Deaf to Menieres have funded research into successful treatment protocols and funded treatment programmes on individual volunteers.
This is the before and after scoring from Frances Mudie who filmed this testimonial after her treatment programme you can watch <here> .
The research into successful treatments has been done by Jan Clementson our Practitioner Partner who has a website page on her findings <here>
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>
You can see the slides from Jan’s 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
(See Dr Arianna Ferrini, Ph.D. in Tissue Engineering and Regenerative Medicine : https://www.kolabtree.com/find-an-expert/arianna-ferrini/ )
For the latest information on how our research is going for stem cell treatment and the success of our fund raising activities please click on this link
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.
If you would like a free 30 minute discovery session with Jan to see if she could help you manage your symptoms then you can contact her and book it via her website here
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.
You can access the survey by clicking on this link
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.
You can help us by registering and donating to our charity. We are an entirely voluntary organisation. All funding raised will be 100% utilised into achieving our objectives
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.
JOIN WITH US TODAY AND RECEIVE 3 FREE GIFTS:
– A GUIDE ON HOW TO HELP YOU FIND YOUR OWN ROOT CAUSE, SHOWING 17 POTENTIAL ROOT CAUSES TO INVESTIGATE
– A GUIDE TO A TREATMENT PROGRAMME TO ADDRESS YOUR POTENTIAL ROOT CAUSES BASED ON PROVEN FUNCTIONAL MEDICINE PROTOCOLS
– A SUMMARY OF THE FIRST 100 RESPONSES TO OUR QUESTIONNAIRE WHICH CONFIRMS THAT MENIERES DISEASE ATTACKS ALL AGES
The Root Cause guide has been built up from patient feedback supplied by our members.
ALSO BY JOINING HERE TODAY YOU WILL REGISTER TO RECEIVE REGULAR UPDATES ON OUR CURRENT RESEARCH AND TREATMENT REVIEWS.