Our organisation would like to wish the best of luck, lots of friends and good grades to all HAE juniors for the new school year 2023/2024! Because HAE awareness in the school environment is especially significant, as every year, we want to offer parents, relatives or guardians helpful educational materials as well as recommendations on how to get through a school year with good health and, ideally, without many missed classes.
Talking openly about a rare disease like HAE is challenging for adults, let alone children. One way to communicate about such uncomfortable topics is through art and stories. A great example is the short story "The Rare Boy and the Little Talkative Balloon" by author Natasa Angjeleska, the regional HAE patient advocate from North Macedonia. The story depicts the adventures of a little boy on his birthday as he experiences a party, an emergency trip to the hospital and an unexpected encounter with a talking balloon. Initial disappointment and sadness are followed by a positive experience of new friendship and mutual understanding.
The Czech translation of the story is available for download here or we can send by post a printed booklet on request. We would appreciate it if you could help us distribute the story to the schools or kindergartens!
School classes as well as after-school clubs, sports activities and trips can cause more stress to young HAE patients than to healthy schoolchildren. The parent’s task is therefore to minimise the impact of the disease via prevention, education of the school staff, but also instructing the children themselves.
We wish all HAE juniors and their parents good health, enough energy and enthusiasm necessary for the new school year 2023/2024!