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SYNGAP1 Stories

Syngap Research Fund, 501(c)(3)

SYNGAP1 Stories

A Kids, Family and Parenting podcast
Good podcast? Give it some love!
SYNGAP1 Stories

Syngap Research Fund, 501(c)(3)

SYNGAP1 Stories

About
SYNGAP1 Stories

Syngap Research Fund, 501(c)(3)

SYNGAP1 Stories

A Kids, Family and Parenting podcast
Good podcast? Give it some love!
Rate Podcast

SYNGAP1 is a rare disease that affects Ashley Frye's son Nathan. As of January 1, 2024, there are 1,339 people in the world diagnosed with SYNGAP1. There is no treatment. There is no cure. In each episode of SYNGAP1 Stories, Ashley will chat with SynGap parents, volunteers, caregivers, researchers, and partners about their journey with SYNGAP1 in their lives. Their joys and successes, as well as heartaches and advice, will be discussed in this heart-warming series as we support the SynGap community.#841128

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Podcast Details

Created by
Syngap Research Fund, 501(c)(3)
Podcast Status
Active
Started
Jan 24th, 2023
Latest Episode
Apr 11th, 2024
Release Period
2 per month
Episodes
29
Avg. Episode Length
39 minutes
Explicit
No
Language
English

Podcast Tags

This podcast, its content, and its artwork are not owned by, affiliated with, or endorsed by Podchaser.
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