Dr Maddy Walker from Thrive Acupuncture and Wellness discusses stress the impact it can have on our cycles in Traditional Chinese Medicine (TCM), emphasising a holistic approach that recognises periods not only as an event of the reproductive system, but one affecting our whole selves . She also discusses how acupuncture can help alleviate the impact of stress, and the other ways in which you can optimise your experience based on the principles of TCM.

Mel from House of Beauty Tofu talks about her new wellness space and journey to healing and self love that inspired this passion project and labour of love. As a fellow Endo Warrior, Mel has made The House of Beauty Tofu an endo friendly space and donates to QENDO to support her fellow endo warriors on their wellness journeys. Read about the space and what inspired Mel to start her wellness business.

Heavy bleeding is a common symptom for those experiencing adenomyosis and endometriosis, and is also associated with other gynaecological conditions such as uterine fibroids. It can be an incredibly frustrating, embarrassing and exhausting symptom to cope with. Read up about what needs assessment, some of your options to tackle heavy bleeding, and looking beyond pads and tampons to deal with your flow.

Our support coordinator Dannielle and HR/management consultant Tracey Stewart continue discussing this essential topic of chronic illness in the workplace with part two! In part two we discuss leave entitlements, flexible working arrangements, using your QENDO App as a tool to improve your workplace experience, and how employers can support employees with endometriosis. Dannielle also shares her experience of coping with endometriosis and adenomyosis in the workplace.

Sharing one’s chronic illness story is an act of both bravery and compassion, and doing so can inspire and empower others on their journey. Today we hear from Emily Johnson, who shares her adenomyosis journey, and how one odd symptom pushed her towards a diagnosis despite having other symptoms ignore since early adolescence. Emily is the instagram account @_livingwithadenomyosis_ an account that promotes awareness and education surrounding adenomyosis.

Conversations in the workplace about endometriosis can be difficult, but armed with the right information, expectations and your rights in the workplace, you can make the conversation easier. In this two part blog series, we’ll give you a comprehensive overlook of some of the most frequently encountered issues in the workplace when it comes to talking chronic illness, and some strategies to overcome them, as well as the support available to you.

We’re continuing our stories from the international QENDO community with the UK and endo warrior Neha Chudasama, who describes her endometriosis journey as hard but enlightening. In this blog she talks about the challenges of talking about a taboo subject in her family, as well as feeling alone and isolated before receiving her diagnosis. Read all about her journey here.

In this blog we share the perspectives of some of our LGBTIQA+ chronic illness community and the unique challenges they face every day in their endo, adeno, PCOS, infertility or pelvic pain journeys. Only through awarenesses and listening to the many unique voices in our community can we better understand how we promote empowerment, inclusivity and advocacy for any individual affected by these illnesses. Hear these perspectives and learn about some of the safe spaces within QENDO where you can find support!

Your partner is often one of the most important people in your life, inevitably they become part of your chronic illness journey, but while some partners naturally step into the role of support person, for others it can be a challenge understanding what that role is and how they can support you on your journey. Today, let’s talk about how you can talk to your partner about chronic illness, what resources are available to support both of you, and starting that journey to understanding.

We announced our new 1800 number today to ensure anyone affected by endometriosis, adenomyosis, PCOS or infertility is able to feel safe, supported and included when accessing the 24/7 support line. Our new number, 1800 ASK QENDO (1800 275 573636) feels right and more reflective of our views within the organisation. For more information as to why we felt it was right we changed our number, read on.

Sharing one’s chronic illness story is an act of both bravery and compassion, and doing so can inspire and empower others on their journey. In this blog we hear from a member of our international QENDO community, Jesica Mazzone from Boston, USA. Jessica shares her journey from adolescence to a diagnosis with endometriosis in her twenties and finding an endometriosis surgeon who was able to give her the care she needed. She hopes sharing her story will help others and is thankful for the online community of other endometriosis sufferers she has found.

Whether you have endometriosis or adenomyosis, there are a myriad of symptoms that may affect you, but one that so many of us have in common is pain. There are many options for pain management both pharmacological and non-pharmacological, and knowing which ones are right for you comes down to understanding your symptoms and body, as well as communicating with your healthcare team! Support coordinator and recovery nurse Dannielle takes you through the ins and outs of pain management and tracking your progress with the QENDO App.

Have you downloaded the QENDO App? Our app team takes you through a video tutorial on the basics of tracking with emphasis on adding, editing and deleting symptoms. 

Meet Ella Swan, an incredible Endo Warrior from New Zealand who is passionate about advocacy and education surrounding endometriosis. Bells is a teacher, nutritionist, and ambassador for anyone affected by endometriosis, as well as mental illness. Though her endo journey has featured some hard moments, she believes that the friends, support and community she’s gained from her fellow warriors has made it almost worth it. Bells shares this inspiring piece with the QENDO Blog about some of her achievements and why she’s passionate about empowering those with endometriosis to live their best lives.

Tracking your cycle, do you do it? In this blog our support coordinator Dannielle goes through the benefits of tracking your cycle for overall health and management of your chronic illness, exploring how the QENDO App can help you do this comprehensively and in a way unique to your symptom profile.

In this blog our Support Team Coordinator Dannielle will talk through how you can utilise the QENDO App to better communicate with your healthcare team and the positive changes this can have on your management of endometriosis, adenomyosis, PCOS, infertility and pelvic pain.

Today, QENDO announced the launch of the QENDO App! Following extensive Beta testing from our wide, varied and inclusive community, the QENDO App will be available for immediate download from the app and Google Play stores.

This week we travel to the United States and meet Shamitris Kirby, adenomyosis advocate and creator of My Peach Fuzz, a blog sharing her experiences with diagnosis, treatment and ongoing management of adenomyosis, and a safe space for sharing resources for anyone experiencing pelvic pain. Here she shares her journey to diagnosis and why she’s a passionate advocate for anyone affected by adenomyosis.

You’ve met our incredible management team over the last few weeks on the blog, heard their stories and the experiences that are the drive for why they do what they do. But we thought it was important that you met our recently repatriated Vice President Jaime White, who returned to her hometown in New Zealand recently, to shine a light on her contributions to QENDO. Our Support Coordinator and Blog Coordinator Dannielle reflects on Jaime’s achievements and on behalf of all of Team QENDO says, thank you Jaime for you drive, compassion and ambition. You’ll always be part of Team QENDO.