Join our brand new training series – Decoding Diagnostics
In the world of rare diseases, navigating the diagnostic journey can often feel like a complex puzzle.
With 72% of rare diseases being genetic in nature, obtaining an accurate diagnosis is crucial for patients and their families. However, the landscape of genetic testing and diagnosis can be daunting, filled with new terminology and processes.
Taking place across May and June 2024, our Decoding Diagnostics series will shed light on this journey, providing clarity and guidance to individuals and groups within the rare disease community.
Through a series of webinars and discussion sessions, we’ll explore the fundamental principles of genetic testing, delve into the methods and applications available, and provide practical insights on accessing, interpreting and supporting genetic diagnostic results.
This free series is primarily for rare disease patient groups, however anyone with an interest in improving their knowledge on diagnostics is welcome to attend.
What to expect from the series
Part one: Exploring the world of genetic testing
Part one of our Decoding Diagnosis series will provide an overview of genetics and genetic testing. Before participating in these sessions, we highly recommend completing our free “Introduction to genetics” course on The Resources Hub.
Each session will take place 11am – 12:30pm BST (GMT+1).
11am – 12:30pm, 1st May 2024 – The fundamentals of genetics and genetic testing (webinar)
Explore the basics of genetic testing and rare disease diagnostics. Learn about DNA, genes, and how changes in these components can lead to a rare condition. Discover the journey of DNA from clinic to lab.
11am – 12:30pm, 8th May 2024 – Understanding the genetic testing landscape (webinar)
Discover the various genetic tests available and their insights into an individual’s genome and disease. Learn about the information each test provides, who they are best suited for, and how to interpret results for patients and clinical teams.
11am – 12:30pm, 22nd May 2024 – Discussion and Q&A
Join our interactive discussion on advancements in genetic testing and their impact on patient experiences. Hear from experts in result analysis and communications and individuals who have navigated the genetic testing journey. Ask your questions and get some answers!
These sessions are like building blocks, with each adding new layers to your knowledge. As a result, we recommend participants endeavour to attend all sessions.
Part two: Navigating a genetic diagnosis
Part two of our Decoding Diagnosis series will focus on the pathways to diagnosis in the UK and the real world implications receiving a diagnosis has on patients and their families.
Each session will take place 11am – 12:30pm BST (GMT+1).
11am – 12:30pm, 5th June 2024 – Accessing genetic testing in the UK (webinar)
Gain an overview of the genetic testing pathway in the UK, including key players and steps. Discover how patient groups have influenced and improved genetic diagnosic services. Learn about expectation management and support options for patients when the journey isn’t straightforward.
11am – 12:30pm, 12th June 2024 – What happens after diagnosis? (webinar)
Explore the practical implications of receiving a genetic diagnosis and what comes next. Demystify the genetic counselling process and learn how genetic tests inform treatment and care pathways.
11am – 12:30pm, 19th June 2024 – Discussion and Q&A
Join our interactive discussion on implementing effective communication in the diagnostic journey and beyond. Hear insights from genetic counsellors, clinicians, and individuals who have experienced the importance of genetic testing for timely treatment.
These sessions are like building blocks, with each adding new layers to your knowledge. As a result, we recommend participants endeavour to attend all sessions.
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Please note: the ticket window may take a few seconds to load. If you experience difficulties, you can register directly here.
