Izdw Police: Charlotte comedy club evacuated before man fires gun
An 11-year-old reporter is landing some major interviews at the upcoming Super Bowl.Jeremiah Fennell was born with several brain abnormalities, including a missing gland in his brain. Despite being born 10 weeks premature, he has learned to read, write and most importantly, enjoy football play-by-play broadcasts.Although his medical issues mean he is unable to play contact
stanley cups sports, Jeremiah has honed his journalism craft.This week at the Super Bowl, he has landed interviews with the likes of 49ers star Deebo Samuel and Chiefs tight end Travis Kelce. NFL Network used his interviews. You re very well-spoken, man, Kelce told Jeremiah after the youth reporter introduced himself.SEE MORE: CBS to air Super Bowl in 4K, but there s a catchJeremiah showed off his football knowledgealongside Chiefs quarterback Patrick Mahomes earlier this week as they created their all-time fantasy football rosters. Jeremiah, however, might have disappointed Mahomes when he chose Barry Sanders as his running back. You ve got a great team, Mahomes
stanley cups told him.Jeremiah, who is from Las Vegas, the site of this year s Super Bowl, has landed other major interviews. He had interviews with Vice President Kamala Harris and second gentleman Doug Emhoff.He is a fan of the hometown Raiders,according to his biography. He never lost his love for the game of football, the art of commentating and especially his love for the Raiders. When he was four years old he would practice interviewing the players on
stanley tumblers the Raiders te Qekn Juneteenth celebrations across the U.S. commemorate the abolition of slavery
A Colorado family is reaching out to the public for help in treating their 15-year-old sons rare and debilitating skin condition.For seven years, Jaiden Rogers has suffered from stiff skin syndrome, a disease that causes the skin to harde
stanley cup n. When they said it was stiff skin syndrome 鈥?I was like oh good its only that, said Natalie, Jaidens mother. But the doctor said, oh no I dont think you understand. They said his skin would turn to stone. Within a month, he was in a wheelchair. It spread so fast. Within just a few months, he was starting to get it everywhere. The condition has caused his skin to gradually tighten and
stanley cups uk harden, spreading from his legs to his hips and then to his stomach and neck.It started as a growth behind his knee. Jaiden has since lost mobility. The syndrome is a painful one as the skin thickens, limiting joint mobility. The syndrome is sparked by a mutation change, and an exact treatment is unknown.With no cure for the disease, Rogers and his family are now banking on an experimental procedure to save his life. Doctors in Ireland are working with doctors in London. This is very expensive, Natalie said. The whole treatment is $1.5 million, because they actually have to make something for him, because he is the only child. Its our only hope,
stanley cup and we are running out of time. Natalie says her son is turning to stone, leaving him unable to walk and sometimes giving him trouble breathing. He sees six doctors and takes chemotherapy drugs to slow the disease
