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In this very candid episode, SYNGAP1 Mom Monica Harding opens up to Ashley about her 17-year-old son Jaxon.

In this very candid episode, SYNGAP1 Mom Monica Harding opens up to Ashley about her 17-year-old son Jaxon.

FromSYNGAP1 Stories


In this very candid episode, SYNGAP1 Mom Monica Harding opens up to Ashley about her 17-year-old son Jaxon.

FromSYNGAP1 Stories

ratings:
Length:
60 minutes
Released:
Jul 11, 2023
Format:
Podcast episode

Description

Show Notes:
In this very candid episode, SYNGAP1 Mom Monica Harding opens up to Ashley about her 17-year-old son Jaxon. She describes his first seizures, aggression, going to church, the impact of COVID changing his schedule, and how it affected the entire family. This is an important glimpse into the struggles and joys a strong family living with SYNGAP1 faces.
Monica's SRF bio
Jaxon's Warrior Story
More links:
  Jayden’s Juice
Follow ⁠⁠⁠⁠⁠Ashley Frye⁠⁠⁠⁠⁠:
⁠⁠⁠⁠⁠LinkedIn⁠⁠⁠⁠⁠
⁠⁠Facebook⁠⁠
⁠⁠⁠⁠⁠Instagram⁠⁠⁠⁠⁠
⁠Nathan’s Warrior Story⁠
SYNGAP1 Stories ⁠⁠Episode 001⁠⁠ - Ashley Frye
SYNGAP1 Stories ⁠⁠Episode 005⁠⁠ - Panda
Panda’s News Story:  ⁠⁠Nathan’s Dog⁠⁠
SRF & SYNGAP1 Info:⁠⁠⁠
⁠What is SYNGAP1?⁠ ⁠⁠⁠
⁠ Syngap Research Fund⁠
Donate: ⁠⁠⁠⁠https://Syngap.Fund/Donate⁠⁠⁠⁠
⁠SYNGAP1 & Epilepsy⁠⁠⁠⁠
⁠Why Getting a Genetic Diagnosis Matters⁠⁠⁠⁠
⁠How to Get Free Genetic Testing⁠⁠⁠⁠
⁠⁠⁠ ⁠Special Needs Trusts⁠⁠⁠⁠
Connect with SRF (@curesyngap1):
  ⁠⁠⁠⁠Facebook⁠⁠⁠⁠
  ⁠⁠⁠⁠Twitter⁠⁠⁠⁠
  ⁠⁠⁠⁠Instagram⁠⁠⁠⁠
  ⁠⁠⁠⁠LinkedIn⁠⁠⁠⁠
  ⁠⁠⁠⁠TikTok⁠⁠⁠⁠
  ⁠⁠⁠⁠SYNGAP10 Weekly Video Podcast⁠⁠⁠⁠ w/ Mike
SYNGAP1 Conference 2023, hosted by SRF - ⁠⁠⁠Hotel Reservations⁠⁠⁠
SRF Newsletter Special ⁠5th Birthday Issue⁠ 6/27/23
Wednesday SRF Family Zoom Meeting:
⁠⁠⁠⁠Syngap.Fund/SRFfam⁠⁠⁠⁠ Meeting ID - 972 0059 2178 Passcode - 848417
Comments: ed@curesyngap1.org
Music: ⁠⁠⁠⁠In the Forest... by Lesfm from Pixabay ⁠⁠⁠
Episode 012 SYNGAP1 Stories, July 11, 2023
#SYNGAP1StoriesJaxon #Syngap #SYNGAP1 #SYNGAP1Stories #epilepsy #epilepsyawareness #autism #autismawareness #intellectualdisability #id #anxiety #raredisease #rarediseaseresearch #SynGAPResearchFund #careaboutrare #advocacy #patientadvocacy #neurology #genetictesting #therapy #family #militaryfamily
Released:
Jul 11, 2023
Format:
Podcast episode

Titles in the series (29)

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