Stephanie Herzog: Board Member for Cure Rare Disease, Working on Finding Cures for Duchenne Muscular Dystrophy for Her Son Max
Team Never Quit
Marcus Luttrell
4.9 • 6K Ratings
🗓️ 5 October 2022
⏱️ 54 minutes
🧾️ Download transcript
Summary
- When we learned about our son’s condition, we put together a golf tournament to raise funds because it was A: Our only option, and B: Our best option to cure our kid.
- 80% of boys with Duchenne Muscular Dystrophy have a gene deletion in the dystrophin gene. Max has a duplication of the dystrophin gene.
- In what should be the best time ever with your child, that’s when we find out he has this horrible disease.
- We had like a funeral in our house for like a month.
- The weight of his future was heavy.
- Our team, through Crispr technology, hope to edit Max’s gene mutation.
- 6 years ago, this was science fiction.
- Boys usually get diagnosed between the ages of 4-6. They lose their ability to walk between the ages of 10 and 12. They usually lose their battle in their early 20s.
- They’re literally knocking out the gene duplication along a string in his DNA on the cellular level.
- Using the Crispr technology, the muscle cells are auto-correcting, producing dystrophin on their own.
- You wonder: “How am I going to live with this? And you do.”
- Faith is everything.
- You need somebody to pray to.
- When the going gets tough they have prayer.
Transcript
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