Had an appointment with my ENT doctor today. Told him about the bad experience I had with the Radiation Oncologist when he scoped me some weeks back. I asked if he could scope me in the future and report to the Oncologist his findings. He said I could request that from the Oncologist and see what happens. He wants to see me again in two months.
I then went in to the Cancer Center for my treatment. The nurse greeted me and asked how I was doing. I again told her I was still having light nausea and she again dismissed it as not being caused by the radiation. I replied that I relieve it when I increase my food consumption as well as drink more water. She ignored this.
The treatments seem to get easier and easier each time. Today I saw the eye of Electa 3 times and then it was over. I hadn't noticed this before but that is a good way to gauge my time on the table. Also, there is a noticeable reduction of my lymph node which is amazing to occur just after 3 treatments.
Then I met with the Dietician. Very pleasant person who gave me information on how many calories I will need to ingest daily (1879) and how many grams of protein (92). She also recommended Boost Glucose Controlled and Glucerna 1.2 or 1.5 in a can due to my diabetes. Encouraged lots of fruits and vegetables. I think I'll try doing that with smoothies. There is a Smoothie King across the street from my house. Very positive meeting. I will be meeting with her on Wednesday from now on.
Drove myself to both appointments today. Not a problem.
Instead of the commercial Boost product (look at the label of ingredients!), would you be able to just add powdered milk to a smoothie? That would give you a good boost in protein. Do you know if they are recommending such a high intake of protein because of the radiation? I've read that the usual amount for a healthy person is .8 grams per kilo (2.2 pounds) of body weight.
ReplyDeleteI am appalled that the staff shows such little concern for your well being. Even if the nausea is not caused by the radiation, they should not just dismiss the problem, but try to find a solution for you.
Is there a National Cancer Society volunteer where you go? They are usually cancer survivors, or spouses of patients who have passed away with cancer, and are very kind and gentle. They love to make a difference in your life.
If there is no one at your clinic, you might try calling your local society and asking questions. Someone with experience with the disease may have more solutions than a nurse who is busy and not really tuned into your needs other than whatever she is doing to facilitate your treatment.
There is usually some sort of weekly meeting of a help group for patients. We never attended any of them, so I don't know how useful they are, but there were always flyers all over the clinics advertising them. As far as I know, there is no charge to attend. It's just a help group.
Virtual hugs,
Judie