The ultimate point of reference for those who deal with LYMPHEDEMA and LIPEDEMA

• Latest news. Updates from the scientific world, clearly explained and always linked to the sources.
• Insights highlighted. Thematic dossiers to really understand what studies and guidelines say.
• Agenda. Calendar of upcoming scientific congresses and training courses for operators.
• Patient space. Testimonials and communities, practical indications, regulatory references and tools for the social management of the disease.
• Verified sources. Selected content from certified social network accounts.
• Treatment centers. Up-to-date information to help you find your way around and find the most suitable services.

Our web apps

• Map of the reference centers. A web app to quickly identify centers dedicated to the treatment of lymphedema and lipedema, with filters by region, services and access times. —>
• Interactive lipedema. A guided path that you can choose as a doctor or as a patient, to obtain explanations, protocols and tailor-made tools. —>
• Data from the National Rare Disease Registry. A web app that makes the data available on the register available for consultation, with clear indicators and understandable visualizations. —>

ITALF SCIENTIFIC PARTNER