I developed a new unilateral tinnitus during ENT treatment using Fluticasone nasal drops. The ENT doctor didn't think they were related and basically felt the tinnitus was untreatable. I went back to my GP (I'm in the UK), who did nothing but agreed with the ENT doctor's judgement. I showed him some research papers, and reiterated that I am deeply distressed by tinnitus because I am an extremely light sleeper, but he was not empathetic.
Now I'm almost 2 weeks into tinnitus and I think I'm running out of time to save my neurons, feeling extremely sad. My only hope now is on finding another ENT doctor who can analyse the cost and benefit for my specific case. But how should I persuade them?
I'm considering medical tourism, but I'm wary of the risks too. Are there any countries that are relatively open to trying the Prednisone treatment if no remarkable hearing loss is detected under regular audiometry?
Now I'm almost 2 weeks into tinnitus and I think I'm running out of time to save my neurons, feeling extremely sad. My only hope now is on finding another ENT doctor who can analyse the cost and benefit for my specific case. But how should I persuade them?
I'm considering medical tourism, but I'm wary of the risks too. Are there any countries that are relatively open to trying the Prednisone treatment if no remarkable hearing loss is detected under regular audiometry?