My mother and father came to England to visit us for a holiday. Her cancer was in remission, miraculously and it was time to visit the grand children she loved so much. We were all so very excited. I’d planned visits to Santa’s grotto. A Christmas Train ride, visit to a Christmas through the ages exhibit. I bought a huge Christmas tree. We had things planned for every day. Winter Wonderland. Fairytale Wander. A visit to Pooh Corner. So many plans.
I went to the airport to collect my parents, only to find that my mother had been taken directly to A&E, where she would spend the next four days getting scans and tests. Whether it was the flight, or whatever it was, a new tumour had sprung up, a malignant, vicious, angry sucker, growing 21cm in just 3 weeks. It was phenomenal, and once again, there was nothing they could do for her.
The hospital arranged a hospice for my mom in the next town up from ours, but also said she could come home while she was ‘well enough’ to do so. There would be community nurses that would come round daily and check on her, and refill her morphine driver.
The decision would be mine, my mom said – my home, my children, my choice. I felt strongly that she should be home with us and that we would send her to a hospice when she was no longer able to go to the toilet on her own, or we felt that we were no longer able to cope. But I believed that while she still had awake and lucid moments, her place was with us, in our home, surrounded by the noises and sounds of her family.