Laatste Nieuws

NF Brochure in Arabic

arabische-tekst The Nina Foundation is extremely happy that next to the Dutch, German and English brochure now the Arabic brochure is added.

Call the expert center

Anyone can now visit the Expert Center for the Angelman Syndrome by simply calling or sending an e-mail. Children who are already receiving medical attention from the Erasmus Medical Center in Rotterdam

New website

FotoWebsite As you might have noticed, we have completely redesigned the Nina Foundation website. We have tried to make it more intuitive. Currently we are putting our effort into the translation of the content, but this can take some time.

Raffle for the Nina Foundation

The Nina Foundation Austria organised a raffle with the support of the Dutch organisation in Vienna ("Nederlandse Vereniging Wenen").

Christmas donation from Maxima

The Austrian Magazine Maxima (www.maxima.at) oranised a christmas party at their offices. During this party they collected 480 Euros for the benefit of the Angelman children. This money was received by Martine Schramm with her daughter Nina and has been passed on to the Nina Foundation for funding of research.

Mouse being created

muis_in_de_maak

The big question is whether the Angelman Syndrome (AS) can ever be cured. To test whether AS is in principle a reversible process, a new mouse is being created. This mouse has the AS mutated gene, but can restored to normal at any random moment.