February 16, 2020 - SCN2A Australia

Clinical Features of SCN2A-Related Disorders

Post author:David Cunnington
Post published:February 16, 2020
Post category:Webinar
Post comments:0 Comments

Mutations of the SCN2A gene can result in a range of different clinical syndromes. Understanding these clinical presentations can help to guide treatment.

Exploring Families’ Needs

Post author:David Cunnington
Post published:February 16, 2020
Post category:Podcast
Post comments:2 Comments

What are the needs of families when their children with genetic epilepsy become unwell? Kris Pierce discusses the outcome from a recent roundtable.

SCN2A Australia and Asia Pacific

2 days ago

You can donate today and your generosity will be doubled.www.walkforepilepsy.org.au/fundraisers/krispierceGIFT MATCH ALERT 📢Donate today and double your impact! Thanks to a very generous sponsor, all donations made to the Epilepsy Foundation will be matched - up to $15,000!! When you choose to give, your donation will have double the impact - double the support, information and resources families need to better understand and manage their child’s epilepsy. For today only, every dollar you raise will be matched - that means if you raise $5, we receive $10! If you raise $25, we’ll be given $50. And for every $100 donated, $200 will be added to the Walk for Epilepsy total. Can you help us unlock the full $15,000 by donating today? Your support will help us empower 250,000 Australians living with epilepsy 💜 If you would like to donate today, head to walkforepilepsy.org.au. ... See MoreSee Less

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SCN2A Australia and Asia Pacific

5 days ago

INTERNATIONAL PREGNANCY AND INFANT LOSS REMBERANCE DAY.We are thinking of those in our community who have lost a child in pregnancy or infancy. Our thoughts are with you and your extended family. #SCN2A #LOSS #remember #community #support #family ... See MoreSee Less

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