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Who We Are?
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Hi, I'm Jana

- founder of PKU Magic.

 

This is how our PKU story began:

9 days after my daughter Vanesa was born, she was diagnosed

with phenylketonuria (PKU) through a newborn screening.

From that moment on, our daily lives began to follow

the strict rules of a low-protein diet.

We knew absolutely nothing about PKU. We gradually learned

to understand values, weigh ingredients, calculate protein intake, and

find a balance between safety and a normal childhood.

 

I realized very quickly that I didn't just want to follow the rules -

I wanted to understand them in depth and create a system that

would work in real life. I started creating my own recipes.

I experimented, wrote down weights, adjusted ratios,

tested procedures, and rewrote recipes over and over again –

until the result was accurate, safe, and delicious.

Gradually, experimentation became a process.
From the experiments system.
From uncertainty to certainty.

 

And that’s how the PKU Magic project was born.

 

PKU Magic is a platform focused on modern low-protein recipes

with an emphasis on accurate calculations, detailed procedures,

and the real needs of families living with PKU.

Each recipe is tested in our own kitchen and created

to be practical in everyday life.

 

The name "PKU Magic" was born from moments when strict rules

were transformed into food that brought joy. It is a reminder that

even special diets can be creative, aesthetic and full of flavor.

 

Today, PKU Magic is growing as a blog, a community,

and a upcoming cookbook that summarizes our

most popular and time-tested recipes.

 

Welcome to our PKU kitchen 🪄💗

Hodnoty použité pri výpočtoch v našich receptoch boli prerátané podľa tabuliek priemerného
Hodnoty použité pri výpočtoch v našich receptoch boli prerátané podľa tabuliek priemerného
Hodnoty použité pri výpočtoch v našich receptoch boli prerátané podľa tabuliek priemerného
Hodnoty použité pri výpočtoch v našich receptoch boli prerátané podľa tabuliek priemerného
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Collaborations & Partnerships

For brand partnerships, sponsored recipes, product features in recipes, cookbook collaborations and media inquiries:

We’d love to hear from you.

  • Pinterest
  • Facebook
  • Instagram
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What is PKU
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Phenylketonuria (PKU) is a rare inherited metabolic disorder.

 

People with PKU are unable to properly break down ​phenylalanine – an amino acid found in protein-containing foods.


As a result, phenylalanine builds up in the body.

What is Phenylketonuria?

 

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If phenylalanine is not properly processed, it gradually accumulates in the blood.


High levels can be harmful, especially for brain development and the nervous system.


That’s why it is essential to carefully control its intake every day.

How PKU affects the body?

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How is PKU treated?

The foundation of treatment is a strict low-protein diet that limits phenylalanine intake.

​​

What does PKU management involve?​

PKU management is a daily routine that includes:

tracking phenylalanine intake
calculating protein intake
• accurately weighing foods
• regular blood testing

(e.g. dried blood spot) to monitor levels

Hodnoty použité pri výpočtoch v našich receptoch boli prerátané podľa tabuliek priemerného
Hodnoty použité pri výpočtoch v našich receptoch boli prerátané podľa tabuliek priemerného
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Hodnoty použité pri výpočtoch v našich receptoch boli prerátané podľa tabuliek priemerného
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