Hi. My mum was diagnosed with T Cell intestinal non Hodgkin’s lymphoma in April 2023. She had 6 rounds of chemo followed by a stem cell transplant (autologous). She was given the ‘all clear’ in February 2024 then in May 2024, after presenting with fatigue, weakness and confusion, attended A&E, had an MRI and was diagnosed with Lymphoma in the brain. Things seem to change so quickly. One minute we’re told she can go home and have chemo as an outpatient, next minute the steroids haven’t worked, her condition has worsened and she’s lost use of her left hand side. She’s now been in hospital for 3 weeks and has just finished her first round of chemo. We’ve been told the tumour is incurable but the aim is to shrink it with chemo so she can go home at some point. Her diagnosis seems so rare and I’m struggling to find information/stories of people who have been through similar. Anyone out there experienced/experiencing similar?