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In
Loving Memory of
Joseph Dominic Lillo
Borrowed from Heaven
June 4, 2008
Little
I knew that morning, God was going to call your name, in life we loved
you dearly, in death we do the same. It broke our hearts to lose you,
you did not go alone, for part of us went with you, the day God called
you home.
You left us beautiful memories, your love is still our guide, and
though we cannot see you, you are always by our side. Our family chain
is broken, and nothing seems the same, But as God calls us one by one,
the chain will link again.
Given back to Heaven
August 29, 2008
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What's
New! |
Fall Excitement!
3rd Annual Family Pasta Night
THANK YOU TO: ROBBINS REEF YACHT CLUB AND EVERYONE WHO DONATED THEIR TIME, SKILLS, CULINARY DELIGHTS, AND FABULOUS AUCTION ITEMS!!! THANK YOU TO EVERYONE WHO ATTENDED AND CONTINUE TO SUPPORT OUR FOUNDATION!!!
The Joseph Lillo Memorial Scholarship
Applications are now available and due no later than February 1, 2012. Click the Joseph Lillo Memorial Scholarship link for more details and to print the application.
Recent Donation from our Foundation: 150 Leachco Bath Pads to Families of SMA
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Overview of the
Organization |
Thank you for
expressing an interest in our foundation, as well as Spinal Muscular
Atrophy.The Joseph Lillo Spinal Muscular
Atrophy Foundation for Children is an organization that was founded in
2008 in memory of Joseph Dominic Lillo. Joseph succumbed to Spinal
Muscular Atrophy (SMA) Type I at three months old. SMA is the #1
genetic cause of death for infants. The statistics show one in 6,000
babies are born annually with some type, and one in 24,000 babies are
born with Type I, considered the most progressive type. SMA is a
neuromuscular disease characterized by degeneration of motor neurons
resulting in the wasting away and weakness of muscles, including
respiratory musculature. SMA is caused when both parents are carriers
of the recessive genetic gene found on Chromosome 5, in which 1 in 37
people are carriers. This deadly genetic disease is far from rare,
although many people have never heard of it.
The Joseph Lillo Spinal
Muscular Atrophy (SMA) Foundation for Children is a non-profit
501(c)(3) organization committed to raising awareness, as well as
raising money for research and medical equipment for families
affected by SMA and other disorders.
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