Dear Editor
September is Blood Cancer Awareness Month, and as part of our Let’s talk lymphoma campaign, Lymphoma Action is inviting people affected by lymphoma to write to their MP, MSP or MS and ask them to raise important issues about lymphoma treatment and care in Parliament.
The campaign aims to make it easier for decision-makers to understand the realities faced by people affected by lymphoma, and to encourage practical action to improve diagnosis, treatment and care.
Lymphoma is officially categorised as a rare or less common cancer. The recent National Cancer Plan recognised that people affected by rare and less common cancers often face major challenges with diagnosis and care. Lymphoma is the most common type of blood cancer, but too many people still experience delays in diagnosis, limited access to treatment and unequal care.
For the first time, the National Cancer Plan gives rare and less common cancers dedicated focus and commits to improvements in treatment and care. It recognises that people with these cancers must receive the same priority as those with more common cancers. But making promises is only the first step – they need to become reality.
This September, we want to hold the government to account and make sure the plan is put into action, leading to meaningful change for people affected by lymphoma and other cancers. If you are affected by lymphoma, you can write to your representative this September and ask them to raise lymphoma in Parliament.
Together, we can push for the improvements people affected by lymphoma deserve and help make sure the National Cancer Plan delivers real change.
Find out more about how you can get involved at www.lymphoma-action.org.uk/BCAM.
Once you register your interest, we’ll send you a draft email with the information your representative needs and details of how to send it.
Yours sincerely
Amanda Harris
Lymphoma Action