INDIGOMED is the only platform that specializes in rare diseases. Families often feel lost and adrift when the diagnosis is a rare disease. Please note that European doctors do not always use the same drugs to treat the same diseases as do their counterparts in the US. Rare diseases such as Bartter’s syndrome, macular corneal dystrophy (MCD), Tay-Sachs disease, Huntington’s disease, dilated cardiomyopathy with ataxia (DCMA), to name a few, may require a second opinion, either to choose a more cost-effective quality of care or to improve the existing treatment plan.