Finding Support
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Finding Support

Support Group Overview


"We have faced a common trauma – coping with an acoustic neuroma. Face-to-face group meetings give the opportunity to be with others who truly understand. By sharing how we have coped and been helped by receiving medical information from professionals who may be new to us, we can restore ourselves by the strength furnished by a caring community." Ginny Fickel Ehr, ANA Founder. 

Support groups are a vital extension of the support network that ANA members can provide for one another. The  support groups provide an opportunity for networking and are able to assist in social and personal support for all acoustic neuroma patients including newly diagnosed, watch and wait and previously treated acoustic neuroma patients, their family members and any interested persons in the local area.


Benefits of joining a Support Group include:

  • Communicating in a nurturing, non-judgmental environment with others who have shared a common acoustic neuroma experience.
  • Sharing information on dealing with specific problems, overcoming handicaps and reassuring others that better times lie ahead.
  • Educating and informing each other about the latest acoustic neuroma topics of interest.
  • Providing emotional support to all patients, both pre- and post-treatment. This helps in reducing the isolation and loneliness that many acoustic neuroma patients feel.


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Testimonials from ANA members describing the positive impact  received from attending a support group meeting:

I remember how desperately I wanted to be able to talk with someone. I feel one of the many benefits provided by our group, is its ability to provide encouragement and compassion for the newly diagnosed. --Greg from DC
I have found all the meetings that I have attended to be very informative and have made several ´friends´. I have found it best to talk with individuals who have just started their AN journey and share my successful outcome. --Joe from New Jersey
My greatest reward from attending this group is watching newly diagnosed patients attend a meeting and having the opportunity to meet a variety of people with many treatment types as they weigh all their options. I see the hope in their eyes appear as they learn we have all survived, and life after an AN is possible. --Joan from Florida
I had great support from my family and friends, but they could not understand my concerns, thoughts and feelings. I never knew anyone who had any type of brain tumor, so it seemed, at times, that I was going through this alone. Coming to the support group allowed me to meet people who also had a vestibular schwannoma. Even though our conditions may differ, it is a great feeling to relate to others. --Jennifer from Florida
The group gave me hope and made me realize that I wasn´t alone. There were many others out there who shared similar problems to mine, and we were bonded on that basis. Together, we can make a difference for others who are newly diagnosed and those who have difficulty dealing with their present reality. --Carol from Florida
It has been very meaningful for us to share and learn from others who can truly understand the daily challenges we all face with acoustic neuroma. We are constantly seeking out solutions to make our lives better. We are reminded at each meeting that there is life after acoustic neuroma! --Gail and Elaine from Michigan.


Dealing with the New NormalTips and Suggestions for Coping

Membership in ANA provides the following benefits:

  • ANA Quarterly newsletter, Notes
  • Patient information booklets
  • ANetwork, Nationwide Peer Support Program
  • Website availability with ANA Discussion Forum



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