Our first annual gala 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
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Thank you to all that attended the first annual Gala. If you are interested in donating or attending future events please see the links below.
We heartily invite you to attend our first annual 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.
All 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 and President,
Nicholas Tersigni Memorial Foundation, Inc.

The Nicholas Tersigni Memorial Foundation, Inc. is a 501(c) 3, Non-Profit organization. All donations are tax deductible. Monetary donations made be made through our website or checks may be made payable to: Nicholas Tersigni Foundation and sent to the address above.
For information on how to donate items to the silent or live auctions, please see our website for details or call 203-746-1074.
Tell us more about how you'd like to get involved.
175 Ball Pond Road, New Fairfield, CT 06812
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!”

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