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Stories, statements and updates from Rett Syndrome Europe and our member associations across Europe.

  • RSE February 2025 E Newsletter

    RSE February 2025 E Newsletter

    Research updates, events and family focus stories plus an opportunity to hear from Tom Pulles and Stephanie Kim from Acadia on 4th March 2025, 7pm CET – you will need to register first to join the webinar.

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  • Latest Update From Taysha

    Latest Update From Taysha

    We are delighted to share the very positive update from Taysha on their gene therapy programme for Rett syndrome. Ten participants have now received the therapy which has generally been well tolerated with no serious adverse side effects. They are in discussion with the FDA about moving to the next phase which is dosing more…

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  • Family Focus – Adventures in Accessibility: Exploring the World with Rett Syndrome

    Family Focus – Adventures in Accessibility: Exploring the World with Rett Syndrome

    Many thanks to Usree and Kalika for sharing this amazing account of their trip across several European countries and India during the monsoon season! It is a such an interesting and inspirational reading but also full of really helpful tips of what to take and things to consider when travelling with someone with Rett syndrome.…

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  • Acadia confirm submission to the EMA for approval of trofinetide (known as Daybue in US and Canada).

    Acadia confirm submission to the EMA for approval of trofinetide (known as Daybue in US and Canada).

    You can read the full press release here . They expect it will be 10-14 months before a decision is known. You might also like to read this plain language summary Trofinetide Treatment Demonstrates a Benefit Over Placebo for the Ability to Communicate in Rett Syndrome.

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  • Latest update from Taysha …

    Latest update from Taysha …

    You can read their latest letter to the Rett community here. All patients dosed are generally tolerating the therapy well with no serious adverse side effects. Third patient in the adult cohort has been dosed with the higher dose now, and the second paediatric patient enrolled for the higher dose.

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  • Latest update from Taysha

    Latest update from Taysha

    We are delighted to be able to share the latest update from the Taysha gene therapy programme. Highlights include the first person who received the higher dose has had no serious adverse side effects, they have the go ahead to dose the second patient with the higher dose and agreement reached to expand the trial…

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  • Latest Update from Taysha

    Latest Update from Taysha

    In the latest update published today we learn that there have been no serious adverse effects from the treatment in both the adult and paediatric trials so far. Both groups are reporting improvements in seizures, motor skills, communication/socialisation and autonomic dysfunction from parent carers and clinicians view points. A further update will be shared later…

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  • Nightwatch – A non intrusive, reliable device to alert parent carers to nocturnal seizures.

    Nightwatch – A non intrusive, reliable device to alert parent carers to nocturnal seizures.

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  • Latest update from Taysha

    Latest update from Taysha

    Taysha today shared updates on their REVEAL Adolescent and Adult Study. Here is the letter to the community. Also read their press release though as there is much more detail there about the improvements seen across a number of different symptom areas.

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  • Family Focus – Niki Konstaninou Without Wings

    Family Focus – Niki Konstaninou Without Wings

    Many thanks to Niki and Petros who live in Cyprus for sharing their wonderful story.

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