health

'I was 5 days into parenthood when a midwife found me on the floor. It was a sliding doors moment.'

 

Warning: This post contains mentions of post-partum depression and psychosis, and may be triggering for some readers.

Have you ever had a moment when your answer to a question determined whether your life imploded?

I have.

It came five days into parenthood. I was lying on the floor in my maternity hospital room crying because I was trying to outrun a jaguar chasing me towards a cliff. Things were starting to go very wrong in my brain.

How to talk to people with anxiety. Post continues below.

In the following months, when my mind warped and writhed in the grip of psychosis and later catatonic depression, and when what started out as postnatal psychosis turned out to be a first episode of Bipolar 1 disorder, I could not imagine things being worse.

But they could have been.

My sliding doors moment occurred soon after my midwife discovered me on the floor and said:

“I think you have more going on than the baby blues.”

And before anything else happened she asked me this question:

“Do you have private health insurance?”

Because I was able to answer ‘Yes’ then, my life now is very different to what it could have been had I answered ‘No’.

Thirteen years on I have two healthy, happy children and a strong marriage. I have a roof over my head and many nourishing relationships. I was able to continue working as a small animal veterinarian, finish my Master of Arts in Writing, Editing, and Publishing, write a memoir detailing my experience with a severe mental illness, and develop my passion as a mental health advocate, both independently and as a SANE Peer Ambassador.

I take none of this for granted.

Because here’s how things could have gone had my answer been “No”:

I wouldn’t have had access to the Mother Baby Unit (MBU) in the private psychiatric hospital I was referred to, courtesy of my private health insurance.

I still would have had my first psychotic episode two days later. But instead of being in the safety of the MBU where postnatal psychosis could have been diagnosed and treated immediately, I would have lost touch with reality while attempting to look after my one-week old baby at home.

Had my husband recognised I was being tortured by psychosis and called an ambulance; I would have been taken to the nearest public psychiatric ward.

I may not even have been admitted because (at that stage) I was not suicidal or a danger to anyone else. And yet in the private hospital setting I was (accurately) assessed as being unwell enough to not only remain hospitalised but to be moved from the MBU into the hospital’s SCU (Special Care Unit).

If I had made it onto a public psychiatric ward, I might have been given a chair to sleep in because sometimes there are not enough free beds.

Public psychiatric wards are under-resourced. And their dedicated, compassionate staff risk burn out because they work in stressful conditions with inadequate support.

For patients, being ‘looked after’ in these conditions can mean being put in a room and told to ‘cry it out.’ It can mean requests for PRN (as needed) medication are not acted on for over eight hours. (That is like asking for pain relief after major surgery and having to wait over eight hours before someone has time to get it for you.)

Had I been admitted I may have been assaulted by another patient, whose care was inadequate.

I would have been discharged too soon. I may even have been discharged whilst suicidal, and my husband would have been instructed to watch me for 24 hours a day to keep me safe.

Over the years I would have seen different mental health professionals at different times. Continuity of care is rare in the public system. I may have received my correct diagnosis. I may not have.

My experiences in the public mental health system may have been so traumatic they left me distrustful of all psychiatric care. I may have self-medicated with alcohol or illegal drugs because I felt I had no other options available to dull my excruciating symptoms.

I may have slid down the slippery slope of self-medication onto the black ice of addiction.

Without the correct management, this illness could have left me jobless, homeless, and with no functional relationships to support me. It could have left me a criminal.

If suicide didn’t kill me, an accidental drug overdose or living on the streets might have.

With high quality care people living with severe mental illness, like me, can return to a fantastic, functional quality of life. But it sickens me to know that in this country access to that care is not a right but a means dependent privilege.

That knowledge sits like a rock in my stomach.

That knowledge makes me ache and work for a future when my children’s generation can access excellent mental health care regardless of their ability to afford private health insurance.

And the first step into that future is holding the terrible state of our public mental health system, and the politicians who turn away from its state of disrepair, responsible for breaking some of our most vulnerable people.

Each of the scenarios I have described as potentially happening in the public mental health system have happened to people I have had conversations with over the last 13 years.

This post was originally published on Thought Food and was republished here with full permission. 

Anita Link is a writer, a mother of two, a small animal veterinarian and a passionate mental health advocate. You can read more from Anita on her blog.  

If you think you or someone you know may be suffering from depression, contact PANDA – Post and Antenatal Depression Association. You can find their website here or call their helpline – 1300 726 306.

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Top Comments

Amandarose 5 years ago

I couldn’t agree more about the terrible state of mental healthcare in Australia.
Public hospitals are great for the majority of issues but mental health for serious mental conditions gets little attention. We here alot about depression of the less severe variety and anxiety but god help those with psychosis or suicidal depression.
I have two brothers with schizophrenia with a 32 history of dealing with it.
Back when my elder brother was diagnosed in the 80’s I was in year 4 at school. Back then we could force him into care. He was hospitalised for months while the tried to work out the right medication and he had good care living at Richmond Fellowship where they live in and get fed, entertained and medicated. It may have had a rehab element also - but I can’t recall being 10.

He bounced in and out of hostels, and flats. And in and out of psychosis. He did not do well out if assisted care and was violent at home ( as kids I recall him hospitalising my mum a few times).

Come the 90’s they put him in Clozapine which was a wonder drug for him at the time but being oral he needed supervision to take it or he would not and end up doing something violent/crazy due to psychosis. He was terrifying unmedicated.
Eventually good assisted living ( think uni dorm style with own room, nice gardens/shared spaces and nurses 24hrs a day. Perfect for 25 years or so.
Then in the 2000’s so idiot decided to shut the place down and send all those seriously unwell people to live alone and “rehabilitate” them for two years before sending them to commission flats. This nearly killed my brother, as he suffered neuroleptic malignant syndrome and was found on his floor in a coma. They did not notify his family for “privacy reasons” and we only found out as a friend was visiting someone at the hospital and saw him there. I can see why they would try and cover it up judging by the terrible overprescribing and drug interactions evident.
Basically non for profits are funded by how well they “rehabilitate” someone to live alone and push it when all common sense and reason shows it will not work.
After much fighting with his revolving door of case workers he was eventually placed back into assisted care. He had to throw a brick through a neighbours window first, punch a bank teller and get banned from the local bakery for violence.

I think his current housing is actually private- it’s basically a huge house with two to a room with meals provided. They get NDIS funding for people to come in and shower him and help clean his room , take him on outings etc. they get most of his pay and give him pocket money. Run by a compassionate father and son. Better then living alone in filth.

Serious mental illness is not a vote winner so it’s unlikely to get funded.
I think the best care my brother got was the 90’s model. They had moved on from institutions to a nicer half way point with lots of care and support funded and run by the government. People were treated in the community with extensive support if they could be with the hospitals there if needed without the bed pressure with have today. The entire Not-for-profit sector is bull shit with funding model that does not serve the people.