Sunday, November 24, 2013

T Minus 2 Days Til' Transplant

11/24/13 – So, I was really a trooper with the ATG infusion. I handled it great. I was a little tired from the premeds (Benadryl knocks me out every time). Today I will get an increased dose of the ATG and the Tacrolimus will begin. I am done with getting the Fludarabine and the Cyclophosphamide as of last night’s doses.

I am doing excellent with my exercising, I walked over 2 miles yesterday and already have logged a mile for today. I have been putting on weight at about 5 pounds per day. This is caused by all the fluids I am getting through my IV. It kind of reminds me of the Willy Wonka movie when the girl gets overloaded with grape juice and needed to be de-juiced.

Again, I want to stress that I feel well and that I am ready for my big day on Tuesday when I will have the transplant. I am truly feeling very peaceful.

The LORD gives strength to his people; the LORD blesses his people with peace.


Saturday, November 23, 2013

T Minus 3 Days Til' Transplant

11/23/13 – Yesterday went great. I actually got to play my guitar, walked about 2 miles around the nurses station (22 laps makes a mile). I really haven’t had any effects from the last couple days of chemo. I had visitors of my wife, Sue and daughter, Alli. Today they will be back and also my other daughter Jill will be joining us.

The plan for the day is to get my doses of Fludarabine and Cyclophosphamide. In addition I will also get ATG. Tomorrow I will get another dose of ATG and start with Tacrolimus.

WOW these are some big words. Let me help by giving some brief descriptions.

  • ATG is an infusion of horse or rabbit-derived antibodies against human T cells, which is used in the Gee I wonder prevention and treatment of acute rejection in organ transplantation and therapy of aplastic anemia. Gee, I wonder if I am going to start craving raw carrots.
  • Cyclophosphamide is a drug that is used primarily for treating several types of cancer. In order to work, cyclophosphamide first is converted by the liver into two chemicals, acrolein and phosphoramide. Acrolein and phosphoramide are the active compounds, and they slow the growth of cancer cells by interfering with the actions of deoxyribonucleic acid (DNA) within the cancerous cells. In addition to slowing the growth of cancerous cells, cyclophosphamide also suppresses the immune system and is referred to as immunosuppressive.
  • Fludarabine or fludarabine phosphate (Fludara) is a chemotherapy drug used in the treatment of hematological malignancies (cancers of blood cells such as leukemias and lymphomas). It is a purine analog, which interferes with DNA synthesis.
  • Methotrexate, abbreviated MTX and formerly known as amethopterin, is an antimetabolite and antifolate drug. It is used in treatment of cancer, autoimmune diseases, ectopic pregnancy, and for the induction of medical abortions. It acts by inhibiting the metabolism of folic acid. I will start taking this after the transplant.
  • Rituximab (trade names Rituxan and MabThera) is a chimeric monoclonal antibody against the protein CD20, which is primarily found on the surface of immune system B cells. Rituximab destroys B cells and is therefore used to treat diseases which are characterized by excessive numbers of B cells, overactive B cells, or dysfunctional B cells. This includes many lymphomas, leukemia, transplant rejection, and autoimmune disorders.
  • Tacrolimus is an immunosuppressive drug that is mainly used with allogeneic transplants to reduce the activity of the patient's immune system and so lower the risk of rejection. 

 I just have to thank God every day for all the blessings in my life, my wonderful loving wife, the best daughters any one could wish for and so many great family and friends.

And I guess I need to thanks our animal friends, after all some rabbit or horse has “donated” the key components for the ATG I will get today.

And God created great whales, and every living creature that moveth, which the waters brought forth abundantly, after their kind, and every winged fowl after his kind: and God saw that [it was] good.


Friday, November 22, 2013

T Minus 4 Days Til' Transplant

11/22/13 – So I did make it into the hospital last night. I was in my room at about 7PM. To keep things on track I settled in quickly, was given some pre-chemo drugs followed by IV doses of Fludarabine and Cyclophosphamide. I will get both of these again today.

So far I am feeling fine. The nurses here on the transplant floor (9th Floor, Pavilion East) of Hackensack University Medical Center are simply awesome. And as far as it goes with Dr. Rowley, the more I see him the more I like him. Also his team is just great.

I did decide to bring a small travel guitar. I have already had it out to help time pass. I think this was a good move.

I had a few visitors from the hospital staff. The nutritionist stopped by to review how they work. Being an old pro here, I am very familiar with how this works. My personal eating challenge centers more on smells versus the taste of the food. As soon as I pick up a bad smell I lose my appetite. The one smell that gets me is the smell of plastic. The food is typically transported to the rooms in a plastic serving dish with a cover. When the cover is removed, the first smell that is released is the hot plastic. After explaining this to the nutritionist she said I could request that my food be wrapped in aluminum foil. This will help me a lot. It just shows you how accommodating they are here.

I also met with one of the resident Catholic Priests. He offered to help me in any way that I need. He gave me the televised mass schedule and will be stopping by periodically to bring me Communion.

On a personal note… Both my daughters (Jill and Alli) have made the cast of the 2014 tour of “Bring it On – The Musical” which will travel throughout the US and some parts of Asia (mostly Japan). I am so proud of them. Their tour schedule has them in New Jersey (my home state) in May of 2014. I am thinking I can make this. This is certainly something I will shoot for.

O come, let us sing unto the LORD: let us make a joyful noise to the rock of our salvation.
Psalms 95:1 


Thursday, November 21, 2013

T Minus 5 Days Til' Transplant

11/21/13 - Yesterday I had my triple lumen installed. It was a very quick procedure that left me with 3 tubes sticking out of my right shoulder. After a few hours I already forgot it was there. This should go a long way in saving my veins while I am in the hospital.

Speaking of the hospital, I get admitted today. I just have to wait for the hospital to contact me that they have a bed available for me. I will start chemo today when I get to the hospital

In a strange kind of way my biggest concern is keeping myself from being bored for the time (about a month) I am in the hospital. I am very confident that all the medical stuff will go great with the wonderful team of doctors I have. To keep myself occupied I will bring a computer and ipad and I am still debating with myself on if I should bring my travel guitar with me. I do remember from when I went through chemo last time (in 2008) that playing the guitar kept my fingers from experiencing neuropathy. This may be a medical study I need to pursue in the future.  

Similar to last time, I have been asked to bring workout cloths. Keeping me active during my stay in the hospital is considered a critical part of getting me on the path to good health.

So I guess my new journey really starts today. I am feeling very positive and exciting that this will lead me to getting my life back.

For I know the plans I have for you, declares the Lord, plans for welfare and not for evil, to give you a future and a hope.
Jeremiah 29:11

Wednesday, November 13, 2013

T Minus 13 Days Til' Transplant

11/13/13 - What a difference a day makes. I am really feel so much better. If you could believe it, I ever feel like I have more energy than I did before my fevers.

Today I had my dose of Rutuxan as an out patient. The does was proceeded by a dose of Benadryl. Boy does that stuff knock you out. I pretty much slept through the entire Rutuxan infusion. 

I am still feeling great, just a little drowsy. 

Then Jesus said, “Come to me, all of you who are weary and carry heavy burdens, and I will give you rest.”
Matthew 11:28 

More to come…

http://mantlecell.blogspot.com/

Tuesday, November 12, 2013

The Long and Winding Road... begins

As I said with my last post, my transplant was moving forward. An unrelated near match has been identified, contracted and has agreed to be the donor. The match is a near match (8 of 10) but the areas of mismatch are not one that are of concern for my doctors. We have come up with a plan that we are in the process of executing one thing at a time. One of the early tasks was to get dental clearance. 

11/1/13 – At my dental clearance appointment I was found have two teeth in question. One that possibly needed to be pulled.  I was able to get an appointment with an oral surgeon on 11/4.

11/4/13 – at the appointment with my oral surgeon it was decided that the tooth needed to be pulled. After consulting my oncologists and transplant doctors, the oral surgeon was given to go ahead to pull the tooth. This ended up being the correct decision being a fairly large infection was found at the root of the tooth. Also on 11/4 I went back to my dentist and had a tooth filled.

11/5/13 - I had my visit with Dr. Feldman of the The John Theurer Cancer Center with I continue to receive positive results. I was given the OK the begin cycle 12 on Ibrutinib.

11/6/13 – I went to work and had a fairly normal day but at the day went on I began to feel like I had the chills and had a bit of a headache.

11/7/13 – At around 2:00 AM my wife noticed I had been sweating heavily. She took my temperature and it was 103.7. She immediately called The John Theurer Cancer Center. She was told to give me Tylenol and if my temp didn’t come down to bring me to the emergency room at Hackensack University Medical Center. The Tylenol worked. I went to my family doctor, Dr. Eric Hansen and he gave me a thorough exam and put me on a stronger antibiotic. In addition he ordered a chest x-ray and blood tests. We had the x-ray right away (which came back clear) but were not able to get the blood test done being we had to head off the Hackensack to meeting with Dr. Rowley, my transplant doctor, to review a number of things for the transplant. Knowing about the fevers, Dr. Rowley made sure all the blood tests were completed plus he had some additional tests run(all test were negative). When I left Dr. Rowley my temp was normal but I did feel like I have the chills.

11/8/13 – At around 12:30 AM, my chills had gotten worse. My temp was 103.3. My wife called the Cancer was told to bring me to the emergency room. The emergency room again put me through a battery of test and I was official admitted into the hospital a few hours later. I was put on broad span IV antibiotics. Dr. Goy came to visit me in my room to examine me. He ordered a CT of my head (which came back negative).

11/9/13 – The trend of having a high fever in the early AM continued. At about 2:00 AM my temp was 103.3. I was given Tylenol and it brought my fever down. I went for a PET scan in the late morning, I was feeling pretty good. When I returned my fever was normal. Over the next few hours I remained that way. At 10:00 PM my temp was 98.9.

11/10/13 - I was wondering what my temp would be at 2:00 AM. Well, 2:00 came and went but I slept right through it. I guess the nurses didn’t want to awake me. At 4:00, the time when they come and take my blood, I had asked for my temperature to be taken. It was 102.7. Not 103… but not what I wanted to hear. I had a good day. As the night nurses are coming into work I am taking a pool as to what my temperature will be at 2:00 AM. By the way… the nurses here at Hackensack University Medical Center are awesome.

11/11/13 – My temp was 99.0 at 2:00 AM. This was great news. I felt strong all day. When I met with Dr. Mateo he said I should be able to go tomorrow.

11/12/13 – My Temp was 99.0 again at 2:00 AM and 98.4 at 7:00 AM. And truly am ready to go home today. I think this storm has past. Hopefully this is not a sign of things to come. Maybe it was God’s way of putting me through some marathon training as my transplant approaches.

Did the dental work have something to do with the fevers? I don’t think we were able to prove that one way or the other. It does make sense that if an infected tooth is pulled that maybe the infection could get into your system. I guess the lesson learned here is that next time to prepare for a transplant I will not take the dental piece so lightly and get it covered much more in advance.

So what does this all mean from the prospective of my transplant? How does it impact my transplant? Maybe not at all. At this point all our plans for transplant are still on. The plan is:
11/13/13 – Receive Rutuxan as out patient
11/18/13 – I go to a transplant class
11/20/13 – Catheter installed
11/21/13 – I’m admitted into the hospital for chemo
11/25/13 – The donor makes the donation
11/26/13 – The stem cell transplant happens

So my new journey has begun. I look forward to telling you about it.  

No evil shall be allowed to befall you, no plague come near your tent. For he will command his angels concerning you to guard you in all your ways. On their hands they will bear you up, lest you strike your foot against a stone.
Psalm 91:10-12 

More to come…

Monday, October 28, 2013

Remission Accomplished Again… Transplant is Next


10/8/12 – Today I met with Dr. Goy for my normal cycle follow up and to review the results of a PET scan I had last week. Dr. Goy said: “You are in full remission…. This makes me very happy”. After a couple of moments of silence he then said, looking at the research nurse, “So where are we with the transplant?”
10/28/13 - From that question until now the entire process has really accelerated. It is looking like the transplant with begin within the next couple of weeks.

Although my daughters and brother did not pan out as being good donors (even as half matches) there have been two near matches found. This mismatch part is in areas where it is not seem as being critical. With this being said, a request for donation has been made. Assuming the donor says yes and gets through the pre-testing… it sure looks like I will have my transplant before Thanksgiving.

To prepare for this I have a dental appointment scheduled for October 30th to make sure I have non issues with my teeth. On Friday, November 1st I will go through all my work up tests at Hackensack University Medical Center. On Tuesday, November 5th I have my normal cycle visit with Dr. Goy. On Monday, November 11th I have a Transplant Class where I will get an education on what I am really getting myself into. According to my Transplant Coordinator, this is a very good chance I will be in the hospital before November 11th. On top of that I have begun getting all the other details of my life in order (leave from work, etc…).

The way it works is that once the donor is fully committed to provide me the gift of his bone marrow and a date to extract the bone marrow is set, we need to count back about 9 days. That will be the day I check into the hospital. I will get chemo for about 8 days and on the very next day the bone marrow will be infused.

I just know that everything will work out for me.

This bring me back to a prayer that my pastor taught me back in 2008:

"Jesus, I believe in you and you will take care of me.
Jesus, I believe in you and you will give me peace"


All the battles of my life are the Lord’s. As I stand in faith, He fights them for me. 1 Samuel 17:47

More to come…