LHON

LHON Main

New support group will help families adapt to LHON

Personal experience of helping her son juggle sight loss and adolescence means Francesca Müeller understands all too well the importance of peer support.

Disease Spotlight

Adaptations and positivity are key to living in the light wi...

It took 30 years for Krister Inde to find out the visual impairment that developed when he was 19 was caused by the rare genetic condition LHON.

Disease Spotlight

Living with LHON: Blindness doesn’t mean losing sight of you...

Losing your sight is every bookworm’s worst nightmare, but former English teacher Paula Morandi has not let her diagnosis hold her back.

Views & Analysis

Imparare a convivere con la LHON

Ogni paziente affronta il viaggio della vita a modo proprio, imparando a conoscere la malattia al meglio delle proprie possibilità e attraverso gli strumenti a disposizione.

Disease Spotlight

Finding the roadmap for living with LHON

Every patient faces their own journey through life, learning about their condition with the best tools available to them.

Views & Analysis

LHON diagnosis: Opening peoples’ eyes to the invisible suffe...

Maryse Roger has firsthand experience of Leber’s hereditary optic neuropathy (LHON), having first assisted her two brothers as their sight deteriorated and then leading the care of her son

New support group will help families adapt to LHON

Adaptations and positivity are key to living in the light wi...

Living with LHON: Blindness doesn’t mean losing sight of you...

Imparare a convivere con la LHON

Finding the roadmap for living with LHON

LHON diagnosis: Opening peoples’ eyes to the invisible suffe...

Gene therapy firm Kate Tx snapped up by Novartis for $1.1bn

Coming soon: The Life Sciences Industry Report 2025 – insigh...

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LHON

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