Moira Cheung

@ADC_BMJ @GOSH_NeuroSurg Great work led by @moiracheung concluding that all infants with achondroplasia AFMS3 should have MRI at 6m of age.

Natural history of spinal cord compression stage AFMS3 in infants with achondroplasia 40% progress and undergo neurosurgery Suggest all have MRI at 6m Retrospective cohort study 🇬🇧 @ACOffiah @GOSH_NeuroSurg adc.bmj.com/content/early/…

@UkXlh Congratulations! This is wonderful news for all our patients! Well done on such a strong patient advocacy group. It makes ALL the difference

Just 4 days to go until #ICCBH2024 and it's not too late to register!

There are still a few places left on the ISCBH/@ern_bond Achondroplasia workshop at #ICCBH2024 so register soon! theiscbh.org/iccbh/iccbh-20…

Only 4 replies from uk so far! Come on uk!

This will be shared with top international doctors involved in the care on Achon.. please help to more fully inform them

We would love to hear your voice on this! This is going internationally but would especially love UK representation in the results.

@GreatOrmondSt I remember sister Lindy from my Sho gosh days on parrot.. over 20 years ago… she was someone who showed me what great leadership looked like. Congratulations! Wonderful News!

Wonderful news! 🎉 Nurse Lindy, who dedicated her 42-year career to GOSH’s neurosurgical department, has been awarded an MBE in the 2024 #NewYearsHonours list! ✨ Read more about Lindy's story 👉gosh.nhs.uk/news/nurse-con…

@ACHONforum Thank you for beautiful lectures. It’s important that if there is Obstructive SA not to delay screening for Foramen magnum stenosis as a cause. It’s also why we don’t use sedation for the MRI and it can lead to an unsafe airway.

Please tune in to listen of the EAF workshop on Understanding Sleep Studies in Achondroplasia: Which? When? Why? Great presentations and discussions on this key topic to develop guiding principles for all clinicians. achondroplasiaforum.com/workshops/

SDMC working hard 2023

SDMC Denver

The BBS & friends in the Rare Bone Alliance celebrated the launch of the NHS Rare Disease Collaborative Network for Adult Rare Bone. It was a successful day of networking and informative talks with reps from the 19 NHS Hospitals who have joined! Read more: shorturl.at/jzI28

@UkXlh @DMAILhealth @EnnalsEthan @rebecwhitt Pleading for help here! @GeneticAll_UK @rarediseaseuk

What a fantastic meeting! Making friends across the pond. 🇺🇸🇬🇧 Autumn UK Skeletal Dysplasia Meeting: “Stick or Twist” Larsen Syndrome, Multiple Synostoses Syndromes and so much more!

👏Congratulations to @LChan_3 @QMUL, one of our Senior Editors on winning the @Soc_Endo Starling Medal for contributing to exceptional scientific advances in #endocrinology. At #SfeBES2023 Dr Chan explores Melanocortin Receptors & their accessory proteins in health & disease.

Delighted with this research award for our study “Collaborative devt of national education standards & resources for emerg. mgt of adrenal insufficiency: mixed-model multiphase study” led by @LucyBray9 #BSPED2023 @mayng888 @AddisonsUK @Pituitary_org @BritSPED

@JudeBubbear Amazing Jude. Hope you enjoyed it ❤️

So last night this happened. It’s been a while 🎶