You are not alone. Millions of people experience vestibular dysfunction. By sharing with others, your own experience is validated, which can give you hope, as well as useful tools for coping with the daily impacts of a chronic illness.
Find out more about:
– In-person and online support groups
– VeDA’s online forum
– Support for your family and friends
Keep up-to-date on new and developing topics in the vestibular community. Join VeDA’s mailing list to receive our monthly e-newsletter, with links to original articles and patient stories, and stay connected via social media.
VeDA exists for you and because of you. We are a non-profit organization supported entirely by your gifts. You can help people like you learn to live a life-rebalanced.
Vestibular disorders are misunderstood. You can advance vestibular research by participating in clinical trials and sharing your medical history through VeDA’s Patient Registry.
Members of VeDA's Sustaining Circle provide reliable funding for VeDA to carry out our mission throughout the year by making a monthly gift. To join the Sustaining Circle, or learn how you can help VeDA
Concussion recovery may be complicated by vestibular involvement. Vestibular rehabilitation can help.
Spread the Word You are welcome to download and distribute these materials in hardcopy or electronic format. We encouage the use of our presentations to educate your community about vestibular disorders. The Road to Balance
Navigating the Medical Billing System Medical billing can be a long and drawn out process, especially for vestibular diagnostics and treatment, where many procedures do not easily fit into a specific insurance codes. While VeDA
The friends and family members who care for vestibular patients provide essential support. Without firsthand experience, these individuals are challenged to learn about vestibular disorders in order to lessen the impacts of their loved one’s illness. VeDA seeks to focus attention on this important part of our vestibular community and to support their efforts.
Increasing awareness about vestibular disorders is the key to reducing the time it takes for a vestibular patient to receive an accurate diagnosis. VeDA promotes continuing education for vestibular professionals and encourages patients to become their own healthcare advocates by learning as much as they can about their condition. It can also be therapeutic for a patient to listen to another patient’s journey so that they know they are not alone, and to gain valuable coping tips.
VeDA’s annual call to all “Vesties” — those living with vestibular dysfunction, their loved ones, healthcare providers, and support partners. Let’s all celebrate the steps we are taking together on the journey to finding “Life Rebalanced.”
בתחילת ינואר 2015 הסתכלתי מחדש באתר כאן ומצאתי מאמרים חדשים שהסבירו את כל הסימפטומים שאני עוברת ומצאתי בכך נחמה וכח. החלטתי שהגיע הזמן לבנות אתר בעברית ברצוני להודות לארגון וודא ולד"ר טימותי היין שנתנו לי רשות
CANVAS Syndrome is named with an easy-to-remember acronym for cerebellar ataxia, neuropathy, and vestibular areflexia. There are only a very few patients reported who have the requisite combination of two rare clinical findings (cerebellar ataxia and vestibular areflexia), and the very common peripheral neuropathy. Patients with CANVAS combine cerebellar ataxia (i.e. coordination problems — the CA), peripheral nerve damage (neuropathy – N), and loss of vestibular function (vestibular areflexia — the VA). This combination causes major disturbances to balance as each of these systems alone contributes to balance. Of course, when all are out at the same time, balance is much worse than when only one or two happens to be malfunctioning.