New Resource Helps Caregivers Identify Involuntary Movements Linked to Tardive Dyskinesia

New Resource Helps Caregivers Identify Involuntary Movements Linked to Tardive Dyskinesia

Developed by Caregiver Action Network with support from Teva.

FOR IMMEDIATE RELEASE

Oct. 2, 2025
Caregiver Action Network
Contact: Allison Borthwick
Email: aborthwick@caregiveraction.org
Phone: 202-780-9978

————————————–

WASHINGTON, DC – Caregiver Action Network (CAN) has released a new, free resource to support caregivers of individuals living with Tardive Dyskinesia (TD). Titled “Seeing the Signs: A Caregiver’s Guide to Involuntary Movements and Tardive Dyskinesia (TD),” this guide provides culturally informed, easy-to-understand strategies to help family caregivers recognize early signs, advocate for treatment, and overcome barriers to care. 

“Tardive Dyskinesia is often underrecognized and misdiagnosed, leaving caregivers frustrated and unsupported,” said Marvell Adams Jr., CEO of Caregiver Action Network. “This tool equips families with the knowledge they need to act early and push for the right care.” 

“Living with Tardive Dyskinesia can be debilitating from a social, psychological and physical perspective,” said Stacy Finkbeiner, PhD, Senior Medical Director, Teva North America Medical Affairs. “That’s why Teva is proud to partner with the Caregiver Action Network to help family caregivers better understand TD, recognize it earlier, and find appropriate support and care for their loved ones.” 

The tool includes: 

  • A breakdown of common signs and symptoms 
  • Guidance for navigating healthcare systems and insurance challenges 
  • Culturally relevant insights for underserved communities 
  • Real caregiver stories and practical advice

The tool is available now at: https://www.caregiveraction.org/td-caregiver/

##

About Caregiver Action Network (CAN):

Caregiver Action Network (CAN) is the nation’s leading nonprofit dedicated to improving the quality of life for the more than 63 million family caregivers in America. From parents of children with complex health needs to spouses, friends, and adult children caring for loved ones with chronic conditions, disabilities, or Alzheimer’s, CAN supports the full spectrum of caregiving families. Through free education, peer support, and resources, CAN empowers family caregivers nationwide to provide care with strength, resilience, and hope.