Do like our godmother Muriel HURTIS (world champion 4X100m relay) Take part in the challenge to cover 100,000 km with the Tape à l'œil foundation in aid of the charity Les Petits Mec P2 https://youtu.be/QBSGJ4QubDA
At the Spotlight in Lille. We look forward to seeing you there!
Théatre Sébastopol, Lille. Song/Cabaret/Magic/Hypnosis/Humour 2 hours of entertainment for all the family! Come one, come all! https://www.facebook.com/watch/?v=4164604122154
General Meeting les petits MeCP2 : Election of the bureau
Help researchers learn more about the sensory abilities of people with MECP2 gene duplication syndrome, which have been little studied until now.
This major event will provide an opportunity for doctors, scientists and families to meet and discuss current developments in the search for treatment and patient care. New therapeutic approaches will also be presented. To register: 2022 MECP2 Duplication Family Conference Registration (office.com)
Come and join us at the Esquibien swimming pool to support research into the syndrome! All proceeds from the event will go to the Les petits Mec P2 association. On the programme: freestyle swimming, slides, games on inflatable structures, introduction to freediving... and much more! And all in a musical atmosphere! For more information, call [...]
Cure MDS is organising "Giving Tuesday" on 29 November 2022. We can't cure duplication of the MECP2 gene without you! Contribute to the event by sharing the information and taking part in Giving Tuesday! To support and donate: Donate to the Rett Syndrome Research Trust to Advance Rett Treatments (reverserett.org)
Take part in the Cure MDS survey to help researchers understand the needs of families affected by duplication of the MECP2 gene. The information gathered will be used to identify needs in terms of resources, support and care centres. Care Center Information (google.com)
The meeting will take place online on 27 January 2023 at 8.30pm and will be held in German. Participation is open to all. The following topics will be discussed: MECP2 duplication syndrome and the state of research Our members Our missions and actions Job vacancies and how to become a member To take part in the [...]
Huda Zoghbi is Professor of Paediatrics, Molecular and Human Genetics, Neuroscience and Neurology at Baylor College of Medicine in Houston (USA). She has made major scientific advances in MECP2 gene duplication syndrome and Rett syndrome, and has received a number of prestigious awards for her research. Her work [...]
Huda Zoghbi is a professor of paediatrics, molecular and human genetics, neuroscience, and neurology at Baylor College of Medicine in Houston (US). She has made groundbreaking discoveries on MECP2 duplication syndrome and Rett syndrome and has received numerous prestigious awards for her research. The work of Prof. Zoghbi gives hope that one day a cure [...]
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