Runner/blogger at The Scientist Runs, scientist and now Senior Policy Officer @MyelomaUK trying to improve diagnosis and quality of life for myeloma patients.
I'm on maternity leave but can't help shout out for the incredible work of my team @MyelomaUK. Help us reach 1000 responses to our latest survey on unmet needs 🧡
Thank you to the 996 patients and carers who have taken part in our @MyelomaUK Unmet Needs survey. We have extended the deadline until 5pm tomorrow. Please help us get over the 1,000 mark and have your voices heard. Let’s make #myeloma history together. See the link below
Myeloma patients, family and friends - help us shape the future of research, diagnosis, treament and care!
What matters to you most? What changes do you want to see? Tell us by completing this major new @MyelomaUK survey, which will drive our strategy in years to come.❤️🫂💊🏥🩸
Come and see my poster @BritSocHaem this evening and talk to me about the impact of delayed diagnosis on #myeloma patient quality of life.
#BSH2022@MyelomaUK
THREAD: Today, we launched a new report A Life Worth Living which shows the hidden impact of delayed diagnosis on the quality of life of thousands of patients living with myeloma in the UK: https://t.co/ZJzMTlZI5a
#Myeloma#MyelomaUK#BloodCancer
Borders XC series done for another year! A muddy one, slip and sliding, two river crossings but worth it for a high five from Annabel at the finish. @ Gala Policies https://t.co/2riAt8NCal
This #WorldCancerDay, we want to #CloseTheGap in cancer care. Myeloma still has one of the longest times to diagnosis of any cancer. We're working hard to fix this so that all myeloma patients get a timely diagnosis and the best possible outcomes.
#myeloma#BloodCancer
Today is #WorldCancerDay, a day that unites people around the world to take action against cancer 🌎 It also marks 20 years since our organisation was formed 🥳 Thanks to your support, we've come so far in that time - and we will go much further. Donate: https://t.co/H9ZiYJtq20
It can be hard to spot the signs of #myeloma.
You may feel fatigued, have easily broken bones and/or bone pain, or have low blood cell counts. Spotting it early is key to helping patients start treatment ASAP before complications arise.
#wordle#wordlechallenge
1/2 Kerry sadly lost the love of her life when her husband Jeremy, and father to their two daughters Charlotte and Emily, died of #myeloma in November 2020. The family are supporting our Christmas campaign this year to help spread hope this Christmas: https://t.co/nJHrA69k75
This #BloodCancerAwarenessMonth, we’re turning the spotlight on those working behind the scenes to improve #myeloma diagnosis.
Dr Ross Sadler, Clinical Lead for Lab Immunology at @OUHospitals talks about educating and empowering clinical scientists: https://t.co/F7bLVbWwZP