thewhitworthgroup
@whitworth_group
Be part of the conversation.
ID:1171816829876133888
http://www.rare-d.com 11-09-2019 16:04:55
287 Tweets
264 Followers
260 Following
open.spotify.com/episode/0H1179…
In this episode, we discuss how migration influences our practice and the central value of Genetic Counselling Nichola Garde Mariangels Ferrer Duch Sofia Douzgou Houge European Society of Human Genetics (ESHG) Genetic Counselling
#GeneticCounsellors
We are still buzzing from #RareDiseaseDay 🌟
Very grateful for the videos sent so far, and a kind reminder for everyone who hasn’t uploaded the videos yet – please send them our way 🎬
QR code & link in poster
Unique Genetic Alliance UK EURORDIS-Rare Diseases Europe Gene People Manchester Rare Conditions Centre
Thanks to everyone who uploaded their videos to our 'rare film' project on Rare Disease Day. Great to see clips from all over the world!
The window for uploading is open until March 18, so there is still time to send us your submissions:
rare-d.com/rare-d-2024/
#rarediseasday2024
Unique have had a great week raising awareness for #rarediseasday2024 .
2. Sophie Sainty and I attended the Genetic Alliance UK parliamentary reception, meeting up with Unique Patron, Baroness Pauline Neville-Jones and many others!
#UniqueandRare
29th of February 2024 is International Rare Disease Day, and thewhitworthgroup are looking to produce a collective, crowd-generated film that captures what a day looks like for those living with rare conditions. To get involved and find out more, go to rare-d.com/rare-d-2024/
Today is Rare Disease Day ! Help us to highlight the voices of people living with rare health conditions and be a part of a 'rare' collective film:
rare-d.com/rare-d-2024
#RareDiseaseDay #storiesbehindthestats #ShareYourColours #LightUpForRare
Just 1 day until Rare Disease Day ! Send us your video clip to be part of a collective film:
rare-d.com/rare-d-2024
#RareDiseaseDay #storiesbehindthestats
Just two days to go until Rare Disease Day 2024!
A rare condition is any condition that affects less than 1 in 2,000 people. There are at least 7,000 rare conditions with more being discovered via scientific progress. Genetic Alliance UK
#RareDiseaseDay #StoriesBehindTheStats
Be as creative as you like. We look forward to seeing your video!
For further details see: rare-d.com/rare-d-2024/
Genetic Alliance AU
Anneke Lucassen
Dr Danya Vears
Dr Simon Stones
@unique_charity
Patient Voices
SamebutDifferent
ViewPoint in Health
Kathryn Asbury
BSGM
🖥️ Can AI help in the study of human genetics? Collaboration and education for a brighter future
New episode of #geneticsounds from European Society of Human Genetics (ESHG), thewhitworthgroup & eshg_young
🎧Listen to the experts Peter Krawitz, Tanja Zdolsek Draksler and Kleefstra Syndrome #kleefstra ➡️open.spotify.com/episode/1ICrgp…
🌟 Mark on your 🗓️ Feb 29: It's International Rare Disease Day! thewhitworthgroup is creating something unique and special. If you're a scientist/clinician or living w/ a rare condition, show us what is rare to you! #RareDiseaseDay #RareFilm
➡️ rare-d.com/rare-d-2024/
On #RareDiseaseDay 🌍thewhitworthgroup wants to capture a day in the lives of people and families living with rare conditions
Share some video clips filmed on February 29th 🎥
The footage will contribute to a short documentary film 🎬
Manchester Rare Conditions Centre NWGMSA The University of Manchester
Proudly introducing the 3rd series of the European Society of Human Genetics (ESHG) podcast #GeneticSounds . With great thanks to thewhitworthgroup, Chaya Nautiyal Murali and Abraham Mamela / Genome Adventures open.spotify.com/episode/7sCoGh…
One of our greatest joys thewhitworthgroup is bringing together scientists, clinicians, artists and public, to approach complex conversations in creative ways
🗓️ May, Monday 15th HOME
Grateful for the support from NWGMSA MFT NHS Manchester Rare Conditions Centre Evolution, Infection and Genomics (EIG) UoM The University of Manchester
New episode of the European Society of Human Genetics (ESHG) podcast: Profs Roos van Westrhenen, Katherine Payne, Graeme Black and Wayne Thompson, a patient who took part in a gene therapy trial for Choroideremia discuss treatments of genetic conditions, breakthroughs, and costs
eshg.buzzsprout.com/1931247/121699…
Really enjoyed learning about the Team of Life today, which is a narrative therapeutic approach used to improve self esteem and identify support systems for CYP. I really resonated with the strengths-based values! Thank you Riverbank Psychology 👏 #twitterEPs #adayinthelifeofa_tep
Very much looking forward to meeting you all in Vienna! Do not forget the live #eshg2022 podcast event in Hall E1 at 12.15 on Saturday 11th June! Mariangels Ferrer Duch, Nichola Garde and an amazing line up of guests will discuss 'What is the future in genetics? eshg.buzzsprout.com