June 3: It was a long day and thankful it is now behind me. I started at the lab where they drew 7 tubes of blood. After leaving, I was not feeling too well. I ate a small breakfast and was working hard on my hydration to boost the veins for the infusion, but it was not enough. After the physical, Pat and I had a some time to slip out for a salad before my chemo. My physical and blood results all came back favorable. All steps in the right direction. It was a little easier going in for this infusion after having one behind me...but still, not right.
The Infusion Nurse had problems with her first attempt with the IV, and my vein collapsed. It took her several minutes for her to locate another good vein. Once the IV was in, it was ok. However, as the medications were going in, I experienced stinging in my arm for the duration of the infusion. With 6 more treatments to go, it is time to have the discussion with Dr. Garg about a port. I don't think I can do this 6 more times knowing these drugs are very hard on the veins and they can only use my right arm. My follow up with him is June 9.
My infusion took longer than my first one, 3 3/4 hours, as expected. My side effects are the same as the first, but not as bad. I think this is the result of slowing it down. Right now, the hardest side effect is fighting the fatigue.
June 5: I returned to the hospital in the morning for my Neulasta shot. I am already experiencing bone pain in my chest, a normal side effect. Tolerable.
This week: Physical Therapy appointments, Blood Work, and Dr. Garg. If possible, I would like to schedule the appointment with the Doctor who will perform the Port Surgery and get this scheduled before my next Chemo Treatment, June 17.
I continue to appreciate all the emails, texts, cards, and calls. Thank you all!
XOXO
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