How you can help
Spread the word about misophonia and Sensory Processing Disorder! If you haven’t done so already, please make sure you get yourself on the free Misophonia Bulletin email (just click here). This is where I share the very latest news, research, user stories and more. One of our biggest challenges right now is to get the right information out there to the people who need it most.
Donate to Misophonia Research
Misophonia is not currently recognised as a disorder in the UK or in the US, which means it currently gets no government funding for research or treatment. Despite this there is some incredible research taking place. One such programme is being headed up at the Le Doux Lab in New York by some of the world’s leading neuroscientists, but it is in desperate need of funding. Please donate whatever you can here. You can find out more about this incredible work here.
Help Support Others
We run a safe and friendly forum on Allergic to Sound – no trolls, bigots or snake oil salesmen allowed. If you want to join in the debate and help others navigate a happier path through their misophonia journey please drop by the forum here. You can also talk to others, share information and positive advice on the Positive Misophonia Facebook group here and the Misophonia Research Facebook group here. We’re on Twitter here.