See all the latest news, blogs and updates from the medical sector.
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...
MPS Society’s Group CEO elected to the ABPI’s new Patient Advisory Council
We are thrilled to announce that our Group CEO, Bob Stevens, is one of the eight leaders from across the patient and health charity...
Rareminds: MPS Society counselling launch
We are pleased to launch our new counselling service at the MPS Society for patients and family members.
COVID-19 vaccination for children and young people aged 12-17 years
It is recognised that a small number of children and young people aged 12-17 years with specific underlying health conditions may be at...
Willow Foundation Special Days and Treats
For people living with a life-threatening illness, every day is precious. The pressures of diagnosis, treatment and recovery can have a...
APPG on Newborn screening
On 9 June 2021, we attended a virtual APPG (All Party Parliamentary Group) meeting on Rare, Genetic and Undiagnosed Conditions about...
MPS Society's chance to win £1,000
MPS Society are asking for nominations to win a £1,000 Movement for Good award from Ecclesiastical Insurance Group. MPS Society is...