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Mes Nacional del Cuidador Familiar: Los grupos de apoyo de la AFTD están aquí para ayudar
The FTD journey can be an isolating experience for people with a diagnosis and care partners alike….
Actualización de promoción: AFTD ofrece comentarios en la reunión de NAPA
As part of AFTD’s advocacy efforts, Advocacy Manager Matt Sharp virtually attended the National Alzheimer’s Project Act…
Atleta del mes de octubre: Steve Perlis
Our Athlete of the Month for October is Steve Perlis from Illinois. Steve has been a member of…
Consejos y sugerencias: conducción y FTD
Driving is a cognitively demanding activity; for people with FTD, it can be especially difficult. While a…
Consejos y sugerencias: uso de medicamentos para aliviar los síntomas de FTD
While there are currently no FDA-approved therapeutics to treat FTD directly, some people benefit from asking their…
Palabras de aliento: compartir el camino hacia el diagnóstico
World FTD Awareness Week 2022 began on Sunday. To mark this yearly event, AFTD asked people to share…
Voluntaria del mes de septiembre: Nicole DeLeve
When Nicole DeLeve’s father was diagnosed with ALS with bvFTD in 2016, she found herself exhausted from…
Sugerencias y consejos: desarrollar una rutina para mantenerse activo
A daily routine can benefit both care partners and people with an FTD diagnosis. Trying to fill…
Palabras de aliento: collages de libros para colorear
Coloring Book Collages by Cathey Merrill Ron and I married when I was 17 and he was…
Conexión comunitaria: horario de oficina abierta para voluntarios del grupo de apoyo
AFTD Support Services Coordinator Erin Ficca has started hosting Open Office Hours for Support Group Volunteers twice…
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