We heartily invite you to attend our first annual "Craving a Cure" gala which will be held on
Saturday, October 3, 2026 from 6 p.m. until 10 p.m. at Anthony’s Lake Club, 10 Christopher Columbus Avenue in Danbury, CT. We will celebrate both the life and memory of little Nicholas Tersigni who was born with Prader Willi Syndrome, and we will raise funds to support research on this syndrome. There will be a buffet dinner, cash bar, raffles, and a silent auction.
Proceeds will go to the Prader Willi Syndrome Association.
If you are unable to join us, please consider making a monetary donation, becoming a sponsor or donating to our Silent Auctions. Together, with your assistance, we will be able to make a difference in the lives of Prader Willi children and their families.
Thank you in advance for your support.
With heartfelt gratitude and warmest regards,
Lara Tersigni
Nicholas’ Mom
President
The Nicholas Tersigni Memorial Foundation, Inc.
PLEASE SUPPORT US and help Make a Difference
Nicholas, a handsome boy who brought joy to everyone around him. He spoke only a few words, yet, he truly had no need for words at all. He spoke his own language. His bright eyes spoke volumes. With his unconditional love, he would take you by the hand and show you better than any words could ever say. Nicholas’ love overflowed and one would never guess he suffered from Prader-Willi Syndrome (PWS).
His trademark greeting was a love-filled, “Hi-Ya!”
