May 25: I experienced the normal side effects from chemo: nausea, loss of appetite, fatigue, and low energy. Dr Garg appeared concerned over the painful headaches I experienced several days after treatment 1. At this time, the cause is unclear. His orders were noted to slow the drip next time. He is also considering this could have also been a rare side effect from the Neulasta shot. Time will tell, my next treatment is June 3.
Pat and I were confused about the frequency of my treatments. Our notes from Dr. Garg reflected 6 treatments, every 3 weeks for 18 weeks. The Infusion Nurses had a different schedule. When we brought this to Dr. Garg's attention he confirmed the following: 8 treatments with for the first 4 every 2 weeks and the last 4 every 3 weeks. Of course, I was not pleased. I believe the change occurred after knowing I am at high risk for recurrence and that my immune system was already compromised before the breast cancer diagnosis. So, they are hitting me strong! The change was not known to us - I do not like surprises! What can you do...start recounting, 1 down 7 to go!
Following this appointment, I had routine Bloodwork. Then, home. I was exhausted and took a long nap. I am trying very hard to walk every day. This is a very important piece when dealing with Chemo. Fight fatigue with exercise!
This week: Physical therapy, bone scan, and treatment 2.
Have a Happy and Safe Holiday Weeekend!!
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