Join us for our two-part webinar series, bringing together the global CACNA1C community. Whether you are living with a CACNA1C variant, a parent or carer, a researcher, clinician or advocate, you are warmly invited.
Registration: Free
Time: 6.30pm BST
Speaker: Dr Rebecca Levy, child neurologist and neurogeneticist at Stanford Medicine Children’s Health, and TSA Scientific Advisory Board member.
Webinar 1: What does your genetic result mean?
Received a CACNA1C result and felt unsure what it means? This session is for you. We will cover the new consensus guidelines on how CACNA1C-Related Disorders are defined, what health screening to consider, and how to interpret genetic testing results.
Date: Thursday 10 September 2026
Webinar 2: Antisense Oligonucleotide Trial for CACNA1C p.G406R variant
For families affected by the p.G406R variant in exon 8A, also known as Timothy Syndrome type 1, and of real interest to clinicians and researchers. We will share news of an upcoming treatment trial for this variant.
Date: Thursday 24 September 2026
Translation into other languages
This is a language accessible series. Live translation and captions are provided through Wordly, so you can follow in your own language. You choose your language when you join.
Recordings
If you cannot attend on the day, please still register. Both sessions are recorded, and everyone who signs up receives the recording.
Start times around the world
- UK and Ireland (BST): 6.30pm
- Western and Central Europe (CEST): 7.30pm
- India (IST): 11.00pm
- US Eastern (EDT): 1.30pm
- US Central (CDT): 12.30pm
- US Pacific (PDT): 10.30am
- Australia Eastern (AEST): 3.30am, next day
These sessions provide general information, not individual medical advice. For anything specific to you or your family, please speak with your own clinician or genetic counsellor.
Help us provide more support to our community
Your donations will help us stage more events, bringing families together in a supportive environment.
Your contribution will help:
- raise awareness to drive research and clinical development
- enhance scientific understanding
- reduce the isolation faced by families
With your help, treatment and a cure for future generations is closer to being found.
See other ways that you can support us.