Proactive App for Parents and Children

A daily helpful guide during cancer treatment.

Join Our Mission

By supporting this project, you help parents and children fighting cancer.

Onko Notes - Your companion
through the most difficult journey.

Zero costs, maximum help - from parents for parents.

ROADMAP

Q3 2025

Creating the application structure and interface

We are currently designing the core of the application, adapting it to new ideas,
and filling it with content. We are also involved in its initial promotion
and securing funding for the next stages.
Q4 2025

Website - beta version

At this stage, we will launch a responsive website that works like a mobile app,
allowing users to follow key B-ALL and T-ALL treatment protocols.
Parents will be able to review the treatment plan and add essential information.
Q1 2026

Additional Protocols and User Login Strategy

We want to make the app as convenient as possible for parents.
This means unlimited access from any device with the option to log in to their account.
The login and data storage process requires us to take steps
to ensure the security of entrusted information,
including the potential need for encryption and data synchronization.
Q2 2026

Apps for Android, iOS & PWA (Progressive Web App)

At this stage, we use solutions that allow us to quickly deliver full functionality
across different devices. Therefore, in addition to the web version,
we plan to launch the app in the Google Play and Apple App Store.
This will help build greater trust among our patients and reach even more people in need.
These will not yet be native apps, but in later stages we will consider what benefits deeper integration with the Google and Apple ecosystems may bring.
Q3 2026

Community and Language Versions

We believe that one of the key features of the application will be its openness to users’ needs and its ability to evolve in response to feedback from the community.
We will actively listen to parents and young patients from many medical centers to better adapt the app’s features to their everyday challenges and real-life needs.

In addition to improvements driven directly by user feedback, we plan to introduce native language versions that will allow users to navigate the app in a natural and intuitive way.
This will enable people from different regions of the world to receive support and information in their own language — something especially important in such a sensitive area as caring for a child during treatment.
Q4 2026

Communication with Doctors

We want to support not only children and parents but also see an opportunity to assist doctors in tracking progress and verifying protocols.
In the future, we will consider whether direct communication between
patients and doctors through the app could be possible.
2027

Native Apps, New Protocols, Clinical Trials, and Much More...

Onko Notes was born out of a deep belief in its potential.
Already, parents, doctors, and foundations have shared their encouragement and positive feedback.

Every day, new ideas emerge — and from them, we aim to create something truly unique.
Our mission is to make Onko Notes a real source of support for families facing the most difficult moments.

We carefully capture every inspiration and continuously explore new ways this app can empower children and their parents.
Together we can shape Onko Notes into a tool that doesn’t just exist, but truly makes a difference.

"Before setting off,
gather your team.”

Only by working with specialists can we provide verified knowledge
in the field of oncology and nutrition.
 
Our experts are not anonymous.
They are real people with BIG HEARTS.
Thank you for your trust and support,
which gives us the strength to continue our work.
 

You can join too!

We invite open-minded and passionate
doctors, dietitians, psychologists,
and all specialists from across the world
who would like to join us in creating a space
for substantive support for patients and their loved ones
to participate in our project.
 
Contact with us:

"No one of us is as smart
as all of us."

- Kenneth H. Blanchard -
It is thanks to foundations and grassroots projects
that we are where we are today.
These activities are primarily driven by incredible people.
We would like to express our gratitude to you:

Ms.
Alicja Szydłowska-Budzich
from the Kawałek Nieba Foundation
Kawałek Nieba
Ms.
Ewa Majewska
website onkorodzice.pl
onkorodzice.pl
Ms.
Magda Undro-Łokietek
author of the book and website
"Brain Tumors in Children"
Guzy mózgu u dzieci
In helping children, we are supported by:
We are simply onko-parents.
This is our story:
kawalek-nieba.pl/kubus
We invite you to support this project!
www.siepomaga.pl/onko-notes