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IT'S ENDOMETRIOSIS AWARENESS MONTH
Help us make a difference
To support Endometriosis Awareness Month, we have partnered with Endometriosis Australia to launch our most loved styles in Limoncello.
20% of sales will be donated to help fund awareness, education and critical research. Together, we can make a difference.
The collection launches Tuesday 3rd March at 11AM AEDT.
take a look at our
Exclusive Endometriosis Australia Collection
Kate's Story
My name is Kate, I am 35 and I am the Founder of Kat the Label.
I’d always heard about Endometriosis affecting other women but didn’t know much beyond the fact that it causes bad period cramps.
It wasn’t until I was 33 and struggling with infertility, that I found out I’d quietly had it all along.
I didn’t experience the typically discussed symptoms like severe pain and surgeries that many women with endometriosis go through, so it was the last obstacle I’d think of when it came to planning my family.
After my diagnosis, I learned how little I knew about the condition. 1 in 7 women are affected, but many go undiagnosed for years due to the common misconception that painful periods are normal.
And the only way to really find out.. is invasive surgery.
After multiple miscarriages, 6 frozen embryo transfers and 10 cycles of IVF, of what can only be described as a rollercoaster - I am so beyond thrilled and grateful to say as of today I am 20 weeks pregnant with my baby boy.
While I still feel a long road ahead of me, spreading awareness and talking about the milestones and hurdles for women living with Endo is something I am so passionate about.
I am so proud to be raising funds into much needed research and support into Endo with Endometriosis Australia - and those of you who are also affected in the many different ways by this condition I hear you, I’m with you and I am so proud of you.
DID YOU KNOW
1 in 7 women are impacted by endometriosis*
- Endometriosis Australia
Roxie's Story
I was diagnosed with stage 4 endometriosis, one of the worst cases my doctor had seen, after years of being told my severe period pain and bloating were “normal.” Like many women, I was prescribed hormonal contraceptives from 16 and later told there was no cure, only symptom management.
After surgery and having a Mirena fitted, I struggled with ongoing symptoms and began searching for another way to support my body. This led me to explore a holistic approach to my health, focusing on gradual lifestyle and dietary changes rather than simply managing symptoms.
By prioritising nutrition, movement, and daily habits that supported my wellbeing, my health slowly began to improve. After removing the Mirena and making consistent changes, my body continued to heal. Today, I have been symptom-free from endometriosis for nine years.
My journey taught me that healing isn’t always linear, but with consistency and learning to listen to your body, positive change is possible. I share my story to offer hope and empower others on their own health journey.
@roxie.health.coach
New Zealand
DID YOU KNOW
Around 50% of those with endometriosis are challenged by fertility, 30% are infertile and a high proportion of patients in their 20s and 30s require hysterectomy, robbing them of their chance to be a parent
- Endometriosis Australia
Beth's Story
Since I was 13, every period came with severe pain. I was told it was “normal” and relied on pain relief month after month. As the years went on, the symptoms worsened — cystic acne, painful bowel movements, leg pain, bloating and infertility. After years of being dismissed, multiple failed IUIs and IVF rounds, and constant advocating for myself, I finally demanded a laparoscopy.
The surgery revealed Stage IV endometriosis — the worst my gynaecologist had seen in 25 years. Everything was stuck together. Tissue had to be removed and I lost a fallopian tube. A biopsy confirmed endometriosis throughout.
For years I had known something wasn’t right. Finally, I had answers.
Our fertility journey has been long and heartbreaking — miscarriages, failed transfers, egg retrievals that declined to just one egg, and eventually the incredible gift of my sister donating her eggs. We did fall pregnant, but sadly lost that pregnancy too. The grief has been immense, but so has the resilience.
The biggest shift has been in my health.
Since excision surgery and committing to reducing inflammation through diet, acupuncture, naturopathy and prioritising my wellbeing, I am almost pain free. After suffering every single month for over a decade, I no longer live in fear of flare-ups. I don’t rely on pain medication. The constant inflammation and daily discomfort that once controlled my life is gone.
After all these years, I finally feel like I have my body back.
Endometriosis took a lot from me, but it also taught me to advocate for myself, to listen to my body, and to never ignore persistent pain. If sharing my story helps even one woman push for answers sooner, it’s worth it.
I’m not giving up on becoming a mum — it just might look different to what I once imagined. And for now, I’m grateful to be living without the pain that once defined my life.
@beth_reeve_hairstylist
Australia
Elizabeth's Story
I’ve had severely painful periods since I was 13 years old. I was diagnosed with stage 4 endometriosis at 19 years old, as well as interstitial cystitis and adenomyosis during laparoscopic surgery. I have had 6 surgeries/procedures in the last 3 years.
This disease affects me every day. I haven’t been able to work for the past 4 years and even had to quit my studies while searching for a diagnosis. I feel that I truly haven’t been able to live my life. I’ve been stuck in survival mode.
I wish more people would understand that this condition is a whole body inflammatory disease that doesn’t only affect women during their menstrual cycles but every other day as well. Every day I experience new and painful symptoms that have left me screaming on the floor or in the emergency room, just to be told “it’s just your endometriosis, there’s nothing we can do for you aside from pain relief”.
I spend my days bed bound in agony, suffering from symptoms like bladder pain, fatigue, body aches and joint pains, nausea, burning every time I pee, severe cramping, and that’s just a few of the symptoms.
I’ve now started an Instagram blog called _chronicpainchronicles that I started to raise awareness for endometriosis and share my story with others suffering from this cruel disease.
_chronicpainchronicles
DID YOU KNOW?
70% of women have to take unpaid time off work to manage their endometriosis symptoms
- Endometriosis Australia
Lani's Story
Endometriosis is ranked among the top 20 most painful conditions in the world — yet for years, my pain was dismissed. Doctors told me I was being dramatic, that it was just a “bad period.” Instead of real answers, I was put on birth control at 13, which only worsened my symptoms while messing with my hormones, mental health and physical health.
Despite endless doctors’ visits, scans, and excruciating pain that landed me in the hospital, I was misdiagnosed with IBS and put on different contraceptives. Nothing changed. I struggled to get out of bed, spent days lying on the bathroom floor, and relied on heat packs even at work/school that burned my skin — which resulted in toasted skin syndrome.
After seven years of being dismissed, I was diagnosed with stage 4 endometriosis — one of the worst cases they had seen. My options? An IUD or surgery. A few months later, I had a laparoscopy, where they found endometriosis covering my uterus, bladder, bowels, ovaries and some other major organs.
I spent days in the hospital on morphine, ketamine, endone and oxy just to manage the pain. And now, nearly a year post-surgery, I still live with it every single day.
Endometriosis is real. It is not just a bad period. And it needs to be taken seriously.
To everyone fighting this invisible battle — you are seen, you are heard, and you are not alone.
@lianatullochs
DID YOU KNOW?
There is no cure for endometriosis.
- Endometriosis Australia
Ella's Story
I discovered i had endometriosis during my final year of college. It flipped my life around. I was a very social and confident person before and my journey with endometriosis caused everything to change. I went from hanging out with my friends to always being in hospital or stuck at home in to much pain to function, medications i was given caused weight gain and surgical scars aswell as burns from hot water bottles all became apart of my body and it was really hard to accept myself and love my “new body” especially when it was also causing me so much pain.
I dealt with countless people within hospitals dismissing me. My first time in the emergency department for pain a doctor dismissed my pain and instead complained about how women are always coming in for the same reasons and are just “drug seeking”. I was told that i was imagining things and even lied to by medical professionals, they told me i was just being dramatic and even would refer me to psychologists instead of endo specialists.
I have a lot more but if you would like more details or some examples of horrid things i’m more than happy to share, endo needs a lot more awareness and it is horrible how many women get dismissed souly because it is a women’s issue leaving us crying and screaming in pain often even in hospitals.
@ellarosehalll
*Kat the Label acknowledges people in the transgender community and people who are intersex, non-binary and gender diverse who are living with endometriosis and may not identify as women.
