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The Abilities Expo is a traveling event for people with disabilities, as well as the family members, caregivers, and professionals who care for them. The expo allows attendees to discover the latest life-enhancing products and services and learn from free workshops and demonstrations.
The Buoniconti Fund to Cure Paralysis is a nonprofit organization committed to finding a cure for paralysis resulting from spinal cord injury — and to seeing millions worldwide walk again.
The Christopher and Dana Reeve Foundation is dedicated to curing spinal cord injury by funding innovative research and improving the quality of life for people living with paralysis through grants, information, and advocacy.
The Miami Project is the largest, most comprehensive spinal cord research centre in the world. Over 120 research scientists and technicians from around the world are focused on curing paralysis and improving the lives of spinal-cord-injured individuals.
The National Rehabilitation Information Center (NARIC) collects and disseminates the results of federally funded research projects. The NARIC serves anyone, professional or layperson, who is interested in disability and rehabilitation.
The National Spinal Cord Injury Association (NSCIA) is dedicated to improving the quality of life for hundreds of thousands of Americans who are living with spinal cord injury and disease (SCI/D).
This award-winning monthly magazine provides active wheelchair users and members of the United Spinal Association with original stories and feature articles about rehabilitation, accessibility, lifestyle, technological advancements, and more.
The Paralyzed Veterans of America (PVA) is a leading advocate for health care, SCI/D research and education, veterans' benefits and rights, accessibility and the removal of architectural barriers, sports programs, and disability rights.
The Spina Bifida Association (SBA) serves adults and children who live with the challenges of spina bifida. Since 1973, SBA has been the only national voluntary health agency solely dedicated to enhancing the lives of those with spina bifida and those whose lives are touched by this challenging birth defect. Its tools are education, advocacy, research, and service.
The information provided herein is not medical advice and is not intended to substitute for the advice of your personal physician or other healthcare provider. This information should not be used to seek help in a medical emergency. If you experience a medical emergency, seek medical treatment in person immediately.
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