MPS Society
The Society for Mucopolysaccharide Diseases (the MPS Society) is a voluntary support group founded in 1982, which represents from throughout the UK over 1200 children and adults suffering from Mucopolysaccharide and Related Lysosomal Diseases including Fabry Disease, their families, carers and professionals.Registered Charity No. 1143472
£11B has been raised this year by employees. We are extremely proud of this!!!!
For more information
Please email the Payroll Giving in Action helpline at [email protected] or use our live chat facility if you need any assistance or guidance. This may include help with completing the donation form, details of your charitable cause, making multiple donations, calculating financial contributions etc.