Offering hope to those on the path behind me

Tag: thrive (Page 1 of 3)

Beyond Thriving in the Chaos to Thriving Every Day

This week, I attended an online writing summit. I had no expectations of what I might learn. I found out about the summit on my Instagram feed. They had a free registration, and I thought, “Why Not? I don’t have anything to lose.”

First, the entire summit was filled with amazing presentations, and I received excellent insights from each one I watched.

One session in particular made the entire summit worth my time investment. The presentation was titled “How to be a writer when you have a chronic illness.”

You might think “Is metastatic breast cancer a chronic illness?” Believe me when I say I have seen and had this debate. But, for the purpose of managing time and spoons, there are many similarities between metastatic breast cancer (especially after living with it for fourteen-plus years) and chronic illness.

The presenter, Sandra Postma, offered a different way to think about being a writer when living with a chronic illness. For example:

Write when you can. Write where you can. If you can’t write every day, be gentle with yourself. More importantly, she reminded the attendees, “We are worthy of living our best life.”

That statement made me search out her Instagram account and immediately follow her. Scrolling through her posts, one in particular stood out:

“Can I Thrive with a Chronic Illness? YES!”

In the caption, she asked the simple question, yet extremely difficult question

“What does thriving mean to you?”

That question haunted me all afternoon and evening. The next day during a live write-in session I unpacked the question further in my journal.

I realized I had never redefined “thriving” for myself since I was diagnosed with cancer. Or maybe not since J.R. had died.

Society tells us thriving may include a happy marriage, two and a half kids, a dog (or cat if that’s your thing), a well-paying job, and a nice car(s).

We were thriving as a family when I was diagnosed in 2003. I even continued to work during the original diagnosis at the well-paying job. We put cancer behind us after all of the chemo and the radiation. Even after taking Tamoxifen for 5 years, Cancer was our past. We were still thriving in the good old American societal way.

After I was diagnosed with metastatic breast cancer, we had to re-evaluate. At that point, my idea of thriving was living to see our daughters graduate from high school. With a median survival rate of 36 months, I would be lucky to see our oldest graduate.

After a few false starts with medications that didn’t work for me, we finally found one that was keeping the cancer cells in check. I had already watched our oldest graduate and I was well on my way to watching our youngest graduate from high school.

Then renal cancer decided to steal our version of thriving. We switched our idea again, now we wanted J.R. to see our youngest graduate from high school.

Graduation came and went. We both saw her graduate. I wouldn’t say we were thriving. Just a few months later, J.R. passed away. What should have been our time to thrive as empty-nesters was gone in a flash.

Over the past eight years, I have been living (not thriving) while waiting for the next thing to happen. I can’t say it wasn’t without cause: an infected hip prosthesis and subsequent surgery, progression requiring a change in medication, a broken femur, both of my in-laws passing away from cancer, spontaneous fractures in my spine, more progression and another change in medication, a hospital stay due to complications from the new medication, another change in medication, neuropathy from the medication, culminating in another change of medication, and finally four surgeries this year related to side effects of medications that have kept me alive for the past 21 years.

“What does thriving mean to me?”

For me, the definition of thriving is not how society defines it.

Kim’s idea of Thriving is a path to discovery.

In eight years, I have shied away from the opportunity to discover who Kim is. But Kim is more than a widow, a mother, or a daughter.

Through this process, I have defined Thriving as the freedom to discover who I am: what I like, and what I don’t like. Furthermore, it is a chance to shed my Enneagram 9 sloth-ness (as much as possible) that I have embraced like a badge of honor over the last eight years as a protection and recovery method.

If you know me, you know I love a good movie reference. I am proclaiming my Maggie Carpenter (Runaway Bride) era. I have already discovered I like fried eggs, preferably with a side of bacon, hash browns, and possibly some pancakes.

Now that I know what thriving means to me, I am ready to find my true, authentic self.

So tell me, what does thriving mean to you?

The Isle of Grief – Acknowledge, Accept, Find a way off

I feel like I have been living on a deserted island….The isle of Grief.

The Isle of Grief

This weekend marked 11 months since my life drastically changed. The first few days are a blur. There were so many things that had to be done immediately. I didn’t even realize the adrenaline that was cursing through my body to be able to make the decisions and get things done.
Friends were there along the way holding my hand and helping any way they could.
Then the funeral came. The numbness from the shock (and inability to sleep) helped me get through the funeral and the reception. So many people offering condolences and holding me up (some quite literally). It was an exhausting day.
Over the next few weeks friends called and texted me just to check in. Some just sending a heart to let me know they were thinking about me (a sweet friend who had gone through a loss of her own suggested that idea to close friends).
So much change was happening in my life I hardly had time to let the grief sink in. Less than a month after my dad and my husband passed away (four days apart), my youngest daughter started her freshman year in college. I also began house hunting and signed a contract to build a new house before a month had passed (yes, people tell you to wait, but believe me when I tell you I had a lot of friends telling me that my situation was different, and it was).

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Get up and Walk? Are you crazy?

Modern medicine still amazes me!  Here I was with a brand new rebuilt hip and the very next morning the physical therapist tells me it is time to get up and walk.  Just like that. Who did she think she was, Jesus? She might as well have said “Get up! Pick up your mat and walk” (John 5:8).

I looked at her like she was joking, the look she gave me said she wasn’t. Here I was less than 24 hours out of a major surgery and I’m wondering how in the world I’m supposed to get up and walk. I hadn’t been able to walk for the last 10 months.  It was a good thing for pain medications!

My first attempt to get up and walk I made it all the way to the bathroom door. All 5 steps. Wow. That was exhausting.

The next time I was able to get as far as the hospital room door. In other words, I added about 3 more steps.

The physical therapists kept coming back, it didn’t matter if it was the same one or not, they all made me get up and walk. Granted it was with a walker, and they were holding onto me. But those first steps were some of the most exhausting steps I’ve taken in my life.

Surgery was on Tuesday, and by Saturday the doctor was telling me it was time to go to rehab. I will tell you I was excited to get out of the hospital, but I was terrified of how much more they might expect of me at the rehab facility.

Sitting in a wheelchair after arriving at the Physical Therapy Rehab facility Sunday August, 8. 2011.

Sunday morning, it was time to head to rehab where they would teach me to walk again.

They transferred me via ambulance. Check that off the bucket list! Not sure that it was ever on my bucket list, and honestly it was the most painful ride ever. I think the driver managed to find EVERY single pot hole in San Antonio. There were not enough pain medications for that trip!

We finally arrived at my new home for the next few weeks. I was never so grateful to be out of a vehicle.

I guess the therapists at the new facility decided an ambulance ride through San Antonio was enough torture for one day. I met my nurses, got settled in my room and slept really well that night.

If you have never spent any time in a physical therapy rehab facility, let me just say I was significantly younger than 99% of the people staying there.

After being there for a few short days, it became obvious that many of the other patients were not happy about being there. When the nurses and nurses aides came to my room and looked worn out. My husband (J.R.) and I talked to them, asked them about their families, found out their stories. They became our family. I like to think they left my room feeling a little refreshed because we weren’t yelling at them. J.R. had brought a bag of silicone bracelets our church wore all summer they were red and said “God is Big Enough”), he gave one to each of the nurses/nurses aides that came in my room. Many of them wore the bracelet the entire time I was there.

I spent 10 days in the rehab facility, but the people I met there made a lasting impression on me. I hope we made a lasting impression on them.

Time to go HOME!

 

I WILL find a reason to Smile

2016 was going to be all smiles and celebrations. My oldest daughter turned 21, my youngest daughter graduated from high school, and I celebrated half a century on this earth – 13 of them as a cancer thriver.

Last summer my girls and I plotted to talk my husband into taking a family cruise. You see, my husband had promised me for 20+ years that he was going to take me on a cruise one day. We were supposed to go on one for our honeymoon but other factors prevented that trip. Ever since I have waited for my cruise. 2016 sounded like a great year to celebrate all of the milestones in our family.

January was an optimistic month. My husband received good news at MD Anderson. The tests showed that the trial he was participating in was working and his cancer had slowed down. In fact the doctor was extremely optimistic about his status. The cancer was not growing and had become stable.

February that door was slammed. We were not able to continue going to MD Anderson for him to receive treatment. That’s a whole other story, but the long and short is the insurance company no longer contracted with MD Anderson so now we had to pursue options elsewhere.

March came and we found ourselves at the hospital at the end of the month. There was fluid in his lungs and he was having pains in his back. We found out the cancer had spread to his brain and his spine. I thought those were the longest 2 weeks of my life. I was wrong.

He stayed in the hospital almost 2 weeks, and after much dialogue with the doctors and the hospital staff, we were able to go home.

May came and we celebrated my nephew’s graduation from college. It was such a great feeling that we were able to travel together. We spent a lot of special time with family. Things were looking up again. His spine was feeling better and he got a short break from brain radiation. He was enjoying life a little.

By the middle of May he was back in the hospital. His lung capacity could not keep up and when we left the hospital we had oxygen tanks that would be his new lifeline. Every time a new diagnosis was shared with us, the wind in our sails would slow down just a little. Leaving the hospital with oxygen 24/7 was scary, and he set a goal to live to see our youngest graduate from high school on May 27th.

May 27th arrived. We had a pre-party at our house for family and friends. The 2 of us, the oxygen tank, and many friends and family watched my daughter walk across the stage and receive her diploma. It was so good to seem him out on the field hugging her and celebrating her accomplishment.Kaci graduation 2016

June rolled in and we were back to hoping things were turning to the positive. We were talking about goals. Setting new goals. Even writing a book together.

Before I knew it July had arrived. On the 4th my daughter turned 21. On the 7th I turned 50. We celebrated both birthdays by going to a baseball game and having a beer. Unfortunately, the heat was too much and my husband decided he did not feel he could go. We celebrated those milestones without him.

July 17th. He had a restless night. Early that morning I suggested we go to the emergency room. He agreed. Unfortunately he was too weak to get to the car on his own. We had to call for an ambulance. We spent the next few days at the hospital and learned that his latest scans showed more progression of the ugly cancer. The doctors suggested that we make arrangements with Hospice.

We came home on July 19th. I believed we would be making friends with the hospice nurse. I believed I would see them regularly over the next weeks. I have heard many great stories about people living for months on hospice or even better “graduating” from hospice and finding a new goal to look forward to.

Unfortunately, none of that came to fruition. Saturday night it became obvious that I would not be developing that long-standing relationship with the hospice nurse. My best friend and husband passed away on July 24th.

It has been one month. Life for the rest of us continues on. It is not the life I envisioned. It is not the life I wanted. But it is the life I have. He sent me a last love letter, with the help of his beautiful cousin, In it he said “I hope you find a reason to smile.” Everyday I try to find a reason to smile. and when I do I know he is smiling too.

Now we have the opportunity to make the rest of 2016 a good year. While I know everyday will not be good, I can find some good in every day.

And yes, I am going on a cruise before the end of the year!

What does it mean to be Strong?

I have always thought I have to be the strong one for everyone around me.
Last night I learned being strong is not what I was really doing.
I have a habit of taking on everyone’s troubles as my own. I care deeply for those around me, therefore, I take on their problems and try to fix them. If I can’t fix them, I worry about how to fix them. I carry this weight around like an anchor. The more I take on, the more the anchor sinks to the bottom.
From the outside, I am able to give the impression that I am gently treading water, but on the inside, the anchor is pulling me down into a whirlpool I can only escape from if I let go of the anchor. But I refuse to let go (cue the song from Frozen, yes, I hear you singing along).
Why do I do this? How can I learn to be strong by letting God take my anchors.
This morning I listened to a short meditation (you can the meditation here). The meditation asked me to see a bright light and let it surround me. The light, representing God was enveloping me. As I visualized the light the old children’s song played in the background of my mind “This little light of mine I’m going to let it shine.” As the words played over and over in my mind, and I tried to visualize the light, I found myself wanting to rewrite the words.  It is NOT a little light. It is as LARGE as we can imagine and then continues to grow to proportions that are beyond our imagination.
After the brief meditation, I took my morning coffee and a small devotional book and sat out on my deck. The devotional was a book I hadn’t picked up in months.
Not normally my habit (I usually start at the beginning and read everything in order), I opened the book to a random page. The first words I read were “you are in Me and I am in You” (from Jesus Today by Sarah Young). As I read further it said “you are filled with my Divine presence.” I’m constantly amazed by the presence of God in our lives when we take the time to invite him in and we are willing to listen.
So today I begin a new way of thinking about being Strong. I am letting go. Letting go of things that I have no control over. I am giving that anchor that has been weighing me down to God. He is so much more capable than I am.
I am going to ask the Light to come in each morning. And each night, knowing that I will resort to my old ways, I will ask God to take the anchors I have picked up along the way and tell him Thank You for taking the burden off of me.
What anchors are you carrying?
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