
Monday, March 21, 2011
I meant well.

Sunday, March 20, 2011
The Truth is Revealed at Last
I want mention that I am still doing good. Just a little tired and sore. As of now I will be having the SIRT procedure on Thursday but, that may change if they weren't able to get the radiation beads. Then it will be next week. Thank you all for the prayers and well wishes , it makes me feel good with all the support that I have received.
Friday, March 18, 2011
He's Back
We are back home from University of Illinois at Chicago. In spite or despite my driving. Bill is giving me a complex about my driving because of his comment on facebook. I spent all day with him. Making sure he was well taken care of and this is the thanks he gave me. What a guy.
Today, went well for Bill. Of course, it is rare for Bill to go anywhere without causing laughs and making a scene or two or even three. Today he didn't fail himself. He began by putting the hospital gown on wrong. It was already tied in the back and he was told to slip the ties around his neck. This is proof Bill doesn't listen. He didn't slip the ties around his neck and instead the tie that is suppose to be in the back was around the front part of his neck. It looked like he was being choked. He didn't realize anything was wrong until I started laughing at him. After that was fixed, he was carted off to the holding room. I followed to give him moral support, hold his hand, and to wipe the tears and sweat away from his face. The nurses explained the procedure to him once again to make sure he understood what was going to happen. He cringed every time someone would remind him the procedure was going to be performed through his groin. After, they were done talking to him he said to me in a serious tone, "If you hear a bunch of laughter coming from the room you know they started on me". The nurses heard and started to laugh. The more the nurse talked about it, the redder his face got. He managed to embarrass himself this time. During the procedure he wouldn't fall asleep. When more medication was administer to sedate him, his blood pressure dropped. I think he was seriously afraid he would be laughed at when they looked at this groin so he fought to stay awake.
After it was all over, he had to spend the next 6 hours laying flat. He still managed his clownish ways and made the nurses laugh. He asked one if she was married because she put sugar in his tea for him. Made it sound like I do nothing for him. Even, though he kept sending me down stairs to buy him food. I just realized something. Maybe he wasn't hungry, he just sent me away so he could flirt more.
Like I said earlier, he is doing well. He has a little discomfort which is normal. He can't drive until Sunday and is not able to lift anything that is more than 5 pounds. No pushing or pulling either. Let's see if he will listen. I am willing to make a wager that he will not. We were told that they were able to map out the veins that lead directly to the tumors.The doctor feels confident that the SIRT will work. He is scheduled to have it done on March 24, unless they are not able to get the radiation spheres by then.
Hopefully, Bill will be able to write a post over the weekend. I am sure he will have a thing or two to say about this post. However, I am only saying the truth and it's not fair to his blog followers to omit information even if it does make Bill look like a goof.He is what he is and he is loved for that.
Sally
Thursday, March 17, 2011
Angiogram in the Morning

Bill is slaving over the fish tank as I am sitting here writing this post.
Yesterday, he went to UIC to speak to a doctor about the next steps into treating the cancer in the liver. For the most part, we understood what was going to happen because of the visit we had in November. The doctor wanted to act quickly so Bill can resume the chemo treatments as soon as possible. We appreciate his concern. Yesterday, all the paper work was faxed to the insurance company and today (in the later part of the afternoon) his nurse called me. The insurance company had approved everything and Bill will be at the UIC 6:30 in the morning tomorrow. He will be having an angiogram. This is done to map the veins to his liver. The procedure it self isn't very long but he will have to lie flat and still for 6 hours following it.
Next week he will go back to have the SIRT procedure done. This is where radiation beads are injected directly into the tumors. This too should be an outpatient procedure.
Bill has this weekend off from work and should be able to go back to work on Tuesday. He will be on light duty for 2 weeks since he will not be able to lift anything that is over 5 pounds. This is why he is cleaning out the aquarium now. Two turtles can become smelly after awhile.
I know everyone has been praying for us and we really appreciate it. Bill is doing amazingly well. It's hard on him having all the medical stuff dictate his life. Hopefully, next week we will get the results back for the KRAS mutation and after that life will go back to a new normal state whatever that will be.
Thursday, March 10, 2011
A huge blow
Bill had a routine CT scan done on Monday. This time we were not nervous about the results. As long as he is on chemo, we knew everything was going to be OK. At the very worse, the tumors were not shrinking as quickly as we would like. It was a change from the last time. The last time, I received a phone call 3 days prior to his chemo treatment saying the doctor needed to talk to us about the CT results. Of course, they wouldn’t say about what. So for three days we worried. I tried not telling Bill about the call but I couldn't stop crying and I was worrying him. Not knowing and worrying about the results is dreadful. Especially, when you know the results are bad and you are in the doctor’s office waiting for a long time for the doctor to walk through the door. The anticipation is unbearable and the worst case of scenario goes running through your mind. Hearing the “bad” news has been easier to handle then the waiting for the results.
This morning I woke up thinking positive thoughts. Bill was scheduled for chemo and had an appointment to see the oncologist. Bill was at work and I was just about to get ready and the phone ring. It was the nurse asking where Bill had his surgeries at. Of course she said she didn’t know anything but I knew it wasn’t a good sign. I tried to act like nothing was wrong when I saw Bill. He went to have the infusion first. The nurse started the IV and the doctor walked into the room and said he needed to talk to us and told the nurse to stop treatment. My stomach fell and I could tell Bill was very concerned. Chewing on his nails is always a given sign when he is upset or worried.
We were moved to an office and didn’t have to wait long for Doctor Mboama. As soon as he walked through the door and by the look of his face we knew it was bad. We just didn’t realize at that point how bad it was. He said that the 2 tumors in the liver had grown. Then the nurse came in the room and told the doctor he had a phone call. He stepped out and left us hanging. Which I could tell he was relented to do but I knew the phone call must have been important. When he came back he told us the tumors have doubled in size and that there are 1 or 2 more additional tumors in the liver. The cancerous lymph node has grown as well and there are 2 more cancerous lymph nodes now.
Usually, the doctor will give us a couple of options to choose from. This time he did not. He said he knows that we have young children and he is going to act aggressive and as quickly as possible. First step is to have the tumor that was removed from the colon tested to see if the cells are genetically mutated or non-mutated. If it’s non-mutated there is a new chemotherapy drug that will be used. If it’s mutated the chances of him beating this is not as high. It takes about 2 weeks to get the results.
The second step will be going back to UIC and have the SIRT procedure to the liver. http://www.umgcc.org/sir-spheres/about_sirt.htm He will have this as soon as possible, since he has to be off chemo for a month. With the 2 weeks wait for the other test result, doctor thought this would be the best time to have it done.
The third step is to wait for the test results so a new chemotherapy regiment can begin. Obviously the chemo pills, Xeloda, did not work. So Bill will have to go back to 5-fu which means he will be wearing the portable pump again. Which of course Bill is not happy about. He didn’t complain about it and the doctor said it’s his only chance for survival. He was also told he will have more side effects. Basically, he was told he is going to be feeling like crap.
Right now, we are trying to absorb everything. It’s terrifying news but the doctor still remains optimistic and so are we. We will be praying for non-mutated cells and just try to live life the same way we did yesterday. Bill is amazing. I know he is scared and worried but he is trying so hard not show it. He and Kaity are at Omni while I am writing this. Which means he hasn’t given up and still determined more than ever to beat this.
Friday, February 25, 2011
An Omission of Guilt
It all began on Super Bowl Sunday. Our friends had invited us over to their home to watch the game. Sally had made a couple of snacks to take with. One of the snacks were meatballs in a sauce. There was snow drifts all over so I was trying to be considerate and I dropped Sally and the kids off in the drive way. They grabbed the food out of the trunk and I went to park the car on the street. As I was walking towards the drive way, I looked at my family from a distance. There was my family with there hands filled with food. I felt a little guilty walking up empty handed. Sally had the container of meat balls and I spotted a trail of sauce leading from the drive way going towards the porch just in case we may forget our way back to the car. I knew she must have had sauce all over her too. Which is funny because I am the one that usually ends up with food all but over himself and then everyone laughs at me. I didn't yet make it to the drive way when Sally yelled from the distance "Are you sure this is the right house?". I of course said "Yep!" I looked at the house again and thought oooooh wait a minute, but decided not to say a word in case I was wrong (wink wink). I decided it was best for me to stay put so I stopped and watched the plot unfold from a far. I saw Sally knock on the door. The door opens and I see Zach walk inside and started to wipe his feet on a the floor mat. I then look at the guy who opened the door and I didn't recognize him. I heard him say everybody is downstairs. I then heard my wife apologize to him and she and the kids walked away with all the food and another trail of sauce. The whole time staring at me. "What I do?" is all I could say (if looks could kill I would have been a corps right then and there). I was more concerned about getting everyone back in the car as quickly as possible. With the trail of sauce and the mud Zachary left behind I knew the evidence of us being there was compelling so I quickly sped away from the scene.
I drove 5 houses further down the street to Ron and Lynn's house. During the short trip I could not help but laugh at her. She did mumble something like "I am going to get you for this". I am glad it was only a five house drive because it didn't give her anytime to say any more to me. When we got to the "right" house I knew because their 3 kids were hanging out the door waiting for us. Next time I told her we will have to make up a checklist of their outside contents to make sure she won't do this again. Most importantly their house address. I wouldn't want to see her embarrass herself again.. Periodically, throughout the game, I would peer out the window to make sure we weren't being followed by angry neighbors with blazing torches.
After the incident, my wife did not mention it again to me. So I thought maybe she had forgotten it. But that was foolish of me, because Sally never forgets things like that.She stills brings up things that happened 12 years ago. She may pretend to forget but she doesn't. If she tells you she will get you back she will but she will wait until you least suspect it. I know I shouldn't do this but Sandy (Sally's sister) you better beware. Sally will get you back. I am not sure and I don't know when but I can promise you she is planning something in that evil mind of hers. There is something about Sally and her sisters. When they get together they usually don't act their age. Sandy thought it would be funny to stick on a maxi pad on Sally's car as she was driving away. Sally knew nothing about it and it fell off the car between their mom's house and the grocery store. It amused Sandy and their mom very much. I still haven't yet to find the humor in it but maybe it was because they littered the street with a maxi pad. Sally swore on that day there will be war. So I thought it is best to warn my sister in law.
I'm scheduled for a CT scan on March 7th so prayers will be very much appreciated. Thank you for reading and hope you enjoyed it, God Bless!!
Sunday, February 20, 2011
This isn't goodbye.
Why are we so gloomy? Today we celebrated my mom's 73rd Birthday. Happy Birthday Mom! That wasn't the reason for the blues. The reason for the sadness, is that today will be the last time I will see my big sister, Dawn for a very long time. Well I hope it's for a very long time. If I see her sooner than a long time , it would mean something bad has happened or is happening. So in that aspect, Dawn I hope I don't see you for a very long time. Dawn and her husband Dave have bought a house in Alabama. Since they are able to receive senior citizen's discounts they feel they are now to old to endure the long Chicago winters.
It's been along time since we actually cohabited together during our childhood. It's been a very long time since she had snatched all my chocolate candy in my Christmas Stocking, shared her bag of Doritos by giving me about 3 after I walked 2 miles in blistering heat in the summer and 5 ft of snow in the winter, bare footed and holes in my coat, when I was able to wear my coat because she would wear it around the house to keep herself warm,( and our furnace worked fine) to buy them for her, I had to endure her singing in the car(that was the worse of the worse), and it's been a very long time since I pulled her hair. Even though it's been a long time and she lives one state over and 40 plus miles away from me now, I am really going to miss her when she moves 15 hours away from me.
Thanks Dawn and Dave for being there for me when I was at my worse. I am not going to say good bye it seems so final. So I am going to say have a safe move.
Love,
Bill
Tuesday, February 15, 2011
It's All About Me.
I live life to the fullest based on my ability. Of course if I had money, I would be doing many things that I am not able to do now. However, I would still live life the same. Spending it with my family and enjoying the time I have with them. There is saying "live life as if it's your last". I do not agree with that. If you live today as if it were your last then what do you have to look forward to for tomorrow. Eventually, you would be exhausted trying to live every day as if it's your last. Rest is very important to my healing process, so that wouldn't be good. My advice is to do something you love each day. It doesn't have to be something earth shattering. For I find that often the simplest things in life are the most satisfying and most meaningful to me. Whether it's sitting on the couch watching a tv show with Sally or cuddling up with the kids reading them a book, those are the times that mean the most to me and hopefully it's the things my family will remember. I try as much as possible to create memories. The memories aren't for me but for my family. They are something for them to hold on to in case I am no longer around.
One more quick note to Ann. I am proud to consider you a friend and have to say that this article was in my humble opinion your best effort to date. So good luck trying to top it. What is better subject matter than me?
Here are the links to Ann's writings. I encourage you to take the time to check them out.
http://www.examiner.com/frugal-family-in-chicago/ann-marie-walker
http://www.examiner.com/psychic-in-chicago/ann-marie-walker
http://livingafrugalfamilylife.blogspot.com/