Kate Learoyd
@pkufamily
Mum, charity trustee, ask awkward questions, trying to cope with this icky platform: support @NSPKU for better future for #RareDisease #pku, tweeting own views
ID: 481512234
http://www.nspku.org 02-02-2012 21:11:57
12,12K Tweet
1,1K Takipçi
1,1K Takip Edilen
The importance of patient advocacy was a recurring theme at the 2025 #MJAAwards. Our chair Shaun Lintern spoke of his family's experience of the strengths and weaknesses of the NHS following his mother's diagnosis with motor neurone disease youtu.be/yXWfhUospXs
The Metabolic team RMCHosp are thrilled that Georgie Wood presented her audit on Low Protein Prescription Foods for children with #PKU at the #ESPKUconference2025 in Hamburg, well done Georgie!! 👩🔬📈🍞 MFT_CSS ESPKU British Dietetic Association BDA Paediatric Group
If you ever spent time with someone deteriorating because of MND or saw the impact on their family, you would not hesitate to make sure treatment was given once available. There can be no good reason for this Wes Streeting NHS England MND Association MND Campaigns #MND
How can we end the cycle of tragedy that sees 2000 babies lose their lives every year in NHS maternity units? My The Guardian piece published today theguardian.com/commentisfree/…