Tinnitus - what should VeDA's role be in providing info on?

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Cynthia Ryan
Tinnitus - what should VeDA's role be in providing info on?

During the November board meeting, Matt pointed out that we talk about tinnitus on social media, and asked what our role in educating patients on it is/should be.

Cynthia pointed out that according to a VeDA poll, 75% of vestibular patients have tinnitus. It can be very debilitating, so we do provide some educational resources (short article, webinar), but don't dive all in, since there are other organizations that do this (e.g. ATA, BTA).

According to Gary, the ATA doesn't provide much good info.

Matt feels like this could be an opportunity for us to access a wider audience.

Thoughts?

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