Saving Neil Verner's Life from MND


The aim of this is simple, to save Neil Verner’s life.  A lot of you will know Neil from his work, his inventions, his rugby & sport and know what a thoroughly nice unassuming person he is.  Neil has been suffering from the ALS version of motor neurone for over 4 years.  During that time he has become quite an expert in neurology, treatment and available medication.  This page sets out why we need the funding, what it will do and the wider implications of success on anybody suffering from a neurological condition. 

Dr Neil has become convinced that bio chemistry(pills and medicines) will never solve the problem as bio chemistry is designed to work on the symptoms and not the cause.  Bio chemistry also requires molecules to react to, but what if the fault with ALS isn’t molecular but a fault with the motor signal that is either electrical or sub atomic.

Over the years we have studied deeply neurology, bio chemistry, quantum biology, epigenetics, neuroplasticity to name but a few.

We aim to map out his brain activity using a quantitative EEG machine and then try to remap his brain using techniques like photo bio modulation.  The following presentation sets out the reasons why we are doing what we’re doing and the techniques we will apply to save Neil's life.

I will produce a monthly blog and when we have saved Neil we will publish and seek to offer the solution to the wider world.

So please help us save Neil and give as generously as you can.

Please post the GoFund me link and the above video to all your social media with a positive message to help anybody who has ever witnessed neurological conditions. Support Neil and his plans.
  • Eamon Ryan 
    • £20 
    • 4 mos
  • Andrew Barton 
    • £20 
    • 8 mos
  • Luke Minshall 
    • £50 
    • 12 mos
  • Simon Fowler 
    • £150 
    • 12 mos
  • Matthew Whiteley 
    • £10 
    • 12 mos
See all

Organizer and beneficiary

Sue Verner 
Hall Green, Yorkshire and the Humber, United Kingdom
Neil Verner 
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