Who are we? Maybe it would be better to say who aren’t we. We are not supporting club, whose members are holding their hands in a circle, speaking about their suffering. We are not Internet forum, where frustrations are spreading like a disease. At the end we are not nonprofit organization that is raising funds for the research, but the truth is that 80% of their budget I spent on employees’ wages. So, who are?

We are dynamic and the young team 😊, that consists of people, who share the same suffering reality. Phrase tinnitus sounds kind of trifle. If you are reading this, you know that trifle is the worst description of the situation. You might heard “get used to it”, “there is no cure,” or in the best scenario (if you are treated by a person with certificate provided by the well-known tinnitus researcher) you might be hearing that after therapy is finished you will still hear tinnitus, however you will be not bothered by it…

In most cases doctors are not interested in tinnitus research. It’s quite frustrating as tinnitus research is quite optimistic recent times. Stakeholders agree, that never in history we had such impressive effort invested in a search for cure. Are we experiencing a breakthrough in the field? – We are not allowed to provide such statement. However, it would be unwise not to have at least some level of optimism.

OUR MISSION

Through creation of communicational space, we would like to strengthen interaction between communities, so in the future tinnitus disease will be curable.

OUR VISION

• To create initiatives and support international interactions, through contact with foreign patient`s organizations.
• To be in the permanent contact with research centers in Poland and abroad. To support and publicize scientist`s efforts for finding tinnitus cure. To help fighting bureaucratic obstacles that, researchers might come across.
• To inform patients and doctors about latest research and therapies.
• To popularize tinnitus and hearing protection awareness in society.