She is incredibly brave during this difficult time. She doesn’t always understand what’s going on, yet she still manages to smile. Sara isn’t alone in this struggle; every step she takes is alongside her loved ones.
April 14, 2026
1,617 PLN (5%)Shortfall: 28,383 PLN
Sara is fighting NF1 and glioma❗Help start treatment❗.
Highlights
Update
The diagnosis is ongoing
Sara is currently in a situation full of questions, with no clear answers. Every day brings new information and new results. Sometimes it brings hope, and other times anxiety. Sara is still undergoing diagnostic tests; more tests, consultations, and more waiting lie ahead. The doctors suspect she has epilepsy.She is incredibly brave during this difficult time. She doesn’t always understand what’s going on, yet she still manages to smile. Sara isn’t alone in this struggle; every step she takes is alongside her loved ones. April 14, 2026
Explore the history of
Disturbing signals and first hospitalization
The year 2024 brought Sarah a series of severe infections: RSV, bronchitis, pneumonia, ear infections and painful mouth ulcers. The girl was taken to a hospital on Koszarowa Street in Wroclaw, where detailed tests were performed, including genetic testing.
It was then that it was confirmed that Sarah suffers from neurofibromatosis type 1. This disease is not due to external factors, as it is written into the genes and develops unpredictably. In her case, the consequence became the formation of a glioma in the left orbit, which requires further specialized diagnosis.
The disease is spreading in the shadows
NF1 is a genetic disease that disrupts the functioning of the nervous system and soft tissues. Its symptoms include numerous café au lait spots, and Sarah has more than 120 of them, one of the earliest and most characteristic markers of the disease.
In some patients, NF1 leads to the development of tumors in the nerves, soft tissues and central nervous system. In Sarah's case, such changes led to the development of a glioma in the orbit, which can affect vision and requires special diagnostic care.
Detention before treatment threshold
A diagnosis of NF1 does not end the process of diagnosis.
Doctors must determine the nature of the glioma, the rate of growth and its effect on the structures of the eye, as well as rule out other complications arising from the genetic disease.
Until this information is known, there is no way to implement appropriate treatment.
It's a time of difficult uncertainty, especially for the mother of a six-year-old girl, who must lead a daily life based on patient waiting. It's also an emotionally and organizationally taxing stage, especially since mom is raising Sarah alone.
Everyday life requires tremendous strength
Sarah stays alternately at home and in the hospital. Each day brings new questions and more visits to specialists. In addition to neurological and oncological care, the girl requires ophthalmology consultations, rehabilitation and dermatological care related to NF1.
Single motherhood puts the entire burden of organizing treatment, commuting, testing and therapy on one person.
It's a huge financial, emotional and physical burden. Every form of support gives Sarah a chance to begin proper treatment, and provides her mother with a bit of a breather in a battle she is waging all alone.
Not everything can be understood, but you can be next to it. For Sarah, this is already a great deal.
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- Step 1 - log in to the e-Tax Office and use the e-PIT service.
- Step 2 - in the PIT return form, click on Select an organization.
- Step 3 - in the list of organizations, search for Cancer Fighters Foundation or enter the KRS number 0000581036.
- Step 4 - in the field with the specific goal of 1.5%, indicate the Ward by entering the following data:
Contributions and words of support
PLN 9,200.00(18%)
shortfall to target - PLN 40,800
The collection was supported by: 32 people
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Sara is fighting NF1 and glioma❗Help start treatment❗.
PLN 9,200.00(18%)
shortfall to target - PLN 40,800
The collection was supported by: 32 people
Highlights
Collection target and updates
The diagnosis is ongoing
Sara is currently in a situation full of questions, with no clear answers. Every day brings new information and new results. Sometimes it brings hope, and other times anxiety. Sara is still undergoing diagnostic tests; more tests, consultations, and more waiting lie ahead. The doctors suspect she has epilepsy.
Explore the history of
Disturbing signals and first hospitalization
The year 2024 brought Sarah a series of severe infections: RSV, bronchitis, pneumonia, ear infections and painful mouth ulcers. The girl was taken to a hospital on Koszarowa Street in Wroclaw, where detailed tests were performed, including genetic testing.
It was then that it was confirmed that Sarah suffers from neurofibromatosis type 1. This disease is not due to external factors, as it is written into the genes and develops unpredictably. In her case, the consequence became the formation of a glioma in the left orbit, which requires further specialized diagnosis.
The disease is spreading in the shadows
NF1 is a genetic disease that disrupts the functioning of the nervous system and soft tissues. Its symptoms include numerous café au lait spots, and Sarah has more than 120 of them, one of the earliest and most characteristic markers of the disease.
In some patients, NF1 leads to the development of tumors in the nerves, soft tissues and central nervous system. In Sarah's case, such changes led to the development of a glioma in the orbit, which can affect vision and requires special diagnostic care.
Detention before treatment threshold
A diagnosis of NF1 does not end the process of diagnosis.
Doctors must determine the nature of the glioma, the rate of growth and its effect on the structures of the eye, as well as rule out other complications arising from the genetic disease.
Until this information is known, there is no way to implement appropriate treatment.
It's a time of difficult uncertainty, especially for the mother of a six-year-old girl, who must lead a daily life based on patient waiting. It's also an emotionally and organizationally taxing stage, especially since mom is raising Sarah alone.
Everyday life requires tremendous strength
Sarah stays alternately at home and in the hospital. Each day brings new questions and more visits to specialists. In addition to neurological and oncological care, the girl requires ophthalmology consultations, rehabilitation and dermatological care related to NF1.
Single motherhood puts the entire burden of organizing treatment, commuting, testing and therapy on one person.
It's a huge financial, emotional and physical burden. Every form of support gives Sarah a chance to begin proper treatment, and provides her mother with a bit of a breather in a battle she is waging all alone.
Not everything can be understood, but you can be next to it. For Sarah, this is already a great deal.
Donate 1.5% of your tax
Your e-PIT is the easiest way to settle your taxes. The IRS pre-fills your tax returns, and you can verify, approve or correct them.
Promote the collection
Contributions and words of support
2,208 PLN (4%)Shortfall: 47,792 PLN
2,348 PLN (5%)Shortfall: 47,652 PLN
PLN 2,020 (4%)Shortfall: PLN 47,980
7,727 PLN (15%)Shortfall: 42,273 PLN
2,664 PLN (5%)Shortfall: 47,336 PLN
28,990 PLN (58%)Still needed: 21,010 PLN
52,250 PLN (105%)Goal achieved!
