The Paralyzed Veterans of America is a veterans' service organization in the United States of America, founded in 1946. The organization holds 33 chapters and 70 National Service Offices in the United States and Puerto Rico. It is based in Washington, D.C. The organization was founded in 1946 by a band of service members who came home from World War II with spinal cord injuries. These service members wanted to live with independence and dignity and as contributors to society, so they created the organization to be governed by its members, veterans of the armed forces living with spinal cord injury or disease such as multiple sclerosis (MS) and amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig’s disease.
PVA's team of legislative advocates, architects, medical professionals, lawyers, and other highly trained professionals strives to ensure that every veteran regains the freedom, independence, and quality of life they fought for. The organization is a major support system for our nation’s paralyzed heroes, their families, and caregivers, through ensuring quality health care; securing earned benefits; fighting for disability civil rights; making America more accessible; helping veterans find meaningful careers; empowering them through sports, recreation, and wellness programs; and funding both research and education in search for a cure and improved care and autonomy for individuals with paralysis. PVA helps paralyzed veterans and all people with disabilities live fuller, more productive lives.
The group holds a congressional charter under Title 36 of the United States Code.
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