Baby Leontýnka and Lilly Are Battling Lung Failure

❤️ Every Breath Counts – Let's Give Little Lungs a Big Hope ❤️

Together we supported the little fighters at Bulovka 

One is only just beginning her life. The other is standing on the threshold of adulthood. Nearly sixteen years separate them, yet they share something no child should ever have to experience – their world is confined by four walls and lungs that are failing them.

100% of your donations go directly towards helping those in need. The operating costs of the Our Lungs Foundation are covered by other sources.

 

For little Leontýnka, we want to provide monitoring equipment that will help her family through the challenging transition from hospital to home care.

For Lilly, we want to provide an oxygen concentrator so that her world no longer has to end at her front door.

Leontýnka

Leontýnka came into the world much earlier than expected. She was born extremely prematurely, at just 23 weeks and 2 days of pregnancy, weighing only 420 grams. Instead of spending their first days together at home, her parents found themselves fighting for their little girl's life.

No one knew whether her tiny body would be able to cope with challenges it was not yet ready to face. After several days, doctors even discussed the possibility of palliative care with her parents.

But her mum and dad kept believing in her.

"We never even considered that option. We believed in her."
Leontýnka's mum

And Leontýnka chose to fight. From a tiny 420-gram baby emerged a little fighter who shows every day just how much strength can be hidden in such a tiny body.

A Hospital Room Instead of a Crib

Leontýnka has been in hospital since the day she was born. Her mum stays by her side 24 hours a day, seven days a week, and the family still does not know exactly when the moment they have been waiting for so desperately will finally come – the day they can take her home.

Leontýnka needs continuous oxygen support. Due to additional health complications, she undergoes numerous examinations and procedures. Every day, cerebrospinal fluid is drained from her Ommaya reservoir.

She is also learning something that comes naturally to a healthy baby – drinking from a bottle. But even ordinary feeding is exhausting for her tiny body. Her mum therefore still has to give her part of her nutrition through a feeding tube directly into her stomach.

One of the consequences of Leontýnka's extremely premature birth is bronchopulmonary dysplasia.

Her lungs were not sufficiently developed when she was born. Breathing is therefore much more difficult and exhausting for her tiny body than it is for a healthy baby, and she continues to need oxygen support.

An Oxygen Monitor Would Make Caring for Her Easier

Leontýnka's mum is especially worried when her daughter is asleep. Leontýnka experiences breathing difficulties during sleep, and her lungs are not always able to provide her body with enough oxygen. In hospital, she is constantly surrounded by monitors, alarms and medical professionals.

With the Owlet Dream Sock smart monitor, Leontýnka's mum was able to monitor her heart rate and blood oxygen levels. If the device detects that something may be wrong, her mum immediately receives an alert through an app on her phone.

"At home, monitoring would make so many things easier for me. It would ease my fear that something might happen and I wouldn't notice. At the same time, I would also be able to think about the needs of my older daughter."
Leontýnka's mum

At home, her ten-year-old sister Tonička is also waiting for them. She is starting fifth grade and, like any other child, she needs her mum too. The family used to love spending time outdoors, going for walks and train journeys, swimming, picking mushrooms and going to football matches together. But for the past few months, their lives have revolved around the hospital.

For Leontýnka's mum, the monitoring device could provide greater reassurance while caring for her little girl, while also allowing her to devote some of her attention to Tonička.

Because Leontýnka has already spent long enough fighting for her life in hospital. Now we want to help her take the next step – towards home.

Lilly Is Sixteen. Her World Shouldn't End at Her Front Door.

In September, Lilly will start secondary school and hopes to become a chef. She loves singing, takes solo singing lessons at an arts school, and is learning to play the guitar. She enjoys social media and, just like other teenagers her age, what she wants most is to spend time with her friends. Her mum says she has an incredible sense of humour and can make everyone around her laugh.

Lilly has experienced health problems since early childhood. For a long time, she was treated for allergies until further examinations revealed a serious chronic lung condition associated with a mutation in the FLNA gene.

Today, her lungs need oxygen support. She sleeps with oxygen at night. In the morning, after getting ready, she takes her medication and checks her oxygen saturation. If it is too low, she needs oxygen support even while resting. When she moves around or does anything physically demanding, she regularly needs supplemental oxygen.

As a result, even something as simple as going out into the garden to see her dog can no longer be taken for granted.

"It mainly limits my mobility. I can't do the things I used to do, and I can't go where I would like to go. For example, meeting up with friends or going to dance classes. I spend most of my time at home."
Lilly

Lilly used to dance K-pop. She rode her bike, sang, performed on stage and lived the active life of a teenage girl. Today, she can no longer dance. She cannot ride a bike, swim or dive, and she has to significantly limit physical activity.

But her illness has taken away more than just her freedom of movement.

It has also taken away a part of life that should be completely normal at sixteen. Spontaneously meeting up with friends. Going to the cinema. Going to a concert. Spending the night at her grandmother's. Spending a weekend with her older sister.

And Lilly's mum watches as the illness affects not only her daughter's body, but her emotional well-being too.

"As her mum, I wish for Lilly to be happy and to truly experience her teenage years. Her first love, going to the cinema or concerts with friends, or simply being able to meet up with them whenever she feels like it."
Lilly's mum

Oxygen That Can Travel with the Family

Lilly requires long-term oxygen therapy at home. According to her family, her current oxygen supply lasts approximately three hours.

This is where the Philips Oxygenate 5 oxygen concentrator could help. The concentrator draws oxygen from the surrounding air and produces concentrated oxygen for oxygen therapy. The Oxygenate 5 provides a continuous oxygen flow ranging from 0.5 to 5 litres per minute.

It is a stationary but transportable oxygen concentrator. This does not mean that Lilly could carry it with her on a walk. However, her family could transport it by car – to her grandmother's house, her sister's home or on a family trip – and plug it into a power supply once they arrive.

Her safe space would no longer have to end at home.

The specific settings and use of oxygen therapy will, of course, always be determined by Lilly's treating physician according to her individual medical needs.

Little Lungs. Big Hope. ❤️ Let's Help Open the Door to a Bigger World. ❤️

Breath for Others

Breath for Others is a long-term fundraising campaign organized by the Naše plíce Foundation Fund.
Thanks to donations, we can finance medical equipment, help specific patients, and support projects focused on lung health.

What your donations support:

  • medical equipment for respiratory support

  • rehabilitation aids

  • assistance for specific patients

  • support for hospitals and healthcare facilities

How your help makes a difference:

  1. Donors contribute to the Breath for Others campaign.

  2. The foundation selects projects and patients in need of assistance.

  3. The funds are used directly for specific support – equipment, aids, or treatment assistance.

Breathing is something most of us take for granted.
For many patients, however, every breath is a struggle. 

Your support can help change their everyday lives. 


100% of funds go directly to specific help

The Our Lungs Foundation was established by Y&T Luxury Property – a real estate agency that has been helping people find their dream homes for over 15 years.

We would like to emphasize that the Our Lungs Foundation Fund does not keep a single crown from donors' contributions. All operational costs of the foundation are fully covered by Y&T Luxury Property, ensuring that your donations go directly to specific aid. 🤝

More information can be found in the annual report and financial statements here.

THANK YOU FOR HELPING!

For more information, please refer to the annual report and financial statements here.
Your help can make children's lives easier and improve their health. Every donation brings them closer to breathing more freely.


JOIN AND FIGHT WITH US

Completed projects

Handover on March 3, 2026 - Let's give the children at Bulovka Hospital a cough assist device

Handover on March 7, 2025 - Let's give Anička a breathing vest

Handover on October 20, 2025  - A Breath of Hope for Daniela


Handover on August 28, 2023 - Give Vanessa a second breath

Handover on March 15, 2023 - Let's give Honzíček a better life 

Handover on April 4, 2022 - Let's donate a lung ultrasound together with Rytíři Kladno

Handover on April 19, 2021 - Let's donate a lung ultrasound to VFN at Karlák 



Bank account Unicredit Bank

1387887332/2700


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