My father passed away on 10 July and I'm really struggling, he was my best friend and I miss him every day.
He had been ill for a couple of years. The local GP tried various antacids, nothing seemed to ease the issue. Eventually, they took blood and urine samples. There was blood in his urine, which triggered several appointments at urology departments in the area. They all seemed to find the same thing, a buildup of fluid in his abdomen, which may need further investigation.
After a month or so of various tests, I called in to see him after work (as I did every day) and found him vomiting blood. He was admitted to hospital, and after a few days, an OGD was performed. He had a 10cm mass where his oesophagus joined his stomach. He was discharged and told "There is nothing we can do".
I was told that the hospital would be in touch within a couple of weeks. After a week, I rang them and was told that they had referred him to another hospital, and we had to wait for an appointment date.
He sat at home waiting for a month, with no treatment aside from antacids and Fortisip, waiting for his appointment.
He had an appointment on 7 July, where the consultant asked him if he knew what was happening, he replied "I'm dying".
My father passed away on 10 July. Three days later.
I'm so sorry for your loss. My mums treatment took 5 weeks for doctors in make a diagnosis despite what other doctors said in the same hospital. She was transferred to another hospital 2 hours away and cried the whole way
Many thanks for your reply. That sounds awful, it must have been so traumatic for you all.
I have to admit that I have lost all faith in the NHS, despite my treatment for CML over the past 22 years.
My poor father didn't even get a chance to start any treatment. I've made a formal complaint, but I don't expect it to go anywhere.
I understand exactly what you mean about the NHS. In my mothers case I lost count of the number of mistakes that were made.
I wish you all the best
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