By Kristin Bogart|2024-01-11T18:04:09-05:00Jul 15, 2022|Daily Living, FXS, School and Education, Webinar Conference|
How you can get involved in Fragile X research, featuring Elizabeth Berry-Kravis, Craig A. Erickson, Randi J. Hagerman, David Hessl, Tracy King, Angel Wang, Jean Luan McColl, Laurie Bridges, Kara Frech, Emily Mack, Amie Milunovich, and Missy Zolecki, and moderated by Hilary Rosselot.
By Kristin Bogart|2024-01-11T18:57:14-05:00Jul 15, 2022|Daily Living, FXS, School and Education, Webinar Conference|
This family-friendly presentation focuses on considerations for school-age children with Fragile X syndrome. Presented by Kerrie Lemons Chitwood, Laura Greiss Hess, and Anne Hoffmann.
By Kristin Bogart|2024-01-11T19:00:30-05:00Jul 15, 2022|Daily Living, FXS, Webinar Conference|
Learn how to navigate medication strategies and approaches for children with FXS. Presented by Karen Regan, RN, and Nicole Tartaglia, MD.
By Missy Zolecki|2022-07-20T21:06:42-04:00Jul 6, 2022|Blog|
The always popular Bike To X Out Fragile X fundraising event draws almost 70 riders for a unique bike ride through Des Moines and Waukee, Iowa. Learn more about their day.
By Dany Petraska|2022-05-05T08:20:30-04:00May 4, 2022|
Consensus of the Fragile X Clinical & Research Consortium Seizures in Fragile X Syndrome Reading Time: 51 min.—|—Last Updated: April 2022—|—First Published: June 2011—|—Download PDF General Seizure Information: [...]
By Dany Petraska|2023-06-15T13:22:42-04:00Apr 25, 2022|
Fragile X Info Series Introduction to Assessing Individuals With FXS In this summary we cover principles, strategies, limitations, and accommodations. ENGLISH SPANISH [...]
By Jayne Dixon Weber|2024-02-02T17:39:52-05:00Mar 13, 2022|Webinar|
Jayne Dixon Weber and Dr. Craig Erickson discuss new medications and review existing medications used for various issues related to Fragile X syndrome.
By Hilary Rosselot|2024-06-10T12:24:22-04:00Mar 1, 2022|
Randi J. Hagerman Summer Scholars Research Awards The Randi J. Hagerman Summer Scholar Research Awards will fund one or more summer students’ research at $2,500 each. Student work can be focused on Fragile [...]
By Dany Petraska|2022-08-02T19:17:16-04:00Feb 25, 2022|Blog|
Corey Gershenson lives with Fragile X syndrome. Thanks to his determination — and employers willing to embrace employees with disabilities — he also works two jobs and volunteers at Mercy Hospital in St. Louis.
By NFXF|2024-06-20T10:14:51-04:00Jan 7, 2022|
Fragile X Advocacy We actively advocate in Congress for Fragile X research funding, and policies that facilitate treatment development and create opportunities for individuals with intellectual and developmental disabilities. [...]