The Lynn Surprenant Memorial Fund has been established to support the AFTD’s research efforts and to help provide resources to individuals and families impacted by FTD.

When Lynn was diagnosed with behavioral FTD in 2018, we struggled to understand her diagnosis and what to expect as it progressed. The AFTD helped us navigate the condition and provided resources like caregiver support groups which offered both emotional and practical support.

Lynn was an outstanding mother, sister, daughter and friend. She cared deeply for those around her, and she will be remembered for her sincerity, grace, strength, and humor. Even as her symptoms worsened, Lynn always saw the best in others and never lost her radiant smile.

Since Lynn’s passing in 2020, her family has sought to honor her legacy by raising awareness for FTD, driving research efforts and supporting affected families and caregivers.

About FTD: Frontotemporal degeneration (FTD) is the most common form of dementia for people under the age of 60. It strikes in the prime of life, gradually eroding an individual’s personality: their ability to speak, make sound decisions, control their movements, behave within social norms and relate to those they love. FTD devastates familial relationships, finances and even the health of family caregivers themselves. Currently there are no approved treatments, and most providers lack knowledge of appropriate care. Average life expectancy is 7-13 years after the start of symptoms.

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