“When the cure for Parkinson’s is found, and it will be,” says Michael J. Fox, “it will be because of all of us.”
Telehealth: A Valuable Asset to Those Living with Movement Disorders
Will Medicare Patients Lose Key Protections?
Member Feature: International Essential Tremor Foundation
Life with essential tremor can be frustrating. Simple tasks like tying shoes, brushing teeth or drinking from a glass become difficult challenges.
International Essential Tremor Foundation, a Movement Disorders Policy Coalition member, is working to improve patients' lives through education and empowerment, celebrating the perseverance and ingenuity of people living with the condition.
“Essential tremor has no cure. And since there is no medication specifically designed for it, patients struggle to find effective treatment options,” says Executive Director Patrick McCartney. “We can't offer these patients a cure, but we can make sure they are educated, connected and empowered to take on the challenges of life with essential tremor.”
This March is National Essential Tremor Awareness Month. Join International Essential Tremor’s 2021 campaign, “Let’s Talk About ET”, to support advocacy efforts.
The Movement Disorders Policy Coalition is proud to call the International Essential Tremor Foundation a partner. Together, we can increase public awareness and advance research initiatives for treatment options and a cure for essential tremor.
To learn more about the International Essential Tremor Foundation’s advocacy efforts and membership visit essentialtremor.org or contact Executive Director Patrick McCartney at pmccartney@essentialtremor.org.
America’s Spectrum of Support for Patients
Member Feature: American Brain Coalition
An active member of the Movement Disorders Policy Coalition, the American Brain Coalition uses education and advocacy to improve public understanding of functions of the brain.
The group also empowers people living with brain conditions, including movement disorder conditions such as ataxia, dystonia, Parkinson’s and Tourette’s.
“The 50 million people living with disabling brain disorders deserve more research initiatives,” says Executive Director Katie Sale. “That will encourage additional treatment options, services and support that will improve patients’ quality of life and build a national commitment toward finding cures for these disorders.”
Bringing together organizations representing patients, families, providers and other stakeholders, the American Brain Coalition works to reduce the burden of brain diseases and increase funding for neurological disease research.
The Movement Disorders Policy Coalition is proud to partner with the American Brain Coalition to advance better care for those living with movement disorders.
To learn more about the American Brain Coalition’s advocacy efforts and membership visit americanbraincoalition.org or contact Executive Director Katie Sale at ksale@americanbraincoalition.org.
New Medicare Approval Requirement Delays Treatment
Living with Huntington’s disease
Now More than Ever, Access to Mental Health Treatment Matters
“I’ve been working with a patient, a male in his late 20s, for a few years now. He showed some early signs of schizophrenia in high school but worked through them and went to college across the country. It was there, away from everything familiar, that he had his first symptoms of psychosis. He left school and moved home.”
Ataxia Awareness Social Graphics
Dystonia Awareness Social Graphics
COVID-19 Introduces New Balancing Act for Caregivers
Sometimes the caregivers who call our help desk need assistance finding local resources for their loved ones. Others just want to talk with someone who understands how stretched they feel.
Insurers’ Rx Switching Disrupts Neurological Care
Telemedicine Bridges Gap for Patients in Hawaii
Time to Make Telemedicine Policy Permanent
World Brain Day Spotlights Parkinson’s Disease
This year’s World Brain Day unites advocates in highlighting a disease that devastates families and communities across the globe: Parkinson’s.