We are a patient led small global charity ran from the UK who are dedicated to researching ways of managing the symptoms of Menieres Disease.
We have now completed phase one of our investigation into Stem Cell research with our research partner Dr Arianna Ferrini who is an expert in stem cell and gene therapy. As a result of this work we believe stem cell treatment has potential to make a great difference to the lives of people suffering from Menieres Disease.
We have also established some successful protocols based on guidance from Functional Medicine practitioners which we have documented within these pages.
We now have a Functional Medicine partner Jan Clementson who is very familiar with Menieres Disease and has been working with a number of our members to relieve their symptoms using Functional Medicine based testing and protocols.
Jan works remotely and has clients globally, so she can help you where ever you are in the world.
Running a legal entity Charity is an expensive operation in the UK to ensure we conform with the necessary regulatory and compliance legislation in place. To keep Deaf to Menieres continuing in it’s current form it would really help if you would join us. The more members we have the stronger we can be.
Joining us is free but if you could afford a small donation to our running costs involved in satisfying the regulatory framework and to help keep this website going then that would be greatly appreciated, however small the donation. Every little helps but free membership is also fine.
I wish you the best of health and if you are a Menieres sufferer reading this then I hope you find this website useful and starts you on the road to symptom management.
Director, Deaf to Menieres
While you are here :
We are a patient led global charity registered in the UK dedicated to helping you find your ROOT CAUSE and find TREATMENTS THAT WORK.
The Root Cause guide has been built up from patient feedback supplied by our members.