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Latest

See all the latest news, blogs and updates from the medical sector.

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Sophie, Head of Patient Services and Clinical Liaison at MPS Society, stands by a poster she is presenting about LAL D at WORLDSymposium 2024.

Highlights from the team at WORLD 2024

Sophie, Bob and Fiona, part of Team MPS attending WORLDSymposium, shared their news and what they have been up to. With plenty of meetings and presentations to attend there are lots of opportunities to expand our knowledge of lysosomal diseases.

Together we can transform lives

Read our latest Fundraising Round Up and your inspirational stories that enable us to support over 1,750 people every year.

Together we can transform lives

Read the inspirational stories of some of our amazing fundraisers and be introduced to the first of our eight TCS London Marathon runners.

Together we can transform lives

Read all about our incredible fundraisers, from marathon runners to mountain climbers and learn how you too can get involved.

Together we can transform lives

Thank you to our amazing fundraisers for the support you have shown us over the past month, let's celebrate your achievements.

Receive a gift this Christmas in our toy giveaway

We are pleased that our charity has been lucky enough to receive donations of toys and gifts that we are able to share with our community.

Christine Lavery Memorial Fund opens a call for applications for summer vacation studentships 2023

The MPS Society are delighted to announce that we are launching the Christine Lavery Memorial Fund on 21 November, Christine’s birthday,...

Bob Stevens attends the SSIEM Annual Symposium

Bob has had a busy month, attending the SSIEM Annual Symposium 2022 in Freiburg, Germany. The SSIEM, is the Society for the Study of...

Footsteps Dance School raises funds in honour of Isaac Turner

The MPS Society has been working with Footsteps Dance School on their annual dance performance 'Steppin' Out 2022' as they wanted to...

MPS Society celebrates after receiving £10,000 in National Lottery funding

The MPS Society is celebrating today after being awarded £10,000 in funding from The National Lottery Community Fund, the largest funder...

Think Rare, Think MPS

The Society for Mucopolysaccharide Diseases (MPS Society) is committed to bringing about change in the diagnostic journey of children...

Hunter Outcome Survey

The latest Hunter Outcome Survey (HOS) for 2020 has been released. We hope that this report will help patients and caregivers who are...