We're back from the hospital. I'm waiting for my body to get weak, get nauseous. It'll come in full force in the next hour or two.
Like I said earlier, the oncology clinic at the hospital is a depressing place. And it's true, as soon as I entered the clinic, there were a lot of patients, more than the last time we were there. The first thing I saw were three patients receiving chemo. They all look so sick and weak. I told Mark right away that when we get to my "spot" I want the curtains closed. I cannot bear to see other patients.
Everytime we go to the clinic, a nurse tells us what chemo unit or area we need to go to. I was told to go to number #26. That spot was taken by another patient. I was told to use #25 instead. I sat down. As soon as I did I was sitting right in front of another patient, an older man, who looked like he was gasping for air. It was such a sad sight. I asked Mark again to close the curtain. Then I felt claustrophobic because I sat so close to the next patient in such a small area. I was uncomfortable. Fortunately the male nurse told me if I want to move to a private room. We did before he changed his mind ;) That was much better. At least I do not have to see other older patients who are so weak and seeing them only makes me sad.
The chemo didn't go on schedule. I think it was around 11:30 before the guy nurse put the IV in. It hurt this time and Mark forgot to hold my hand. It was alright, he made up for it afterwards. :)
I don't know why it hurt this time. The nurse thought the saline was going too fast so he lessened the amount going through the IV. A warm blanket was also placed over the IV and that helped a wee bit. Then came the red stuff (5-Fu), it was cold but painless. The last medicine (clear one) had the same effect on me the last time I had it, pins and needles on my head and a mild headache. It really hurt, I shed some tears and they gave me Tylenol. I told the nurse that I experienced the same (headache) during my first chemo. The nurse told me they'll try to inject it slower next time.
I feel tired and getting sleepy. I will have to take the nausea pills soon. Drink lots of fluids to flush the chemo meds off my system. Take lots of rests and sleep. :)
And that's two chemo treatments down and four more to go. Before we know it will all be over. :) My next chemo is Monday, March 2nd.
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