ATP1A3 Symposium in Disease – Reykjavik 2019
The ATP1A3 Symposium in Disease was held in Reykjavik, Iceland on October 2-4th 2019 The President of Iceland, Gudni Th. Jóhannesson opened the symposium with a message that we should …
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ABBY AHC AWARENESS VIDEO
This is a video about Abby who suffers from a rare disease AHC. Additional footage from the “Human Timebombs Documentary” has been included in this video. ABBY AHC AWARENESS VIDEO …
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The voices of AHC
The voices of AHC video was showed at a Hope for Annabel fundraiser where 830.000$ were raised.
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Ollie´s Story
Ollie was born with Alternating Hemiplegia of Childhood, meaning any muscle in his body can become paralysed at any time, including his lungs and heart. Like any other seven year …
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Carmel Hartman in the news
Carmel daughter of Sophie Hartman in the news
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How CRISPR-Cas9 works
Geneticist Jennifer Doudna co-invented a groundbreaking new technology for editing genes, called CRISPR-Cas9. The tool allows scientists to make precise edits to DNA strands, which could lead to treatments for …
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Can we cure genetic diseases by rewriting DNA?
In a story of scientific discovery, chemical biologist David R. Liu shares a breakthrough: his lab’s development of base editors that can rewrite DNA. This crucial step in genome editing …
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A wish mom’s story: Sophie
Wish mom Sophie shares her family’s story and how her daughter’s (Carmel) wish transformed their lives.
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Carmel in a Make-A-Wish Interview
Carmel is an amazing little girl battling Alternating Hemiplegia of Childhood. She was able to Make-A-Wish in 2017 and she was chosen to be the featured wish for WISH NIGHT …
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