Californians Can Be a
Hero at Tax Time and “Get the 414 on ALS” to Help Fund a Cure for
Lou Gehrig’s Disease with State Income Tax Contributions
February
21, 2013 –
This
tax season, Californians have an opportunity to make a difference in the fight
to defeat Amyotrophic Lateral Sclerosis (ALS, also known as Lou Gehrig’s Disease)
by giving $25 or more to the ALS/Lou Gehrig’s Disease Research Fund on line 414
of their state tax return.
The
four California chapters of The ALS
Association have launched a grassroots, public awareness campaign about the
disease to inform taxpayers that they can make a donation on state tax returns
to support cutting-edge research to discover new ALS treatments and a cure. The “Get the 414 on ALS” campaign seeks to
inform both California taxpayers and tax preparers that regardless of income,
any state resident can help conquer ALS. More information about the campaign is
available online: www.GetThe414onALS.org.
Amyotrophic
lateral sclerosis (ALS, also known as Lou Gehrig’s Disease) is a progressive,
neurodegenerative disease that causes people to lose their ability to walk,
speak, swallow and eventually to breathe; while in most circumstances, all five
senses and mental functions remain intact. Once diagnosed, most people with ALS
survive an average of two to five years.
Currently,
there is no known cause and no known cure. However, scientific advancements
identifying new genes and drug pathways are vital to revealing new targets for
treatment and are occurring at an unprecedented rate.
“The progress in ALS research over the last
few years gives us every reason to believe that new discoveries are right
around the corner,” said California ALS Advocacy Committee Co-Chair, Jim
Barber, who has been living with ALS since 2006. “We’re depending on the
generous support from California tax payers to help get us there.”
This essential fundraising initiative would
not be possible if it weren’t for the dedicated work of passionate California
ALS advocates, the leadership of Senator Juan Vargas and President pro-tem Darrell
Steinberg, and the approval of Governor Edmund Brown., To date, the annual
campaign has raised nearly $500,000 in voluntary contributions.
“We
want people to understand that ALS affects people from all walks of life, and
above all, to know that their donation makes our quest for a cure possible,”
said California ALS Advocacy Committee Co-Chair, Jared Gill, who lost his
father to ALS in 2000. “Californians are incredibly generous. We know their continued
support will again send a strong message to our state legislature regarding the
importance of supporting programs and research initiatives that benefit people
with ALS and their loved ones.”
California
is one of 41 states allowing all taxpayers to make a voluntary, tax-deductible
contribution to one or more worthwhile causes in the “contributions” section of
the state tax return. Every year, the organizations must raise a minimum of
$250,000 or be removed from the tax form. Even a small donation will have a
significant impact on funding programs that support a range of important issues
from medical research to the environment; reduction of violence and child
abuse; to assistance to seniors; and honoring our men and women in uniform.
The ALS Association is the only
non-profit organization fighting Lou Gehrig’s Disease on every front. Our
mission is to lead the fight to treat and cure ALS through global research and
nationwide advocacy while also empowering people with Lou Gehrig’s Disease and
their families to live fuller lives by providing them with compassionate care
and support. Our vision is to create a world without ALS.
The four California chapters of The
ALS Association, (from north to south - Greater Sacramento, Golden West, Orange
County, and Greater San Diego), spearheaded the efforts that led to the fund being
added to the state’s income tax form.
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