The effects of Hyperacusis

People do not understand it's the opposite to deafness and there is no control what happens when you have had exposure to your triggers. Emotionally it has been devastating as I began to have panic attacks and was later diagnosed with Post Traumatic Stress Disorder (PSTD). This is a condition that affects me and has prevented me from securing employment. I'm interested to know how it has had an impact on others both in work and socially. 

During my journey, I found information regarding Dr Silverstein procedures helpful, I must emphasise I've not had the procedure done but it gave me hope for the future. 

http://www.earsinus.com/inventions-procedures

Whats your opinion? Whats been your experiences?



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So its been a while now since I've been on here- apologies to all! I must confess I wanted to write but have had many challenges and here are just a few; I've been put onto Universal Credit and this  means I now get, almost £200.00 less benefit per month.  I still have the fighting spirit to get a job though and this can only be achieved if the behaviours towards disabled applicants changes. I would consider working from home. In one recent telephone conversation I was asked why don't I have hearing aids? I was stumped by the question but really I should have responded by asking why they don't have hearing aids as (1) had they heard and understood my explanation of what its like to have Hyperacusis - the opposite to deafness (2) if they had they would have understood that a person with Hyperacusis hearing is like being in the middle of an orchestra and trying to have  a conversation with someone that is 20 foot away being expected to hear and understand  then give  
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