“Let’s go fly a kite, up to the highest height…” Ah, the lyrics to one of my favorite tunes from the production of “Mary Poppins”. My wife and I went to see this classic and fun Broadway-style musical at the Arizona Broadway Theatre (ABT) last night in Peoria, AZ.
Now, this particular theatre is a dinner theatre. The night begins with a dinner that is, of course, included with the ticket price. The meal choices are outstanding. They have several choices that are included or you can pay a little extra for upgraded meals or dessert during intermission. I chose the chicken tikka masala dish and my wife upgraded to the lamb chops. The menu had a British food theme including traditional dishes like shepherd’s pie and sticky toffee pudding for dessert.
Now the best part of our night was the fact that our tickets were free, compliments of the H.O.P.E. team at Cancer Treatment Centers of America (CTCA). This team puts together all kinds of outings and events for cancer patients treating at CTCA. We have been to sporting events, plays, and day outings in scenic Arizona. This group raises funds throughout the year to make these events possible. It gives patients a chance to meet other patients and share their cancer journey and to get out of the hospital and have some fun.
As for the production itself, the sets were very creative using multiple set pieces that moved seamlessly in transition. The cast put on a great show with not only the songs but also with the choreography. We have been to several shows now at this theatre and have not been disappointed with the food or the performances. Now, a couple of years ago, I would have told my wife that I don’t like musical theatre. But, in fact, she convinced me to attend the performance of “Fiddler on the Roof” at ABT and I have been hooked ever since. I have added some level of “culture” to my personality.
Thank you so much to the H.O.P.E. team for putting this all together and giving us a wonderful night out.
There’s a new kidney cancer-fighting cocktail out there and I am about to try it out. No, you can’t buy it at your local supermarket or health food store. This one is only available from a licensed oncologist.
As a current cancer patient, I am about to embark on my sixth type of treatment in four years to battle stage 4 kidney cancer. What a statement! Four years of receiving five previous types of treatment and by the grace of the Lord, I am still alive and kicking. Now I am getting ready for treatment #6.
This new cancer-fighting cocktail I am going to receive is a combination of two immunotherapy drugs. The first drug I have previously been treated with and is called, OPDIVO. Perhaps you have seen the commercial on television with the tagline, “A chance to live longer.” The second drug is called, YERVOY. What a name, Yervoy. It sounds like something you could pick up at Russian deli.
This combination has been shown to be very effective in treating metastatic kidney cancer in clinical trials. The FDA has put this treatment in the fast lane for approval for general use for kidney cancer. That is great news for kidney cancer patients like myself, especially now during kidney cancer awareness month.
Immunotherapy drugs are designed to boost a person’s own immune system to fight cancer cells with the body. These drugs have less toxic side effects than traditional chemotherapy drugs for fighting cancer. I am very optimistic that this will treatment will be effective in beating the cancer cells into submission for myself and other patients.
Well a few days ago I had my first PET scan. No, it wasn’t done to determine whether I should get a cat or a dog as a pet. This is a scan to help my oncology team to determine the status of the current cancer treatment I am on. I usually only get a CT scan. However, I am not able to do a CT scan with contrast dye. I only have one kidney left, my left one, and my GFR is too low. So, this scan will allow my oncologist to get a better view of what is going on.
Apparently before the scan I was injected with a radioactive sugar solution. I had to wait in a special room with a very thick door and scary radioactive sticker on the door.
After a short while, I was brought into the room for the scan. It was a larger looking CT machine. I am very familiar with CT scans on this cancer journey. It usually takes 5 minutes and I’m done. This PET scan however was slightly different. It began with a short CT scan. Then the machine moved me all the way through the scanner. It would begin a series of scans from my head to the bottom of my abdomen region. Each set took about 3-5 minutes. The only problem I had was that my left shoulder began to ache from holding a “Superman” flying position with my arms during the scan. Finally, when I thought I could stand it no longer, the test came to a conclusion.
My wife and I met with my oncologist a couple of hours later. One of the aspects of being treated at Cancer Treatment Centers of America (CTCA)that I love is getting lab and scan results quickly is. We got good news, the tumors in my lungs, liver, and lymph nodes seem to be stable with no new growth. So, the plan is to continue using Cabometyx
(aka Caboazantinib) for treatment and we will scan again in 3 months. He also reminded me that he has several other treatment options if Cabometyx ceases to be effective. So far I have been on this drug for one year and it is still providing me progression free survival. Thank you Lord Jesus!
As some of you may or may not be aware, I have been battling stage 4 kidney cancer since 2013. Let me rephrase that. My wife Tanisha and I have been battling this cancer since 2013. This cancer has invaded my body, but my wife is battling it just as hard as I am. I couldn’t make it on this journey with Jesus Christ and Tanisha by my side.
Since last December, I have been receiving treatment at Mayo Clinic in Phoenix, AZ. I have received excellent care from my oncology team. However, the distance to the clinic has always been a struggle. So, I have had to say “goodbye” to Mayo Clinic and go “home” again.
Where is home you may ask? Well in for my cancer care it’s a place in Goodyear, AZ called Cancer Treatment Centers of America (CTCA). Why do I call it “home”? Well, I began my treatment for stage 4 cancer at CTCA in 2014. I spent two and half years surrounded by a staff of stakeholders, clinicians, and doctors that genuinely cared about my treatment and well-being. These wonderful folks have been with my wife and I when the cancer closed in and nearly took my life in the early months of treatment. Then they rejoiced with my wife and I when the tumors began to shrink and some of the severe effects began to loosen their grip. This team of people make a hospital for cancer patients feel more like a home than a hospital. They are like family.
Do you remember the TV series “Cheers”? Each time the character of Norm would walk into the bar, his friends erupted and said, “Norm!”. They knew him and were excited to see him enter this fictional bar. Each time I walk through the sliding doors of CTCA I can hear someone on staff say, “John!”. What a great feeling!
It is for this reason, that I am so glad I have made it back home. I was able to meet with my new oncologist this week. I was very glad to hear the treatment plan he has in mind moving forward in this fight against cancer. Once again, I can walk the main corridor of the center and meet fellow patients as we encourage each other in this journey and fight.
Houston. We have shrinkage.
My wife Tanisha and I received some great news last week concerning my treatment for stage 4 kidney cancer. The tumors are shrinking. I have been on my 5th line of treatment in the past 3 years. I am now on a targeted oral therapy called Cabometyx. I have been on this drug for 3 months now. I started off at a low dose of 40 mg and am now tolerating 60 mg dose. The scans showed that many of the tumors that are spread to my lungs, liver, and lymph nodes have shrunk by almost half of their size from a scan 3 months ago.
They also did some lab work and an echocardiogram. The test showed my heart is still healthy and functioning well. The labs showed my thyroid has a low function. They have put me on a low dose thyroid medicine for now. The next CT scan is scheduled for late June.
We are so thankful for this wonderful, encouraging news. The Lord Jesus has been faithful throughout this journey of battling cancer. I thank Him for sustaining me through all the procedures, treatments, and side effects. Thank you all for your prayers.
Well it has been too long since my last update. A lot has changed since then so I will bring you up to date. I had been receiving treatment for stage 4 kidney cancer at Cancer Treatments Centers of America in Phoenix (CTCA). As of December of 2016 my wife and I decided to change treatment centers to Mayo Clinic in Phoenix. We had been thinking of changing care facilities for several months prior to making the change.
CTCA was a great place for cancer care for my first two years of treatment. However, this last year we noticed that the changes management was instituting were not positive to my overall care.
My new oncologist is an expert in the area of kindey cancer and runs the clinical trials at Mayo Clinic Phoenix. He ordered a battery of new scans and blood tests to get a baseline to start my treatment. I had never had a CT scan using contrast before. I finally received a CT scan with the contrast and it proved most valuable in determining what was going on in my body. It showed that the cancer was more widespread than previously thought. It has now invaded my lungs, liver, lymph nodes, and left kidney.
I have been given a new targeted therapy drug to attempt to combat the cancer. It is called, Cabometyx. It was approved by the FDA recently and has had good success in clinical trials. This drug is now my 5th line of treatment. My oncologist has told my wife and I that if this doesn’t slow down or shrink the tumors my survival will be spoken of in terms of months. However, we are trusting in Christ our Lord for complete healing of this disease. I thank all of you for your continued prayers and support.
I recently had an MRI on my brain. I had been experiencing headaches and they wanted to make sure the tumors hadn’t spread to the brain. Praise the Lord! There was no evidence of tumors in the brain. The LORD is definitely at work here.
Hello faithful followers of this blog. I apologize that it has been a while since my last post.
I recently had a CT scan at Cancer Treatment Centers of America (CTCA) in Phoenix. Again, I have been treating at CTCA for two and half years for stage 4 kidney cancer that has spread to both lungs.I am currently being treated with an immunotherapy drug called Opdivo.
The scan showed that the tumors in both lungs are fairly stable. There has been some growth but it is not significant enough for my oncology team to state that it is growing. That’s good news! Yet, the scan also showed that the mass that is where my right kidney used to be is growing. My team thought that it might be pressing against my colon and intestines. I had a colonoscopy last week. Fortunately for me the colonoscopy showed that the mass is not invading that area. On a side note, the procedure was very easy, but prepping for it was not. I had to drink this solution called Moviprep on two separate occasions. It tasted like a thousand lemon flavored sweet tarts in water. Needless to say I had to stay close to the bathroom after drinking this stuff.
The next step in this process of determing what to do about this mass will be a CT guided biopsy of the tissue. I am having this procedure this week. From my own observations of previous scans of this mass I am pretty sure it is cancer. It responded to treatment with the drug Votrient and was shrinking along with the other tumors. So far some of the options to removed this tumor include possible surgery or radiation therapy. But, I will leave the final determination up to the experts and my wife and I will determine what treatment option will will take.
More updates soon.
I just had a CT scan a few weeks ago to check on the state of things in my lungs. The scan had some good news and some bad news. The good news is that the pneumonia I was dealing with has finally cleared up. The bad news is that the tumors in both lungs are growing not shrinking after 2 months of treatment using Opdivo. Again, I am being treated for stage 4 kidney cancer that has metastasized to both lungs at Cancer Treatment Centers of America in Phoenix.
My pulmunoligist has recently begun treating one of my symptoms with something called Photo Dynamic Therapy. The drug used is called Photofrin. So, the upper part of my right lung in not only partially collapsed, but it is also blocked by the tumors. This new treatment is designed to open that part of the airway up by burning away the tumors using the drug Photofrin.
I had the drug injected into my body on Monday. On Wednesday I had a bronchoscopy procedure where a cool laser was placed into my airway and turned on to activate the drug internally. Basically, the tumors are now light sensitive and by using the laser it will destroy the tumors by burning them and flooding them with oxygen. Oxygen is a natural enemy to cancer cells. I will have up to four more procedures in the next week or so to clean up the dead tissue from the soon to be dead cancer cells.
While this will help to improve my breathing and overall quality of life, it is limited to only clearing up this one particular symptom. The remaining cancer cells in my lungs will have to be dealt with in other ways by my oncologist. I am hopeful that I will be cancer free soon.
I had yet another CT scan to check on the progress of the stage 4 kidney cancer in both lungs. The scan showed no new growth in the tumors. That’s great news.
Now my pulmonary doctor wants to go in and look around with another bronchoscopy procedure. This is scheduled for next Tuesday. I take this news as my Christmas present. The cancer will not beat me.
Thank you for your prayers.
Well last week I had yet another CT scan to check on the status of the tumors in both lungs. The scan showed that the tumors are stable. My oncologist at Cancer Treatment Centers of America is going to continue my treatment using the oral medication Votrient. He has a couple of other treatment options ready to go in the event the Votrient ceases to be effective. Votrient is a targeted therapy rather than a form of chemotherapy. This means my healthy cells won’t be damaged by the treatment.
I have been learning quite a lot from a 9 part internet documentary series from www.thetruthaboutcancer.com. ICancer does not mean a death sentence any longer. It can be cured. In the last week I have been making the transition to a more plant based eating plan. I am using my Nutribullet quite a lot these days.
Since I am being treated for stage 4 kidney cancer that has spread to my lungs I also found out that my one remaining kidney has begun to lose quite a bit of its filtering ability. I met with my kidney doctor and he has made some changes to my blood pressure medications. He told me that he is making these changes to “buy me time”. I am not accepting this statement and I am believing the Lord Jesus to restore my kidney as I make the necessary dietary and lifestyle changes. Thank you all for your prayers and support.