Jan 24ADVOCACYAbout LilianI’ve always been an empathetic person and someone who has enjoyed helping others. This is why the career pathway I chose as a young adult...
Oct 30, 2023ADVOCACY7 Tips on Being an Effective CarerBeing in a caring profession as a social worker and caring for a child/young person with a long term illness as a carer are two very...
Oct 18, 2023ADVOCACYRARESummit23I was invited to attend the RAREsummit 2023 and talk about the long lasting impact of having a rare disease. Despite not being able to...
Jun 11, 2023KATTYMy Life, My Genetics - Genetic Inheritance I was a part of Rare Youth Revolution's Genetics Project. I worked alongside Rare Youth Revolution to talk about different topics...
Feb 15, 2023ADVOCACYRARETalksI was interviewed by RARE Youth Revolution about what it's like living with Lupus. It was a great opportunity to talk about Lupus with...
Mar 27, 2022ADVOCACY7 Stages of Managing a Long Term IllnessThese stages relate to my own experiences of being diagnosed, processing and living with Lupus. I believe it can be used as a guide for...
Mar 18, 2019ADVOCACYWorld Young Rheumatic Diseases DayFind out more about more about a new World Wide event to raise awareness awareness about the lives of young people living with rheumatic...
Jan 30, 2019ADVOCACYMcPin YPAGIn December I became a member of the McPin Foundation Young People Advisory Group (YPAG). This is an organisation that through research...
Jan 30, 2019ADVOCACYDecade of LupusThe following article was published in Lupus Uk's News & Views magazine,Winter 2018 edition. I've posted it on my website because this...
Jan 30, 2019ADVOCACYCochrane Conference Edinburgh 2018In September I was invited to the Cochrane Conference in Edinburgh, Scotland by the lovely Dr Erin Walker ( Patient Insight and...
Sep 13, 2018ADVOCACYRARE Revolution Magazine ArticleI recently had the opportunity to write an article for the RARE Revolution Magazine. Click below to find out more. LINK TO FULL ARTICLE...