SynGAP Stories

SynGAP Stories
1
Global Rank
TOP 1%
Creator:
Syngap Research Fund, 501(c)(3)
- Parenting
- Kids & Family

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Podcast data
Created By Syngap Research Fund, 501(c)(3)Podcast Status activeStarted 24/01/2023Latest Episode 18/04/2023Release Period EpisodicEpisodes 7Partner Reviews 0Language EnglishFrequency 335Average Length 32 minutes and 34 secondsCountry United StatesGlobal Rank TOP 1%Description
SYNGAP1 is a rare disease that affects Ashley Frye's son Nathan. Fewer than 1,200 patients have been diagnosed as of January, 2023. There is no treatment. There is no cure. In each episode of SynGAP 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, will be discussed in this heart-warming series as we support the SynGap community. -
Episodes
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#522275 - It's Ashley's turn, as she talks about her beginnings of volunteering for SRF and what she's working on now! Pickleball, anyone?
2 years ago -
#522276 - How Can a Service Dog Help Your SYNGAP1 or Other Rare Disease Child? Listen as Cecilia Anastos Chats with Ashley.
2 years ago -
#522277 - Kali Worth, SYNGAP1 Mom to Kailyn (Kai) is Ashley's guest.
2 years ago -
#522278 - Ashley's Guest - SRF Community Activation Leader Corey Baysden
2 years ago -
#522279 - Ashley talks to SRF Co-founder Mike Graglia
2 years ago
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