First Follow-Up Today

I just got home from my 1st chemo follow up and it went pretty good. My bloodcounts are better, but still on the low side.

I told my oncologist about the tightness in the chestport area, the ongoing neuropathy and my short term memory loss problems. He said it's typical for a chemo patient after finishing the folfox treatment of chemo.

The tingling in my fingers is still pretty bad, but he said it might take from six to nine months before that goes away, but it WILL go away! They flushed the implanted mediport with saline and heparin (both sides - dual port) with both needles at the same time!

If I play guitar for a few hours, I have to skip the next several days because of the neuropathy in my fingertips from bending strings, so I play keyboards :)

So, my next follow-up is in 2 months, March 24th, then I'll have another two months from then and next will be be CEA bloodtests, scans and colonoscopy. All in all, he said that I'm progressing very well :)

5 Months of Chemo finished !

I went for my treatment today and it was another short one. I got a great informative publication from my oncologist about "living with, during and after cancer" and some great informative links that I'll post a little bit later.

I had my port flushed with a heparin lock and then was disconnected from the portable infusion pump...ah...what a great feeling!

Not sure what I'll be feeling like later or tomorrow, but I'm hoping to be well enough to go to my nephew's house for a little while. My platelets and white blood cell counts are pretty low and that makes my system's immunity level very low, so I'll have to stay away from anyone who is sick, or possible not go, but I'm hoping that everything work's out okay.

4th Cycle Complete (1/3 of the way)

I started and finished my 4th cycle of the Folfox treatment this past week and for the most part it went well. My next milestone will be finishing my 6th cycle (the halfway point) which should occur in early October is no setbacks.

The week started with a little bit of a pinch when the oncology nurse inserted the needle into my mediport, but I was able to whisper to the oncology nurse whose technique from last cycle gave me NO pain at all (zilch!) and she said that she would make a point to look for me to do the "poke in the port" on my next scheduled cycle start. I told her that I don't know how or what she did, but she has been the only one so far, to insert it with no pain at all.

As for the chemo, it was the same routine, a long first day with the infusion and sent home with the pump of 5-FU, then a little shorter on the second day with the IV and then more 5-FU in my holster pump to infuse overnight until I got in today for the exam and disconnect, where they flush the port with saline and give it a heparin lock.

I had an early appointment today, so I was out by 10am and had a nice breakfast (with hot coffee and not my favorite iced coffee) with my sister, Cathy, who recently had her colonoscopy. Even though they only found and removed one polyp, her doctor wants to see her in a year, due to my situation (sibling/family history?).

It got very hot and humid over the past 2 days, but all in all, it's been a cool August and the heat isn't bothering me like it did during July.

I can't stress enough to get yourself checked (scope) because it is a LOT easy than having surgeries and chemotherapy for six months. Early detection is a key factor and I truly believe that it is what saved my life along with the help of God!