Harriet talks about the importance of not giving up after 17 years of failed treatment and misdiagnosis for her exceptionally rare T-cell skin lymphoma, Hypopigmented Mycosis Fungoides (HMF).
Diagnosed with indolent B-cell non-Hodgkin lymphoma, Alan talks about treatment and periods of active monitoring (watch and wait).
Lauren shares her experience of doing a work placement with Lymphoma Action.
Diagnosed with Hodgkin lymphoma at 24, and during a pandemic, Cassie talks about finding the treatment tough, and the challenge of losing her hair.
Richard shares his experience of high-grade B-cell non-Hodgkin lymphoma with central nervous system involvement, also known as primary central nervous system lymphoma (PCNSL).
In this podcast, Emma talks to us about her experience of supporting her sister, Sarah, who has a diagnosis of lymphoma.