Internet enthusiasts have been swapping gleeful fist bumps, now that the Federal Communications Commission has voted to regulate online connectivity more aggressively, in the name of "net neutrality.

It was meant to be the trip of a lifetime for 9-year-old Braeden Lousier-Hicks of Airdrie, Alberta, who has an extremely rare genetic disease. After the family waited five years to go on a charity ...

It was meant to be the trip of a lifetime for 9-year-old Braeden Lousier-Hicks of Airdrie, Alberta, who has an extremely rare genetic disease. After the family waited five years to go on a charity ...

Shares of Rosetta Stone are lower after the company lowered fourth quarter earnings and revenue forecasts due to weak demand in the US and the bankruptcy filing of Borders The company expects ...

Last month, Google's VP of Infrastructure made an unusual request to computer hardware manufacturers: build hard drives that are less reliable. It seems silly — why would Google want its data ...

"It's gonna be a little scary out there for kids like ours," said Lia Lousier, whose 10-year-old son Braeden has a rare genetic disorder. A COVID-19 infection could send him to the ICU.

Today’s Daily News story about the slower, more crowded trains we can expect from the MTA with the next budget — thanks to the end of 1,500 jobs and the Z and W line, and trims to G and M ...

Braeden Lousier-Hicks, or Baby Braeden, was born with a number of rare health conditions that has kept him in hospitals for most of his young life. His mother Lia Lousier says Braeden might not ...

Lia Lousier of Airdrie, a bedroom community just north of Calgary, says nine-year-old Braeden is one of 100 people in the world to be diagnosed with a rare inherited connective tissue disease ...