Bertrand was born in Scottsdale, Arizona on December 9, 2007 to Matthew Might and Cristina Casanova Might. They moved to Salt Lake City, Utah when he was 8 months old, and lived there until moving to Birmingham, Alabama in 2017. As the first patient diagnosed with the rare disease N-glycanase (NGLY1) deficiency and as a youth advocate for rare disease, Bertrand leaves a rich legacy of legislative, digital, communal, medical and scientific achievements. In the hearts of those who knew him, he has left an even greater legacy of love.
He will be remembered as a boy who loved to smile and make others laugh; the world’s best daddy to his pet fish; a lover of music, lights, and Elmo; someone skilled at snuggling and cheering others up; and the proudest older brother to his younger siblings Victoria Elizabeth Might (age 9) and Winston John Might (age 6).
Bertrand was a student at Mountain Brook Elementary School where he excelled at making friends and touching hearts.
Buddy is survived by his family, many friends, and a global community who loved him.
His life will be celebrated at St. Luke’s Episcopal Church in Mountain Brook on All Saints Day, Sunday, November 1, 2020 at 3:00 pm.
More information will be available at http://bertrand.might.net/
“The good life is one inspired by love and guided by knowledge.” --Bertrand Russell
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