Offering hope to those on the path behind me

Tag: #lifer (Page 2 of 6)

Enduring the Pinktober Fest

enduiring-pinktober

As you might have guessed, Pinktober is not my favorite month. Every year when October rolls around we are inundated with Pink Ribbons and Facebook posts asking us to do something silly like posting the color of our underwear or other such foolishness.

I will admit for the first 7 years after my original diagnosis I was sucked into believing that it was all a good thing. I have tons of breast cancer awareness shirts, cups, mugs, wristbands, etc that I purchased over the years, or that others purchased for me.

I fell into the trap of thinking I had done everything right and that because of that I was GOOD. After 7 years, I had been lulled into believing that I HAD BEAT CANCER.

If you have read any of the previous posts, you know I did not BEAT CANCER.

what-stage-4-looked-like

In August 2011 I had surgery to repair my hip destroyed by metastatic breast cancer. This photo is in the rehab hospital. Note I’m sporting the Pinktober shirt.

Just as I celebrated 7 years of being cancer free, I got the phone call.

My journey took the Stage 4 Exit onto a new cancer highway.

Last week was my cancerversary for my stage 3 diagnosis 13 years ago. This week I can celebrate my Stage 4 cancerversary. The celebration is that I am still here to share my story. But it is a bittersweet celebration. One that I wish no one would have to celebrate. Continue reading

I’m OK (and that is OK)

im-okIt is OK to just be OK

The other day an acquaintance asked me how I was doing. If you know me at all, you know my standard answer to that question used to be Awesome!

Now when I’m asked, my answer is OK.

She looked surprised and said “that doesn’t sound good.”

My first thought as she seemed surprised with my answer was “How would you answer the question if your husband (and father) had just passed away 2 months ago?”

I’m not Awesome. I still cry for what seems like no reason. I am still adjusting to living without my best friend. In the past 2 months my life has completely changed. Some changes were expected (like my youngest daughter heading off to college), some were anticipated, but unexpected (like my husband and father passing away just 4 apart from one another).

I am learning how to live alone for the first time in over 24 years.

Cut me a break if my response is that I’m OK.

OK is pretty good right now.

If I answered honestly, you might not want to hear the dark details of the sleepless nights, or the trips to the store so I don’t feel alone. You don’t want to know that the smallest thing can make me cry…like hearing a song, or something I read, even a commercial for something that he hated or loved.

I know that I am here, he is gone and (I believe) there is something God has planned for me, but my life today is not Awesome. I am working towards it, and I want it to be Awesome, but right now I am OK with being OK.

We all see things differently. Allow me to experience my grief in my own way. Do not push me to grieve the way you think it should be done.

Do not push me to grieve longer, or to grieve less, or to grieve in any way that I am not comfortable. It’s mine and I will do it as it fits me.

This is my grief, and I am OK.

One day my answer may change to better, good, great….even Awesome.

But not today.

And that is OK!

 

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!

Hip Hip Hooray – Time to get a new Hip

I had a new deck, now it was time to get a new hip.

Now that I had the hysterectomy, it was time to move forward…again.

The hysterectomy was done so I could take Arimidex, another hormone blocker for ER+ breast cancer. This was going to be easy. All I had to do was take 1 pill a day for the rest of my life. Easy.

Oh, but wait, there’s more. Since I had bone metastasis, I also got to have monthly infusions of Aredia. It’s purpose is to strengthen bones in an effort to keep the cancer from attacking them and to keep from having any bad breaks.

In the meantime, now that the hysterectomy was behind me, I was taking the hormone blocker, and getting the monthly Aredia infusion, it was time to find out if I would ever be able to walk on my own again. In December, my radiation oncologist and my regular oncologist recommended the same local hip surgeon. With glowing recommendations I was able to get an appointment with one of the best hip surgeons in the area.

My husband and I had hope based on all of the positive recommendations. Unfortunately, when we met the doctor, the air was knocked out of us – Again.

I need to give credit to the surgeon. He was very nice and completely honest about his abilities. After looking at my scans and reading the reports he told me “I’m sorry. I can’t help you. There is too much damage.”

You could have knocked me over with a feather. The wind was gone from my sails and with only one hip, I wasn’t very stable (ha ha).

As I was still trying to catch my breath, he followed up by saying “There are only 4 or 5 surgeons who can help with this. One of them happens to be in San Antonio. I’m going to send your records to him.” In fact, it was better than that, he was actually friends with the doctor and called his office before we left.

In 2011 we met my orthopedic oncologist. He was amazing. He looked at the scans, reports and x-rays and started talking about options. My head was spinning. I don’t think I really understood anything he said. Thankfully, my husband was there and understood the language (he majored in kinesiology in college). What I remember most is the equipment he wanted to use was not available in the US yet. It was stuck in a government approval process.

I was excited he was talking about options, and then, just like that, the air was out of the sails again.

We made a follow-up appointment and drove home. Over the next few months, we drove to San Antonio several times to meet with the doctor. Each time he would talk about options. I was beginning to get a little frustrated, wondering if I would be using a walker the rest of my life. Finally, during our trip in July, my husband and I were wondering aloud in the car ‘Why do we continue to drive two hours to see this doctor if there isn’t anything he can do?’

When he walked in, it was as if all of those other appointments had been his way of processing everything. Instead of us asking why we kept driving to San Antonio he shocked us by saying “It’s time. When do you want to have surgery?” What? Did that just happen?

After the shock wore off, my surgery was scheduled for August 3, 2011. It was time to get a new hip!

 

 

Community is an amazing gift

We have belonged to an amazing church community for many years. If you don’t belong to a giving community, I strongly suggest you find a group that you can resonate with. They can make all the difference in the world to you, both emotionally and physically.

We decided to have the surgery to put my body into menopause. The doctors both agreed that would be the best course of action. The surgery was scheduled for mid November 2010.

What does this have to do with community?

Let me tell you a story.

Every year in November our church youth group plans a Fall Mission Trip. Even though I call it a trip, it is done over a weekend, therefore they look for local needs in the community. The kids and adults work all day Saturday, then spend the night at a local church. It is a great weekend for the youth and the adult volunteers to experience what it is like to give back.  Everyone from middle school to high school is invited to participate and they work at different locations throughout the community. Close to 100 people participate in this event each year.

As a family, we had participated in this event with our kids before. This year, it was our turn to be a recipient.

While we were at the hospital, my husband received a phone call. One of the projects scheduled for the upcoming weekend Mission had to be cancelled. Scrambling to find a project for 20 or more kids and adults to work on, the church leaders reached out to my husband. They wanted to build a deck on the back of the house that would have a ramp to allow me access to the backyard.

Let me just say, it is so much easier to be on the giving side than the receiving side, especially for my husband.Deck Youth Mission

His first reaction was NO. We would just be getting home from the hospital, and he did not want me to be bothered by the noise and chaos of the volunteers working just outside our living room.

A plan was hatched.

When God puts people in your life to offer you a gift, He does not let you say NO. One of our friends from church offered to come to the house, pick me up, let me sit in her recliner and pamper me at her house while the youth worked at our house. It was an offer we couldn’t refuse.

Saturday morning, I was whisked away before 8 am. A little later, more than 20 people were at our house building, cleaning and painting. A beautiful deck was built, our yard was raked and mowed and the ramp my father-in-law had built for our main entrance was painted with non-slip paint. These kids and adults did an amazing job.

I’m not sure it was God’s plan that I have a beautiful deck. More likely God’s plan was to remind us that we are all part of a loving community and that community is ready and willing to help if we just ask (or even if we don’t).

A huge shout out to the youth and families at First United Methodist Church Round Rock. I am so thankful to have this community of friends in our lives.

« Older posts Newer posts »

© 2024 BuiltaLife

Theme by Anders NorenUp ↑