The comedians have told the Court that they invited persons with disability during these shows and encouraged them to share ...

In November last year, the Supreme Court ordered Samay Raina and other comedians to organise events/shows to raise funds for ...

10-year-old Myer Gallant, a Pittsburgh Penguins fan with spinal muscular atrophy, got to live his NHL dream through a special one-day contract arranged by the Make-A-Wish Foundation. He met favorite ...

Louis has a genetic disorder called spinal muscular atrophy, or SMA, and a couple of months ago, on his 10th birthday, he learned his dream would come true -- he's ...

Nuvo Intl Group Inc. today announced that pregnant moms can lease the FDA-cleared INVU wearable solution , a cloud-based pregnancy monitoring platform designed for use at home or at work, directly ...

Moose Jaw’s Shailyn Taylor says she’s thrilled to be returning to the Telemiracle cast this year and to take on a new role as a co-host in the telethon’s expanded Backstage Lounge livestream. “It’s an ...

Finance Minister K.N. Balagopal announces budget allocations, including wage hikes and support for students and workers in ...

ETCO Incorporated has introduced a line of connectors for attaching wires to laminates and other flexible circuits that must bend, fold, or fit into tight, moving, or weight-sensitive spaces in ...

Over three million patients identified with more than 130 rare and hard-to-treat diseases are covered by Salamat Health Insurance Organization.

Finance Minister Nirmala Sitharaman’s announcement that seven additional rare diseases will be added to the customs duty exemption list brought significant relief to many families ...

‘Like Jesy Nelson’s twins, I have SMA. I want to show you can live a full life and be disabled’ - Kelly Gordon, 36, was ...

Jesy Nelson’s new documentary is shockingly candid about her high-risk pregnancy, and all the better for it - IN FOCUS: The ...