Oliver Gardiner

XLH UK, International XLH Alliance

[Oliver Gardiner @otronics]

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

[Oliver Gardiner @otronics]

@GeneticAll_UK @rarediseaseuk The community is devastated by this decision. Are you behind us?

[Oliver Gardiner @otronics]

@MediaplanetUK @UkXlh @newscientist @AllianceXlh Thank you to @sanz_dawson and @GiniaJo for all your support too!

[Oliver Gardiner @otronics]

@NVIDIAGeForceUK #UltimatePlay @BryonyAshman

[Oliver Gardiner @otronics]

@Joyce_Inman Incredible to think that the crew will hurtle across little old England just 17 minutes after launching from Florida 🔭

[Oliver Gardiner @otronics]

@Se_Railway @TLRailUK Ebbsfleet or Gravesend, can you honour a journey to one of those?

[Oliver Gardiner @otronics]

@Se_Railway why aren’t you letting @TLRailUK customers on your lines when nothing else is departing from St Pancras?

[Ingunn Westerheim @ingunn_w]

Nice to exchange ideas & experiences with patient representatives from other European rare bone organizations: HPP, XLH, achondroplasia and other skeletal dysplasias. A lot of challenges in common!

[International XLH Alliance @AllianceXlh]

Well deserved dinner with the team after a great 1st day at @childrensbones Looking forward to more exciting news and networking tomorrow! #xlhawareness #ICCBH2019

[International XLH Alliance @AllianceXlh]

Meet the founding members of our International #XLH Alliance! We are committed to improving outcomes for patients and families impacted by #XLH and related disorders. Visit our website for more information:https://t.co/Of25xHy8gZ

[Oliver Gardiner @otronics]

@FDSSUK Great photo! X

[Oliver Gardiner @otronics]

@KLM please help us. We need our lost luggage tonight. I have PM’d you

[Oliver Gardiner @otronics]

@FatherQuizmas 64% #havas

[Brittle Bone Society @BrittleBoneUK]

THANKS @ScotParl @NicolaSturgeon @ShonaRobison not just 50th Awards for care, research, philantrhopy . . . #OstegenesisImperfecta we are building bridges with @XLH_Network & @Softbonesuk & @FDSSUK @JoeFitzSNP @AnnieWellsMSP @SheffChildrens @EdinburghUni @dundeeuni @Craigie_High

[NICE @NICEComms]

We've recommended burosumab as an option for treating X-linked hypophosphataemia in children and young people. Find out more here: https://t.co/xA4LcpzR0A

[ECTS @ECTS_soc]

Excellent news for our field: NICE Backs Crysvita® (Burosumab) for Rare Metabolic Bone Disorder, X-linked Hypophosphataemia #XLH #Kyowakirin #rarebonediseases #rarediseases https://t.co/HdpiPJpSHq

[Oliver Gardiner @otronics]

@HavasXmas the answer is #White https://t.co/BywLfKqh19

[Oliver Gardiner @otronics]

@HavasXmas the answer is #NuggsForCarter https://t.co/PiQIWHrxRR

[Oliver Gardiner @otronics]

@HavasXmas the answer is #Rudolph https://t.co/4jXc9wD3r8

[Oliver Gardiner @otronics]

@HavasXmas I think it's #280characters https://t.co/h1yUdQSCde