jueves, 20 de agosto de 2026

CHILDREN WITH LYMPHEDEMA – PEDIATRIC AND PRIMARY LYMPHEDEMA – The Galician Lymphedema Association (AGL) supported a French lady’s charity challenge to walk 200 km along the "Way of Saint James" (Camino de Santiago) to raise awareness of lymphedema.




The Galician Lymphedema Association (AGL) supported the initiative of the French association ‘Vivre Mieux le Lymphedème’ (AVML), its counterpart with which it shares the objectives of raising public awareness and improving the quality of life of people with lymphoedema. The meeting between the AGL and the AVML representative, Delphine, took place on Tuesday 26 May at 11.30 am in the Plaza del Obradoiro in Santiago de Compostela, in a space dedicated to the exchange of experiences and the strengthening of collaborative ties between the two associations.

Delphine is a nurse at Marcy Hospital in Metz and has been living with lymphedema for over ten years. She currently holds the post of regional director for Alsace-Lorraine at the AVML and is the association’s national communications officer. Committed to raising awareness of the reality faced by people living with this condition, and in particular by affected children, she decided to embark on a personal and charitable challenge: to walk 200 kilometres of the "Way of Saint James" (Camino de Santiago) in ten days.





Through this adventure, Delphine aims to raise public awareness of lymphedema, a chronic and debilitating condition that remains largely unknown and which significantly affects the quality of life of those who suffer from it, with a particular impact on young people. Alongside the physical challenge, a fundraising campaign was launched to help children with lymphedema through AVML.

AGL emphasises the importance
of building collaborative networks with organisations in other countries: when AGL learnt of this initiative, it contacted Delphine to find out more about the project and arrange a meeting.

The project’s objectives include
: raising awareness of lymphoedema and its consequences; giving visibility to children affected by this condition; and raising funds for their care.

“This challenge is much more than just a journey. It is a way of turning my personal struggle into concrete actions to help other children and families,” says Delphine from AVML. 





REFERENCES:


Confederación Galega de Persoas con Discapacidade | COGAMI

Diario Compostela (Digital Newspaper)

Asociación Vivre Mieux le Lymphoedéme





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