When Veronica Wolfe’s mother was diagnosed with bvFTD in 2018, her family initially struggled to find information about the disease. Once her mother’s neurologist pointed them to AFTD’s website, however, Veronica committed to learning all she could about FTD and AFTD’s resources. She joined a support group and attended a few virtual Meet & Greets, and in 2020 she was compelled to become an AFTD volunteer herself.

Siden da har Veronica været en aktiv fundraiser - organiseret en uafhængig begivenhed, deltaget i Food for Thought og sluttet sig til AFTD-teamet til New York City Marathon. "Det er let at se fordelene ved at skaffe penge og bidrage til AFTD's overordnede mission," fortæller hun. "Det, jeg har fundet for at være endnu vigtigere, er den synlighed, fundraising giver til sygdommen, selv i mit lille samfund. At skabe opmærksomhed har været ekstremt givende."

In February, Veronica hosted a virtual Meet & Greet to bring together those with the unique experience of being an only child with a parent who has FTD. “Although these have all been completely different [volunteer] experiences, I feel like it’s a small way to support my mother, connect with others going through a similar situation, and process things for myself,” she said. “Volunteering has been rewarding and extremely satisfying… each experience has provided a slightly different sense of fulfillment.”

When asked what she would tell someone considering becoming an AFTD volunteer, Veronica said, “Do it! AFTD makes it easy, regardless of whether you’re filling a pre-existing need or creating your own event! The support from AFTD has been great – the process of organizing individual events, Meet & Greets, and fundraisers has been seamless. I was guided every step of the way. I hope to continue to contribute to the organization however I can in the future!”