Follow up CT scan

My experience during the second round of chemo treatment was similar to the first. The day of and after the treatment I felt fine, but the following 5 days were uncomfortable. During this time I get fatigued easily and experience general aches and pains. Thus far my appetite has been great, but this round of chemo was difficult on my digestive system. After some research, I found certain nutritional plans are much easier (and healthier) for the body to process.


I have adjusted my diet drastically before. Just after the twins were born I was my heaviest, 265lb on my 6'6" frame.


At that time I decided that I didn't want my kids to see me as an overweight father. I cut my caloric input by 1/2 and did weight training exercises 3 times a week. I lost 40lbs in about 6 months.

I have kept the weight off by eating less than I used to, but I haven't utilized the healthiest diet. I tend to eat lots of processed foods, red meats, and refined sugars. I switched to diet soda when I originally lost my weight which helped reduce my caloric intake, but it's certainly not the healthiest way to hydrate.

For the last 2 weeks, I have switched to a vegetable focussed nutrition plan that has a moderate amount of lean white meat (to get me the appropriate amount of protein). This nutrition plan provides loads of nutrients, vitamins, and enzymes that my body can process much more easily. I don't know if this diet will help my fight against cancer, but it certainly can't hurt eating a diet full of foods that are natural provided for us (Genesis 1:29). In addition, I drink about 100 oz of water a day.

Deb and I went to Karmanos yesterday for my 3rd scheduled chemo treatment. We first met with Dr. Flaherty to discuss the follow up CT scan taken the week before. The oncology field uses results from the CT scan in conjunction with other indicators such as blood work (each of the 100+ cancers is different, but for liver melanoma one blood indicator is LDH, an enzyme that can indicate liver disease). A normal LDH level is 250. At my first consult my LDH was 800. By my second treatment it had fallen to 300. On Friday the LDH was just under 200. We took this as encouraging news.

The CT scans were a mixed story. The mass in my left lung (not known if it is cancerous) has decreased in size by 60%. There is also no evidence of fluid in my lung. The liver CT scan was a different story. The new images looked significantly different than the previous ones. On the CT scan report, the tumor is larger than before, but Dr. Flaherty thinks that the official measurements don't tell the whole story. Since all of the indicators of my health (i.e. energy, pain, sleep, appetite, blood work) have been improving, he feels that changing my treatment now based only on the liver CT results would be a knee jerk reaction. I agreed with him and elected to proceed with 2 additional chemo treatments.

My white blood cell count came back slightly low for the chemo protocol, but it was still high enough to adequately fight infections. This means that I will have to wait a week before getting my 3rd chemo infusion. Every day I realize more that this is going to be a long road for me. In a world that expects fast and quantifiable results, cancer doesn't fit. Faith and patience will be what gets me to the end of this road, wherever it leads.

Please keep me in your prayers for the chemo drugs to be effective over the next two treatments, that I'll avoid infections during this difficult time of the year, and that I'll keep hope and strength through this process. In addition, please keep Deb, the twins, and the rest of my family in your prayers. Cancer can be just as difficult for those close to it.

Thanks to everyone for your comments on my blog, as you have been sources of inspiration, joy, kindness, and love. It is comforting to know there are lots of people pulling for me.