Whether you want to learn more about Waldenstrom’s macroglobulinaemia, or have questions on a specific topic, our experts have the answers.
Pour yourself a cuppa and settle down to watch our webinars with lead specialists in WM, mental health, cardiology, research and more.
Dr Owen talks about laboratory research and the part it plays in answering our most pressing questions about WM
Dr Shirley D’Sa talks about Bing Neel Syndrome, a condition linked to WM.
Dr Rebecca Auer talks to Bob about the Rainbow Trial, a clinical research project she is currently undertaking.
Dr Shirley D’Sa and Professor Mike Lunn take a closer look at peripheral neuropathy, a condition that can affect people living with WM.
Dr Dr Dima El-Sharkawi answers your questions and concerns about getting the third dose of the COVID-19 vaccine.
In rare cases, WM can transform into a faster-growing type of lymphoma. Here Dr Edward Libby talks us through what happens when this occurs.
Peripheral Neuropathy (PN) is a common condition among WMers. Here Dr Gita Ramdharry from UCLH talks physiotherapy and other ways to help manage PN.
Still have questions?
We’re here to help. Don’t hesitate to get in touch by phone or email.
You can find up coming webinars on our What’s On pages.