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In 1994, the relatives of patients suffering from Thalassemia thought of joining a committee to try to have more strength in finding new therapies, more suitable treatments for different ages, experimentation with new drugs and psychological help different from the current one. . Thus was born the Committee of Thalassemia Families Hope to Live, and in the first 25 years of activity we have brought a great advantage to our children both in clinical care and in the experimentation of new drugs, under strict control of a very valid medical team of the Meyer Hospital in Florence. . Unfortunately, as everyone knows, the current Health Service does not provide particular economic support, which is why the Committee organizes events for the collection of funds to finance pre-established projects.

Contact Comitato Famiglie Talassemici (Committee of Thalassemic Families)
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