Welcome to The Neuro Foundation
The Neuro Foundation’s vision is to improve the lives of those affected by Neurofibromatosis.
Everyday a baby is born in the UK with Neurofibromatosis. There are over 25,000 people in the UK affected by the condition and as yet, there is no cure.
Raising funds to support you
The Neuro Foundation's work includes funding a team of Specialist Advisors and a Telephone Helpline, as well as supporting research and raising awareness about Neurofibromatosis.
The Neuro Foundation Specialist Advisors
Our Advisors have a depth of knowledge and understanding of neurofibromatosis which benefits individuals, families and professionals needing their expertise.
No matter how large or small, we are always grateful for your donations.Read More
Statement from the Board of The Neuro Foundation - March 2014
Following my announcement in December regarding the joining of forces with Children with Tumours (CwT), I can now confirm that, with effect from Friday 14th February, CwT has become part of The Neuro Foundation and has ceased to operate as a standalone virtual charity.
Should you have any questions then please refer to the 'Frequently Asked Questions’ on the website (see link below under Read more) or telephone The Neuro Foundation, 020 8439 1234 and speak with either Mike or Hazel.
Dr. Tim Corn – Chair, The Neuro Foundation.Read more
Get in touch, find latest news and interact with the NF Community on our Facebook page.Visit us on Facebook