Showing posts with label Bill UIC. Show all posts
Showing posts with label Bill UIC. 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, March 24, 2011

The Backside View

Today Bill had the selective internal radiation treatment done to the liver at UIC.  It went very well.  We will know in 2 to 3 months if the procedure killed the tumors in the liver.  So far, Bill is fairing well.  He is not nauseated and the pain is minimal so far.  It is not unusual for pain and nausea after this procedure.  Maybe tomorrow he will be feeling the effects.  Because of the radiation, he needs to stay away from the little ones for the next week.  He can hug them but they are not allowed to sit on his lap.  He needs to stay 3 feet away from them and do not spend no more than 2 hours with them at a time.  It is going to be hard but he will be going back to work on Sunday which will help with the situation.  Another side effect he might have to deal with is major fatigue.  He is on steroids to help combat the fatigue. He was told the fatigue lasts for about 2 weeks.  Hopefully, it won't be so bad for him.  Right now him and Zachary are having a contest on who can snore the loudest.  Bill is in the lead.  I need to add ear plugs to my shopping list.

I know it's Bill's blog but I thought it would be different to show my perceptive.  Today, I spent 12 hours at the hospital with Bill and I wanted to share a little about my day.  Instead of making it all about Bill's day.

We arrived at the hospital around 7am.  At 10:30 they began the SIRT on Bill and he was finished at noon.  I sat in the waiting room by myself bored.

When we went back to the room, I was sent on a food room.  I had the privilege of looking and smelling all the delicious hospital food.  How someone can eat that food day in and day out baffles me. I can barely tolerate it for a day.  I then had to go to the gift shop to get the rest of the food items (candy) that were on his list.  One good thing that came out of it, I met a lady on the elevator and she gave me a menu for a local restaurant that has good food.  Hopefully, we will never have to go back to UIC again, but if so I am bringing the menu.

I get back to the room and help Bill with his food since he had to lay almost flat.  First, was the liquid tray.  Then we the regular tray. I had to cut up his turkey and butter his role. He also had a grilled cheese sandwich, peaches and cottage cheese,stuffing, green beans, and a yogurt banana smoothie.  I was thinking the entire time. this resembles nothing of a liquid diet he was told to be on to help prevent him from getting nauseated
and vomiting everywhere. 
After that he watched TV and slept.  He rattled the room with his snoring.

Once again, I was bored.  So I decided to paint my nails since it's rare to be able to paint them and not move long enough for them to dry at home. I recently discovered a new brand on nail polish called Zoya.  It stays

on longer and is safer then other brands. 

I realized there was a beautiful window view from the room.  I stared out, while he snored away.


Ester, the nurse practitioner, came in the room to check on Bill and woke him up.  She talked to us for awhile and shortly later Bill was able to sit op and move around.  Ester asked Bill what he wanted for dinner.  He told her to surprise him.  So he waited with anticipation for his dinner surprise.  And he was surprised.
Publish Post

A liquid diet is not what he had in mind.  So I was off to down stair for another food run. In the mean time he took over my chair and watched more TV.  I got the pleasure of watching court shows all day.


The  joys of the cafeteria.  Reminds me of high school but I think the food in high school was a tad better.  Then another trip to the gift shop for more candy.

Bill cramming down a hot dog.  He couldn't have a Snickers until he ate his hot dog.

Then we sat some more while he watched TV and slept some more.
 
When he did wake up again, I managed to make him him a little agitated but I can't remember exactly what I did.


I think that was when I told him the gift shop closed and there would be no more candy runs.

I also saw a lot of this.


Unfortunately. I think a lot of people got to see that.  His gown was on the shorter side as well.  So there was a lot of front exposure too.  I would have taken a picture of it but I was afraid Bill would lose all of his blog fans.  Plus, there were enough pictures taken of that area for a medical publication in Brazil. I hope Bill is enjoying his sleep while I am taking pleasure of being a good wife and writing a post for him.

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.

Thursday, November 18, 2010

Another visit to UIC and than again.

It's been a busy week to say the least. Went to UIC on Monday and spoke with Dr. Warso, the cancer surgeon. He discussed treatment options and what he felt was best for me. He didn't recommend surgery. He thought right now surgery isn't the best option. The location of the lymphnode will pose a great risk to remove. Right now my oncologist feels the best option is the chemotherapy. If the chemo doesn't work then radiation will be the next option and surgery will remain the last option.

As for the cancerous tumor , the surgeon recommended radio frequency ablation (RFA). Tomorrow I will be going back to UIC to speak with an radiologist and to make an appointment for that. It's an out patient procedure and I should be able to return to work the next day.

As for me, I am feeling well. Tired goes with out staying but I am still able to keep up with life's demands. I still haven't had a full dose of chemo therapy yet which might be one of the reasons I am feeling good. The first round of chemo pills there was a misunderstanding I was only taking half of the dosage. Second round of the chemo pills were cut short because my liver wasn't tolerating it. Today I went into start my third round. There was an error with the infusion medicine and treatment was stopped. I go back in Tuesday and start all over again. Stinks I have to have it on Thanksgiving week but mistakes happen especially to me and I make a couple every now and then.Just a couple mind you,But than again It's usually Sally's fault I make them,I think.

A good thing came out of today though. I had to go into work for a couple of hours this morning.We had a fire drill and I was a auditor, but anyways. When Sally picked me up we went to have lunch which is something we normally do before chemo. It's the only time we really get to spend time alone with each other. Sad but true. We have my mother in law watch the kids for my treatments, appointments and when ever we need a sitter so we feel guilty to have her watch them so we can have a night out. Like I was saying we went out for lunch, there is a new Italian restaurant across the street I have been wanting to try. It's called Ciao Bella Ristorante. I was told this is as authentic to Italian cuisine as it gets.That was told to me by the Italian workers that are working on our new Metallizer machine and they should know. I will say it was very good. I highly recommend it if you want a true Italian meal.

I know I said I was going to write part two of my Halloween adventures but with everything going on I haven't had a chance. I was going to write it today but Sally demanded I write about me. I am sure though the Halloween blog would be more entertaining. The real reason she wanted me to write about me is because she still does not have the Halloween pictures ready for the blog. Bad wife. A punishment is forthcoming.

Will try to write again as soon as possible. Take care and God Bless.

Thursday, June 11, 2009

Day 2

<span class=I am here with Bill. It's amazing, he looks so good. If he wasn't hooked up to IV's, it would be hard to believe he under went surgery yesterday. He is doing well. He says he is in a lot of pain. It's worst then the last surgery. He is tired as well. The medical staff kept coming in his room though out the night. He said they did a chest X-Ray at 1 AM. He is up and about today. The catheter is out. We walked around the hall way and he did well. He is on a clear liquid diet and is waiting patiently for his spaghetti dinner.

He has his cell phone. It's OK to call Please do not call pass 8 so he can get his sleep. The kids are doing well. Zachary is having a lot of fun with his aunt and cousins. He misses home and wants to go home today. I miss them to and will be happy to have them home, It was sad last night to see an empty crib next to my bed. Last night, Zachary was home sick. We were able to do video chat and he felt better. Hopefully he will be able to do video chat with his dad today.

Bill did not feel like writing the blog today because of the pain. I did read him all the comments and guest book. He enjoyed hearing them.