It's been great to be part of the #UniqueCharity Family Information Day in Cardiff for those affected by rare chromosome and gene conditions.

We were highlighting our work along, with that of #GenomicsPartnershipWales, #AllWalesMedicalGenomicService, and #geneticallianceuk.

#PatientEngagement

Today is Pallister-Killian Syndrome (PKS) Awareness Day!

Let’s work together to raise awareness and celebrate the diversity that makes our community so special.

Download our guide to PKS here: bit.ly/P-Ksyndrome

#PKSAwarenessDay #RareChromosome #UniqueCharity #PKS

💛 Today is Global Developmental Delay Awareness Day 💛

We're proud to stand with our members and families affected by GDD. Show your support today by wearing yellow and sharing why you care!

#GDDawareness #GlobalDevelopmentalDelayDay #InvisibleDisability #UniqueCharity

📅 It’s 10 weeks today until #RareChromo Day – a day to celebrate and raise awareness about rare chromosome and gene disorders. 💙✨
#RareChromo #UniqueCharity #RareButMighty #10WeeksToGo

New Guide! 🧬

We’re excited to share our latest guide on HIST1H1E syndrome! Available online as: a brand-new Single Gene Disorder Guide, a My Gene Story, An Easy Read version.

Check them out now at: bit.ly/alluniqueguides

#HIST1H1E #RareChromosomeDisorders #UniqueCharity

A rare condition diagnosis can feel isolating, but it doesn't have to be. For 40 years, #UniqueCharity has connected families worldwide, offering support and understanding for those navigating rare chromosome and gene disorders.

#ChromosomeDisorder #GeneDisorder #rarediseases

Fertility can be challenging, especially for couples with rare conditions like balanced translocation presenting unexpected hurdles in starting a family. We want you to know that you are not alone.

#RareDiseases #UniqueCharity #ChromosomeDisorder #GeneDisorder

Swipe to read truly #UniqueStories from parents of young adults living with a rare chromosome disorder. We're proud to offer support for those impacted by rare disease. #UniqueCharity offers scientifically accurate guides, peer support, and events that bring families together.

Swipe to read truly #UniqueStories from parents of young adults living with a rare chromosome disorder. We're proud to offer support for those impacted by rare disease. #UniqueCharity offers scientifically accurate guides, peer support, and events that bring families together.

📢 Today is PACS1 Related Syndrome Awareness Day!

Learn more in Unique’s PACS1-related syndrome guide: bit.ly/PACS1Guide

#PACS1 #RareChromosome #UniqueCharity

Today is Bainbridge-Ropers syndrome Awareness Day! 🧬

🔹 Learn more about Bainbridge-Ropers syndrome by reading our disorder guide: bit.ly/B-Rsyndrome

#BainbridgeRopersSyndrome #RareChromosomeDisorder #UniqueCharity #BainbridgeRopersAwareness #BRPSAwareness #BRPS

Today is #TBCK Awareness Day! 🧬

To read our quick read guide on TBCK syndrome head to: bit.ly/TBCK

#TBCKAwarenessDay #RareButNotAlone #UniqueCharity #GeneticDisorders #ChromosomeDisorders

🎄✨ Happy holidays from Unique! ✨🎄

Please note, our office will be closed from 24 December 2023 and will reopen on 2 January 2024.

If you need urgent support over the holidays please visit: www.rarechromo.org/c...

#MerryChristmas #HappyNewYear #ThankYou #UniqueCharity #HolidayGreetings

🎭✨ Join Head 2 Head Sensory Theatre for the Rumpelstiltskin Panto! ✨🎭

📅 Check out the flyer for all dates and details: h2hsensorytheatre.com/

#Rumpelstiltskin #FamilyFun #PantomimeSeason #HolidayMagic #UniqueCharity #RareChromo