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Podcasts from Fragile X professionals and experienced family members. If you have any questions or suggestions, email NATLFX[at]fragilex[dot]org
We speak with the Foundation's Support Services Coordinator Jayne Dixon Weber about her holiday experiences with her FXS-diagnosed son Ian. She gives a few tips on how to deal with the holidays, which can also be applied to other situations.
You can reach Jayne Dixon Weber at treatment@fragilex.org
The National Fragile X Foundation Podcast
Podcasts from Fragile X professionals and experienced family members. If you have any questions or suggestions, email NATLFX[at]fragilex[dot]org
