Endometriosis is something that’s often overlooked—even though it affects 1 in 7 women globally. It’s more than just “bad period pain.” It’s a chronic condition that can be debilitating, painful, and frustratingly misunderstood.
In March, at Payless Promotions, we decided to support Endometriosis Awareness Month in our own fun and engaging way—with a “guess the number of lollies in the jar” competition that had the whole office talking!
We created a moment of connection and conversation with something everyone can relate to: lollies! While awareness is serious business, the education journey can include some fun and sugar along the way!
What Is Endometriosis?
Let’s start with the basics.
Endometriosis occurs when tissue similar to the lining of the uterus (called the endometrium) begins to grow outside the uterus. This rogue tissue can attach itself to the ovaries, fallopian tubes, the bladder, and even the bowel. Like regular uterine lining, it thickens, breaks down, and bleeds with every menstrual cycle. But because it’s outside the uterus, there’s no easy exit route.
That can lead to:
- Severe pain (especially during periods)
- Inflammation
- Scar tissue
- Fertility issues
It’s like your body is fighting itself every month. And for many women, it’s not just physical—it affects mental health, relationships, careers, and social lives.
Common Symptoms of Endometriosis
Endometriosis doesn’t look the same for everyone, which is one of the reasons it’s so tricky to diagnose. But here are some symptoms many people experience:
- Chronic pelvic pain
- Painful periods
- Pain during or after sex
- Pain when going to the toilet
- Fatigue
- Bloating (aka “endo belly”)
- Difficulty getting pregnant
If you or someone you know has these symptoms, it’s worth speaking to a healthcare professional—and pushing for answers.
HOW Long to Get Diagnosed?
Here’s the shocking part.
It takes an average of 6.5 years to be diagnosed with endometriosis.
Yep… SIX AND A HALF YEARS.
That’s a long time to live in pain without answers.
Many are told:
“It’s just period pain.”
“Try Panadol.”
“You’re exaggerating.”
“This is normal for women.”
Spoiler: it’s not.
“It wasn’t until I was 17 that I got diagnosed—after years of severe abdominal pain and being brushed off. I heard everything from ‘You’re too young for that’ to ‘Just tough it out.’ Finally, one GP listened. It made all the difference.”
Payless Promotions Team Member
This isn’t rare.
Too many women are made to feel like they’re overreacting when, in reality, they’re living with a serious condition.
Laparoscopy: The Only Way to Know for Sure
Endometriosis can only be officially diagnosed with a laparoscopy—a surgical procedure where a doctor uses a tiny camera to look inside the abdomen and check for endometrial tissue.
It’s invasive, and that can be scary – but for many, it’s the only way to get a clear answer.
“Once I had the laparoscopy, they found extensive endometriosis and removed as much as possible. It didn’t solve everything, but it finally gave me some relief and peace of mind.”
Payless Promotions Team Member
A Laparoscopy can also help guide treatment options like hormone therapy, pain management, and in some cases, fertility support.
Endometriosis & Fertility: What You Need to Know
Another major challenge people with endometriosis face? Fertility issues.
Around 30–50% of people with endo experience trouble getting pregnant. For some, it’s the first clue that something isn’t right.
“I was told at 17 that I might never have children. And then another doctor told me that getting pregnant would ‘fix it.’ Those two conversations happened within weeks of each other. It was heartbreaking and confusing.”
Payless Promotions Team Member
The emotional toll of this kind of medical whiplash can be overwhelming. That’s why it’s so important to raise awareness—not just among patients, but among doctors, too.
The Lolly Jar Challenge ?
Who doesn’t love a guessing game?
We filled a jar with a colourful mix of lollies, and asked staff to guess the number. Simple, sweet, and a great way to spark conversations.
Some guesses were hilariously off (we won’t name names!), but the best part? It created a lighthearted space to talk about a very serious topic.
And we didn’t stop there! Alongside the competition, we shared facts, personal stories, and resources around endometriosis, helping everyone better understand what so many people silently go through.
Why It Worked
- Everyone could participate
- It sparked genuine curiosity
- It created a non-intimidating entry point for learning
- It brought people together for a common cause
We think awareness doesn’t always have to look like a ribbon or a fundraiser. Sometimes, it looks like a jar of jellybeans and a few honest conversations.
How You Can Support Endometriosis Awareness
Whether you’re an individual, a small business, or a large organisation, here are some easy ways to show support and raise awareness:
1. Talk About It
Conversations break down the stigma. Share stories, ask questions, and encourage openness in your workplace, school, or social circle.
2. Educate Yourself
The more we know, the more we can support each other. Check out trusted resources like:
3. Share on Social Media
Use your platforms to spread awareness. Post infographics, personal stories, or even photos from your own awareness activities. Hashtags like #EndoAwareness, #1in7, and #EndoWarrior help expand the conversation.
4. Host a Morning Tea or Fun Office Game
Follow our lead! Whether it’s a bake sale, trivia quiz, or lolly jar guess, interactive activities help people engage and learn in a low-pressure way.
5. Donate or Fundraise
If you’re able, support organisations like Endometriosis Australia through donations or fundraisers. Every dollar goes towards research, advocacy, and support services.
A Message from Our Team
To anyone out there living with endometriosis: we see you.
Whether you’re undiagnosed, recovering from surgery, navigating fertility questions, or just trying to get through the day—your pain is valid. Your story matters.
And to everyone else: let’s keep the conversation going. Awareness isn’t just for one day or one month. It’s about changing how we listen, how we speak, and how we treat those around us.
Why Payless Promotions Cares
We’re not a medical organisation. We sell branded merchandise, but we care deeply about the people who make Payless Promotions —the individuals who show up to work, share their stories, and support one another through tough times.
Final Thoughts (and a Big Thank You!)
We’re proud to have supported Endometriosis Awareness Month in a way that felt true to our team—fun, engaging, and meaningful. Our lolly jar competition was more than a game; it was a symbol of how small actions can lead to big conversations.
We’re committed to continuing this journey, supporting our team and community however we can. Because when we talk openly, listen deeply, and learn together, we can create real change.
If you’re experiencing symptoms of endometriosis, or want to learn more, we highly recommend visiting Endometriosis Australia for trusted resources, support groups, and expert advice.
