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Team Tommy Foundation Birthday Bash Ready To Pop December 9th

Team Tommy Birthday Bash

The Team Tommy Foundation is pleased to announce they’ve moved the “Crawl to Hall” with their popular Pub Crawl heading west to the Firefighter’s Union Hall at a one stop Birthday Bash commemorating Tommy’s birthday this year.  A fun fundraising night like no other, the Birthday Bash will feature birthday party games, contests, raffles, cake and dancing!  Admission is only $10 and may be paid in advance and may be purchased at the door.

The Birthday Party Bash will be held at the Firefighter’s Union Hall at 11201 W. Midway Road in Fort Pierce (34945) from 7:00 - 11:00 p.m.  Guests will be treated to contests, games, prizes plus a lot of fun and laughs for a small donation of only $10.  The Bash is a BYOB event but food will be available for purchase from Creative Ched on Wheels and Mad Dogs.  Traxx Entertainment will keep the party moving with their second to none DJ and Crew.  Dress for the Decade Contest with winners awarded amazing prizes from local businesses, Busch Gardens, Uber and others.

Sponsorships are still available and are $100.  Team Tommy Foundation has a reputation for getting social media exposure, therefore you can be sure your business will get great coverage on all popular media platforms as well as on its internationally recognized Myositis Awareness website, for this nominal donation.  Team Tommy would like to thank the Edge Family at the Tax Shoppe and Bruce Lamoureaux from Bruce’s Cool Sunscreens for their sponsorship. Please visit the website, for complete more information on sponsorships or find the event on Facebook at

Team Tommy Foundation is a local, 501(c)(3) not-for-profit organization established to raise funds for families with Myositis diseases, finance research and promote awareness.  Team Tommy Foundation was started in honor of Tommy Worthington, a St. Lucie County Sheriff’s deputy who succumbed to Dermatomyositis in July 2012.  All proceeds will go towards providing financial assistance to patients and their families living with Myositis disease and to The National Myositis Association for Dermatomyositis research. Visit us at for additional information.


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