"My advice to anyone that's got something wrong with them that they're just not 100% sure what it is, and it's out of the ordinary, is without doubt, to speak to a GP." - Shaun
Learn more about #myeloma: https://t.co/12144qgrZK
#MyelomaAwarenessWeek#DontMissMyeloma
23 years ago today I was diagnosed with #myeloma and told I had 2-3 years to live. Am so grateful for the support I've received from HCP's, family, friends and importantly @MyelomaUK and others working collaboratively to gain access to effective new treatments #thankyou#hope
1/2 A new study investigating #COVID19 vaccine effectiveness, led by The ICR London and @royalmarsdenNHS has found that 70% of #myeloma patients had an immune response to the first dose of either the Pfizer-BioNTech or Oxford-AstraZeneca COVID-19 vaccine: https://t.co/lwj1Fbnu0z
Hey @marksandspencer can Colin and Cuthbert be besties? We’re bringing back a limited edition Cuthbert and want to donate profits to cancer charities including your partners @macmillancancer & ours @teenagecancer. Let’s raise money for charity, not lawyers #caterpillarsforcancer.
💊 This is great news for multiple #myeloma patients in England.
This therapy could be offered to around 2,000 patients, with clinical trial evidence showing that it gives longer periods of remission and people live longer compared to current treatments.
https://t.co/NveRkB6cKt
1/3 Last year, we spoke to #myeloma patient @mrscottnunn about how #COVID19 impacted his treatment journey.
Our Hopeful Futures Appeal aims to tackle the legacy of COVID-19 but we need your help. Please donate whatever you can to help us safeguard lives: https://t.co/y0Ef7SFEAk
📆 Today marks the halfway point of #MyelomaAwarenessMonth!
📢 We hope you'll join us in helping to raise much needed awareness around #Myeloma, such as what signs and symptoms to look out for.
But first, let's start by answering a very important question 👇 1/