Nathan's Fight For Life

A RACE AGAINST TIME.

Hello this is my son Nathan he was diagnosed with motor neuron disease 3 years ago.

MND is pretty much a death sentence with no cure the average life expectancy is two years so things looked rather bleak indeed.

So I guess you could say he’s been lucky getting three years.

Since then we have watched him wither away his photography business closed down, the guitar he loved playing so much, gone. Once a vibrant loving family man full of life now reduced to a wheelchair and becoming increasingly dependent on full time care.

We’ve all been praying for a miracle and it’s finally happened a treatment has been found, but its not cheap $600 for a months supply.

Its called the Deanna Protocol invented by Dr. Vincent Tedone who’s own daughter Deanna, contracted the disease and now seems to be in remission.

Since its launch the Protocol has given hope to thousands worldwide afflicted with this dreaded disease.

The Deanna Protocol is not a cure, but it has been effective in either slowing or stopping the advance of this fatal disease.

Watch this video about “Deanna Protocol”

https://www.youtube.com/watch?v=ZOx1-KG1vHA

The moment Nathan went on the Deanna Protocol he experience a definite turn around in strength, muscle tone, and his brain fog lifted so it's helping him big time.

The family need your help to raise the money to keep him supplied with the medication, running raffles and cutting firewood simply can’t sustain this for any length of time thats why I started this appeal.

My wish is to string it out as long as possible in the hope that a cure can be found before his time runs out.

If you are reading this and know of someone who has this deadly disease please tell them about the Deanna Protocol, you may just save their life.

Here’s the link to the medication http://www.simplesanutrition.com/deanna-protocol/