We need to better support First Nations women with violence-related brain injuries. Here’s how
- Written by Michelle Fitts, ARC DECRA Fellow, Institute for Culture and Society, Western Sydney University
Please be advised this article contains details of family violence.
Domestic violence causes disability for women through lasting impacts on their brains.
Traumatic brain injury refers to damage to, or alteration of, brain function due to a blow or force to the head. This leads to bruising, bleeding and tearing of brain tissue.
Such injury can have short-term (acute) effects or cumulative effects (over months or years).
A 2008 study by researchers in Adelaide found Aboriginal women experience head injury – including traumatic brain injury – due to assault at 69 times the rate of non-Indigenous women.
We spoke to Aboriginal and Torres Strait Islander women and communities in regional and remote Australia about their experiences of traumatic brain injuries from violence and their decision-making about health care access.
We also spoke to family members about what they observed in other women who were important to them and had experienced traumatic brain injury.
Here’s what we found – and how it can inform the development of better health care and support services.
Not feeling like the person I used to be
Violence-related traumatic brain injuries are not isolated experiences. The Aboriginal and Torres Strait Islander women we spoke to reported repetitive, violence-related head injuries over prolonged periods. Most women reported dozens of head injuries or had lost count of the number of injuries suffered.
The violence experienced was usually from Indigenous and non-Indigenous current or former male partners.
Aboriginal and Torres Strait Islander women reported living with and managing many common changes from traumatic brain injuries, including:
- memory troubles
- dizziness and headaches
- difficulty with concentration and organisation
- trouble with taking in information and thinking (sometimes described as “mixed up thinking”)
- finding it hard to start a yarn or keep conversations going with family and friends (described as “losing the words or having the words disappear” or feeling like “my brain went blank”)
- mood swings and impulsivity.
Coral shared:
Black out, now suffering from memory loss, like finding hard to be telling a yarn. These are stories that have happened to me. But I can’t remember it.
Kirra said about her own experience:
I put something somewhere, like, book, keys, phone. If I can’t see it, I forget where I put it. I have troubles keeping focused on one thing.
The women we interviewed also frequently mentioned being strangled. Non-fatal strangulation is also harmful to the brain because it reduces blood flow to the head and deprives the brain from getting oxygen.
When and why women access health care
Women felt accessing health care and support services after violence-related traumatic brain injury was not always an option for them. This was primarily because they were experiencing coercive control or were worried they would be reported to child protection authorities.
The characteristics of the injury also influenced their decisions about accessing health care. If there was no visible bruising, lacerations or marks, blood or recalled loss of consciousness (or blacking out) many Aboriginal and Torres Strait Islander women did not go to hospital and managed their own symptoms.
As Cathy explains:
Then one night he hit me. There was no hospital, no blood, bleeding, no one would have thought there was domestic violence that happened to me. Didn’t think it was serious enough to go.
How women manage symptoms of traumatic brain injury
Authors: Michelle Fitts, ARC DECRA Fellow, Institute for Culture and Society, Western Sydney University
