8th Annual Jack Martin Bevacqua Dinner Dance & Auction

To Benefit PWSA-USA and NJ

Saturday, October 22, 2011 , 7 pm to 11pm

VFW Post 2179, Port Monmouth, NJ

We can't believe it is that time of year again!  Join us to support PWSA-USA and PWSA-NJ to raise money for research to battle this disease.

Our son Jack was born 9 years ago with Prader-Willi syndrome (PWS).  PWS is a genetic disorder that affects muscle tone, appetite and overall development.  The most devastating part of this disease is that it causes an insatiable appetite.

Jack is a happy 9 year old, but has had global developmental delays as a result of the PWS.  Jack did not walk until he was 3 or talk until he was 5. Our most challenging aspect of life is watching everything Jack eats.  Despite his delays, Jack is a charmer and lights up everyone's face.

PWSA USA and NJ are wonderful organizations that fund research, provide mentoring and crisis counselling for families afflicted by PWS.  We would not have survived the early years without these organizations and continue to lean on them today.

This benefit was born 8 years ago, and thanks to our wonderful support network of family and friends we have raise over $100,000 for this cause.  Without you, this event would not be possible.

So, reach deep into your phone contacts, your FaceBook friends and your email contacts and get a group of people to come out for a FUN night out!

Join us on October 22nd to raise money to battle this disease!

Tickets are $40 and include dinner, dessert, beer and wine.  If ordering tickets on this website, please write "tickets" in comments.  For further information,

Contact me via:

FaceBook

email:  captainjack816@msn.com

cell:  732.859.4588

Kevin Bevacqua

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Many thanks for your support -- and don't forget to forward this to anyone who you think might want to donate too!