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MPS Society

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Family stories

Meet some of the children, adults and families that we support and read about their experiences of living with MPS, Fabry and related diseases.

Naomi (Fabry Disease)

MPS Society

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

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MPS Society, MPS House,

Repton Place, White Lion Road,

Amersham, Buckinghamshire,

HP7 9LP, United Kingdom

mps@mpssociety.org.uk

0345 389 9901

Registered Charity No.1143472 & SCO41012. Registered Company No. 7726882.
Images and stories may not be reproduced without express written permission.
© 2023 Society for Mucopolysaccharide Diseases

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MPS Society

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Family stories

Miya (MPS I)

Oliver and Sam (MPS II)

Ella (MPS III)

Joanne (MPS IV)

Oliver (MPS VI)

Naomi (Fabry Disease)

MPS Society

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Registered Charity No.1143472 & SCO41012. Registered Company No. 7726882.
Images and stories may not be reproduced without express written permission.
© 2023 Society for Mucopolysaccharide Diseases

Family stories

Registered Charity No.1143472 & SCO41012. Registered Company No. 7726882. Images and stories may not be reproduced without express written permission. © 2023 Society for Mucopolysaccharide Diseases

Registered Charity No.1143472 & SCO41012. Registered Company No. 7726882.
Images and stories may not be reproduced without express written permission.
© 2023 Society for Mucopolysaccharide Diseases