Advice as a newly diagnosed - PMOS
I have had PMOS for almost a year now…
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The AskPMOS App is for those who think they may have PMOS, those who already have a diagnosis, and those supporting women with PMOS.
The AskPMOS App is a trustworthy, comprehensive PMOS App developed by leading PMOS experts worldwide and co-designed with individuals living with PMOS. It will answer your PMOS questions and help you better manage your condition.
AskPMOS has a range of features, including:
TOTAL USERS
155K+
and growing
COUNTRIES
195
of 195 worldwide
AVAILABLE SINCE
2018
IOS & Android
EVIDENCE BASED
Free
backed by doctors and researchers
Pick a feature to see it in the app. Every screen is interactive, so tap around.
Easy to understand information based on the latest research evidence on PMOS.
I have a particular symptom that worries me, is it related to PCOS?
What do my test results mean?
I’m newly diagnosed with PCOS, what do I need to know right now?
Track your symptoms by logging them every day or at least once a week. This will help you track the different aspects PMOS has on you and will help with communicating with your doctor.
↻ November 5th, 2026
POSAA is Australia’s leading organisation committed to addressing the challenges faced by women with PMOS.
We bring together medical professionals, researchers, advocates, and the community to create a unified
platform for change. Learn about them here.
10 New Things about PMOS from the 2023 International Guideline – download it here.
Click on the icons to open a series of fact sheets which we hope will help you better understand PMOS.
The Yarning about Polycystic Ovary Syndrome (PMOS) booklet aims to provide Aboriginal and Torres Strait Islander women with information about the condition.
The Question Prompt List is a document intended to help women with PMOS obtain professional medical advice. It lists questions that are OK to ask your doctor or health professional. It is for women of all ages, weights and backgrounds. You may have been diagnosed recently or a long time ago.
Yumi Stynes catch up with ladies who have been battling PMOS for years and finds out how they get on top of it. Featuring Professor Helena Teede. Listen here.
Watch Professor Helena Teede busting myths and misinformation about PMOS on a TikTok produced by the ABC.
Watch Professor Helena Teede talk to Professor Joyce Harper
ABC journalist & PMOS consumer, Sabra Lane, and leading PMOS experts, MD & Endocrinologist, Prof Helena Teede and MD & OBGYN, A/Prof Jacqui Boyle host a Q&A session about PCOS/PMOS and discuss the AskPMOS App. (22/9/2021)
We are working with partners to develop a best practice framework for optimal PMOS care. This is modelled off the guidelines.
In Victoria, a statewide service is available, linked to the guidelines and resources.
The Victorian Statewide Polyendocrine Metabolic Ovarian Syndrome Service is unique and is the first of its kind nationally. The service is co-designed by women affected by PMOS and staffed with a multidisciplinary team who are world leaders in PMOS. It is supported by funding from the state government and affiliated with the NHMRC Centre for Research Excellence in PCOS/PMOS. It is a public clinic offered through Monash Health.
To be seen in the PMOS Monash Health clinic patients will need to be referred in by their GP to Monash Health. More information for GPs on the referral process is here.
This program is for Victorian residents only.
A healthier lifestyle is the first step to managing PMOS. This starts with a nutritious diet, regular physical activity and maintaining a healthy weight or reducing weight if in the unhealthy weight range.
Life! is a free healthy lifestyle program for Victorian residents that gives you knowledge, support and expert advice.
Watch more webinar recordings and events on MCHRI’s YouTube channel