Why Early Diagnosis of Endometriosis Matters More Than You Think

In Australia, it takes an average of 78 to 84 months that’s 6½ to 7 years for most people to receive an endometriosis diagnosis after their first symptoms appear.

Seven years.

Seven years of unexplained pain.
Seven years of uncertainty.
Seven years of missed opportunities for early intervention and support.

During that time, endometriosis can quietly progress, affecting not only physical wellbeing but also emotional health, relationships, and fertility.

What Exactly Is Endometriosis?

Endometriosis occurs when tissue similar to the uterine lining grows outside the uterus, commonly on the ovaries, fallopian tubes, or pelvic surfaces. Each month, this tissue responds to hormones just like the lining inside the uterus it thickens, breaks down, and bleeds.

But because the blood has nowhere to go, it leads to:

• Inflammation

• Scar tissue and adhesions

• Cysts

• Sometimes, infertility

Symptoms vary widely. Some people experience severe, debilitating pain. Others have almost no symptoms at all. That variability is one reason diagnosis takes so long but it shouldn’t have to.

Why Early Diagnosis Matters

Recognising endometriosis early can make an enormous difference. Early diagnosis can:

• Reduce pain and suffering by enabling timely treatment

• Preserve future fertility, minimising damage caused by long-term inflammation

• Empower informed decisions, including options like egg freezing for those not ready to grow their family yet

Knowledge truly is power and in the case of endometriosis, it can also be protection

If You’ve Been Putting It Off… Consider This Your Sign

If you’ve been suspecting endometriosis, or if getting checked has been sitting quietly on your “I’ll deal with it later” list since January this is your gentle reminder.

We’re continuing to see patients before the end of the year.

It is never too late to seek clarity, comfort, and a plan forward.

Your health matters. Your pain matters. And support is available.