MND is devastating. 150 years since it was discovered, it remains a terminal condition with no treatment or cure.
30 years ago, no inherited forms of MND had been identified. Now, there are over 40 known genetic mutations. Despite this, genetic research is still chronically underfunded.
We say, that sucks.
EVERY MUTATION MATTERS
We believe answers will be found in researching inherited forms of MND. No form of MND is too rare to deserve our attention. We are ruthlessly thorough and leave no stone unturned in our search for answers.
COLLABORATION IS IN OUR DNA
We believe that we’ll find a cure and treatments faster if we all work together. We operate with an open access policy, sharing resources and results with a consortium of top minds in MND research.
GOING FULL TILT AGAINST MND
We believe we must move faster. Time is not on our side but commitment, brain power and a determination to crack the hell on with it is. That’s why we’re dedicated to funding the most efficient and impactful projects ASAP.
We’re here to supercharge progress because every moment matters.
MND, we’re coming for you.