Settle's Sam Lewis blogs for CMT Awareness Month on living with the disease
A WOMAN from Settle is spending September letting the world know what it’s like to live with a debilitating condition […]
Continue ReadingA WOMAN from Settle is spending September letting the world know what it’s like to live with a debilitating condition […]
Continue ReadingAfter years of bullying at both school and in the workplace, one woman hopes to use her experiences to help […]
Continue ReadingTwo small pieces have appeared in these popular magazines!
Continue ReadingLike many young girls 11-year old Aaliyah Jones started secondary school last week, looking forward to a new challenge in […]
Continue ReadingHER struggle coping with a rare neurological disease has caused Wick woman Claire Fraser to speak out in a bid […]
Continue ReadingA DISCOVERY by scientists at the Institute of Neurology and Genetics (CING) in Nicosia may open the way for gene […]
Continue ReadingOur friends at Mini Matt Films in Grimsby have just completed their marathon 72 hour “Stay-Awake-Athon”, streaming the event […]
Continue ReadingTWO young brothers are refusing to let a debilitating genetic disorder stop them achieving their dreams, as they this week […]
Continue ReadingCMT.ORG.UK CMT stands for Charcot-Marie-Tooth, the names of the three scientists who discovered this inherited neurological disease, […]
Continue ReadingMember Catherine Martin has been featured in the Daily Record:
Continue ReadingLast Updated: Monday 9th February, 2015