Welcome to the
Heart of a Giant Official Website.

Until the patient speaks or writes, no story will glorify him.

Sharing an unfiltered account of my journey with my congenital heart condition and how surviving I am giving more meaning and purpose to my life through social entrepreneurship in health.
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BOSTON MA. - SEPTEMBER 7: VADP recipient Bouba Dieme looks out over the crowd at the start of the Boston Heart Walk at the Esplande on September 7, 2019 in Boston, Massachusetts. (Staff Photo By Jim Mahoney/MediaNews Group/Boston Herald)
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BOSTON MA. - SEPTEMBER 7: VADP recipient Bouba Dieme second from left standing and Julius Johnson, standing eight from left, a young man who shares a VADP and who Bouba has helped at the Boston Heart walk at the Esplanade on September 7, 2019 in Boston, Massachusetts. (Staff Photo By Jim Mahoney/MediaNews Group/Boston Herald)
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HeartOfAGiant Blog

Engineer, Entrepreneur, Author, Heart Patient Ambassador​

6feet8 born with a heart defect, waiting for a heart transplant, living with an LVAD pump system.

In 2017, after recovering from my open-heart surgery, I began sharing my experience with my congenital heart condition and the support system that helps me stay alive. With time, I started to add how I am successful in aspiring to self-actualization.

I blog as a patient because I believe it is essential that the patient’s point of view is made more public, more relevant, and a primary source of information in improving therapies and healthcare systems. Read Posts>

Story Featured In:

HeartOfAGiant Foundation

Power To The Patient

Project Launch – Dec 2020. Learn More >

Nonprofit Incorporated in MA

Tax-exempt status under the US Internal Revenue Code (Section 501(c)(3)) – Application pending.

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