô¹ÏÍøCouncil on Palliative Care, aims to use her years of work in palliative care, caregiving, and grief to educate. Together, with research-practitioner and associate professor at the 51³Ô¹ÏÍøSchool of Social Work, Professor Pam Orzeck, the Caregiver Grief Connexion will provide insights into the issues of caregiver grief and available resources at Palliative Care McGill’s upcoming National Palliative Care Week. Ìý

Lexa Frail (LF): Can you tell us a bit about your talk?
Zelda Freitas (ZF):ÌýThe goal is to explore caregiver grief in a way that focuses on the impact of caregiving on the grieving process. Caregiving doesn't occur in isolation; it often goes unseen or overlooked, and we want to bring attention to the fact that ¾±³Ù’s happening. Most people that live with illness, even advanced illness, are either living at home or in a residential setting. Most of the time, there are family members, partners or friends that take on the role of caregiving, and this discussion is centered on caregiver grief and the critical need to provide support to caregivers.
LF: What distinguishes caregiver grief from other forms of grief?
ZF:ÌýThat is a very good question and one for which we »å´Ç²Ô’t have a lot of research to draw from for answers. We're working in an area tha³Ù’s less explored, so we're looking at the research we do have available. What we do know that grief is different for caregivers; compared to other family members, partners or significant others experiencing or have experienced the death of that person. We know that caregivers continue to be impacted by their caregiving. This means there are certain factors that may increase caregivers’ vulnerability during their bereavement. The impact of the caregiving journey alone has many different factors that come into play. It could also be impacted by their relationship to the bereaved or the timing of the caregiving in their lives. Then, ³Ù³ó±ð°ù±ð’s the place that caregiving held: was it an added burden to an already very stressful life? Were they better prepared? Were they prepared at all for caregiving and their commitment? All these factors influence the ³¦²¹°ù±ð²µ¾±±¹±ð°ù’s sense of self and their relationships with others, further impacting their grief and then their bereavement.
We can also talk about caregivers transitioning out of caring into a role of no longer being a caregiver, which can impact several factors, including ´Ç²Ô±ð’s identity. If someone strongly identified with being a caregiver, that can shape how they grieve. They might also feel exhausted or alone, because caregiving often takes up so much time and energy that other parts of life—like social activities or other roles—get put on hold. As a result, they may end up feeling more isolated in their grief, just when having support is most important.
LF: Sounds like there's a lot to explore there. What do you want your audience to take away from your lecture?ZF:ÌýAbove all, supporting caregivers during their active caregiving can have a crucial impact on their grief process afterwards. We must ask: what are some of the things that we could do to better support caregivers while they're caregiving? What are some of the risk factors that could be present, and how could we help mitigate them? We're not talking about extraordinary measures. We're essentially talking about helping caregivers find their place and be in the community, with the rest of the care team validating their role and their experience. I³Ù’s about helping them prepare for that transition as well and identifying what might be helpful to them after they're no longer providing care.
Also, it's about knowing what existing resources could be helpful to them afterwards, given the fact that when they are caring for someone, there's usually a team around them. Then, when that person that they're caring for dies, that team also disappears. This can leave them feeling disconnected. We want to make sure we can bridge them to resources and recognizing themselves as individuals after caregiving.
LF: Is there anything else you want to add that I haven't mentioned?
ZF:ÌýWe are getting better at recognizing caregivers and the contribution that they make not only to the lives of the person they're caring for, but to society. 80% of care that's provided in the community is provided by caregivers. Caregivers are the backbone of our health and social care system, so making sure that their role is recognized, acknowledged, and that they have access to the support they need. Luckily, various organizations advocate for and promote support for caregivers, such as the Canadian and . Society is making progress, but caregiver grief still needs to be more fully acknowledged as an important part of the overall caregiving journey. People are caring for others every single day and tha³Ù’s been largely invisible. I believe we need to emphasize and fully recognize that this is happening.
Caregiver Grief Connexion’s presentation, “Understanding Caregiver Grief: Anticipatory and Post-Caregiving Grief,†will be held at noon on Wednesday, May 8. You will not want to miss this invaluable talk. For more details and registration info, as well as information on all the exciting activities being offered for National Palliative Care Week 2025, see our schedule.