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Amyotrophic Lateral Sclerosis (ALS) and the ALS Association
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On January 5, 2000, BWZA's CEO Bruce
W. Zimmerman was diagnosed with Amyotrophic Lateral
Sclerosis (ALS). He succumbed to ALS on March 28, 2002. What is ALS?
Also referred to as Lou Gehrig's disease, ALS is a progressive fatal
neuromuscular disorder that attacks nerve cells and pathways in the brain
and spinal cord. Motor neurons, among the largest of all nerve cells, reach
from the brain to the spinal cord and from the spinal cord and from the
spinal cord to muscles throughout the body. When these motor neurons die, as
with ALS, the ability of the brain to start and control muscle movement
fails. Simple voluntary movement in one's arms, hands and legs, as well as
speaking, swallowing and breathing, eventually become impossible. With all
voluntary muscle action affected, patients in the later stages of ALS are
totally paralyzed, yet their minds remain unaffected. To date, over 60 years
since Lou Gehrig's death from ALS, there is no known cause, prevention, or
cure for ALS. |
There are approximately 15 new cases of
ALS diagnosed every day. Every 90 minutes a person loses his or her battle with the disease; every
90 minutes another person is told he or she has ALS. Each of us is vulnerable - ALS knows no
boundaries.
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The ALS Association (www.alsa.org)
is only national not-for-profit, voluntary
health organization dedicated solely to finding the cause and cure for
Amyotrophic Lateral Sclerosis. It carries out its mission at the national
level and through its nationwide network of chapters and support/resource
groups. We ask that you please support the ALS Association. |
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The ALSA Chapter is a
multi-faceted grass roots organization that carries out the Association's mission and strategic
goals at the community level. ALSA Chapters are registered within their own states as non-profit
corporations and are governed by a volunteer Board of Directors. ALSA Chapters come under the
umbrella of The ALS Association as a tax-exempt 501(c)(3) organization. ALSA Chapters provide
services free of charge to people with ALS and their families within their designated service
areas. |
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To learn more about ALS or The
Association, please contact us at
717-657-6240 or any or all of the organizations
below:
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Throughout the first several months of
2001, Scott Zimmerman and Jody Laverty had the privilege and
honor of chairing the Harrisburg area's first ever Walk to D'Feet ALS. By
all measures, the Walk was an overwhelming success! So many
people contributed their precious time, energy and resources to help organize and conduct this
special event for the benefit of Persons with ALS (PALS) and their families. We can't thank them
enough. Jim Pinciotti, Executive Director of the ALS Association Greater Philadelphia Chapter,
expressed our sentiments so eloquently in his thank you letter to our sponsors. |
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To learn more about the
Walk to D'Feet ALS, please contact us or the ALS Association's Greater Philadelphia
Chapter at www.als-phila.org/dfeet.html. |
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