cagnotte santé

Tudor The Dino Kid

Date de création, 28/12/2025
Qui organise? Caroline Le LAY
0 € sur 30 000 €
Fin il y a 4 mois
0€ 30 000 €

A propos de cette cagnotte

Our son was diagnosed with epilepsy at just 3 years old. For years, doctors couldn’t explain why. This year, after his latest MRI, we finally got an answer — and it broke our hearts. He has a small glioblastoma, and part of his brain is no longer functioning properly.
Over the past seven months, his condition has rapidly worsened. What used to be 2 or 3 seizures a month has become daily seizures. Watching your child suffer like this, knowing there is a solution but not knowing if you can reach it, is unbearable. 
A few months ago, doctors offered us hope: a highly complex brain surgery that would remove the tumor and the damaged part of his brain, and implant a pacemaker to help control the seizures. Unfortunately, we couldn’t afford it at the time.
Today, we have been given a second chance. This life-saving operation can be performed — but only in Austria — and it costs €180,000.
We have done everything we possibly can. We put in all our savings. We took out a loan. I sold my car. We borrowed money wherever we could. Despite all this, we are still €30,000 short.
That is why we are asking for help.
Every donation, no matter the amount, brings us closer to giving our son a future without constant seizures, without daily fear, and with the chance to live like a child should. If you can’t donate, sharing our story also means the world to us.
Thank you for reading, for caring, and for helping us give our son a chance at life.


 


 

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