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Hit the nail on the head with these! All 10 perfectly represent the questions that my cardiomyopathy patients ask me on a regular basis!

80% of rare conditions are genetic, and our clinical genetics team are proud to support families with rare diseases each and every day! #shareyourcolours #RareDiseaseDay2024 #RDD2024

RYR2 Variant associates with Sudden Death and Dilated Cardiomyopathy - another new paradigm for RYR2 related disease #yaelbenhaim ⁦Marta Futema⁩ ⁦Alan Michael Pittman 💙⁩ ⁦⁦Mary Noelle Sheppard⁩ sciencedirect.com/science/articl…

Researchers at Great Ormand Street Hospital are developing a simple cheek swab to monitor arrhythmogenic cardiomyopathy (ACM) in children. independent.co.uk/news/uk/patien…

🔬 Researchers identify factors that affect the risk of developing dilated cardiomyopathy (DCM) in people with a genetic change that can cause the condition but who don't yet have symptoms. 📰 medicalxpress.com/news/2024-04-s…

🧬Don't miss this chance to come together, meet others, and learn about supporting #LynchSyndrome genetic testing in cancer MDTs. 🧬 🌟FREE event-July 4th-Leeds-REGISTER TODAY!🌟 West Yorkshire and Harrogate Cancer Alliance North East & Yorkshire Genomics

'There's cancer in my family, what does this mean for me?' In our next #genomic Lunch & Learn #webinar on 13 June at 12pm, Dr Jude Hayward explains how to manage patients with a family history of #cancer, from a primary care perspective. Sign up here re-url.uk/WIO2

🔝 Check the recommendations for carrier testing for partners of MUTYH variant carriers ➡️ The UK Cancer Genetics Group provides guidance to address the current inconsistencies in clinical practice. 🗣️ Terri McVeigh et al bit.ly/3XdBDmU

Research alert 🚨 Do you have #LynchSyndrome? We need you 🙏 Do you feel you receive adaquate support and information when interacting with healthcare professionals and services? Short survey co-designed with the patient community to explore this. qualtricsxm2t8gtw5xb.qualtrics.com/jfe/form/SV_7Q…

Help in this research appreciated. Thank you.

#Lynch syndrome genetic testing in the cancer MDT. Wonderful engagement at our day in Leeds with over 65 CNSs from the North East & Yorkshire Genomics region. Thank you to all who travelled to us, to my fantastic co-hosts, and especially Anita and Nathan for sharing their experiences 🧬

Work starts on a cancer vaccine for people with #Lynchsyndrome ⁦Cancer Research UK⁩ news.cancerresearchuk.org/2024/09/10/lyn…

Have you tried our Heart to Heart service? ❤🔁❤ Our Heart to Heart network offers you 1-to-1 support with a trained volunteer who knows what it's like to live with #cardiomyopathy. To find out more, and to request support, head to our website: cardiomyopathy.org/heart-to-heart

My lovely colleague Jo!

Busy week ahead! Currently travelling to Cambridge for the #AICC conference. Looking forward to some great talks! Back home for a couple of days before heading back down south to present at the fabulous Cardiomyopathy UK 2024 patient conference with lovely Tahni-Ann Wilson ❤️🧬❤️🧬❤️🧬

Getting ready to talk about my favorite topic cardiac genetics 💙🧬 at Cardiomyopathy UK UK’s fabulous annual patient conference. Slightly nervous! Good job it’s for a fantastic cause 🙂

📢We're hiring! Genetic counsellors or clinical nurse specialists with experience in cancer genetic counselling. This opportunity will be to work on the PROTECT-C research study as well as counselling participants in the study. Learn more below! qmul-jobs.tal.net/vx/mobile-0/ap…

Interesting report with lots of important points raised from genetics/healthcare professionals, but also some very valid points raised from insurance professionals which I had not considered before

Research reveals why hypertrophic #cardiomyopathy may be underdiagnosed in women. theguardian.com/science/2025/j… Learn more: bit.ly/3WdhhJb #HCM

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