Australia Recognise Endometriosis As A Disability

The issue

1 in 10 females suffer from endometriosis. This chronic illness can cause debilitating pain among other symptoms.

Many women also have to endure multiple surgeries and are left unable to work and yet the illness is NOT recognised as a disability.

This disease is destroying lives and even pushing young women to take their own life due to the mental and physical pain that this disease puts them through. Many employers are unfairly dismissing women from work due to 'too many sick days', many private health funds don't cover the surgeries and specialists we need to see...the public wait lists are long and it's difficult to see anyone who actually cares. Often women will have 4-5 laparoscopic surgeries before being diagnosed and the mental anguish that we go through during diagnosis is extreme. It puts pressure on all relationships in a woman's life and makes everything so much harder. With the UK recognising Endometriosis as a Disability in 2017, we want a push to follow suit!

Australian women need EXPOSURE on this disease so employers, partners, family and friends understand what we go through. We want to be HEARD and UNDERSTOOD. Mostly we need more funding towards finding a CURE... or at least something to ease the pain so that we can find some quality of life and we want our disease recognised as a DISABILITY so we can receive the help and support that we need and deserve.

If you care about women's health and women's rights, you will sign this petition and help us to boost the understanding of endometriosis, recognise it for the disability it is and help support more research which that women are in such desperate need of.

Victory
This petition made change with 5,281 supporters!

The issue

1 in 10 females suffer from endometriosis. This chronic illness can cause debilitating pain among other symptoms.

Many women also have to endure multiple surgeries and are left unable to work and yet the illness is NOT recognised as a disability.

This disease is destroying lives and even pushing young women to take their own life due to the mental and physical pain that this disease puts them through. Many employers are unfairly dismissing women from work due to 'too many sick days', many private health funds don't cover the surgeries and specialists we need to see...the public wait lists are long and it's difficult to see anyone who actually cares. Often women will have 4-5 laparoscopic surgeries before being diagnosed and the mental anguish that we go through during diagnosis is extreme. It puts pressure on all relationships in a woman's life and makes everything so much harder. With the UK recognising Endometriosis as a Disability in 2017, we want a push to follow suit!

Australian women need EXPOSURE on this disease so employers, partners, family and friends understand what we go through. We want to be HEARD and UNDERSTOOD. Mostly we need more funding towards finding a CURE... or at least something to ease the pain so that we can find some quality of life and we want our disease recognised as a DISABILITY so we can receive the help and support that we need and deserve.

If you care about women's health and women's rights, you will sign this petition and help us to boost the understanding of endometriosis, recognise it for the disability it is and help support more research which that women are in such desperate need of.

The Decision Makers

Greg Hunt
Minister for Health
Responded
Time for action on endometriosis The Turnbull Government will create the first National Action Plan for Endometriosis, providing much needed support for women who face this often misunderstood medical condition. The Plan will seek to improve the treatment, understanding and awareness of endometriosis, which affects around one in ten Australian women. It will be developed in collaboration with the Australian Coalition for Endometriosis, and members of the Parliamentary Friends for Endometriosis Awareness. The Plan will focus on how to improve the lives of women who face this terrible condition. Diagnosis of the condition currently takes on average around eight to nine years, placing a significant toll on individuals, families and the community. This condition should have been better acknowledged and acted upon long ago but today we are taking action so the struggle that women face will no longer be silent or their battles private. We will work with the medical community and key stakeholders to look into what gaps might be present in training, support and care. Importantly medical research will be critical to uncovering new options for diagnosis, treatment, care and understanding of endometriosis. We will therefore issue a targeted call for endometriosis research under the Medical Research Future Fund. The Turnbull Government will also provide funding of $160,000, through the National Health and Medical Research Council, for Professor Grant Montgomery to use genomics to investigate better treatments for women with endometriosis. The Jean Hailes Foundation, supported by Turnbull Government funding, will also make endometriosis a key feature of next year’s Women’s Health Week, to raise awareness of the condition. All participants of the Australian Coalition for Endometriosis should be congratulated for the advocacy and voice they give to the thousands of women who suffer from endometriosis. We look forward to developing this new national approach with all involved in the battle against endometriosis.
Malcolm Turnbull
Former Prime Minister of Australia
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Petition created on 18 July 2017