Hi all, I was diagnosed with MS in March 2015. Since then, I've undergone 2 bouts of Lemtrada chemotherapy.... and cycled over 45,000 miles on my bike. It's been quite a journey. I think that other MS sufferers would benefit from aspects of my story - especially the newly diagnosed or those considering Lemtrada treatment - and I've now finished the book that I've been writing about my experiences. I attach a link to my book, "CyclingWithMS", which is now available for purchase on the amazon website - both e-book and paperback. https://www.amazon.co.uk/CyclingWithMS-Ewan-Johnston-ebook/dp/B07HZ2MW97/ref=dp_kinw_strp_1 (All profits are going to the "MS Society" - I am making no profits, direct or indirect, from any sales - and I know the site doesn't allow advertising but I've cleared this with the moderators!) Several readers have encouraged me post on this website - I'd be happy to answer any queries about my experiences with Lemtrada, my book... or other.... either via this site, or on my wordpress blog: https://cyclingwithms.wordpress.com/ As background: I’m not a writer. I’m not even a cyclist, not a professional one anyway. But I do have MS. To try and organise my own thoughts, I started to write a diarised blog entitled “CyclingWithMS”. I found this exercise enormously therapeutic and was hugely buoyed by the messages of support that it elicited. As my blog grew and grew, it became harder for readers to find a coherent story so, this year, whilst I was laid low by ill health, I spent my bedbound time transforming my various diary extracts into a single book. The result is that my book is not necessarily in chronological order and has had to be heavily edited from its original form but I feel that it now best-represent the trials, tribulations and joys of a life with MS. I hope that it provides you with an entertaining read.