I believe in self-help as an effective way of dealing with stress, hardship and pain. . . . Mending people, curing them is no longer enough; it is only part of the total care that most people require. The benefits of mutual aid are experienced by millions of people who turn to others with a similar problem to attempt to deal with their isolation, powerlessness, alienation, and the awful feeling that nobody understands.
~Former Surgeon General C. Everett Koop, M.D.
Dr. Koop’s inspirational statement pretty much sums up what ANA/NJ is all about. Being diagnosed with a brain tumor can be a devastating experience. Often, although they try, even family members never fully understand. It helps tremendously to be able to meet or talk with someone who has been down the same road. Our president and founder, Wilma Ruskin, had this experience in 1993. “The night before surgery, feeling frightened and alone . . . I called [a woman] in Chicago . . . and she spent nearly an hour of her time answering my questions, acknowledging my fears, and comforting me. That was my first introduction to the self-help and support concept, and it was to help me time and time again.”
So ANA/NJ was founded in 1995 to help bring acoustic neuroma patients, their families and friends together for mutual support and to share experiences and information. This is basically what we’ve been doing for these many years. We try to help new patients through rough times, and along the way we have also tried to increase public awareness of the symptoms of acoustic neuroma and the benefits of early intervention.
Our organization has grown. We have a dedicated planning group, which we call our Executive Board, and a very supportive Medical Advisory Board of prominent regional doctors. We publish a newsletter twice a year, and in 1999 we introduced our Directory of patients and friends, which has been especially helpful for putting people with similar concerns in touch with one another. We also maintain this new website, to stay up-to-date and keep in touch with the broader community of ANers and medical professionals.
But our basic reason for being remains the same -- self-help. The Internet
is amazing and wonderful, but we still believe it’s most important for
the newly diagnosed patient to have personal contact with someone who
has already made the journey. We’re here. Give us a call,
or send an email. Anytime!
Services provided by ANA/NJ
• Two meetings a year, to include both informal gatherings and biennial Mini-Conferences, with speakers and programs of interest to acoustic neuroma patients and caregivers.
• A semi annual ANA/NJ Newsletter of special articles, notices, reports on personal experiences with acoustic neuroma, and reviews of recent research in the field.
• A Directory of members and friends to facilitate personal contacts and sharing between acoustic neuroma patients.
• Support through local/satellite meetings
planned by members in different areas of NJ
• Scholarships to encourage local meetings initiated by members, and to assist in attendance at ANA/NJ Mini-Conferences.
• A website (www.ananj.org) for providing up-to-date information, notices and sharing experiences,
and for linking with other important sources of information for acoustic neuroma patients and
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no medical decision should be made based on such information. For medical
advice, consult your physician.