Patchie: CYSTIC FIBROSIS CHILDRENS THERAPY APP
Crowdfunding successfully finished
Raised
The goal: Free of charge teach in an easy and playful way about the everyday therapy and make everyday life easier for children who have cystic fibrosis (6-16 years). Many children suffer from a chronic disease and must sometimes spend several hours a day for therapy measures. This presents a major burden for the children and their family environment. Using the example of cystic fibrosis our app "Patchie" shows that therapy can also be fun. The app will be available for Smartphone and Tablet.
Funding period
4/2/15 -
7/31/15
Realisation
9 Month
Minimum amount (Start level): €
75,000 €
City
Hamburg
Category
Technology
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Cooperations
Mukoviszidose e.V.
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.
Legal notice
Birds and Trees UG (haftungsbeschränkt)
Marc Kamps
Schloßmühlendamm 11
21073
Hamburg
Deutschland
E-Mail [email protected]
UST-ID: DE295207838
Amtsgericht Hamburg, HRB 132049
Vertretungsberechtigte Personen: Marc Kamps, Sebastian Lenk
5/1/15 - We are often asked if Patchie could also help...
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)
