Rare Disease Day 2022: Young People Living With A Rare Disease (Part 2)
Jaden Lim, Living with Growth Hormone Deficiency and Pituitary Microadenoma
You can share this podcast by copying this HTML to your clipboard and pasting into your blog or web page.
One person living with a rare disease may feel unseen and unheard, among the minority. But collectively, the voices from the community of people with rare diseases are significant, and can make a difference. In December 2021, the first-ever UN Resolution on “Addressing the Challenges of Persons Living with a Rare Disease and their Families” was adopted, giving visibility to the rare disease community on the global policy landscape. This Rare Disease Day, we hear from two young people on how their rare condition affects their lives, presents challenges to growing up, and what kind of actions they would like to see from society to support them. In the second part of this special feature, Jaden Lim tells us about being diagnosed with a growth hormone deficiency and a tumour on his pituitary gland.
Image credit: Yap Sook Yee
Produced by: Tee Shiao Eek
Presented by: Tee Shiao Eek
Download the BFM mobile app. Stay at home and stay up-to-date.