Our Commitment to RETT Syndrome Awareness Month

We participated in the RETT Awareness Month throughout October.

10 November 2023

In collaboration with Chloe’s RETT Cure Research Institute we organized a series of initiatives spanning the entire month to amplify awareness. Julia Ramlogan is the RETT Institute's founder and mother of Chloe, a RETT syndrome patient, and our students Justine, Amelie, and Charlotte.

Our programmes featured educational sessions led by international professors specializing in genetics, a visit from Chloe, a fundraising bake sale, and an art creative competition.

RETT syndrome, a rare genetic mutation predominantly affecting girls' brain development, is the focus of our efforts. Encouragingly, recent research suggests the possibility of reversing RETT syndrome, offering a glimmer of hope.

The event has attracted media interest. Check out the article here.

Get in touch if you would like to support this cause or learn more.

Photos: David Biedert Photography AG/ IMZ

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