See all the latest news, blogs and updates from the medical sector.
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Wearing it blue for Noah
July marks National Bereaved Parents Awareness Month and we would like to share a heartfelt thank you to Shauna and Steven who have supported the MPS Society with an extraordinary fundraising campaign in memory of their precious son Noah.
25/07/2024
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Cody's journey in powerchair football: A dream come true
Hear from our member Cody who shares her passion and journey of powerchair football from national to premier league.
18/07/2024
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Of course I love to score goals!
Hear from Tyler who, after a bilateral hip replacement, is fully embracing his passion for football. He shares how sheer determination to achieve his goals rewarded him places in the Danby Rovers and Mencap England football teams.
21/05/2024
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Sam just does "normal stuff"
We recently caught up with Sam to reflect on our first Adult Social Weekend in Manchester and covered even more important topics such as TV’s Taskmaster, Manchester United (his favourite football team), writing theatre plays and aerial acrobatics.
27/02/2024
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Conclusion of an epic challenge
After 12 months, Steven Gill completes his heroic effort of challenging himself across 59 events to raise funds for the MPS Society.
04/01/2024
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Believe in yourself
Read Morgan's inspiring story on how becoming an ambassador at her school made her feel more included and proud of herself.
25/09/2023
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My daughter Eva
For Leukodystrophy Awareness Month we hear from Catrin, whose daughter has Metachromatic Leukodystrophy (MLD). My daughter Eva Rae...
18/09/2023
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My son Joey
For Leukodystrophy Awareness Month we hear from Katie, whose son has Metachromatic Leukodystrophy (MLD). Joey was born a happy healthy...
11/09/2023
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Robert's story - A father's love
During MPS Awareness Week this year we heard from Robert and how he chased a diagnosis for his son Nathan. In the second installment of...
18/06/2023
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Robert's story - MPS Awareness Week 2023
For MPS Awareness Week, we are looking at chasing the signs of MPS and raising awareness of the disease. Read Nathan's story.
