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The SANE Blog

‘Discover More’: the power of choir and community to expand horizons

Jenni and Niall standing in front of the Voices of Frankston banner at the Frankston Uniting Church

From singing alongside acrobats, community and acceptance, to improvement in mental health symptoms, Niall and Jenni chat about the empowerment that comes from ‘finding their voice’ in Voices of Frankston.

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'Discover More': how my husband's schizophrenia led me to Oxford University...twice!

Sandra is standing outside, smiling and wearing a patterned shirt. Sun is shining on her and the trees and plants behind her.

I eloped with my partner in November 1985, wearing huge ‘leg of mutton’ puff sleeves and listening to Starship’s ‘We built this city’. I worked in marketing and he was a registered nurse. He was funny, quirky, different and we were in love. We did what everyone was doing; buying a house, partying, dinners, birthdays, Christmas and in a blink, ten years had passed.

In 1998 our son was born, and everything seemed perfect. Seemed.

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'The death sentence didn't eventuate': the importance of discovering hope and purpose

Sandy is on a hockey pitch with her hockey stick in position to hit a ball. She is wearing a purple uniform and rainbow coloured socks.

From poet and violinist, to hockey player and advocate, Sandy Jeffs OAM is also one of SANE’s longest serving Peer Ambassadors, sharing her experience of living with schizophrenia for 45 years to shape public policy and help others. 

This Schizophrenia Awareness Week, which coincides with SANE’s 35th anniversary, we chat to Sandy about the ‘heady’ early days of SANE, becoming a public figure, and ‘curating’ a life towards wellness, despite the daily challenges.   

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OCD: the symptoms you don’t see

A photo of Tim from the shoulders up looking into camera calmly.

You might have seen Tim on ABC’s You Can’t Ask That sharing his experiences of Obsessive Compulsive Disorder (OCD). Here, he gives even more insight into living with OCD, the symptoms people don’t see and how acceptance gives him strength.  

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ECT and me - my pathway of recovery

Photo of coral under the ocean

This post originally appeared on Dr Deb Robert's blog here.

There is no one all ‘fixit’ for those who suffer from mental health conditions.  I’ve searched far and wide since I was a teenager for a therapy that can give me a lasting reprieve from the bouts of anxiety and depression I have suffered from for most of my life.  Whether my condition is a genetic predisposition or has developed from adverse experiences, I can’t conclude for certain but what I do know is that a combination of factors has contributed to my reality.

Traditional methods and farfetched therapies, I’ve explored them all.  I’ve seen psychologists who provide Cognitive Behaviour Therapy (CBT) and Dialectic Behaviour Therapy (DBT), and I’ve seen psychiatrists who provide psychotherapy and pharmaceuticals. I’ve explored Transcranial Magnetic Stimulation (TMS) and Eye Movement Desensitisation and Reprocessing (EMDR). I’ve tried kinesiology, chiropractic work, osteopathy and naturopathy. Acupuncture, yoga, yoga therapy and massage therapy.  Heck, I’ve even attempted equine therapy.  But, nothing has provided sustainable, long-lasting relief. 

Many of us, including me at times, have put barriers up to historically controversial therapies.  One such therapy is Electroconvulsive Therapy (ECT). 

For a long time, I sided with societal prejudice about ECT, so my decision to try ECT was not an easy one.

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Your no-bullshit mental health story

SANE-Youth-Peer-Ambassadors_thumbnail

As part of Be Kind to Your Mind, we asked young people who've lived with mental illness questions about their experience. Here's what they told us.

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How has diagnosis affected your sense of self?

As part of Be Kind to Your Mind, we asked young people who've lived with mental illness questions about their experience. Here's what they told us.

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When did you first seek help?

As part of Be Kind to Your Mind, we asked young people who've lived with mental illness questions about their experience. Here's what they told us.

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What does 'be kind to your mind' mean to you?

As part of Be Kind to Your Mind, we asked young people who've lived with mental illness questions about their experience. Here's what they told us.

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STIGMA: dismantled, revealed artists in conversation

Dax-Artists-In-Conversation
the knots we make

On Thursday 28 March, Julia Young, Curator at The Dax Centre, sat down with four artists from their current exhibition—STIGMA: dismantled, revealed to talk about their experience of stigma, self expression and art making.

Once the audience had indulged in cheese platters and drinks, they gathered around Cornelia Selover’s oil on board artwork, The complex heaven of a broken mind, to hear Simon Crosbie, Lucy Hotchin, Kylie Steinhardt and artist in residence Jessie Brooks-Dowsett participate in a Q&A style panel conversation.

“What are your experiences of stigma, and how do you feel we can dismantle and reveal it?,” Julia asked the artists.

“I think my own self stigma was my biggest obstacle,” Kylie said.

“Emergency room stigma from doctors, nurses and the medical system is the worst. That’s the part of the stigma that gets in your soul,” Lucy added. “The whole idea of doing well whilst experiencing mental illness—you can actually be in a state of flux and still be doing well in life.”

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