In some cases, spasmodic dysphonia may run in families and is thought to be
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Support and advocacy groups can help you connect with other patients and families, and they can provide valuable services. Many develop patient-centered information and are the driving force behind research for better treatments and possible cures. They can direct you to research, resources, and services. Many organizations also have experts who serve as medical advisors or provide lists of doctors/clinics. Visit the group’s 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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Have any cases of spasmodic dysphonia been documented as having partially reversed spontaneously (i.e., non-medically and non-surgically)? I have spasmodic dysphonia and have experienced a dramatic and spontaneous improvement of my symptoms. Is there a medical explanation for this? See answer
My mother has spasmodic dysphonia and I believe that I may have it too. How is this condition diagnosed? Is genetic testing available for this condition? See answer