MND-ALS Treatments

Hi, My name is Alistair, and my brother Stuart (that’s him in the photo) was diagnosed with Motor Neuron Disease (MND/ALS) on 24 November 2022. More information on this condition can be found at this link; The only treatment offered/available to him in the UK is called Riluzole and it’s effectiveness is minimal with horrendous side effects. Since his diagnosis through our own research it appears there are treatments available outside the uk, however these are very expensive, but effective in treating the illness. These range from Stem Cell treatment in Europe and Asia to holistic therapies in South America. Any donations received will go towards finding treatments that will not only help my brother in his own fight, but also the thousands of other MND/ALS sufferers in their own fight against this cruel and horrible disease, for which there is currently no known cure. Stuart is 47, and used to lead a very active lifestyle, working extremely hard, in order that he could also play hard, be this Snowboarding, Mountainbiking, water sports and even visiting Thailand to train in his first love, Muay Thai boxing, none of which he is able to do anymore. Hopefully, through the kindness of others, we can do our best to at least slow down, halt or even reverse the progression of this disease.https://www.nhs.uk/conditions/motor-neurone-disease/

You can follow Stuart’s journey on TikTok searching [email redacted]