Support

People with MS, and those affected by the Leukodystrophies, are often lonely, frightened and confused. We are unique in that we provide 24 hours a day, 7 days a week, information and support. The support is provided by laypeople that are also affected by these diseases and can relate to experiences and mixed emotions our members may go through.

All support and information is provided absolutely free of charge. We do not charge members a yearly fee nor ask for money to receive our newsletters / updates. We, at The British Trust for The Myelin Project, believe that our members have enough financial strain on their families without having to incur a cost when seeking information. We raise our funds solely through public fundraising.

· We are an open-minded, grass-root movement.
· We encourage all who are affected by MS and the Leukodystrophies to be part of their own future.
· We have an honest, positive vision for the future.
· We ensure our research and its application addresses current patient needs.
· We have personal commitment and support from our researchers.
· We provide in-depth information and updates on research and therapies by means of newsletters, fact-files, lectures, videos and personal emails.
· We help and support issues close to patients' hearts and needs.
· We hold information on fundraising ideas, sponsor forms, posters, and collection-boxes.
· We help to organise events.

We also exist as a sounding board for our members to pass on information they might discover through the Internet, media or even personal experiences. We intend to win this race against time, sooner, rather than later!

Click here for FREE online membership form