Posts by: Hal Foster

News

It wasn’t until Gordana Loleska’s son David was 14 years old that doctors in their native North Macedonia diagnosed his kidney, vision, and hearing problems as Alport syndrome. Although ... Read more

June 21, 2019June 20, 2019

Eurordis Unveils Integrated-care Initiative for Rare Disease Patients

News

Europe’s umbrella organization for 800 rare disease associations has developed a sweeping initiative to help the continent’s 30 million rare disease patients and their caregivers learn about their conditions, ... Read more

June 19, 2019June 17, 2019

‘Rare Barometer’ Program Helps Eurordis Shape EU Rare Disease Policy

News

People with rare diseases know that the right government policies can make a big difference in the quality of their own lives, and those of their caregivers. But most ... Read more

Posts by: Hal Foster

Hal Foster

World’s First Alport Stamp Is Macedonian Mom’s Latest Win for Rare Disease Patients

Eurordis Unveils Integrated-care Initiative for Rare Disease Patients

‘Rare Barometer’ Program Helps Eurordis Shape EU Rare Disease Policy

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