On Rare Disease Day, we remember that Primary Lymphedema is a rare or uncommon disease.
For many people, it is unknown why their
lymphatic system did not develop properly from birth, which creates
uncertainty and delays diagnosis.
That is why research is
essential: to better understand its origin, improve diagnosis and
advance for more appropriate care. Researching today means
caring for tomorrow.
WHO WE ARE: LIST OF THE SPANISH LYMPHEDEMA ASSOCIATIONS
FEDEAL - THE LYMPHEDEMA AND LIPEDEMA FEDERATION (SPAIN)


