Coming Soon to iOS

Your endometriosis journey, finally understood

We're building EndoPal – the first app that truly understands the complexities of living with endometriosis.

Currently in development – join our waitlist to help shape an app that works for you.

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EndoPal Preview Coming Soon

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1 in 10

women* live with endometriosis

7+ years

average time to diagnosis

100+

women* consulted in our design

Designed With You, For You

We're building these features based on feedback from women* with endometriosis and guidance from healthcare professionals. Help us prioritize what matters most to you.

Comprehensive Symptom Tracking

Track not just pain, but fatigue, mood, digestion, and other symptoms often overlooked in standard trackers.

Personalized Insights

Discover patterns and potential triggers with visualizations that help you understand your unique experience.

Treatment Tracking & Reminders

Keep track of medications, appointments, and which treatments actually help your symptoms.

Community Support

Connect with others who understand what you're going through. Share experiences and strategies that work for you.

Consultation Preparation

Generate comprehensive reports to share with healthcare providers, helping you advocate for better care.

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Our Mission: Health Justice Through Innovation

Endometriosis affects 1 in 10 women* worldwide, yet it takes an average of 7-10 years to receive a diagnosis. We believe this is unacceptable.

EndoPal is being created to empower women* with the tools they need to understand their bodies, track crucial symptoms, and advocate effectively for their healthcare needs.

Throughout our development process, we've been consulting with healthcare professionals specializing in endometriosis care to ensure our app delivers medically accurate and truly helpful features.

This isn't just an app—it's a movement toward better understanding, treatment, and eventually a cure for endometriosis.

Meet the Team Behind EndoPal

We're a passionate group of healthcare professionals, technologists, and women* with lived endometriosis experience.

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Tanika Naidoo

Founder & CEO

After living with endometriosis for 10 years and experiencing firsthand the challenges of diagnosis and treatment, Tanika founded EndoPal to create the tool she wished she had.

We started EndoPal because we believe women* with endometriosis deserve better tools to manage their health. While our core team brings technology and personal experience to the table, we regularly consult with healthcare professionals to ensure medical accuracy and relevance.

Join us on this journey

Join Our Community of Co-Creators

We're building EndoPal with constant input from women* like you. Here's what some of our early collaborators are saying:

"I've tried so many period trackers, but none of them really understood endometriosis. I'm excited to help shape an app that actually gets what I'm going through."

NA

Nisha A.

Living with endo for 15 years

"Being able to provide input on what this app should include makes me feel heard for the first time in my healthcare journey. I can't wait to see the final product."

AM

Aisha M.

EndoPal beta tester

"I'm thrilled to see an app focusing specifically on endometriosis. The data this will provide could be invaluable for both patients and providers."

DR

Dr. N.

Healthcare Consultant

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Help Shape EndoPal

Join our waitlist to be the first to try EndoPal and have your say in its development. Your input will help create an app that truly serves your needs.

By signing up, you'll receive updates about EndoPal. We respect your privacy and will never share your information.

What happens next?

1

You'll receive updates on our development progress

2

We'll invite you to participate in surveys and user testing

3

You'll get early access when the app is ready for beta testing