All Episodes
A Mama’s Xtra Love — 72 episodes
Small Steps, Big Impact!
Q&A Part 1: Fragile X Treatments, Anxiety and more!
Rare Patient Voice’s Stacey joins Talk FX Host Nicole Smith!
The Raw Realities of Grief & More!
A Fragile X Family’s Diagnosis Journey
An Update on our Fragile X Journey!
An Important Message from Talk Fragile X
Talk Fragile X is Back with News!
Why Should We Advocate for Inclusion in the Workplace and in the Community?
Special Guest: Rob Snow, Director of the CEO Commission for Disability Employment
Disability Employment Awareness Month 2023
An Update from FRAXA Research Foundation’s Katie Clapp & Holly Roos!
Fragile X Awareness Month & A Suprise Announcement!
Life Update!
The One Where It's The First Episode of 2023!!
The One Where It's The Last Episode of 2022!
It's Disability Employment Awareness Month!
What More Special Needs Families Should Be Talking About! With Special Guest: Ashley Zazueta
Life Update!
A Raw Conversation with Andrea Miller
We Must Do Better!
How do we maintain hope? (Part 1)
Special Guest: Stephanie Hanrahan Blogger & Founder of the Non-Profit Labeled and Loved
Fear & Anxiety Part 2 With Kirsten Fowler
THIS is why inclusion is important!
Fear & Anxiety Part 1
It's Fragile X Awareness Month 2022!
World Fragile X Day with Special Guests: Katie Clapp & Holly Roos with FRAXA Research Foundation
A Conversation with Kirsten Fowler, Author of Family, Faith & Fragile X
Exciting News for The Fragile X Community!!
Special Guest: Kate Swenson Author of Forever Boy: A Mother’s Memoir of Autism and Finding Joy
Autism Awareness Month
Another Fragile X Diagnosis Story with The Knudson Five family!
Prioritizing Self-Care in Your Life
Advocacy Day 2022 is here!!
Preparing your Fragile X child for Employment
A raw conversation with family about Fragile X Syndrome
How FRAXA Research Foundation is keeping hope alive for a cure for Fragile X!
My Fragile X Diagnosis Story with Special Guest: My Husband Moe Smith!
Preparing for Doctors Appointments
Transition from Grade School to Adulthood: Part 2!
Giving Tuesday!
Why Advocate?
Transition from Grade School to Adulthood
We’re back! With Special Guest: Dr. Randi Hagerman
World Fragile X Day
Special Guest: Brandy - Two boys with Full-Mutation Fragile X Syndrome
Special Guest: Katie Clapp (President & Co-Founder of FRAXA Research Foundation)
ADVOCACY DAY 2021!
Approaches to Handling Aggressive Behavior & Discipline
What Has Fragile X Taught You??
2020 Wrap Up!
Perspective From a Single Mom of Fragile X Full Mutation Carrier Jaxon
Navigating Distance Learning
Fragile X Author Series: Jayne Dixon Weber
Fragile X Author Series: Cindi Rogers
Fragile X Author Series: Elizabeth Griffin
A Fragile X Diagnosis Story Series: Episode 4
A Fragile X Diagnosis Story Series: Episode 3
A unique Fragile X Diagnosis Story
A Fragile X Full-Mutation Diagnosis story from a Mom of 2 FX Children - Boy & Girl
Step Up for Fragile X with FRAXA Research Foundation
Potty Training & Life Skills for children with Fragile X
Fragile X Awareness Month & The NFXF International Fragile X Conference Virtual Series
A Fragile X Carrier’s journey using IVF (In Vitro Fertilization)
From the Perspective of a Newly Diagnosed Fragile X Family
Special Guest: AMP (Autism Movement Project) Sports & Fitness
Special Guest: FRAXA Research Foundation
Finding out you’re a Fragile X Carrier!
“Fragile What??”
Sibling of Full Mutation Fragile X Child Interview
An Intro to Talk FX