The Fragile X Society has produced a wide range of information and resources about Fragile X to support you and your family. Please visit the website for more information. ow.ly/RsPM50QBOS9

We are delighted that so many of you have already signed up for our Landmark Conference in Birmingham, there is still time to register at ow.ly/w0sJ50QGFrG

Delighted to produce these alongside Kirsten Johnson, FRSA Gaia Scerif Kayla Smith @jojohjhj Hayley Crawford and Angus Clarke The All Wales Medical Genomics Service. Guidelines help professionals and empower those affected by fragile X and their families. Fragile X Society, UK Fragile X International (FraXI) doi.org/10.1111/jar.13…

Our new paper establishing feasibility of eye tracking and atypical social attention in #syngap1. Published online today! Thanks to all the families who took part. onlinelibrary.wiley.com/doi/10.1002/au…

The NHS Lothian learning disability service is at the Royal Infirmary today -come along and see us if you want more information about making your service accessible for people with LD #ScotLDWeek24

Reflecting with izy utley this afternoon on the conversations she had whilst raising awareness of the LD service within Royal Infirmary of Edinburgh Being able to reach those who may not know much about the service & signposting what resources are out there is what this week is all about! ✨

Following on from yesterday's success at the Royal Infirmary Edinburgh, it's the Western General today! Awareness raising in general health services is so important #ScotLDWeek24

We are doing lots of fragile X research in the Patrick Wild Centre at the moment. Opportunities to participate in clinical trials, community surveys and more! patrickwildcentre.com/research/clini…

#ShapeResearchChangeLives Report launch: Shape Research, Change Lives: setting priorities in genetic syndrome research. Gaia Scerif Liz Pellicano Jo Van Herwegen Laura Cristescu To download our report: shorturl.at/X6V75

#ShapeResearchChangeLives We compared the research landscape to priorities for people with Down syndrome (DS), Fragile X syndrome (FXS), and Williams syndrome (WS) and the people who support them. To download our report: shorturl.at/X6V75 x.com/ekfarran/statu…

📊 #ShapeResearchChangeLives. New report on genetic syndrome research. Findings provide a new opportunity to reshape research, so that more research can transform the lives of people living with DS, FXS and WS shorturl.at/X6V75

It’s #SYNGAP1 awareness day so we headed to the water with some friends and family to #Splash4Syngap instagram.com/reel/C8eKmY5Nk…

International Fragile X Awareness Day offers everyone the occasion to know the many strengths of people with Fragile X Syndrome. Today let's talk about IMITATION! fraxi.org. #internationalfragilexawarenessday2024 #10october #XX24 #weareaforce #imitation

Wonderful to be at the UK #syngap1 family day today. SynGAP Research Fund (SRF) SYNGAP1 Global Network (SGN)