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By Marcus Chen
WFLA Statewide
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LEICESTER, Vt. (InvestigateTV) - ALS, often called Lou Gehrig’s disease, is a cruel illness. There is no cure, it’s always fatal, and Vermont has the highest rate per capita in the country with around 27 people living with it now in the state. To help those losing independence and their, a nonprofit is working to restore the ability to communicate with loved ones and doctors.Paul Francoeur’s days didn’t always start like this, but when they did, it was difficult. The cough-assist machine helped the 67-year-old clear his lungs when he couldn’t do it himself. His ALS weakened his muscles and motor skills too much.“I think soon after diagnosis you realize how this road ends,” said Kris Francoeur, Paul’s wife.That diagnosis came in 2019. Kris turned into a caregiver, allowing her husband to remain at home. They get help from their son Ben. But it’s getting more challenging, especially as Francoeur loses his ability to communicate.During a tele-medicine appointment with his doctor, the coup