Winnipeg death doula provides care for the 2SLGBTQ community, chosen family at end of life

A Winnipeg death doula is working to ensure people in the 2SLGBTQ community have care and support at the end of their lives, services that are increasingly sought after across Canada, says an organization that advocates for improved quality of dying.

Rayne Foy-Vachon trained as an end-of-life doula during the pandemic to ensure people approaching death can avoid discrimination because there's a gap in queer-specific services, she said, and not every person has a supportive family member that will be with them at the end.

"There's no queer hospices, there's no queer hospice programs within the hospitals and there is no queer retirement homes or long-term care facilities in this province at all that are addressing the needs of the 2SLGBTQ+ community," Foy-Vachon said in an interview on Thursday.

When people in the 2SLGBTQ (two-spirit, lesbian, gay, bisexual, transgender and queer) community do access health-care services, they can experience homophobia and transphobia, and it makes them reluctant to seek out additional help, she said.

In addition to helping address a person's anxiety around death, Foy-Vachon helps advocate for people, whether with health-care providers or their own family members.

LISTEN | How Rayne Foy-Vachon supports people who are dying:

There are also challenges after death navigating how a 2SLGBTQ person might want to be remembered. 

Foy-Vachon helps ensure that her clients aren't called the wrong name or referred to using the wrong pronouns in an obituary, on a gravestone or in a funeral service. 

The person's chosen family or partner might not have legal rights because they're not married or legally considered family. 

Even on death's door, there can be stigma.

Foy-Vachon worked with people with HIV and AIDS in the 1980s and saw first-hand how people were treated as second-class citizens.

"In the hospital, they had a special ward for people who were HIV positive and dying of AIDS, and they were being treated like people who had leprosy. It was it was mind-boggling, actually, but so upsetting," she said.

Partners and family members couldn't visit them as they died.

"Yes, things have gotten better, but I still see the struggle within the queer community, within the health-care system. And you'd think from 30 years ago, you think that we'd see a larger change, and I don't feel like we have."