Understanding Fabry disease - information for parents and families

    Updated: Jan 30

    This booklet is produced by the Society for Mucopolysaccharide Diseases (MPS Society) and is designed to help those affected by Fabry disease – both patients and their families – understand its causes and effects. While there is currently no cure for individuals affected by Fabry disease, this booklet explores how best to understand and manage the disease. It draws on the experiences of patients, carers, families and medical professionals as well as medical literature.


    You can view the booklet below or download a PDF copy.



    We are the only registered charity providing professional support to individuals and families affected by MPS, Fabry or a related disease in the UK.

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    Registered Charity No.1143472 & SCO41012. Registered Company No. 7726882  

    Images and stories may not be reproduced without express written permission. © 2019 Society for Mucopolysaccharide Diseases

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