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Personlige historier
Historier om FTD Genetics omtalt i "Brain & Life" Magazine
Brain & Life magazine recently told the stories of two people whose lives have been affected by FTD, and who participated in the March 5…
AFTD Founding Board Member Talks about Creation of FTD Caregiver Resource Book
AFTD founding Board member Lisa Radin shared her journey of being an FTD caregiver during Massachusetts General Hospital’s “Community…
AFTD Volunteer Living with PPA interviewet på "Rodger That" Podcast
AFTD volunteer Jennifer Lee discussed how her life has changed since being diagnosed with primary progressive aphasia…
Magasinet "Atlantic" fremhæver person diagnosticeret med FTD
En artikel offentliggjort i The Atlantic beskriver livet for personer diagnosticeret med demens midt i COVID-19-pandemien, herunder en mand diagnosticeret med FTD, og hvordan...
Personer med medlem af FTD Advisory Council deler historien om fortalervirksomhed og frivillighed
Katie Brandt (left), Amy Shives (center), and Sharon Denny AFTD volunteer Amy Shives, MEd, discussed her experience of being diagnosed…
UK kvinde deler mands rejse med ung demens
Michelle Macadangdang mistook her husband’s sudden change in temperament to be a sign that their marriage was in…
Giv en hånd til vores hjælpende hænder! AFTD-frivillig Marc Toles
A former caregiver to his wife, Marc Toles (MI) wanted to give meaning to what he and…
Giv en hånd til vores hjælpende hænder!
AFTD Volunteers: Kati Woodford and Marlene McKian AFTD offers a young-adult Facebook group for people in their…
Giv en hånd til vores hjælpende hænder!
AFTD Volunteer: Amy Almeida AFTD volunteer Amy Almeida and her family used AFTD’s resources for care partners…
Giv en hånd til vores hjælpende hænder!
AFTD Volunteer Nanci Anderson As care partner for Gary, her husband of 38 years, AFTD Volunteer Nanci…
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