Showing posts with label SIRT. Show all posts
Showing posts with label SIRT. Show all posts

Friday, September 23, 2011

The roller coaster continues

Sorry I didn't post yesterday.  I was exhausted by the time we got home last night. Yesterday we went to UIC Medical Center.  Bill was to meet with the oncologist for a second opinion.  We were both very nervous.  We have not spoke to the regular oncologist after the ERCP.  We both feared the oncologist from UIC would tell there are no trial studies and he would recommend discontinuing chemo therapy treatments.  


The oncologist said there were no trial studies in our area that he is aware of.  He did say that he believes Bill should continue with chemo therapy.  It will not cure him from the cancer but it is slowing down the progression.  He said he has seen many patients like Bill who has lived several years.  I asked about the pain Bill is experiencing.  I asked if it could be caused by the gallbladder (ultra sound showed gall stones).  He said that could be causing the pain.  UIC does robotic surgery for this and it's a rather simple procedure.  Bill agreed to meet with the surgeon.  At this point he is willing to do anything to get relief from the pain. I mentioned to the oncologist about traveling in December and he said he thinks Bill should be fine then.


We waited for the surgeon to meet with us.  We were told that the surgeon himself was unavailable and his assistant would speak to us instead.  He looked over the reports and PET scan.  He seemed more concerned about the tumor in the liver that was treated in March with the SIRT procedure.  From what I understand it's no longer cancerous and more like dead tissue.  He wanted the surgeon to go over everything and talk to us.  We had to walk a block to another building to talk with the surgeon's nurse to schedule an appointment.  She told us the surgeon can see Bill in 2 weeks.  I explained to her that Bill has been off chemo for over a month.  With the possibility of surgery he could not resume chemo.  I didn't want him to wait for another 2 weeks to see if he may or may not have surgery.  She said the surgeon was in a meeting and if we would wait he would talk with us.  


We finally saw the surgeon.  He went over everything.  He seemed more concerned with the liver and the bile duct then he did with the gallbladder.  He said he recommends removing a section of the liver.  He explained leaving it can cause Bill to develop jaundiced and could be causing pain.  He also said Bill would respond better to chemo.  He was concerned about the bile duct.  He said the "tumor" could be caused from many things.  It's not near the cancerous areas.  He said it could be a lesion caused from the SIRT procedure.  He said he would like to examine the slides that were taken at the ERCP last week.  He also said he would like to speak to all the physicians that are treating Bill so they can treat Bill collectively and not individually.  He said that after he receives all the information he needs and talks with the other doctors he will call us.


4 hours later we were finally on our way home.  Bill was in a lot of pain. We were both hungry, tired and stuck in traffic during rush hour.  This morning, I called his regular oncologist office.  I wanted to see if there was a different pain medication Bill could try since the current one is helping very little.  The nurse called back and said the doctor wrote out a script for something else and we could pick it up right away.  I called the hospital where the ERCP done.  I needed to get slides plus the pathology report on the tumor.  I was told there was no report and I need to ask the doctor who performed it. 


We went to pick up the script.  The oncologist saw us walk in and told us to take a seat, he wanted to talk to Bill.  He said that Bill is looking good and he doesn't look jaundice any more.  He wanted Bill to have blood work done to see if the liver enzymes are low enough to resume chemo again.  I mentioned the possibility of surgery.  He didn't think it was needed but said that he is going to talk with the doctors at UIC to see what they had to say.  I asked if there was a biopsy done during the ERCP procedure.  He said no that there was no need considering Bill's history.(So there is a chance it's not cancerous)  He also mentioned about trying to find a trial study for Bill but we might have to travel for it.  He didn't seem as optimistic as the doctor at UIC, but he wasn't depressing either.  Bill is going back next week to see him.  Hopefully by then all the doctors will have spoken to each other and we will know what's going on.  


The roller coaster continues..... It's been the longest ride of my life.  

Monday, August 15, 2011

PET scan in the morning


I just found out I have a PET scan scheduled for tomorrow morning.  I have to be there at 8.  I will be cutting it close since I work until 7am.  UIC is requesting this.  It's routine to have it done after a S.I.R.T. procedure.  http://www.uwhealth.org/radiology/selective-internal-radiation-therapy-sirt/10503

Even though it's routine, it is still going to be worrisome.  More so now then ever.  The results maybe another life changing event in my life. I can only think of 4 possibilities it could be.  The first one, there is no change. Wouldn't be the greatest news but at least the cancer is being contained and not growing.  The second possibility the cancer activity has lesson.  Which I will be dancing the jig if I hear this news.  The 3rd possibility could be a miracle has happened and I am cancer free.  Anything is possible and I do believe in the power of prayer but God's will may not allow this.  The forth and most dreadful possibility could be chemo is not working.  Cancer is growing and there for chemo treatments will be discontinue.  This is my biggest fear.  No one wants to hear they are doomed.  Especially me.  


Whatever the results, I know by the grace of God and the help of family and friends I will be able to handle it.  It frightening knowing that this time could be it.  Since there are no other treatment options, scans are scarier then a scary horror flick.  Not a good comparison since I love horror flicks. Let's  just say I am about to be scared out of my britches, waiting for the results.  

I or Sally will update with the results as soon as we know.  As for those who encounter me in their daily lives, I might not be my chipper self.  This is why.  Please understand and avoid me if I am a grump.  Thanks.  

Thursday, June 2, 2011

My Update on Me

Just a little post to let everyone know I am doing well for the most part.  I am working a little less due to production at work has slowed down.  Right now I am on 8 hour shift and I have the weekends off.  Which is nice but a little worried since the overtime will not be there.


Health wise I am good.  Except, for stomach pains I have been experiencing.  The pains are hard to explain.  Sort of feels like the gas pains I had experienced after the surgeries but not quite as severe.  It worries me that the cancer may have spread. My chemo meds has changed so it could be do to that as well.  I mentioned it today at chemo.  Dr. Mboama thinks it's because of the chemo and told me to take GasX.  However, he must have some concerns because he wants me to go for a CT-scan A.S.A.P.  So, tomorrow at 2:30 I will be having one done. The ct will also show if the SIRT procedure I had done in March worked. Now the fun of waiting for the results begin.  The waiting is so cruel.


Please keep me in your prayers and thoughts.  I so desperately need a good CT reading or I am doomed. 


God Bless and Take Care
Bill

Thursday, March 10, 2011

A huge blow


view detailsBill 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, November 19, 2010

Update by Sally (his wife)

Bill had to work tonight and the following 3 nights. So this is the reason I am posting for him. Today, we went to UIC to meet with the radiologist. It's didn't go as we expected. Not that it's a bad thing we were caught off guard a little. We were under the assumption Bill was going to have the tumor ablation. It would be a simple out patient procedure and he would be able to resume normal activities the following day. We found out today the radiologist wants to do a different procedure. He recommends selective internal radiation therapy (SIRT). Instead of using radio frequency energy(which is the RFA procedure) to attack the tumor, tiny radioactive beads are inserted directly in the tumor/tumors.

The reason for the SIRT is because there are two cancerous tumors on the liver. One is about the size of a quarter and the other one is about the size of a pea. The smaller one is near the wall of the liver which can't be treated by the RFA procedure.SIRT will be able to treat both tumors in the liver. SIRT is not as simple to perform as the RFA though. SIRT requires two procedures. The week prior to the SIRT an angiogram is done to map out the vessels. If everything looks good then the SIRT procedure will be performed 7-10 days later. The angiogram would require Bill to be in the hospital for at least 12 hours. He will have to be off work for 48 hours and on light duty until a week after the SIRT is done. He will have to be off work for another 48 hours for SIRT procedure itself but the hospital stay would be much shorter as long as there are no complications. In order for the SIRT to be performed, chemo has to be stopped 2 weeks prior to the angiogram.

A concern which we have about the SIRT is the stopping of chemotherapy. Even though the tumors in the liver will be treated, he still has the cancerous lymph node by the heart. Since September, when chemotherapy was resumed, he still has not had a full dose of the chemotherapy. Which is concerning. Could delaying treatment longer increase the chances of the tumor from spreading or growing? Which is one of our major concerns. The oncologist seems confident the chemo will attack the lymph-node so we don't see why it wouldn't attack the tiny spot on the liver as well. Plus the RFA procedure seems a lot less complicated and a shorter recovery time.

If Bill had to pick of course he would pick the RFA procedure. Spending 6 plus hours flat on the back without moving after the angiogram wouldn't be fun. However, Bil wants what is best to fight the war with in his body. Tuesday, we are going to talk to the oncologist. Hopefully he will be able to answer our questions and give us his honest expert opinion on which one he thinks is best.

Please pray that he is guided to the right procedure for him. Thanks you.