Nonprofit support and advocacy groups bring together patients, families, medical professionals, and researchers. These groups often raise awareness, provide support, and develop patient-centered information. Many are the driving force behind research for better treatments and possible cures. They can direct people to research, resources, and services. Many groups also have experts who serve as medical advisors. Visit their website or contact them to learn about the services they offer. Inclusion on this list is not an endorsement by GARD.
These resources provide more information about this condition or associated symptoms. The in-depth resources contain medical and scientific language that may be hard to understand. You may want to review these resources with a medical professional.
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Is Eagle syndrome genetic? See answer
I have been diagnosed with Eagle syndrome and have ringing in my left ear. Can Eagle syndrome cause tinnitus/hyperacusis? See answer
How rare is Eagle syndrome? Is surgery the best treatment? What kind of doctor would perform this surgery? See answer
How might Eagle syndrome be treated? See answer