Top Tweets for #25yearsofMUK
So... this happened! Thank you @rodstewart for support Gary, who is taking on the infamous SAS Fan Dance challenge in the Brecon Beacons tomorrow for @MyelomaUK. Good luck tomorrow @garydoconnor! #25yearsofMUK #myeloma
He did it! What a wee legend. Sunny, the three-legged rescue pup, smashed his 100km Lost in Lapland challenge in aid of @MyelomaUK. Well done to his two humans too. #25yearsofMUK
https://t.co/k9W3YySwFR via @BedfordIndy
I've written a blog post reflecting on how the #myeloma community has rallied behind us time and time again to give patients and their families more time together and a better quality of life: https://t.co/BTLOhhPGyl
We can’t thank you enough for everything you’ve done 🧡
In 2016, our ‘Life in Limbo’ research gave an unprecedented insight into the difference carers make to #myeloma patients – and the pressures they face. #25yearsofMUK https://t.co/3a1RPTTzct
Myeloma carer Karen told us about how services like the Myeloma Infoline have helped her.
In the last of our 25th anniversary blog series, associate professor of haematology and clinician researcher Karthik Ramasamy explains why he sees nimbleness as the key quality that sets Myeloma UK apart. #25yearsofMUK
Read the blog: https://t.co/HEi5W8Dw4a
Over the past 25 years @MyelomaUK has sent out almost 2 million publications and helped many patients like John Gibson get to grips with their diagnosis. John shares his story ⬇️ #25yearsofMUK
https://t.co/vnF53ZChmW
In 1997 we launched patient & family support services providing information, advice and support. Since then, we’ve sent almost 2 million publications, answered over 60,000 calls, and hosted more than 200 Infodays #25yearsofMUK
https://t.co/ew7JLjrEZk
https://t.co/jba2iqJu9Q
In 1997 we launched patient & family support services providing information, advice and support. Since then, we’ve sent almost 2 million publications, answered over 60,000 calls, and hosted more than 200 Infodays #25yearsofMUK
https://t.co/ew7JLjrEZk
https://t.co/jba2iqJu9Q
Join us Tuesday 15 November, 4:30-5:30pm for a live interactive digital event to celebrate the incredible achievements we’ve made together over the last 25 years of transforming lives.
#25yearsofMUK
Register now and put your questions to our panel: https://t.co/s8sCijDtig
It has been great to be part of the long collaboration between @MyelomaUK and @UKmyelomaforum in producing evidence-based clinical guidelines in multiple myeloma. More detail in the video.👇 #25yearsofMUK.
In the early 2000s, a lack of evidence-based guidelines meant #myeloma patients' experiences of diagnosis and treatment varied hugely.
We linked up with @UKmyelomaforum & @BritSocHaem to develop the first-ever guideline on care for myeloma patients.
https://t.co/uO5sTSDugs
It's amazing to see how far we've come #25yearsofMUK
In the early 2000s, a lack of evidence-based guidelines meant #myeloma patients' experiences of diagnosis and treatment varied hugely.
We linked up with @UKmyelomaforum & @BritSocHaem to develop the first-ever guideline on care for myeloma patients.
https://t.co/uO5sTSDugs
1/2 Join us Tuesday 15 November, 4:30-5:30pm for a live interactive digital event to celebrate the incredible achievements we’ve made together over the last 25 years of transforming lives. #25yearsofMUK
Register now and put your questions to our panel: https://t.co/s8sCijE17O
In 2020, we launched our #COVID19 information hub - discovering how #myeloma patients are affected and sharing advice and support. It was viewed over 66,000 times!
Visit our timeline to see our other milestones: https://t.co/sh1pByihjM #25yearsofMUK
In 2018, daratumumab, the first immunotherapy drug targeting #myeloma cells, was made available. Our Interim Director of Research, Shelagh McKinlay, talks about the process and the role patients play by sharing their experiences. #25yearsofMUK
https://t.co/IFDMEEEYxw
Thank you to @JudyDewinter for sharing her reflections on how far we've come over the past 25 years and what we've been able to achieve by refusing to take no for an answer! #25yearsofMUK
In the latest of our special blogs, Judy Dewinter, President of Myeloma UK, reflects on how our refusal to accept the status quo has inspired life-changing progress for #myeloma patients. #25yearsofMUK
Read the blog: https://t.co/Da3qq0EgcN
It's heartwarming to hear Monica's story - being part of the #myeloma community and the difference we've been able to make to patients and their families through nurse education #25yearsofMUK @mmamynurse
Myeloma UK's Monica Morris has written a blog reflecting on her time as a #myeloma nurse specialist. Monica looks back on how patient support and nurse education has improved over the last 25 years - and the positive impact Myeloma UK has had #25yearsofMUK
https://t.co/PosCtGI0IV
This is a heartening read. Thank you Judy Dewinter for refusing to accept the status quo and for making strides ahead #25yearsofMUK
In the latest of our special blogs, Judy Dewinter, President of Myeloma UK, reflects on how our refusal to accept the status quo has inspired life-changing progress for #myeloma patients. #25yearsofMUK
Read the blog: https://t.co/Da3qq0EgcN
In the latest of our special blogs, Judy Dewinter, President of Myeloma UK, reflects on how our refusal to accept the status quo has inspired life-changing progress for #myeloma patients. #25yearsofMUK
Read the blog: https://t.co/Da3qq0EgcN
MAGIC grew up but still going strong #25yearsofMUK Thanks for the opportunity to reflect @mmamynurse @MyelomaUK Such fond memories and lasting friendships in strong #myeloma #nurse international community @IMFnurseMyeloma @Bethfaiman @marymyeloma @domenica76 @MatthiasNaegele
Congratulations #25yearsofMUK and G’day to all those MAGIC #nurses #myeloma out there. My time @MyelomaUK shaped a lifelong passion/career to help people live longer/better. Proud to have been there at the start with you @mmamynurse @CNRU1 @IMFnurseMyeloma
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