Lorenzo is a baby suffering from Prader Willi Syndrome. The goal is to publish a children's book that tells his story and highlights the importance of early detection and visibility of rare diseases.

CHF 4’307

107% of CHF 4’000

107 %
This is how it worksä

The «all or nothing» principle applies: The project only receives the funds if the funding target is reached or exceeded.

78 backers

Successfully concluded on 10/10/2021


Log in with your profile to comment on this project.

Log In

  • Car il faut qu il y ai tjr plus de visibilité pour les maladies rares .

    Taline Künzler on 10/10/2021 09:48

  • ¡Suerte con el proyecto!
    Las cosas realizadas con dedicación, esfuerzo y cariño, ya de por sí, son un éxito en su proceso. Seguro que Lorenzo nos robará el corazón ;)
    ¡¡Estoy deseando recibir el libro!!
    Enhorabuena por tu trabajo. Un abrazoooo

    TERESA MÉNDEZ on 15/9/2021 02:06

  • We like your project – this is why we’ve added it to our «We Fancy» category! For the next couple of days it will appear on the front page and also in the «Recommended» section. We’d say you can be proud of yourselves and tell everyone about it! Publish some news, make a tweet or write a post!

    Team wemakeit on 14/9/2021 09:12