Thank You for Your
Interest in the A.L.S. Family Charitable Foundation, Inc.
Several years ago, we started this Foundation
in hopes of creating a brighter future
for those living with A.L.S.
Because we know the realities of the disease, we have made it our life's work
to eradicate A.L.S.
We proudly offer several great programs designed to enhance the
lives of those that we seek to support.
We owe a great deal to our wonderful volunteers and
benefactors that are now part of our "family".
Today we remain as committed to finding a cure as we
were when we first formed the foundation. Our focus
centers on raising funds for much-needed research so
that one day there will be no need for what we do,
but we remain acutely aware of the needs of our patients.
We will stop at nothing to help those impacted by A.L.S.

Mission Statement: The A.L.S. Family Charitable
Foundation, Inc. is a federally recognized 501(c)(3)
non-profit organization dedicated to raising funds for
cutting edge research and patient services for those
suffering from Amyotrophic Lateral Sclerosis.
The A.L.S. Family Charitable Foundation, Inc. was founded
in 2001 in loving memory of Clifford Jordan, Jr. and
Edward Sciaba, Sr. to honor all the courageous individuals
and families touched by A.L.S.
Co-founders Mary Ann
(Sciaba) Singersen and Donna Jordan witnessed first-hand
the harsh reality of Amyotrophic Lateral Sclerosis when
they lost family members to the dreadful disease. After
years of working at the volunteer-level, these two spirited
women embarked on their own journey making it their
life's work to eradicate Amyotrophic Lateral Sclerosis,
more commonly known as Lou Gehrig's Disease.
Despite years of research, the cause of A.L.S. has yet
to be determined, making the search for a cure all that
more difficult. The Foundation focuses much of its energies
on fundraising in an effort to provide crucial financial
support to the medical and scientific organizations
that specialize in A.L.S. research. It is imperative
that the Foundation also provides services to patients
and their families while the search for the elusive
cure continues.
The needs of A.L.S. patients and their families run
the gamut from financial and emotional support to extensive
medical and therapeutic treatment and ultimately advocacy.
The A.L.S. Family Charitable Foundation works almost
exclusively to raise money to help fund agencies that
assist patients to ensure that their needs are met.
Meet Our Founders
Two total strangers shared the same vision, now best
of friends, they have combined their efforts and turned
that vision into a driving force in the fight against
A.L.S.
Our Inspirations
The A.L.S. Family Charitable Foundation, Inc. was founded
by Donna Jordan and Mary Ann (Sciaba) Singersen in dedication
to the loving memory of Clifford Jordan, Jr. & Edward
J. Sciaba, Sr. The impact of these two great men had
such a profound effect on their families that they have
left behind not only a legacy of love but of a boundless
hope!
A.L.S. took their lives years before, but today the
spirit of their courage continues to be the foundation
of something wonderful. That spirit is at the heart
of the A.L.S. Family Charitable Foundation, where families
join together to help one another, where families join
together to support each other, where families join
together to overcome!
Clifford Jordan, Jr. was born and raised in Brockton
and resided in Dedham. He was an accomplished carpenter
and welder. Cliff was a devoted father to his daughter
Amanda, a loving husband to his wife, Jean, and a cherished
son and brother. Before he was stricken with ALS at
the young age of 34, he loved to vacation at his home
in Vermont, ride his mountain bike, his motorcycle,
and spend time with his family. Cliff had a unique and
creative personality. He was very loved and is sadly
missed.
Edward J. Sciaba, Sr. grew up in the South End of Boston.
After high school, he worked as a rigger at Bethlehem
Steel Co. in Quincy before joining the Navy in 1944.
After being honorably discharged in 1945, he formed
a construction company, Sciaba & Co., Inc. Over a 45-year
period, he built many buildings throughout the Commonwealth
including schools and other public facilities. Ed was
highly respected in the industry.
Ed was a successful businessman, but more importantly,
he was the loving patriarch of his family. He was tremendously
strong and yet quietly adoring. He and his wife, Adele,
raised four children and had eight grandchildren. Before
Ed was diagnosed with ALS, he would spend hours supporting
his grandchildren by attending their activities. A.L.S.
took many things from him but never his inner-strength,
never his resolve. Through it all, he remained a shining
example for all that knew him.
The A.L.S. Family Tree
In 1999, the A.L.S. Family Charitable Foundation planted
the A.L.S. Family tree as a symbol of hope for the families
and patients affected by A.L.S. Bricks etched with the
names of ALS patients make a circular walkway around
the tree.

A brick in honor of your loved one who is battling or
has battled ALS can be purchased by contacting the A.L.S.
Family Charitable Foundation at (508) 759-9696 or by
downloading the
brick order.
A.L.S. Family Charitable Foundation Organizational
Profile
Mary Ann Singersen
President, Treasurer, Office Manager
Donna Jordan
Vice President
Tara Cronin
Marketing Director
Board of Directors
Jeff Beals
Dianne Farron
Donna L. Jordan
Bill MacLeod
David Phillips
Mary Ann Singersen
Dale Wolbrink
Honorary Board Members
Clifford Jordan, Sr.
Shirley Jordan
Adele Sciaba
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