Final Taxotere

When I last saw my Oncologist he said that I had enough Chemo and that I did really well. He wanted me to start on Radiation. I told him that my Medicare would kick-in by June and could we wait for it. He replied that I should then have at least one more Chemo to hold me over. Since the last Chemo was so brutal, I asked if I could have one more week of near-normalcy and he agreed. So, I had my last Chemo yesterday, 10 May 2013.

Since the Taxotere seems to build-up in my system, I know that the next 2 or 3 weeks will be tough. Last time I had a hard time getting the motivation to write in my blog. That is why I am trying to get through this now.
I have found that wearing my Yoga Toes helps greatly with my peripheral neuropathy in my feet. But, just like diet and exercise I sometimes forget or slack-off until I find that I need to wear them again. I try to wear them every other day. And, I drink a lot of SoBe Lifewater and grapefruit juice. I used to buy other fruit juices but they are putting artificial sweeteners in everything these days! I enjoy a soda pop now and again but they mainly taste too sweet and not enough carbonation. However, I do like Jarrito's Mandarin soda! I also have a bowl of Frozen Yogurt every evening because it seems to keep me from getting acid reflux. I know that if I don't eat a bowl for two or three nights that I get an upset stomach or acid reflux.
The past two weeks, as I have been out and about, I am always astonished to hear people tell me how positive I have been and how well I am doing. Especially when I feel so tired and my hands and feet hurt so much. But, I accept their observation. And, most of them follow it up with how the power of Prayer works so well. I mention that because I have prayed to the Lord to let my Clowning be a ministry. A ministry of Love and Smiles and a testament to the Lord's plan for all of us. But, I have told the Lord that I am not comfortable in initiating a witnessing. He has heard my prayers. When I am visiting businesses and nursing homes and shut-ins and elderly, it is they that begin talking about the Lord. He opens the door for me to give my testimony and listen to theirs. The Lord is great and he answers prayers.
From the very beginning I was never scared. At first I experienced a sadness that it might be my last Summer or my last Christmas. But, I put it out of my mind and told the Lord that I would accept his plan for me and go wherever he needed me--whether it was Heaven or here on Earth.
I prayed for those that were going through this Cancer thing and for the people that had loved ones that were going through it. I prayed for Strength and Comfort and Peace and Healing for them. I prayed that they would trust in the Lord. And, I prayed for Blessings for everyone that was experiencing heartaches and difficulties and doubts. I prayed for our Leaders in the World that they would make the right decisions to end suffering and Wars. That they would lead with compassion and forgiveness and understanding.
I wear a button that says, "Almost Famous". This is an admonition that I am just a servant. When I am Clowning, I bring smiles and humility. I am the Stumble-bum, the ne'er-do-well, the Clown who tries to get it right. I stay on "Almost Famous" or "Nearly Famous" or "Soon to be Famous". I stand on the edge, knowing that to keep something beyond reach will keep me moving in the right direction.
There are so many things that I want and need to do. I can't wait for my energy level to come back up so that I can accomplish more. My mantra everyday, though, is to at least accomplish one or two things because it keeps me feeling that I am still able to do some things. My priorities, then, are if I can't do everything, at least I should do a few things!

I am so thankful that I have my friends and family and my wife and Clown buddies and church family and Facebook friends to share with. And, I pray that I can be there when they reach out to me.
I am going to try to get a lot of clowning and errands done this weekend. And, the next two weeks I will see how this Chemo treats me. I always think that I will be able to work around the side-effects or get use to them...never seems to happen. But, I will come out the other side feeling stronger and I believe that this summer will hold a plethora of opportunities for clowning and activity!
Life is Good...Life is an Adventure !!!

Fighting Back to Normalcy

I saw my Oncologist on the 11th of April to see if I was able to handle another Chemo and, to also get the results of my most recent PET scan. Good News !!! The tumors in my neck and left lung show no uptake...which means that they are not active. And, they are shrinking. There are still some nodes in both lungs that are insignificant and the doc said they didn't appear to be cancerous. He felt that I should continue with 2 or 3 more treatments and he was also going to talk to a radiologist to see if I could benefit from some radiation to finish off the tumor sites.
Originally, when I was first diagnosed--December 2011,  after 3 biopsies (2 needle and 1 w/scalpel) there was not enough tissue samples to give a specific call on the type of cancer with which I was being  taunted. He had not wanted to try radiation at that time because if it was a certain breed of cell the radiation would have caused it to explode and spread. Now he has enough information that he can be safe with some radiation.

I had the Chemo on the 15th and everything went well. I usually am tired for 4 or 5 days afterward and then start returning to normal. I wonder if this Chemo builds up in my system though. I guess it must because I was Really Tired and Weak. I usually go out visiting during the day and try to clown around some. This time, however, I found that after being out and about for half an hour--I need to get back home and lie down. Also, there was a stomach virus that roared through the local nursing home that I like to visit and I stayed away from there. Thanks to a resident who texted me with the warning to stay away !  I have also been lax in that I have been clowning in crowds and with a compromised immune system I guess I have just been lucky. This round I had decided to be a little smarter and just visit people one at a time and one day at a time.
But, the Chemo really got to me. Aside from being very weak, on about the 3rd day I awoke in severe pain in my legs and shoulders and back and neck. This kept up for several days and really wore me out. I usually take my pain meds as needed--or every 6-7 hours. However, the only relief I got was taking them every two hours in the evening times. And, every 3-4 hours during the day. I found myself going to bed more often than usual because I was so weak and in so much pain. Although I still can't get comfortable and wake every night out of a ridiculous nightmare (not scary, just grippingly and startlingly bizarre!) It just usually signals that I am in pain and need to get up.
My hands look and feel like they have been slammed in a car door. The nails have turned brown and the skin is peeling from the knuckles. And, when I try to twist some balloons I get cuts. The literature on the Taxotere says to refrain from shaving because a razor cut could become infected. However, I only get a few stray whiskers every few days, so I use an electric razor maybe once a week.
My hair fell out after the first Chemo and it has grown back to a "peach" fuzz...but no further ! My lower legs and feet swell ever so often but as long as I elevate them and use Arnica gel and wear ankle socks, the swelling doesn't last long. Walking in socks is painful---the threads feel like wire or glass, so when I am walking around I go barefoot (inside the house). I have also noticed that I can't walk very far and it is really difficult to walk in the first place. I have noticed that my toes are curling under and maybe that is the problem with my ambulation.
My appetite is still good and my weight has remained at 160 lbs. since I was first diagnosed in Dec 2011 ! But, my taste buds change up now and again. I still rely on SoBe lifewater and Grapefruit juice (not from concentrate) and eat an egg every morning. I eat liver and onions once or twice a week for the iron and B12. I eat a lot of spinach and beets. I don't seem to like lettuce anymore. Other vegetables don't taste good to me..except canned, diced tomatoes with green peppers that I put on my spinach and eggs (when I microwave the egg---I usually eat boiled eggs). I still enjoy frozen fish fillets. And, salmon--as long as I know where the salmon came from. I'm losing my taste for snicker bars and spearmint lifesavers. I still like cinnamon rolls and tangerines. I like Kona coffee with a teaspoon of Ovaltine. I eat bratwurst now and again if I can find the right mustard (always a challenge!).
When I approached my Doctor about my various complaints, he assured me that they were the result of the Chemo. That is comforting in a way. It means that after the Chemo that they should go away. A lot of the complaints that I have would normally be classified as having to do with aging...but not mine, ha. So, I guess I am missing out on the growing old creaks and aches.
I still try to accomplish some small tasks every day. I think that it is vitally important to stay active and try to do constructive tasks. If one just gets up and eats and decides it is too painful or hard to do anything and then goes back to bed--well, your body will just get weaker and your self-worth will slide and you become a great candidate for depression. I would rather attempt something and find that I am unable to finish it than to not try at all.
Speaking of which...I am working on a new hat:

All in all I am winning this battle---with the help of excellent Medical staff and a wise and caring oncologist. My friends and family along with their caring and prayers have helped immensely. My Church is always there for me--even when I can't attend as regularly as I would like.
I can see the light at the end of the tunnel and I am making sure to put graffiti on the walls of the tunnel and continue to dance along the tracks of said tunnel !!!
Life is Good....Life is an Adventure !!!!!!!!!!!!!

I've come this far...

Back when I was diagnosed with NSCLC Stage IV in January, 2012 I briefly entertained the thought that it would be my last summer and that it would be a safe bet that I might not live to see another Christmas...but, I quickly told myself to stop thinking about such backward, negative things. I have made it this far and so be it.

                                     My good friend, Santa...I'll put in a good word for you!

I went back to Work a few weeks ago! I am working 2-3 days a week and it is going pretty good. They are very accommodating. I don't use my condition to slack-off, and they keep an eye on me to make sure that I don't over-do things or falter. It mainly involves light janitorial duties and driving a shuttle (car or van---not a spaceship!).
The other morning my car wouldn't start when my shift was over so I had to get a jump. On the way home I dropped the car off at the local mechanic which is just 3 or 4 blocks from my house/domicile. I decided I would walk home even though I had just finished an 8 hour shift. One thing I neglected to factor in, though, was that I had a hill to climb. So, I started up the hill and halfway into my trek, my legs gave out. It felt as if I had just finished a 26 mile marathon. I wasn't out of breath. My legs just felt overly tired and ready to buckle. I continued on and when I reached the top of the hill where it was level ground, I felt better. I could see a park bench (there is a park on the way) and I decided to try to make a landing on it. I felt that if I were to collapse that, even though it was 27 degrees Fahrenheit and  a lot of frost on the ground, the landing would be a bit softer than sidewalk concrete.
My phone began to ring. I soldiered on. Made it to the park bench and rested a few minutes before calling my wife (who had been ringing me). I told about my predicament and let her know that I would continue my journey as soon as I recovered well enough.
My chemo, the Alimta, works in the manner of starving cells that ask for nutrients. The Hill was over the limit of my apportioned energy. I waited 20 minutes, drank a bottle of SoBe Lifewater,  and, then continued my way home, knowing that should I collapse that it was rush-hour and, this being a small community, that someone would notice me and come to the rescue.
I made it home.
I had experienced the effects of the Alimta before when I was raking leaves, trimming trees, painting the house or climbing on the roof to clean the gutters. I had learned to pace myself. Of course, climbing the hill was a foolish learning experience. As I said, I wasn't out of breath and my heart rate did not go up. It is just that Fatigue sets in rapidly and the recovery time is lengthy.
Aside from that incident, I am doing pretty well. I have a severe, irritating pain in my neck that concerns me but I am not worried---just snappy and agitated. I have a PET scan scheduled for the 27th of December to see if any cancer has come back. The pain is in the same place at the crook of my neck and collar bone/shoulder that I had the neck tumor. And the lung tumor radiated pain to the same place and also to my shoulder. But, this may be a pinched nerve from driving so much. I have been trying to analyze my driving habits to see if I can prevent it. I seem to be able to move my neck fairly normally, but, occasionally I get a sharp stabbing pain that jerks me low. And, the pain is also a chronic, sharp nuisance consistently. My pain medication helps, but I try not to take any until the pain is absolutely, overwhelmingly an activity stopper. Even then, the medication only brings the pain down to a dull roar.
I say that it doesn't worry me--because it doesn't. It just makes me angry that I can't enjoy my normalcy!  The only thing that I am on guard about at this point is the cancer coming back and spreading to the brain. I don't care if it returns and spreads to the liver or kidneys or bone or somewheres (sic) else...I just don't want it after my brain because I need my mind to enjoy a good book or podcast or sight gag !
Anyway, Christmas is coming up and I need to start on my cards and shopping. No procrastinating!
I have some clown gigs coming up this week and, of course, work. It's nice to be back in the swing of things. Back in the thick of it. I want to devote more time to some Mars stuff, too. Tech Fest is coming up in February and I also want to give some presentations at the Library. So much to do. I will pace myself...
Also, I am attending a Bible Study about Intercessory prayer...we are involved with a book called, of course, Intercessory Prayer by Dutch Sheets. It is an extremely interesting, insightful and inspiring read. Prayer is a very important part of my life and always has been. And, Intercessory prayer is so important. Too often we might be overly concerned with our own problems and neglect some other areas. Praying for goodwill and blessings for others...praying for understanding and guidance...praying the right path and the right knowledge. I have always felt that constant dialogue with God and communication leads to more satisfying prayers. This Bible study sheds light on mediation and meetings and representation. It is an opportunity to be aware of, not just the theological attitude of prayer, but also the understanding that prayer is such a spiritual journey.
Monday I will be clowning around for the Rotary Springfield Christmas banquet for 140 children with multiple disabilities. I have been attending for 5 or 6 years and it is a wonderful time. Several clowns from our Alley will be there and we really have a lot of fun!
Life is Good...Life is an Adventure !!!