 
 A unique educational tool created within VASCERN’s Paediatric and Primary Lymphoedema (PPL) Working Group is reaching a wider audience. The Lymphoedema Colouring Book, designed to help children understand their condition in an engaging and reassuring way, was recently featured at two major international congresses: the Congress of the French Society of Vascular Medicine (SFMV) in Lille and the 12th International Lymphoedema Framework (ILF) Conference in Canada.
Available in ten languages, the book combines friendly illustrations, simple explanations, and a child-adapted version of the Do’s and Don’ts for lymphedema skin care and compression. It is a practical and reassuring tool that helps children learn about compression, skincare, and daily routines in a way that feels safe and approachable.
Helping children understand lymphoedema
Developed as a child-friendly resource, the Lymphoedema Colouring Book transforms medical guidance into playful, illustrated pages that encourage learning and dialogue between children, their families, and healthcare providers.
Each section simplifies essential information about lymphedema care, from compression and skincare to daily routines, allowing children to actively engage with their condition while colouring. The book’s mix of visuals and simple explanations helps reduce fear, build confidence, and promote good habits from an early age.
The project was led by Dr. Caroline Fourgeaud from Hôpital Cognacq-Jay (France) and Manuela Lourenço Marques, Co-Chair of the PPL European Patient Advocacy Group (ePAG) and patient representative from andLINFA, with illustrations by Chrystèle Lim. It was validated by the PPL Working Group and translated into ten languages with the support of patient associations in the ePAG and wider patient community, ensuring accessibility for children and families across Europe.
 
  
 Shared at National and International Congresses
The Lymphoedema Colouring Book was presented as a poster at the Congress of the French Society of Vascular Medicine (SFMV), held in Lille from 8 to 10 October 2025. This national event gathered specialists to discuss advances in vascular medicine and explore innovative ways to improve patient communication and care.
It was also displayed at the 12th International Lymphoedema Framework (ILF) Conference in Canada from 23 to 25 October 2025, one of the largest global meetings dedicated to lymphoedema care. The event brought together more than 600 participants from 35 countries, including clinicians, researchers, and patient representatives.
Having the book featured at both congresses showed how a collaborative project can attract interest far beyond its original community.
A joint effort with a lasting impact
The Lymphoedema Colouring Book shows how patients and professionals can work together to make information accessible and human. It reminds us that communication in healthcare can take many forms, including crayons and colouring pages.
The book is available in ten languages:
Bulgarian: Книжка за оцветяване при лимфедем
Danish: Malebog om lymfødem
Dutch: Lymfoedeem Kleurboek
English: Lymphoedema Colouring Book
French: Cahier de coloriage sur le lymphœdème
German: Lymphödem-Malbuch
Portuguese: Livro para Colorir sobre Linfedema
Slovenščina: Pobarvanka o limfedemu
Spanish: Libro para colorear sobre el linfedema
Swedish: Målarbok om lymfödem
The success of this project reflects VASCERN’s wider mission to connect expertise and compassion in rare disease care. Through initiatives like this, the network continues to promote collaboration across Europe and ensure that patients of all ages have access to clear, reliable, and empowering information.
 
 