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The EUPATI 2013 Conference: A Vision For 2020

By Olga Timutsa. The EUPATI 2013 Conference: A Vision For 2020 took place in Rome in April 19, 2013. The Rome conference, held just 14 months after the launch of EUPATI (European Patient’s Academy on Therapeutic Innovation). More than 180 delegates from 28 countries were there to hear about the plans under way for three […]

3rd Catalan Rett Syndrome Day

By Jordi Serra. On March 2, 2013 took place the 3rd Catalan Rett Syndrome Day: “Update on Research, Emotional Wellness, Disability and Guardianship at the Teknon Medical Center in Barcelona” http://www.teknon.es/jornada-rett/programa In this conference, the Teknon Foundation, and the Catalan Association for Rett Syndrome provided the latest information on Rett research and updates for early […]

The Drug Information Association (DIA) 2013 Euromeeting

By Danijela Szili. The DIA (Drug Information Association) is global-wide working association which provides networking opportunities and information about innovation in science and pharmacy by organising events and training courses over the entire world. The biggest get-together on our continent this year was the Euromeeting 2013 (March 6th RAI centre, Amsterdam) with more than 3,000 participants. […]

3rd European Rett Syndrome Conference “Research Update and Preventive Management”

The 3rd European Rett Syndrome Conference Maastricht, “Research Update & Preventive Management” (ERSCM 2013), will take place on October 17th – 19th, 2013 at the MECC inMaastricht, The Netherlands. For more information on registration and program please visit: http://www.ersmc.eu ERSCM 2013 is an initiative of the GKC (Gouverneur Kremers Centrum), Stichting Terre (Dutch Rett Syndrome Foundation) and NRSV (Dutch Rett Syndrome Association) and […]

Polish Summer Camp

By Eleonora Misiarz (eleonorabaran@wp.pl) The summer camp is organized regularly in June by the Polish Rett Association. Last couple of years we have been meeting in Mielno on the Polish Coast. The camps are a good opportunity to meet other parents and their kids. The idea for the meeting of the families is more to get […]

Rett UK bangs the drums for families in South East England

November 10th saw over 180 people from the South East of England, arriving at The School for Profound Education at the Children’s Trust in Tadworth. Families, specialist medical and therapeutic practioners, staff and board members of Rett UK took part in the largest gathering of the Rett Community in England for many years.   There […]

The 2012 RSE General Assembly

  The 17th November took place the Rett Syndrome Europe general assembly in London, UK where Lorna Jaffa, representative from RettUK, welcomed the delegates to the meeting. 14 countries were represented that day and two researchers; Angus Clarke and Laurent Villard were also invited. Member countries each gave a brief report about their associations. Martine […]

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