Haematologist | PhD candidate in PNH @UniversityLeeds @LIMRLeeds | Specialist interest in #PNH #AplasticAnaemia

Joined February 2018
Photos and videos
Alexandra Pike retweeted
We're teaming up with the International PNH Interest Group to improve care for people with Paroxysmal Nocturnal Hemoglobinuria (PNH) in low-resource countries. PNH is a rare, debilitating blood disease that requires frequent blood transfusions & poses high risk without treatment.
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Alexandra Pike retweeted
Join our PNH Awareness Campaign! 🌟 From Sept 6 to Oct 12, let's raise awareness about Paroxysmal Nocturnal Hemoglobinuria. Share our posts with #PNHAwareness2024, join discussions, and support those affected. Together, we can make a difference! 💪 #DidYouKnow #TreatingPNH
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Alexandra Pike retweeted
Access for all to support is vital
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Alexandra Pike retweeted
It was amazing to represent the wider multidisciplinary team at EHA presenting about PNH with the patients at the centre of everything. #eha2024 #pnh #acp @GlobalPnh @PNHSupport @PNHScotland
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Alexandra Pike retweeted
Fantastic poster session yesterday. 🎉 Congratulations 🎉 to @AlexandraCPike and the team at Leeds, and to @AlexLubin6 & @bethpay and the team at UCL on their ASH Abstract Achievement Awards - a double win for Blood Cancer UK funded grants! 🏆 #ASH23
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Alexandra Pike retweeted
Dr Jens Panse reminds the audience that 80% of #PNH patients have no access to #treatment = significant #inequality As #patients we collectively lobby to address this where we can @lichterzellen @aamdsif @pnhaacontact @hpn_asociacion @PNHCanada @AAundPNHeV @ERNEuroBloodNet
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Alexandra Pike retweeted
Another very nice selected abstract evaluating disease burden and it’s implications for patients with #pnh within a UK-F-G consortium including QLQ-AA/PNH54 developed by ⁦@UniklinikAachen⁩ with strong support and collaboration ⁦@lichterzellen⁩ and ⁦@AAundPNHeV
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Alexandra Pike retweeted
Today musicians gather at 3pm in Trafalgar Square 💛💙#playforukraine @decappeal
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