On Friday’s Morning Focus, we spoke with Sue and Sinead Maguire as they are looking to raise awareness about a rare genetic condition, cystinosis. Sinead was diagnosed with the condition when she was 2 (her sister was also subsequently diagnosed with it), while her mum Sue works as an advocate to help those with the disease, including fundraising for research, through Cystinosis Ireland. More details are available on www.cystinosis.ie and they’re hosting a virtual conference on the condition this weekend.