Prince Frederik of Luxembourgs heroic final act…
Prince Frederik, the youngest son of Prince Robert of Luxembourg and Princess Julie of Nassau, left behind a lasting legacy following his death at age 22 this month.
The beloved royal died on March 1 from POLG Mitochondrial illness — a uncommon genetic dysfunction that impacts roughly one in 5,000 people.
The genetic dysfunction impacts a number of organ systems and the mitochondria, the energy-producing components of cells.
Prince Frederik, the youngest son of Prince Robert of Luxembourg and Princess Julie of Nassau, left behind a lasting legacy following his death at age 22 this month. POLG Foundation
Frederik was recognized with the illness on the age of 14 after enduring unexplained signs for years.
In 2022, Frederik based The POLG Foundation, an group that researches the illness and searches for a treatment.
Despite his short lifespan, the prince managed to create an inspiring legacy by way of his basis, which his father vows to proceed in his son’s identify.
“He had barely been able to speak for several days, so the clarity of these words was as surprising as the weight of the moment was profound,” Prince Robert, 56, stated of his late son.
“Frederik knows that he is my Superhero, as he is to all of our family, and to so very many good friends and now in great part thanks to his POLG Foundation, to so very many people the world over.”
Despite his health battle, Frederik labored tirelessly to raise awareness concerning the sickness in a determined bid to help others.
The beloved royal died on March 1 from POLG Mitochondrial illness — a uncommon genetic dysfunction that impacts roughly one in 5,000 people. Royal Family of Luxembourg/Instagram
He then joined forces with designer Donna Karan to develop the MITO clothes line, promoting gadgets by way of his POLG Foundation to raise awareness and funds.
In addition, Frederik participated in medical trials which helped to develop cell traces for analysis throughout Switzerland, the US and Europe.
His work laid the muse for The POLG Toolbox, a essential useful resource for scientists, his proud father stated.
Frederik was recognized with the illness on the age of 14 after enduring unexplained signs for years. Royal Family of Luxembourg/Instagram
“The POLG Foundation, in only three short years, has accomplished so very much, including funding four major research projects, totaling over $3.6 million,” stated Robert, the primary cousin of Grand Duke Henri of Luxembourg.
Meanwhile, Frederik’s mom, Princess Julie, had been instrumental in tasking the scientific group to push ahead with analysis.
Despite his struggles, Frederik noticed his sickness as a present and alternative to help others.
In 2022, Frederik based The POLG Foundation, an group that researches the illness and searches for a treatment. POLG Foundation
“Speaking to a friend of ours, he told Andrew, ‘I am glad that I am the one who was born with this disease. Even though I’ll die from it… and even if my parents do not have the time to save me, I know that they will be able to save other children,’” Robert stated.
Speaking about his son’s heartbreaking final moments, Robert revealed that Frederik’s final query to him was, “Papa, are you proud of me?”
Prince Frederik had struggled to talk for “several days” earlier than he died, in keeping with Robert, “so the clarity of these words was as surprising as the weight of the moment was profound.”
Robert added that his son’s mission in raising awareness for the illness will proceed by way of his group.
Frederik additionally participated in medical trials which helped to develop cell traces for analysis throughout Switzerland, the US and Europe. POLG Foundation
“With our Superhero’s help, we hope to turn our deep grief into positive results and follow his unwavering example,” he stated.
“His ultimate message is one of hope, compassion, and resilience. We are all so very proud of you, Frederik. I am so very proud of you. We love you.”
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