Showing posts with label cancer journey. Show all posts
Showing posts with label cancer journey. Show all posts

Thursday, July 21, 2022

Parallels in Life

As many of you may remember, I took up the sport of Dog Agility after my recurrence. My dog, Amber, who we believe to be part Jack Russell was full of energy and needed an outlet for all the energy. At the end of puppy obedience class, the instructors, Joe and Rebecca, put out some agility obstacles. Amber ran right through the tunnel. She looked like she would be great at agility. But I wasn't sure if I was ready to start something new. I just had a recurrence the year before would I get started and have to stop for another recurrence? Did I have the energy to learn a new sport? I was experiencing chemo-brain, would that impact remembering the course layout?   For those who aren't familiar with agility,  handlers move around the course directing their dog to take different obstacles. Some handlers can work at a distance from their dog and the obstacles and others like myself need to run the course as the dog runs over , around, on top of and through the obstacles. 

At the same time I came up with reasons why I shouldn't try agility, I thought that maybe something unrelated to cancer would help me recover from the past few years where my life was laser-focused on cancer and treatment. Maybe I needed an outlet from cancer as much as Amber needed an outlet for her high level of energy. 

I know that taking part in agility is a choice I could make and having cancer was not my choice. But there are parallels in how I approached agility and how one could approach cancer treatment.

Amber and I took lessons for a number of years before our first competition. For one piece of equipment the teeter, which is like a see-saw, the dog had to run up to the middle and down the other end causing it to drop to the ground. When other dogs ran the teeter it made a thumping sound when it hit the ground. Amber who does not like loud noises wanted nothing to do with the teeter. If the obstacle didn't move - like the dog walk or A-frame she had no issues.  We slowly trained with it to overcome her fear. I would give her treats to run up to the mid point. Then I would give her treats as I controlled the decent with my hand. I needed her to trust me that it was OK. It took us almost a year for Amber to not hesitate running the teeter. Finally she felt comfortable



When I started my initial treatment I was fearful of how treatment would affect me. How long would it take me to recover from surgery? How would I be affected by the chemotherapy treatments? Would I be tired? Would I feel nauseous and vomit? Would I have bone pain or neuropathy?  I wasn't comfortable with what laid ahead. My chemo nurses and gyn oncs walking me through the process, providing me the necessary nausea medications, answering my questions while assuring me along the way. Did I want to stop after  6 initial treatments? I sure did. But I trusted that the way to ensure the best results was for me to have three more cycles.I felt comfortable with what I had to face.

As we got closer to entering competition we went to a few trials just to scope out the routine of crating with other dogs, signing in, getting to the line on time and getting measured. I volunteered to work the rings so I would see how things worked.  Amber and I did the best we could to prepare for our first competition. 



After I finished my initial treatment, I went back to work. I learned more about ovarian cancer, how to be empowered to make a difference and started volunteering with my local ovarian cancer non-profits so I could be on top of ovarian cancer treatment. I was preparing for whatever the future held for me.

Our first competition and those that followed were not uneventful. I had to deal with different occurrences in the ring. There was the time the helicopter flew over the outside course and Amber hid in the tunnel and would not come out. Or the time she got to the top of the A frame and just stood there watching the dog in the ring next to us.  We were certainly over the course time on that run. Or when chutes were used in competition and she tried to enter the obstacle through the closed cloth end. Or there were the many times she got on the table and then off to smell the cone with the obstacle number on it. 

But there were times when everything went right. We Q'd. We had no faults and finished below course time. Amber even qualified for a few titles. 


When I recurred I was prepared for part of the process but as in agility I had to deal with a number of things. I had an  allergic reaction to carboplatin and ended up in the hospital. I was upset I had lost my best choice to get me back in remission, carboplatin. I had to postpone treatments when my platelets were low. The additional cycles of taxol made my neuropathy worse and caused my toe nails to lift from their bed.  But I dealt with each thing as it came my way. It was not always easy and not without shedding some tears but I did finish treatment.

 An agility friend shared this on Facebook. While written for the agility community I see parallels with what cancer patients experience.

" maybe we ought to take a step back and look at, well, most of us who are there achieving things you can’t see on paper. Those who gather the courage to step to the line for the first time. Who put their embarrassing moments behind them and then do it again. Those who struggle to cope with their dog’s stresses and their own anxieties, yet come to understand and accept them and get back out there again anyway. Those who, little by little, find ways to improve. To celebrate the first time their dog completes a course, or allows a rear cross, or pays no attention to the judge. Or even the first time they didn’t get lost on the course.

What really, truly matters aren’t the letters or a piece of parchment paper. It’s the memories we make.
 
We haven't competed in agility in over a year due to Amber's health issues including her recent diagnosis with Cushings disease. We miss the camaraderie of the other dog and handler teams and the fun times running the courses. But we are happy to celebrate her 12th birthday this week. 

 

 
Dee
Every Day is a Blessing!

Sunday, April 24, 2011

Spending Time

For the past few days I have spent hours in church. Not just the normal one hour Mass on Sunday but the services on Thursday, Friday and Saturday known as the Easter Triduum. Attending those services gave me time to reflect on my cancer journey and my faith.

On Thursday I attended the Mass of the Lord's Supper. The Mass was bilingual, Spanish and English and I loved listening to my fellow parishioners singing hymns in both languages. I watched as the chrism for the Anointing of the Sick sacrament was brought to the altar by a parishioner with very little hair on her head but a look of reverence on her face. I thought of the times I received the sacrament. I was anointed with chrism before both of my cancer surgeries. Sitting in the pew on Thursday, I once again felt the grace and calm of the anointing. There might not be a scientific study to prove that grace from the sacrament calms and strengthens . What I do know is the calm and strength I felt facing my surgeries.

Friday afternoon I attended the Passion Service with Nick. We walked into church as the dark clouds and drizzle began. Was that what is was like as Jesus hung on the Cross? After reading the Passion, a group of parishioners walked a large wooden Cross to the altar. Holding it upright the group invited parishioners to come forward. Row by row parishioners- young and old and some in wheelchairs and walkers came forward and genuflected or gave the Cross a light kiss or gentle touch. The church was full so it was a long wait to get to the front of the line and revere the Cross. I expected that I would start to get antsy waiting. But not this time. The waiting was OK. I thought of times after my cancer diagnosis that I needed to wait - for my chemo to begin, to see my doctor, for my scans, the hour I layed in the PET scan machine having my test done, for the pains in my legs to stop, for my fingers to feel less numb, for my appetite to come back. Sometimes you can't rush the process you just have to wait - patiently. And so I sat. I thought about My Uncle Bruno, my Aunt Dora, a friend who was recently diagnosed with breast cancer and another two friends who have had their ovarian cancer recur. I felt sad and once again in church my eyes filled up. And I prayed for all of them. And I continued to wait.

I thought about my clear scan results, my future grandson, being accepted to a special cancer advocate program and the speech my son, the crew coach, gave at his crew dinner. Life can be tough- Jesus knew that but it can also be very good. So I said a prayer of thanksgiving. It was my turn. Well worth the wait! Two hours later we quietly walked out of church.

We decided to attend the Easter Vigil Mass on Saturday night which meant spending even more time in church: 2 and a half hours to be exact. Not really a long time when you think about the time I was in treatment and was in bed due to fatigue. Two days per cycle I never left my bed. Two times fifteen cycles ( if you include my recurrence) makes thirty days. Those thirty days equal seven hundred and twenty hours. During those hours and many more the chemotherapy drugs were killing off the cancer cells. Two and a half hours celebrating the Easter Vigil was my spiritual medicine.

Happy Easter!

Dee
Every Day is a Blessing!