A man with ALS struggles to find a cure

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A man with ALS struggles to find a cure

The diagnosis of ALS does not prevent the man from helping to find funding, treatments

Christmas Lavasseur strives to find a treatment or treatment for ALS for the next generation. A diagnosis of ALS, also known as Lou Gehrig's disease, was diagnosed in Lavasseur in 2017, just one year after his marriage to his wife, Jen. The disease slowly destroys muscle control and there is currently no cure. He can no longer work on masonry. Lavasseur has become a strong advocate of ALS awareness. "I was ready to fight to get it, where others had this appalling diagnosis that makes them want to curl up and go to a corner, it 's not my style, "said Lavasseur. He has lobbied the Maine state and Capitol Hill in Washington DC, and with the support of several members of Congress, he will soon return to Washington as part of a national effort to find money to fund ALS research. "We are trying to reach 50 states both through the ALS community." The ALS association recently recognized him as a national hero. Lavasseur joked saying, "I'm a Red Sox fan, so nothing to do with the Yankees I hate automatically, so this Lou Gehrig affair was not a good match from the start." Lavasseur is realistic about to his fate, but hopes his work will definitely help defeat this disease. "The reality is that I will eventually be just a statistic, but maybe I can help, so the generation behind me could benefit from this treatment or treatment that gives them more time with their family. "

Christmas Lavasseur strives to find a treatment or treatment for ALS for the next generation. A diagnosis of ALS, also known as Lou Gehrig's disease, was diagnosed in Lavasseur in 2017, just one year after his marriage to his wife, Jen.

The disease slowly destroys muscle control and there is currently no cure.

He can no longer work on masonry. Lavasseur has become a strong advocate of ALS awareness.

"I was ready to fight for this because there are other people who have this appalling diagnosis that drives them to want to curl up and go to a corner, that's not my style." Said Lavasseur.

He lobbied the State House in Maine and Capitol Hill in Washington, British Columbia. With the support of several congressmen, he will soon be returning to Washington as part of a national effort to find money to fund ALS research.

"We are trying to reach 50 states both through the SLA community."

The ALS association has recently recognized him as a national hero, where Lavasseur joked: "I am a fan of the Red Sox, so all that relates to the Yankees that I hate automatically, this film Lou Gehrig has not was a good match from the start. . "

Lavasseur is realistic about his destiny, but hopes that his work will help to definitively defeat this disease.

"The reality is that I will eventually be just a statistic, but maybe I can help, so the generation behind me could benefit from this treatment or treatment that gives them more time with their families."

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