MISSION STATEMENT
We are a Chapter of #MEAction established by Granite Staters to advocate for people with ME/CFS in New Hampshire. We aim to accomplish this by amplifying awareness and understanding of ME/CFS; working with medical providers to offer more in-depth medical education about ME/CFS; fighting for disability rights; and advocating for people and their families concerning issues of health insurance, treatments, and quality and compassionate care.
aBOUT US
We are a New Hampshire ME/CFS advocacy organization. We advocate for our rights and recognition, bring awareness to this disease, and work with elected officials, medical providers, and others to make sure New Hampshire recognizes ME/CFS and provides quality care and support to all.
Each month we will plan and organize for action and we need and welcome your help. We will be working with elected officials, medical providers, and fellow citizens to ensure we are recognized, understood and supported in NH.
We welcome people with ME/CFS, long COVID, and related conditions, those who are undiagnosed, family members, caregivers, healthy allies, and anyone looking to amplify our needs and work to make NH a place that cares for all of us.
UPCOMING EVENTS
Monthly planning meeting – We meet the second Monday of the Month at 4:30pm ET on BlueJeans.
For more information including video conference link and call-in numbers please look on the #MEAction Events calendar for our upcoming call and join details!
Contact
For questions please contact any of our co-leaders:
Leah Stagnone: [email protected]
Michelle Roy: [email protected]
Arna Lewis: [email protected]
Visit our Facebook for updates.