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Today we're honouring Rare Disease Day! At UNIQUE we provide individualised support and information to loved ones of those who have a rare Chromosome or Gene disorder. Visit our website to learn more: bitly.ws/3dXhS #UniqueAndRare #RareDiseaseDay #RareDiseaseDay2024

Have you received a genetic lab report and struggled to interpret it and understand what all the complex scientific language means for you or your family member? We've published a brand new guide for #rarediseasday that will help. See: rarechromo.org/brand-new-info… #genomics #genetics

Please help Unique member Lucy win a Bafta! Lucy amazed everyone in the TV show, The Piano. Her mum asked if everyone could please vote for her. Voting closes TOMORROW so vote now! publicvote.bafta.org/po-cruises-mem…

As today's #nationalsiblingsday we're thinking about all those brilliant people growing up with a brother or sister who has a rare chromosome or gene condition, to let them know how amazing they are. Our guide to supporting siblings is free at rarechromo.org/disorder-guide…

🎉 Exciting news! Our team have been busy creating an original pop song to celebrate Rare Chromosome and Gene Disorder Day this year. The video features community members and is inspired by their stories. Mark the 13th ! 🗓️🎥 #Unique #RareChromoDay #TouchtheSky ✨🎤🌟

It's #RareChromoDay! Celebrating anyone living with a rare chromosome or gene condition and their families and carers. Please show your support... More at rarechromo.org/rarechromoday #unique #RareChromosomeDisorder #GeneDisorder #RareDisease #Genetics #UniqueButNotAlone #rarechromo

Today is a really special day! ⭐️ #RareChromoDay celebrates our amazing Unique members and all those affected by rare chromosome and gene disorders. 🧬 #UniqueAndRare

The wait is over! Our very own pop song for #RareChromoDay, "Touch the Sky," is out now! Share it with friends, family, and loved ones. Available on all major platforms! Check out our lyrics video on YouTube: youtu.be/Nw2G8vKqon8 #TouchTheSky #NewMusic #ListenNow

From the @unique_charity team, a huge thank you to all of you for getting behind #RareChromoday today. If you need help, we're here for you. Visit rarechromo.org/donate to support our work. #rarechromo #uniquebutnotalone

Are you a professional working in #genetics or #healthcare or a related field? How did you first hear about Unique? Please take a few moments to tell us more here.... bit.ly/UniqueProfSurv…

A message from Richard Davidson, Chief Executive, Sarcoma UK. Not enough people know about sarcoma. #SarcomaAwarenessMonth is an opportunity to reach them. When people are aware of the symptoms of this cancer, there's a better chance of an earlier diagnosis. [1/2]

New research shows that “whole genome sequencing is a game-changer for diagnosis and treatment of patients with sarcoma”. Read more via this linl: ow.ly/FzYJ50SC6hg Cambridge University Hospitals NHS NHS East Genomics

Now is your last chance to donate to our Database Appeal! We have been fundraising for a year and it’s now the last month to help us reach our target! Please click here: bit.ly/DatabaseAppeal to donate 💙 #GeneticDisorder #Fundraising #DatabaseAppeal #CharityCampaign

Unique is turning 40! Our story began all those years ago with a little red book … and now we're launching a new digital version where you can submit your story of living with, or supporting someone with, a rare chromosome or gene disorder lnkd.in/eVCi2A_E

Today is the day! An early start made more dramatic by an encounter with a bat (more later!). Looking forward to catching up& speaking about really important Unique preliminary survey findings at 4pm. Please come say hi at our stand, chat new logos & bats! #AGNC2025

It's Undiagnosed Children’s Day! 🙌 🎈 Many families spend years searching for answers, living with the unknown, without a name for their child’s condition. Please consider sharing this post, taking part in a fundraiser, or donating to support SWAN UK’s work. #SWANUK

Join Unique next week for an event not to be missed!

🧬 IT'S RARE CHROMOSOME AND GENE DISORDER DAY 2025, #RareChromoDay We're so excited to share two publications. Have a read, share and let us know what you think in the replies💬 - The Little Red Book: rarechromo.org/little-red-boo… - 'Unique experiences' report: rarechromo.org/get-ready-for-…

📕 Happy #RareChromoDay! All over the world, our members have been sharing their experiences of life with rare gene and chromosome disorders. Join us in celebrating them by visiting our website and reading our Little Red Book today! #MyUniqueStory rarechromo.org/little-red-boo…

In response to the Governments NHS 10 year plan and Industry Strategy The AGNC has drafted a response attached below.