This short film (originally published in February 2015 - see below) tells the story of Lewis and his family. Lewis has Batten disease, a rare neurodegenerative disorder that begins in childhood. Lewis’s mum Samantha talks about their struggle for a diagnosis and the impact a rare disease has had on the entire family.
Dr Nadeem Qureshi provides practical insight and advice for GPs who have patients with suspected rare diseases. Professors Sir John Burn and Mark Caulfield discuss the role that research, specifically the 100,000 Genomes Project, can play in helping to diagnose and treat patients with rare diseases.
*Please note, this film was published in 2015. You can find a more up-to-date resource for GPs and other primary care practitioners here: genomicseducation.hee.nhs.uk/genomics-in-healthcare/genomics-in-primary-care/.
For more information please see genomicseducation.hee.nhs.uk
For more support, these organisations are here to help:
Rare Disease UK
Syndromes Without a Name (SWAN UK)
Genetic Alliance UK
UK Clinical Trials Gateway
Deciphering Developmental Disorders (DDD)