We are a team of medical specialists, physiotherapists, patients, family members and friends.
We have joined forces in order to create an association that can help people affected by this condition and their families, to get all the information and support they need.
We are committed both to promoting better understanding of Lymphoedema, and to talking about prevention, so as to avoid being caught off guard by this condition.
The most recent news about clinical and surgical research, in Italy and abroad;
Details about the care centres and the specialized facilities in which the SSN (Sistema Sanitario Nazionale, Italy’s National Healthcare System) provides Diagnosis and Treatment protocols for Lymphoedema;
The Patient’s Vademecum: a collection of useful advice to help you manage your working day, giving a suggested time needed for treatments and providing you with all the information to learn “do it yourself” bandaging, physical exercises and a diet to follow.
We do our best to make ourselves heard both by institutions and society, and to make the State recognise this serious condition as disabling.
Supporting these projects and achieving significant results is an arduous challenge, but if we work as a team, together we can do much more.
