Most recently I was fortunate to attend Tinnitus Research Initiative’s Tinnitus Conference in Auckland, New Zealand. I hugely enjoyed this event, both because of what I learned and because of who I met. Here were 230 researchers, clinicians, and audiologists from all around the world who made the effort, at considerable expense, to gather and share their knowl- edge about tinnitus—all with the same one goal: to find a cure for tinnitus.
I’ve been able to share what I’ve learned with other tinnitus patients through a patient-support newsletter I edit for the University of Aukland’s School of Public Health, Audiology Section. This monthly newsletter, named Sounding Board, is the premier information resource for tinnitus and hyper- acusis patients here in New Zealand. Readership has grown steadily with each issue, and I’m happy
to provide hope to so many fellow patients.
I am empowered by learning about tinnitus and neurosci- ence, and I’m excited at the work being done to better understand and treat tinnitus. A cure is the goal (tinnitus management is the next best thing), and I know we’ll get there someday soon! I am convinced that the way ahead is for people at all levels of life and all levels of tinnitus to support tinnitus research.
Chris Bedford credits his caring wife and the regular demands of his work and church activities with keeping his spirits up.
Editor’s Note: A version of this article appeared in the April 2014 issue of Sounding Board. ATA is sad to note the recent
passing of Joan Saunders, QSM, founder of the New Zealand Tinnitus Association and lifelong advocate for tinnitus patients in New Zealand.
Advertisement — ATA does not endorse or recommend any tinnitus products or treatments.
Summer 2014 | Tinnitus Today
11
PATIENT STORIES
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