MY STORY

I thought I could deal with my health later.

For a long time I kept functioning through endometriosis, migraines, digestive and hormonal problems, anxiety and poor sleep. Life still had to continue, so I did too.

Ilze Krastiņa

01

WHERE IT BEGAN

I wanted to understand what was happening before the body had to shout.

I lost my father to a heart attack when he was only 43. At 27, I experienced a microstroke myself. I also live with endometriosis, alongside years of migraines, digestive and hormonal concerns, anxiety, poor sleep and prolonged emotional, practical and financial pressure.

I kept going because that was what life required. Eventually, exhaustion and burnout made it impossible to pretend that health could remain a separate issue to deal with later.

I began looking for a way to understand the connections: what could be measured, where the greatest pressure was and which actions were creating real change.

I did not need another reason to try harder. I needed to know what my body was dealing with.

02

WHAT CHANGED

I stopped treating every problem as a separate failure.

Testing helped me see patterns that effort alone could not reveal. It gave me a baseline, helped me make more informed decisions and allowed me to check whether those decisions were changing anything.

But numbers also have limits. A person may be eating poorly because they are exhausted, sleeping badly because they feel unsafe, or unable to recover because their work and family leave no space. Health is biological, but it is also lived.

That is why my work combines measurable health information with relationships between specialists who see different parts of the same person.

As a mother, I want the next generation to recognise pressure earlier and understand that postponing health has a real cost.

03

WHY I SPEAK WITH FAMILIES AND SPECIALISTS

Endometriosis can begin with years of confusion.

This is personal to me. I know how widely endometriosis can reach into daily life: pain, energy, digestion, hormones, fertility, relationships and emotional wellbeing. These experiences do not arrive as neat, separate problems.

I also see young girls facing symptoms and difficult decisions while they and their families are still trying to understand what is normal, what deserves attention, which questions to ask and where to turn. That confusion can begin at an age when a girl is still learning to understand her own body.

This is one reason I speak with families as well as specialists. Families need better information and language for these conversations. Professionals across medical care, nutrition, gut health, stress, recovery and emotional wellbeing hold knowledge that can help people feel less lost.

Diagnosis and medical treatment remain with the appropriate medical specialists. My work focuses on earlier understanding, better questions and more connected support.

Test-based preventive health & international collaboration.

Talk with Ilze