Offering hope to those on the path behind me

Tag: #breastcancer (Page 3 of 4)

Is “Living a Great Story” enough to make the story worthy of sharing?

“You should tell your story.” I can’t count the number of times I’ve heard that. 

But what is my story and who really wants to hear it? More importantly, what can people learn from my story?

I have been hesitant to take the next step as far as writing a book or searching for places to speak about my story. In my head, I don’t have the answer to the questions that I think people want to hear.

  • How do you get up and face the day?
  • How can you keep a positive attitude about life and what’s around the next corner?

 If I don’t have a good answer should I stand in front of people who are looking at me expectantly and just shrug when the questions start?

This past week I had to fill out an application. I was applying to be a model for the Breast Cancer Resource Center’s (BCRC) annual gala/fundraising event: ArtBra Austin

One of the questions asked the applicant to write a brief bio (in 3rd person). I stared at the screen for a solid 15 minutes. I started to write something and then hit the delete button. Then I did it again. And again and again. I finally texted a friend who was also applying and asked what she wrote. As most people would, she started with “xxxxx was born and raised in such and such, Tx”. She went on to say where she went to college and what kind of career she had. 

I started typing “Kim was born in Germany”. Delete. 

“Kim was raised in the military”. Delete

Was that really the story I wanted to say in my bio? I had to discern what really makes Kim, well, Kim. What would an audience want to know about this woman walking down a runway, in a bra, with a slight limp?

Obviously I had breast cancer because you can’t be a model unless you have been a client of the BCRC. But what else makes me unique? Do they want to know the details of the limp – thank you metastatic breast cancer. Or that I have been metastatic for 9 plus years?

After much consternation, I decided to briefly state that I have been metastatic since 2010 and then wrote about my daughters (no explanation of the limp but that’s another story). I followed with a quick sentence about finding new opportunities to express myself through writing. (I mean I am trying to tell my story through this blog and I have a very rough draft of my first attempt to write fiction). 

When it was all said and done, I was not pleased with the bio but it was sufficient for what I was doing. But once again it got me thinking about what is my story and who really wants to know more. 

Live a Great Story Sticker
#LiveAGreatStory

If you were to drive around Austin, you might notice stickers on cars or even signs around town that say  “Live a great story” (you can learn more about that here). I love the simple, yet profound, words. Although I’m trying to tell my story through words, I realize my story is not about cancer or grief. My story is made up of so many more things that have helped shape who I am and how I have persevered through some of the ugly to continue to have the opportunity every day to “Live a great story”. 

My story is still being written. Maybe not eloquently. But every day I can get up, be present and ask “what will I do today to continue the story of Kim?” And maybe I don’t have to have the answer to those questions. Maybe by seeing me “living a great story” it is enough to encourage those on the path behind me that sometimes just getting up and being present is enough. And maybe, it will give them the strength to ask themselves “What can I do to continue my story?”

Now excuse me while I go order some of those stickers to remind me and those that I encounter to “live a great story” 

Bucket list memories – who are the memories really for?

Do you have a bucket list? My guess is you do. Most people have ideas and dreams of things they want to see or accomplish before their time is up. I even wrote a post about bucket lists before my husband was diagnosed with cancer.

I have some items on my bucket list. But lately, I’ve been rethinking my idea of a bucket list. I still want to do some of those things in the link above (yes, I still want to go to the Ellen show and fly on a private plane). However, instead of making these memories for myself, I have come to realize it is the memories we make with our loved ones (be it family or friends) that will be how we are remembered.  

A year after JR died my oldest daughter graduated from college. To celebrate the fact that we all made it through the toughest year of our life the girls and I took a cruise. It was a time to get away from everything. What we discovered (aside from the fact that my snoring had gotten really bad) was that we weren’t really “cruise people.” I wanted to go on a cruise because it had been on my bucket list. JR had planned a cruise for our honeymoon, but plans had to be changed and he promised me for years that he would take me on a cruise one day. Unfortunately, that day never came and I shared this bucket list item with my girls instead.

If you were to ask the girls if they liked it they would say no. However, we did make some good memories on the trip. Like the boat ride where the dolphin played in the water beside us. Or their excursion at Roatan where they played with the monkeys. The mysterious midnight WiFi that brought us text messages even though we didn’t upgrade to the WiFi package. Watching Moana on a big screen at midnight in the middle of the ocean. And even the day we stayed on the ship when most got off (definitely one of the better days).

This weekend my youngest jokingly (but seriously) suggested I take her to Vegas to see the Jonas Brothers. She turned 21 last year and she just graduated from college a semester early. At first my reaction was “I don’t really want to go to Vegas”. The last time I was in Vegas was on my honeymoon. It would be bittersweet to go just a few weeks after what would be my husband and my 27th anniversary. But the more I have thought about it, the more I realize that I should go and make memories with her. Because when we are gone, the sweet memories are what get us through the days of sadness. And who better to make memories with than those you love the most in the world. 

So I’m going to dust off my bucket list and figure out who wants to make memories with me – memories that we can share now and they can use to reminisce when I’m gone (don’t worry, I don’t think that will be anytime soon – I have lots of items on my bucket list and adding more every day).

God’s gentle reminder to take out the trash

If you are new here, welcome. Several years ago I was talking with God. I wanted a sign, kind of like a hand signal, to remind me that He is around me and in control. Like a lot of conversations, I tried to lead it in the direction I wanted it to go. I was determined my sign would be a ladybug. I think I had just read a book where a ladybug was present at many crucial times. But as I was telling God I wanted the ladybug to be my sign, He gently whispered in my ear “Butterfly.” I really didn’t want a butterfly because it sounded so cliche. But there it was. And now, God’s sign to remind me that he is here with me and in control is the butterfly. What does that have to do with a rainy Friday in January, you ask?

Lately, I have been feeling a little out of sorts. Recently, the medication I take for metastatic breast cancer had to be changed because of some slight progression. I am still getting used to the new side effects from the medication which has not exactly been a joy ride. In addition, it is the height of Cedar season in Austin, and with an immune system that isn’t quite as strong as years past, I am struggling with allergies.

Today, God reminded me He is still with me and in control…

Friday is trash day. Last night, in the rain, I was taking the trash can out to the curb. When I pulled the can away from the wall, I noticed something on the wall. I didn’t think much about it. Mostly because it was 10 PM, it was chilly and raining and I just wanted to get the trash out to the street. I had procrastinated earlier in the evening, and then it started raining, so I procrastinated some more. Since it was raining, I knew I just needed to get the trash out and I would have time in the morning to get the recycle out.

In my neighborhood, the trash pickup comes earlier than the recycle. This morning, even though it is still chilly, I caught a break in the rain to get the recycle bin out to the street. I noticed, again, that there was something on the wall behind the trash and recycle bins. With a little more light this morning, I could see that it was a butterfly.

Butterfly
A gentle reminder from God

I don’t know about where you live, but in Austin, Texas you don’t really see a lot of butterflies in January.

There it was, attached to the wall. A butterfly. A gentle reminder from God. Nudging me to move the trash out of the way.

I have all sorts of trash that I allow to pile up. Whether it is my diagnosis and the recent progression, the loneliness of being a widow, the cedar fever, disagreements with friends over small things, or just plain old procrastination – be it taking out the trash or working on my book. All of these things pile up and I find myself separated from God.

But God always finds a way to reveal himself. Today it was ever so gently by placing a butterfly on a garage wall behind a trash can.

What kind of trash do you need to move so you can see God at work in your life?

Where will you be in 10 Years? Reflections on a Decade

10 years…one Decade…Gone in a Flash

I could never have guessed 10 years ago, on the eve of a New Decade what the next 10 years would bring.

What have I learned in 10 years? Just like the Bertie Bott’s Beans in the Harry Potter books, you never know what you are going to get. I have learned to enjoy the highs and use the memories created sitting at the top of the mountain to get through the lows of the valleys. I’ve also learned that friends are there to help carry you when you think you can’t go on anymore and will help you look to the next mountain top and remind you of the view that is just over the hill.

Where will I be in 2029? I have no idea, but I plan to try to capture as many highs as I can before I get there and focus on those when (not if) I find myself in a lowly valley…

Here’s the highlight reel of the last decade…

At the end of 2009, I was married to my best friend. We had 2 beautiful daughters – one in High School and the other in Middle School. Cancer was in my rearview mirror and my husband’s business was beginning to find footing.

2011 Rose Bowl Champs – TCU

2010 – Hello Cancer, my old friend (not really, but it is definitely a constant companion). If I’m honest, I should have been diagnosed much earlier in the year, but October 8th was the date of the Stage 4 diagnosis. Definitely not one of the highs of the year (or the decade). The year brought lots of pain (from the cancer metastasizing in my bones) but we ended it on a high note (thanks dad and Judith for the trip to the Rose Bowl and thanks TCU for the win! #gofrogs).

2011 – Cancer was still the highlight of the year. Since the metastasis practically destroyed my left hip, there were many trips to San Antonio to meet with an orthopedic oncologist. And in August 2011, I spent 2 weeks in San Antonio rehabbing from a surgery that made me feel like the bionic woman – lots of metal in my hip, but it didn’t give me any superhuman powers like leaping over buildings or running as fast as a train, but I was able to walk again by the end of the year.

2012 – Seemed like life was settling back into a routine. Nothing exciting happened. But after the past 2 years, we were fine with no excitement.

2013 – Our oldest daughter graduated from High School and got accepted at my alma mater to study Athletic Training. Super proud frog mom moment.

2014 – Still riding a roller coaster, but the drops are getting smaller and the hills not so large. We learned to live with the cancer diagnosis and even began to think we had it somewhat on our terms. The medicine I was taking was keeping things in check and although I had a minor setback with my hip (unexplained pain after many, many tests). I was stable as far as cancer goes and was still here to watch my kids grow up.

2015 – Cancer once again took control of our lives. Only this time it was my husband and not me, I was still stable (not sure how with all of the stress, but thankful nonetheless). J.R. had not been feeling well for months and on September 22, he ended up in the hospital with a diagnosis of Stage 4 Renal Cancer. Friends and family rallied to support us during this time. My daughter and I even got to welcome in 2016 at the Alamo Bowl. One of the all-time greatest bowl comebacks in history. TCU defeated Oregon in one of the craziest games I’ve ever had the opportunity to see in person.

2016 – We had some highs, my youngest graduated from High School, but mostly the year took its toll on our family. My dad, who was also diagnosed with Stage 4 cancer in September of 2015, passed away on July 20th. My brother and his family had made the trek to Texas to see everyone and I’m so grateful that he was there that week. July 24th, exactly four days later, my husband passed away. The rest of the year is a blur. But, with the help of great friends, we managed to get my youngest daughter moved into her college dorm and she began her college career.

A fresh start in a New Home #BuiltaHouse

2017 – I #BuiltaHouse. – we always talked about building a house, and in March 2017 I moved into my new house. It was bittersweet and I told friends it was an anniversary present (I closed on March 1st and March 6th would have been our 24th wedding anniversary). My oldest graduated from TCU and got a graduate assistant job at Angelo State University (my husband’s alma mater!). The year did not end so well, as I spent 10 days in the hospital and had to have all of that beautifully rebuilt hip removed due to an infection. Once again friends and family rallied to get us through Christmas and the coming months.

2018 – Hey, I’m walking again. No one saw that coming. Who walks without a hip joint? This girl, that’s who. Other than learning to walk, 2018 was a pretty mellow year, but again, didn’t I deserve a pretty mellow year after the rest of the way the decade had gone?? I think so.

2019 – This was finally going to be the year. I was walking, my oldest finished graduate school and got her first “real” job, and my youngest graduated from college a semester early. Unfortunately, cancer had decided it was time to flex its muscle again and after 7 years of being stable, I had some new “spots” show up on my scans, one in June and a couple of more in October.

2020 – I will be welcoming the new decade in with some new medication to try to get back on the stable train. Fingers crossed that we can find a medication that will be as successful as the last one. I plan to finish writing a book I started in 2018 and find as many mountain top views to enjoy as I can.

What are your hopes and dreams for the roaring 20’s?

Traditions – This newest one is something I don’t really want to continue

At this time of year, our family has many traditions. I imagine you do too. We make Christmas cookies together (always a TCU stocking and a purple penguin because we don’t make black icing). On Christmas Eve we have tamales for dinner (it’s a Texas thing), we go to the Christmas Eve service and, either before or after depending on which service we go to, we watch It’s a Wonderful Life. Now that the kids are older we all gather the stocking stuffers we have accumulated and we try not to peek at what others are putting in our stockings.

This year marks the 4th Christmas without J.R., the love of my life and best friend. He passed away in July 2016. For Christmas that year, my girls and I traveled to New York to spend Christmas with my brother and his family. It was nice to not have to think about how to “do Christmas” without my husband and their dad. But it was also a little more difficult than just the first Christmas without him. Part of the trip also involved going to Washington DC to bury my father in Arlington National Cemetery. (He died 4 days before my husband). It was not the Christmas that any of us wanted and some of our traditions were put on hold as we didn’t know how to celebrate with J.R. and dad that year.

In 2017 I moved into a new house and was hoping to start some new traditions. I wasn’t really sure what they would be but we had survived all the firsts and I was hoping to make Christmas a celebration again. Instead, in November I started fighting an infection. I ended up spending 10 days in the hospital in December and came home with one leg 2 inches shorter than the other from the removal of the hardware that had been my hip since 2011, unable to walk without a walker (and even then not more than a few feet at a time) or do much of anything other than give myself the daily antibiotic infusion and watch everyone around me try to make Christmas not quite so depressing. Needless to say, we did not start any new traditions that year.

For Christmas 2018 we celebrated at home, no hospitals, no surgeries, no antibiotics, no funeral, just me and the girls and my mom. It was quiet but after the previous 2 years, it was a welcome change. I was walking with a cane and could participate in helping get things done. All in all not a bad Christmas, but still no new traditions that I had been hoping for. 

This was going to finally be the year – 2019. Both of my daughters are grown – one lives in South Carolina and the other in West Texas. As of this December, they both have now graduated from college. We could start some new traditions. Something that could be aimed toward more adult aged things. {At one point we talked about going to Ireland for the holidays, but with the move by the oldest halfway across the country, we weren’t able to coordinate our plans.} But once again my body decided not to want to play nice. In early December I started a new treatment (thanks to the progression in my spine they found on my last scans). The new meds may have had something to do with the excruciating pain that landed me in the emergency room last Monday morning. Thankfully I haven’t spent 10 days in the hospital, but I did spend 6 hours in the emergency room and another 4 hours in a doctor’s office trying to determine the source of the pain. They finally decided to give me antibiotics and with 3 days left before Christmas, I am beginning to feel like myself again. Not sure what this means for my new treatment plan (since I have stopped taking the drug that the doctor changed me to at the beginning of the month) but now I’m pretty sure we won’t be squeezing in any new traditions that we want to build on.

But one thing is certain… I’m hoping next year will be antibiotic and hospital free (this is not the kind of tradition I want to continue).  And maybe I should quit worrying about any new traditions and just learn to appreciate the wonder of the season for what it is…A Gift.

« Older posts Newer posts »

© 2025 BuiltaLife

Theme by Anders NorenUp ↑