It's #RareChromoDay today & also Tom's 27th Birthday. I can't believe that the baby who they said would be unlikely to survive more than eight or nine months & with whom they twice offered a termination, is 27! Bloody long eight months!
#HappyBirthdayTom
#22q11.2
#UniqueCharity

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

🎄✨ 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

Today is Tetrasomy 18p Day!

April 18th is dedicated to raising awareness about the rare genetic condition, tetrasomy 18p, which involves having four copies of the short arm of chromosome 18. Help us raise awareness by sharing our post.

#Tetrasomy18pDay #UniqueCharity #Tetrasomy

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

🎭✨ 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