News

Pearl Jam frontman Eddie Vedder is releasing a new documentary, “Matter of Time,” this summer on a project he and his wife Jill have been working on to find a cure for epidermolysis bullosa ...
A string of 2023 solo concerts in Seattle are the backdrop for the film, which chronicles Vedder’s efforts to raise funds for clinical research for Epidermolysis Bullosa, a rare genetic skin ...
(CNN) — “Matter of Time,” a documentary featuring Pearl Jam frontman Eddie Vedder that is set to debut this summer at the Tribeca Film Festival, is being billed as much more than a concert ...
To create awareness on rare skin conditions, the Rare Skin Conditions Society (Singapore) and the Dystrophic Epidermolysis Bullosa Research Association, Singapore, will be launching a book ...
Eddie Vedder’s Matter of Time — about the Pearl Jam singer’s fight to cure epidermolysis bullosa (EB), a rare and often fatal genetic disease — will also premiere at Tribeca, where it will ...
The funeral post marks Campbell's first social media update since she shared the heartbreaking news that Elliana died less than one year after she was born with junctional epidermolysis bullosa ...
He has been supporting Isla Grist, 16-year-old girl living with epidermolysis bullosa (EB) - a rare genetic skin condition often referred to as "butterfly skin". Explaining the illness ...
The 2025 Tribeca Festival, presented by OKX, has revealed its lineup of documentary, narrative and animated features, including the premiere of Miley Cyrus’ visual album, a Leonardo DiCaprio ...
Tribeca Festival 2025 is out with the slate of documentary, narrative and animated features for its 24 th edition, a intriguing lineup showcasing music legends, key cultural figures and stories ...
Twenty month old Albi was born with a severe form of recessive dystrophic epidermolysis bullosa (RDEB), a disorder which causes his skin to break out in blisters or tear with the slightest friction.