Hello everyone, as the title says literally confirmed today, I would appreciate any help or advice however small on anything I could or shouldn’t expect
regards Sean
Hello everyone, as the title says literally confirmed today, I would appreciate any help or advice however small on anything I could or shouldn’t expect
regards Sean
Hi! I have recently been diagnosed with a Glioblastoma- Stage 4. It's the aggressive Cancer type, so I know it can't be cured. The tumour was sat in the right frontal lobe of my brain. It was removed by operation a short time ago. I have let any extra tissue that remained be used for research. I know that I will be starting Radiotherapy, and Chemotherapy tablets in a couple of weeks. The thing I have noticed the most is my energy levels aren't great. They fluctuate every day, so have to stick to new limitations on what I can do. You might find yourself feeling more exhausted more quickly. I also seem to be more thirsty at the moment, so have to try and stay well hydrated. I think now that the key is to cope with any side effects I might have, or get when treatment starts. Am already under a Community nurse, who also helps with Palliative care team in my area. I am taking each day as it comes. I am thinking about how to make the most of the rest of my time, however limited it possibly could be.
Hi! I have recently been diagnosed with a Glioblastoma- Stage 4. It's the aggressive Cancer type, so I know it can't be cured. The tumour was sat in the right frontal lobe of my brain. It was removed by operation a short time ago. I have let any extra tissue that remained be used for research. I know that I will be starting Radiotherapy, and Chemotherapy tablets in a couple of weeks. The thing I have noticed the most is my energy levels aren't great. They fluctuate every day, so have to stick to new limitations on what I can do. You might find yourself feeling more exhausted more quickly. I also seem to be more thirsty at the moment, so have to try and stay well hydrated. I think now that the key is to cope with any side effects I might have, or get when treatment starts. Am already under a Community nurse, who also helps with Palliative care team in my area. I am taking each day as it comes. I am thinking about how to make the most of the rest of my time, however limited it possibly could be.