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Lysosomal Storage Disorders Support Society

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LSDSS wins prestigious Global Genes “Champions of Hope” Award

LSDSS was chosen from more than 40 nominated patient organisations worldwide for Global Genes’ “Champions of Hope” award.

12–14 September 2022

San Diego, California

Global Genes

The Lysosomal Storage Disorders Support Society (LSDSS) has been honored with the prestigious “Champions of Hope” award in the Foundations category by Global Genes at the RARE Patient Advocacy Summit 2022 held on 12-14th September at San Diego, California.

The LSDSS, which is the first patient organization to bring the topic of rare diseases and Lysosomal Storage Disorders (LSDs) to the forefront of discussion in India, was selected as the winner from more than 40 nominated patient organizations worldwide.

Each year, Global Genes, a leading global rare-disease patient advocacy organization, asks the community to nominate those deserving of recognition for their extraordinary efforts in rare diseases. The Champions of Hope Award serves as a great recognition of the relentless efforts by LSDSS since its foundation in 2010 to improve the lives of rare disease patients, in particular those affected by LSDs, in India.

The award was received by LSDSS Secretary Mr. Suyog Sathe and President Mr. Manjit Singh.

Conference

25–27 May 2022

LSDSS joined rare-disease patient organisations from across Asia Pacific at Pinnacle Singapore, organised by APARDO.

Meeting

7–8 May 2022

The International Gaucher Alliance, of which LSDSS is a member, held its Biennial Members Meeting in Rotterdam.

Blog

26 February 2023

Why marriages between blood relatives raise the risk of genetic disorders such as LSDs, and how awareness and counselling can help.

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