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The ALS Association is the only national 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.
The Greater Chicago Chapter offers services to patients & families living in Northern and Central Illinois who are affected by ALS, including: Home Visits, Skype Appointments, Support Groups, Information & Educational Materials & Programs, Medical Equipment Lending, ALS Clinics at The University of Illinois Medical Center & The University of Chicago Medical Center, & Professional In-Service Presentations.
We are always seeking passionate volunteers and spirited individuals who wish to join the cause! «Walk — Run — Ride to Defeat ALS» programs & other great events hosted year round. Visit ALSAchicago.org for more information!
History
Established in 2004.
The ALS Association was established in 1985. In 2004, The Greater Chicago Chapter was founded by Martha Kucharski in memory of her late husband, Edmund J. Kucharski.
Vision: Create a world without ALS.
Core Values:
— People with ALS and their families come first in everything we do.
— Scientific credibility and innovation are the hallmarks of our research program.
— Commitment to excellence and professionalism are key tenets at all levels of our organization.
— We are one team with one vision and one mission working together.
— Collaboration and partnership within our organization and with others who share our vision and values are key to sustained success in the fight against ALS.
— Integrity, honesty and ethical behavior guide all our endeavors.
— Mutual respect is the cornerstone for all our working relationships.
— Diversity of ideas, cultures, ethnicities and backgrounds strengthen our efforts.
— Financial strength enables us to accomplish our goals.