Carlos is a sociologist, works in non-profit organizations for hemophilia in Mexico since 1992. Currently CEO of the chapter in Jalisco State and manager of the national registry of the Mexican Federation of Hemophilia, which has increased by 300% under his management. Carlos and his son Juan live with severe hemophilia A.

He has led national advocacy campaigns, also planned and coordinated the main campaigns to locate and register patients in 10 Mexican states, was president of NMO and hemophilia congresses in Mexico, coordinated a twinning program of the World Federation of Hemophilia, and has been a member of some of its committees, he was also a speaker at some workshops and conferences for NMO.

He co-founded the Coalition of the Americas and coordinated its initial projects.

In his local chapter, he leads advocacy and assistance activities for a group of 700 patients who receive care in 10 hospitals in Jalisco.