| Last updated on August 12, 2008 |
OUR VISION
In the quest to create a world without ALS, our vision is to care for and support all people living with Lou Gehrig’s disease as we leave no stone unturned in our relentless search for a cure.
We will achieve our vision by upholding our commitment to be the:
Preeminent organization and catalyst in funding and promoting ALS research;
Most comprehensive provider of care and support services to the ALS Community through our coordinated network of Chapters, Centers and clinics;
Leading advocate and voice for the ALS Community;
Recognized authority and most trusted source of information and education about ALS.
OUR MISSION
To lead the fight to cure and treat ALS through global, cutting-edge research, and to empower people with Lou Gehrig’s disease and their families to live fuller lives by providing them with compassionate care and support.
OUR VALUES
People with ALS and their families come first in everything we do.
Scientific credibility and innovation are the hallmarks of our research program.
Integrity, honesty and ethical behavior guide all our endeavors.
Champion the cause of people with ALS to raise awareness, understanding and support at every turn.
Collaboration and partnership within our organization and with others who share our goals and values promote continued success in the fight against ALS.
Mutual respect is the cornerstone for all our working relationships.
Financial strength enables us to accomplish our goals.
Commitment to excellence and professionalism are key tenets at all levels of our organization.
Diversity of ideas, cultures, ethnicities and backgrounds strengthen our efforts.
Teamwork: We are a unified organization with one vision and one mission.
Description:
The ALS Association is the only national not-for-profit health organization dedicated solely to the fight against ALS. The ALS Association covers all the bases - research, patient and community services, public education, and advocacy - in providing help and hope to those facing the disease. The mission of The ALS Association is to lead the fight to cure and treat ALS through global, cutting-edge research, and to empower people with Lou Gehrig’s Disease and their families to live fuller lives by providing them with compassionate care and support.
ALS Association Northern New England Chapter addresses the needs of persons with ALS in the states of Maine, New Hampshire and Vermont.
The following programs and services are provided through our chapter:
ALS patients and families are provided information and resources about ALS as requested.
Support Groups have been established and maintained providing peer and family support in all three states.
Adaptive devices and equipment can be provided at no cost through our loan closets, located in the three states.
Increased public awareness in our communities about ALS through educational talks by knowledgeable staff.
Supporting ALS advocacy efforts.
Informing patients and families about clinical trial opportunities.
History:
The Northern New England Chapter was founded on August 20, 1999 to serve the needs of those living with Amyotrophic Lateral Sclerosis and their caregivers.
The ALS Association is the only national not-for-profit health organization dedicated solely to the fight against ALS. ALSA covers all the bases — research, patient and community services, public education, and advocacy — in providing help and hope to those facing the disease.
The ALS Association (National Office and the Northern New England Chapter) operates under a shared mission: to help people living with Amyotrophic Lateral Sclerosis and to leave no stone unturned in search for the cure.
We work together to accomplish our mission. The Northern New England Chapter focuses primarily on helping local patients and families live with ALS while the National Office focuses primarily on research and advocacy. The Chapter supports the National Office through revenue sharing and research contributions. The National Office supports the Chapters by providing up-to-date information and materials.
Our accomplishments are made possible by the generosity of others. From the smallest donation to the largest gift, donors touch the ALS community with hope for the future.
Contact person: Kimberly Tonneson, Program Coordinator, (phone), (email)
Office fax number: (603) 226-8890
Address:
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10 Ferry St, The Concord Center, Ste 438 Bx 314
Concord, NH 03301
(See a map) |
Web Site: http://www.alsanne.org
Directions:
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From the North- Take I-93S to exit 15W. At the light take a left. At the next light take a left into The Concord Center(Ferry St).
From the South- Take I-93N to exit 14. Take a left at the light. Take. . . (more) |
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