The ANetwork, Nationwide Peer Support Program, consists of acoustic neuroma patients and family members/caregivers who are willing to talk about their acoustic neuroma experience. These volunteers provide information, encouragement, and support to other acoustic neuroma patients via telephone and email. Personal contact with other patients is a strength of ANA, and we encourage pre- and post-treatment ANA members to take advantage of this important resource.
The ANetwork list includes volunteer participants covering all treatment types, various tumor size and representative demographics from across the U.S. as well as dates and types of treatment and talking points on other acoustic neuroma related treatment issues.
To request a complimentary packet of information and the ANetwork list, please submit your request below. We are happy to provide the packet to any pre- or post-treatment acoustic neuroma patient, family member or friend.