ALS Ice Bucket Challenge Progress

The Northern New England Chapter has new address:

The ALS Association Northern New England Chapter
PO Box 207
Concord, NH 03302-0207

Prevent the Spread of Coronavirus
People with ALS are at an increased risk for respiratory problems associated with viral infections.
Prevent the Spread of Coronavirus

People with ALS are at an increased risk for respiratory problems associated with viral infections.

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Coronavirus Statement
Considering developing news regarding COVID-19 (novel coronavirus), the staff at the Northern New England Chapter is working to continue our support to all the constituents in Maine, New Hampshire and Vermont. Our priority is the safety and well-being of our entire community. Therefore, in an abundance of caution, the Northern New England Chapter is taking the following steps to minimize risk to the families we serve:
 
  • The Chapter staff, located in Concord NH, will be working remotely and still available to our constituents daily.
  • We will be implementing technology to remotely deliver Care Services programs for at least the next 30 days:
    • All Support Groups will be offered by video/voice conferencing. Specifics will be sent to people living with ALS by our chapter care service coordinators.
    • Home Visits will also move towards video conferencing, phone, e-mail and/or mail support.
    • Caregiver Lab programs in Manchester NH and Bangor ME will be rescheduled. A date for the Vermont Lab will be selected soon.
  • As always, your Care Services Coordinators will be available by phone and email to help support you. We will be working closely with our Durable Medical Equipment partners to continue the equipment loan support as best we can.
 
Our plans for the Walk to Defeat ALS events do not begin until August, so we continue to do our work as usual on this front. We anticipate that instead of meeting over a cup of coffee to discuss walk plans, that much of the work will be done via phone or video conference.

  As we remain committed to defeating ALS on every front, we will work to keep all of you informed as we all proceed in this time of uncertainty. Please contact us if you have any questions or concerns. For specific information about symptoms you may be experiencing or questions about personal exposure as someone living with ALS or as a caregiver, please contact your physician directly.

For the most recent information about the coronavirus (COVID-19), The ALS Association recommends that you reference the following websites:

Center for Disease Control
World Health Organization
NH DPHS Website
ME DPHS Website
VT DPHS Website

The Northern New England Chapter supports people living with ALS and their loved ones through services and education in Vermont, New Hampshire and Maine. We leave no stone unturned in search for the cure of this progressive neurodegenerative disease.

To view our current events calendar please click here.
Our Mission
To discover treatments and a cure for ALS, and to serve, advocate for, and empower people affected by ALS to live their lives to the fullest.
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Help create a world without ALS by getting involved in the way that best suits YOU! When you fundraise with friends and family you take us closer to discovering a cure.

Walk to Defeat ALS

More than 180 walks take place in communities across the country February through November. Walk to Defeat ALS draws people of all ages and athletic abilities coming together to honor a loved one with the disease, to remember those who’ve passed and to show their support for the cause.

Find A Walk Near You

Host your own event to support our Chapter

Hold a golf tournament, run a marathon, or donate your birthday to raise funds that will help create a world without ALS.

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Celebrate a Loved One with ALS

Pay tribute to a friend or loved one affected by ALS. Each tribute is a personalized online fund designed to honor or memorialize someone special. Your Community of Hope fund creates a lasting legacy.

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Discover More Ways to Help Fight ALS
The Impact of Your Support in 2016
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Resources

Whether you’re newly diagnosed, navigating your journey with the disease, caring for a person with ALS, or researching the cure, there are resources to support you.

Let us help you and your family cope with the day-to-day challenges of living with ALS.

For People with ALS

Learn about our grant program, upcoming scientific meetings, and opportunities to collaborate.

For Researchers

Caring for someone with ALS is hard work. We offer resources and support to help you.

For Caregivers
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You Can Help Create A World Without ALS

Your gift will help The ALS Association support research to find a cure for ALS and provide much-needed services to patients and their families. By becoming a part of The ALS Association family and making your gift today, you will help sustain hope in thousands of people affected by ALS.