Deaf to Menieres have funded research into successful treatment protocols and funded treatment programmes on individual volunteers.
Feedback from Lee Mcintosh following our treatment programme developed with Jan Clementson, a Practitioner partner of Deaf to Menieres :
“In my near 4 year journey with Menieres symptoms of vertigo and hearing loss, Jan has been key in my recovery. After seeing 5 different types of ENT specialists, Jan was by far the most helpful and I would say had the most impact on my improvement of symptoms. In fact, nearly a year completing my program with her I am almost symptom free and leading a very normal healthy life, The nutritional tips and protocols she has given me have benefited a number of other aspects of my health and mental well-being. Hand on heart, I can say I would be in a far worse place if I had not come across Jan and her expertise. Given her recent focus on Menieres I believe she is more of an expert than any ENT I have dealt with and unlike most of them – she really listens and cares. For anyone suffering through Menieres I really recommend getting in touch with her!”
Jan has presented her findings in a video showing discoveries made from her research into Menieres Disease, how she has been constructing successful treatment protocols and in particular how she went about successfully treating Frances Mudie. You can see the presentation <here>
Stem Cell Research
Other Treatment Options Researched
We have also commissioned research papers looking at the potential success of other protocols in treating Menieres Disease :
- Hyperbaric Oxygen Therapy
- Ozone Therapy
We are running case studies with Menieres Disease sufferers through our partnership with functional practitioner Jan Clementson.
Jan has created a testing programme for our Menieres Disease sufferers using blood samples, nasal swabs, urine and stool samples. We are then using the results from these tests to identify root causes and inform suitable treatment protocols.
We are documenting the results from these case studies to evidence outcomes of the tests and treatments applied.
Jan works remotely and has clients globally, so she can help you where ever you are in the world.
Symptom Management Survey
We are using this survey to collate from menieres sufferers the effective measures they use to manage their symptoms.
If you are a menieres sufferer you can contribute today by completing this survey, it’s a tick box exercise which takes on average 6 minutes to complete.
We aim to share the results of this survey and to use it to inform our research into effective treatment protocols.
Linking up Meniere’s sufferers
Meniere’s is a multifactorial set of symptoms i.e. there can be many causes for the symptoms being displayed.
Using our presence on social media we aim to link up Menieres sufferers with the latest research available to help them manage their symptoms
Raising Funds for Research into Meniere’s Disease
In the UK for example there is no Government funding currently being set aside specifically for Meniere’s. We are trying to raise the profile to achieve significant funding into the research of Meniere’s Disease.
We are committed to raising significant funding into research of Meniere’s Disease.
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.