Patients Have a Voice
VEDA advocates for the vestibular community to increase awareness about vestibular disorders, while implementing programs to reduce diagnosis times and improve treatment effectiveness, thereby improving the quality of life for vestibular patients.
- Read about VEDA's advocacy strategy in our Strategic Plan.
You can be an advoate for vestibular awareness!
- Share your story
- Become a VEDA Ambassador
- Volunteer with VEDA
- Follow VEDA on Facebook - "Like" and "Share" our posts
- Write a letter to your legislator
- Share our "Top Ten Facts About Vestibular Disorders"
- Participate in Balance Awareness Week
- Give a presentation about balance disorders
- Host an information table about vestibular disorders at a health fair
Don't forget to contact us and tell us how you are helping to raise awareness about vestibular disorders!
The FDA Patient Network
The FDA has a long history of working with patients and patient advocates representing specific groups, beginning with the AIDS crisis of the 1980s. Since then, FDA has reached out to advocacy groups, such as the National Council of Rare Health Disorders and other disease-specific groups, to ask for their input on proposed regulations and guidance documents.
More recently, in July 2012, President Obama signed into law the Food and Drug Administration Safety and Innovation Act (FDASIA) which calls for the agency to increase patient participation in the regulation of medical products.
According to project manager James Valentine, M.H.S., the Patient Network helps to bring the unique perspective of patients, family members, caregivers and patient advocates to the decision-making processes of the FDA. There are a number of ways to become involved, including becoming a patient representative on a committee that advises FDA on key issues.
Find out more about the FDA Patient Network by visiting their website.