Radio host makes shocking claim about women's health—expert responds!

In a world where we've made leaps and bounds in understanding and treating various health conditions, it's disheartening to hear that misconceptions and misinformation still run rampant, even among those with a public platform.

This was made painfully clear when a radio host with a penchant for controversy made a shocking and ill-informed claim about a serious women's health issue.


During a recent broadcast, Marty Sheargold, who was already under fire for making sexist remarks about Australia's national women's football team, decided to add fuel to the fire by suggesting that endometriosis, a chronic and often debilitating condition, is 'made up.'

'God, don't ladies carry on. Jesus Christ, there is no end to it. Honestly, endometriosis, and this is controversial,' he said.

'No, I'm going to say it, it's controversial. It's made up.'


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Radio host Marty Sheargold is criticised for calling endometriosis a 'made-up' condition. Credit: Facebook


His flippant comment not only sparked outrage but also highlighted the ongoing struggle for recognition and understanding that many women face when dealing with their health concerns.

Endometriosis is a condition where tissue similar to the lining of the uterus grows outside of it, causing severe pain and a host of other symptoms.

It affects nearly 1 million Australian women and girls, who often endure an average diagnosis delay of 6.5 years.


This delay can lead to a range of complications, including fertility issues, and is a testament to the need for better awareness and medical attention.
Dr Brad Robinson, a Brisbane-based obstetrician-gynaecologist, took to social media to address Sheargold's comments with sarcasm and seriousness.

'Sincere thank you to Marty Sheargold for helping me today sort my scheduling out,' he responded.

'I stupidly—I don’t know what I was thinking—had surgery booked for a patient for likely endometriosis, but of course, it can’t be because endo is not real.'

'So, look, we’ve just cancelled and I have a free slot available now, Thanks Dr Sheargold.'

Dr Robinson shared a story of a patient who had suffered from undiagnosed endometriosis for over half her life, emphasising the systemic failure in addressing women's reproductive and menstrual health.


The response to Dr Robinson's posts was overwhelming, with many women sharing their own harrowing experiences of living with endometriosis.

Stories of being dismissed by doctors told their symptoms were all in their head or being left undiagnosed for years were all too common.
These accounts underscore the importance of advocacy and the need for a medical system that listens to and supports women.

After the backlash, Triple M took action by parting ways with Sheargold.

The network's chief content officer, Dave Cameron, issued a statement acknowledging the need for reflection and review and the responsibility to align programming with the standards and expectations of the audience.

This incident is a stark reminder that words have power, mainly when spoken by those with a platform.


It's crucial for public figures to be informed and sensitive when discussing health issues, as their words can either contribute to the stigma or help in breaking it down.

This story hits close to home for our readers at the Seniors Discount Club, many of whom are women or have women in their lives they care deeply about.

It's a call to action to support the women around us, to advocate for better healthcare, and to educate ourselves and others about conditions like endometriosis.

In other news, it wasn't long since Triple M's Marty Sheargold was back on the airwaves after a sudden, months-long absence.

He took a break after drawing inspiration from two high-profile AFL coaches, citing burnout and the need for time away. You can read more about it here.


Credit: YouTube

Key Takeaways

  • A Brisbane-based obstetrician-gynaecologist criticised radio host Marty Sheargold for claiming that endometriosis is a 'made-up' condition.
  • Marty Sheargold faced backlash and was axed by Triple M after making sexist and misogynistic comments on-air, including dismissive remarks about endometriosis.
  • Doctor Brad Robinson used social media to sarcastically thank Sheargold and highlight the seriousness and reality of endometriosis, which is often unrecognised and can significantly impact women’s health.
  • Women with endometriosis shared their long and painful journeys of seeking a diagnosis, underscoring the challenges and medical system failings in recognising and treating the condition.
Have you or someone you know been affected by endometriosis or other under-recognised health conditions? How do you think we can improve awareness and treatment? Your stories and insights are valuable, and by sharing them, we can work towards a future where no woman's health concern is dismissed or belittled.
 
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I was lucky?? to be born with two completely separate uteruses (uteri?). From the age of 12, I suffered severe period pain every four weeks, with both uteruses contracting together.

It was the 50s, so knowledge of endometriosis and parental sympathy were both in very short supply. I was sent to school on days when the abdominal pain radiating into my legs was so bad I could hardly walk. I went many nights with little sleep. Mum eventually took me to the doctor who knew exactly what was necessary to stop the pain: Get married and have a baby, that'll cure it. To a 14 year old, this goes down as the most ridiculous piece of medical advice I've ever heard.

By the time I was 28, hubby and I had been trying for a baby for six years with many miscarriages. I was losing so much blood every month that even I had to admit that a baby of my own wasn't going to happen, so I underwent a total hysterectomy. I was riddled with endometriosis and also had internal and external fibroid cysts.

I'd love to find a way to make this moron suffer the pain for just one hour, and then tell me endometriosis is 'made up'!
I am sorry you had to suffer so much.
 
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I was lucky?? to be born with two completely separate uteruses (uteri?). From the age of 12, I suffered severe period pain every four weeks, with both uteruses contracting together.

It was the 50s, so knowledge of endometriosis and parental sympathy were both in very short supply. I was sent to school on days when the abdominal pain radiating into my legs was so bad I could hardly walk. I went many nights with little sleep. Mum eventually took me to the doctor who knew exactly what was necessary to stop the pain: Get married and have a baby, that'll cure it. To a 14 year old, this goes down as the most ridiculous piece of medical advice I've ever heard.

By the time I was 28, hubby and I had been trying for a baby for six years with many miscarriages. I was losing so much blood every month that even I had to admit that a baby of my own wasn't going to happen, so I underwent a total hysterectomy. I was riddled with endometriosis and also had internal and external fibroid cysts.

I'd love to find a way to make this moron suffer the pain for just one hour, and then tell me endometriosis is 'made up'!
WOW, you have been through a lot - so sorry to hear!
 
I am sorry you had to suffer so much.
Thank you so much Jen. Hubby and I have a wonderful adopted son who's 47 years old. He's been married for 17 years to our lovely daughter in law. They've given us our adored grandchildren, 14 and 15.

It was hard to go through at the time, but it's made me both strong and empathetic, so it was worth it. And through it all, I still worked full time as an Emergency Ward nurse in a large Sydney teaching hospital, and that gave me perspective.
 
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Reactions: mOiOz
I was lucky?? to be born with two completely separate uteruses (uteri?). From the age of 12, I suffered severe period pain every four weeks, with both uteruses contracting together.

It was the 50s, so knowledge of endometriosis and parental sympathy were both in very short supply. I was sent to school on days when the abdominal pain radiating into my legs was so bad I could hardly walk. I went many nights with little sleep. Mum eventually took me to the doctor who knew exactly what was necessary to stop the pain: Get married and have a baby, that'll cure it. To a 14 year old, this goes down as the most ridiculous piece of medical advice I've ever heard.

By the time I was 28, hubby and I had been trying for a baby for six years with many miscarriages. I was losing so much blood every month that even I had to admit that a baby of my own wasn't going to happen, so I underwent a total hysterectomy. I was riddled with endometriosis and also had internal and external fibroid cysts.

I'd love to find a way to make this moron suffer the pain for just one hour, and then tell me endometriosis is 'made up'!
My heart goes out to you. Had the same “cure” recommended to me. I missed so much school and exams. Even fainted with pain when I had the chance to go to the Melbourne Cup in the sixties. Missed the race altogether. In the end monthly pethedine injections until I was no longer allowed. Thank you menapause
 
My heart goes out to you all who suffered from this I never suffered with my periods and had early menopause thank goodness. ☹️
 

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