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Finn in the media

Everything that has been published about Finn – and everything editors need for their own coverage.

Bertille and Finn laughing in the sand
For editors

Key facts at a glance

Your contact is Finn’s father, David Wulf. For interviews, photos or background talks, reach him by email. We are happy to provide photos of Finn and the family for coverage – please ask first.

Who
Finn Wulf, 4, from Waldbronn near Karlsruhe; parents Bertille and David Wulf, brother Milo
Diagnosis
SLC6A1-related neurodevelopmental disorder, extremely rare; genetically confirmed in February 2025
Timeline
First tremor episodes January 2023; epilepsy diagnosed June 2024 (Städtisches Klinikum Karlsruhe); more than 200 absence seizures a day before the first medication
Hope
Gene therapy; not available in Germany, treatment in the USA, cost around €1 million
Fundraising
Goal: around €1 million for the treatment, first milestone €250,000 (GoFundMe “Finn macht Mut”). Private fundraiser, no tax receipts. Art card campaign “Create to help” on Ulule, proceeds go to the fundraiser
Promise
If gene therapy doesn’t happen (not enough money or too much risk), all donations go to SLC6A1 Deutschland e.V. or SLC6A1 Connect. Finn’s father David Wulf sits on the board of SLC6A1 Deutschland.

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