In Deutschland sind rund 8.000 Kinder, Jugendliche und Erwachsene von der unheilbaren Erbkrankheit Mukoviszidose betroffen. Jedes Jahr werden rund 200 Kinder mit der seltenen Krankheit geboren. Der Mukoviszidose e.V. vernetzt die Patienten, ihre Angehörigen, Ärzte ,Therapeuten und Forscher.
UST-ID: DE295207838
Amtsgericht Hamburg, HRB 132049
Vertretungsberechtigte Personen: Marc Kamps, Sebastian Lenk
We are often asked if Patchie could also help children with diseases other than CF. That’s definitely a yes. However, we’re pretty committed to getting this App done right now for CF. Two of our team members are affected by this disease and we want to do it the right way. The result can (and will) easily be taken as a technological base for apps that support different diseases. You see there’s a lot to do. Please support us, together we can reach our goal!
Denis (co-founder of Startnext)
