Donating Profits – Motor Neurone Disease

Ambrose has lost several family members to Motor Neuron Disease ‘MND’ (known as ALS or Lou Gehrig’s Disease in the USA) including his younger sister Louise who succumbed to the disease at age 47. Few diseases are considered a more debilitating and challenging ending to life, with the mind left intact to deal with a body that wastes away.

Ambrose is determined to commit whatever funding he can to research the disease. An 80% net profit to research model enables Ambrose to operate this platform, whilst driving funds into researching this disease. We must find a cure.

Ambrose is also a participant into MND research through the Royal Women’s and Children’s hospital in Brisbane Australia.  

The Unsent Letter platform is the perfect combination in offering a way to help those in distress from their own past issues, including those who have suffered loss of any kind, whilst at the same time raising funds for MND research.

Some Facts

Motor Neurone Disease (MND), Amyotrophic Lateral Sclerosis (ALS), or Lou Gehrig ’s disease is the name given to a group of diseases in which the nerve cells (neurones) controlling the muscles that enable us to move, walk, speak, breathe and swallow undergo degeneration, weaken, waste and die.

  •         MND is a progressive, terminal neurological disease
  •         MND can strike anyone. 10% of cases run in families.
  •         There is no known cure and no effective treatment
  •         Average life expectancy is 2.5 years
  •         MND is becoming more prevalent
  •         Approximately 58% of people with MND are under the age of 65

Research is continuing around the world and continues to gather momentum. The Ice Bucket challenge is a well known and successful initiative for MND research.