ALSRI is an affiliation of:

• PEOPLE with ALS (pALS),

• ADVOCATES for pALS, and

• VISIONARY LEADERS of the NURSING HOME INDUSTRY.

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ALSRI recognizes that currently available technology and innovation can restore the freedom and independence that disease and injury has so cruelly taken from the physically disabled. It has been proven as demonstrated by the original ALS Residence open since March 2010. Register today as an ALS Advocate to receive the latest information about efforts to open an ALS Residence near you and if you are in the nursing home industry, contact us to schedule a visit and tour of the original in Boston. Seeing is believing. Your support will help influence the decision of the people who can make this a reality for you.

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The Gleason Initiative Foundation Mission is to help provide individuals with neuromuscular diseases or injuries with leading edge technology, equipment and services; create a global conversation about ALS to ultimately find solutions and an end to the disease and raise public awareness toward ALS by providing and documenting extraordinary life adventures for individuals with muscular diseases or injuries.

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THE GREEN HOUSE® Project offers a model for long-term care designed to look and feel like a real home. Over the last decade Green House homes have set a new standard for quality care with a model that is both proven and practical

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Today there are hundreds of Green House homes open or in development in the majority of states. Our evidence-based model has been proven — through independent research — to be effective, feasible and sustainable. Our technical assistance is a big reason why The Green House Project has become a preferred partner in helping organizations meet demands of the changing long-term care market.

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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 in Maine, New Hampshire, and Vermont.

 

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.

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The ALS Association Northern New England Chapter operates under a shared mission with our National Office: to help people living with Amyotrophic Lateral Sclerosis and to leave no stone unturned in search for the cure.

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The Muscular Dystrophy Association is the world's leading nonprofit health agency dedicated to finding treatments and cures for muscular dystrophy, amyotrophic lateral sclerosis (ALS) and other neuromuscular diseases. It does so by funding worldwide research; by providing comprehensive health care services and support to MDA families nationwide; and by rallying communities to fight back through advocacy, fundraising and local engagement.

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