Esophageal Cancer: Anyone else?
I’ve completed 15 chemo treatments and 1/25 proton radiation treatments for my stage 2 esophageal cancer. I’m jst looking for helpful advice from anyone going thru this past or present. I’m a bit frightened wondering how this treatment will affect me.
Interested in more discussions like this? Go to the Esophageal Cancer Support Group.
I have ec and am 71. After 24 radiation treatments and 7 chemo treatments my tumor is gone from esophagus and stomach. The biopsy in August confirmed it.
I have a small spot on liver and have started chemo/immunotherapy and pump therapy sept 19 . I will have treatment every other week for 4 treatments to see if the tumor on liver reduces or goes away. I had a feeding tube for 3 months. Never give up and stay strong🙏
Praying the CT scan in December shows that the tumor is gone. They have to wait a couple of months after treatment (radiation) for the scans as the radiation lingers in our body for that long and is still killing the cancer cells. I just recently found this out from Radiation oncologist. I wondered why they scheduled the PET & CT scans so long (3 months) after treatment. This throat cancer I just recovered from is my second time with cancer. First time was esophageal cancer back in 2020 (chemo, radiation & surgery to remove). I'm doing ok considering. As with anything else some days are better than others. Please think positive!!!!!!!
Hi @sherrybinbin, I'd like to add my welcome. I'm also tagging @katelewis and @naomicanada who are caring for their mother's who have pancreatic cancer.
Sherry, my advice is to keep asking questions even if you're afraid of the answers. Everyone's experience with esophageal cancer is different. But having stage 4 cancer is not an automatic or immediate death sentence. Palliative care is a great option and it is really good in New Zealand. Palliative care is also referred to as symptom management care or comfort care. It is useful at any stage of cancer, not just stage 4.
Oncologist rarely use the word "cure" because they cannot make guarantees that the cancer will never return. That is unfortunately a lingering fear that all cancer patients and their families live with.
So keep asking questions here and of your mum's cancer team. I hope being equipped with information will help. Do you live close to your mum? What do the two of you like to do together?