Sunday, January 10, 2016

My Christmas List


 
  Do you remember writing Christmas wish lists as a kid? In your neatest handwriting, you painstakingly wrote that perfect list of things you longed for that year.
 
It's surprising how the lists change as the years go by.
 
The older I get, the fewer things I put on my Christmas list. As I grow older, my Christmas list gets shorter because the things I want most can't be bought. In fact, the things I wish for aren't things at all. Maybe that's why Amy Grant's song "My Grown Up Christmas List" resonated with me and so many other people this year.
 
If you are unfamiliar with the song, here are a few of the lyrics:
 
"No more lives torn apart,
That wars would never start,
And time would heal all hearts,
And everyone would have a friend,
And right would always win,
And love would never end,
This is my grown-up Christmas wish".
 
Too often, we are caught up with wishing for material things in life. Christmas is not JUST about gifts and "getting". It's about a whole lot more than that! It's about things that are important...things like time, memories and experiences. Those are what people want most.
 
Wouldn't it be great if we could make those three wishes last all year? I believe we can!
 
We can make time to do something with a family member or a friend...lunch, a cup of coffee, an ice cream cone. How about taking in a movie or a walk in the park this summer or delivering a batch of cookies to someone who may need a friend.

Spending time making memories could be carried out as a year long wishTake a picture or two to remember the day, the moment, the fun. Make that memory! 

 Give someone the things they desire the very most...your time, good memories, and fun experiences. It would be time and energy well spent and your family member, friend, or acquaintance would be thrilled. And it would be so rewarding for you too!
Now that the holidays have come and gone, I have had time to reflect on this special season. I really love the Christmas songs, the lights, decorations, and the tree, but most of all, I treasure the time spent with family and friends, the memories made, and the shared experiences.
Now my challenge is to make these three wishes last all year long!
 
My Grownup Christmas List:
 

 

Wednesday, December 16, 2015

Feeling Grateful


The Thanksgiving holiday brings the spirit of gratitude and thankfulness more fully into focus. I realize should never forget to be thankful for my many blessings but sometimes life just seems to get so busy that I need a reminder to keep that "attitude of gratitude" in the forefront.
Tonight was a sharp reminder of all I have to be thankful for...
I just got home from welcoming 29 homeless people to our church.
Our church is the sheltering church this week. I volunteered to go to our church each evening to greet our guests, welcome them to a warm place to stay, and serve them food.
We provide our guests with tangible physical comforts like an air mattress, blankets, lots of food, winter clothes, hats and scarves, and a warm place to sleep. We also provide them with some non-tangible things like hope, comfort, companionship, and safety for the night. 
Our guests tonight are both male and female, some old, many young. Some are solemn and quiet while others return our smiles and readily engage in conversation with us.
They are back and brown and white. They are from all walks of life. One was a farmer, another a builder. One has quite a bit of education while others have little. Some are physically ill while others suffer from mental illnesses. Some were born here and others just recently arrived.
All of them are doing what they can to survive and that is why I was fortunate enough to serve them this evening.

In this season of thankfulness, I am feeling quite lucky. I have a roof over my head, plenty to eat, amazing kids and grandkids, and a multitude of awesome friends.
That is why I am feeling especially grateful, thankful, and blessed this evening.
 

Thursday, October 1, 2015

How People Cope With Cancer

Everyone has a different way of coping with a cancer diagnosis.
 
Shortly after my diagnosis, I had told an acquaintance who was in the field of counseling that I was going to start a blog. She looked and me, shook her head, and said, "Verna, Verna, Verna, what are you doing?"
 
I will never forget that moment nor the words she said. It shook me to the core. Self doubt set in hard!
 
 I thought that writing a blog would be a good thing for me to do. A blog would clarify my thinking. A blog would share my news...good and bad...with family and friends. A blog would help me cope. A blog would inform others and spare me from retelling my story over and over. A blog could educate others that may be going through what I was going through.
 
I almost let her comment deter my belief that writing would be a good thing for me. After all, she was a counselor. She knows "stuff" I don't know.
 
But I didn't back down. I trusted my "gut" instinct and started my blog with the belief that it would be a positive move, a good thing for me!
 
And it has been!
 
 
 
A few weeks ago, I ran across an article I wish I would have had after my counselor acquaintance and I had that conversation. The article was written by a breast cancer survivor who happens to be a writer. It gives an excellent argument for handling a cancer diagnosis in the way that's best FOR YOU!   

      I have included the article below:
 
 
Is There a 'Right Way' to React to Cancer?      By Heather Millar
When I was going through treatment, there was a woman that I used to always see in the infusion ward. We had the same oncologist and we were going through the same scalp cooling clinical trial, in an effort to save our hair through chemo. We were always seated in the same treatment bay. So, from my point of view, we had lots in common.
Being outgoing to a fault, I tried to chat with her. Every infusion. And every time we sat together having poison dripped into our veins, she shut me down. Didn’t want to talk. Seemed angry and unfriendly. So by the last couple infusions, I learned to just smile and nod.
I assumed that she must just be a grumpy person, but she always had a different friend sitting with her. So someone must have liked her…
Then, about four months after our chemo ended, I ran into this woman as I was getting a post-radiation checkup. She smiled broadly and extended her hand. “How are you doing?” she asked in the cheeriest of tones. “Aren’t you glad THAT’s over?”
Her hair looked fantastic; she looked fantastic. Her personality almost seemed to bubble over. She was a completely different person now that treatment was almost finished.
That got me to thinking about how everyone has their own particular way of dealing with the terror and uncertainty that cancer brings into our lives.
Being a journalist, and being gregarious, I turned my cancer into a “story.” Turning my illness into a project kept it at arm’s length. Certainly, if I could explain what was happening to me, I could beat it. I probably asked so many questions that I really annoyed my medical team. I even interviewed the radiologist as she was sticking needles into my left breast to guide the surgeon during my first operation. I wrote about everything that happened. I talked to everyone, endlessly.
Looking back, I now realize that I was just trying desperately to stay in control. I don’t regret what I did but I now realize it was a coping mechanism.
In contrast, I think the lady who sat next to me in the infusion ward responded differently. She turned in on herself. In the face of the scariest thing that may have ever happened to her, she threw up walls. She took care of herself. She didn’t pay much attention to others. She did what she needed to do, even if it made her seem unfriendly. That, too, was a coping mechanism.
The mother of one of my family’s dearest friends is now dying of lung cancer. She’s in her late ‘80s, and the cancer has spread to her brain and her bones. Her response is simply to deny what’s happening to her. Her daughter, our dear friend, says denial has been her mother’s coping mechanism forever.
So when we go to visit this charming old lady in her assisted living facility and she talks about how she’s going to move to Idaho because there’s a doctor there who has a magic bullet that will make her well, we just nod seriously. There’s no point in trying to set her straight. She’s just trying to cope.
For the woman who set up the young survivors group that I joined, I think her response to cancer was to organize. She’s now built a non-profit that runs support groups, pools information, and organizes retreats, parties and other get-togethers for breast cancer patients and breast cancer survivors. She’s a corporate attorney, and I think she channeled her professional skills to create something that’s helped hundreds of women. I also think her activism is a coping mechanism.
There’s no one “right” way to respond to cancer. And, I think, when we’re in the moment, we cancer patients really don’t have much control over how we respond.
Each style of response has its pros and cons. My charm offensive helped me feel that I wasn’t isolated, wasn’t helpless. Yet I wonder if I avoided fully feeling some things. The lady who pulled up the drawbridge and turned in on herself probably protected herself emotionally. But she also missed connections with people who wanted to help. The mother of our friend keeps herself in a haze of delusional hope, but I wonder if it will also get in the way of saying her goodbyes to friends and family. The founder of my young survivors group has helped hundreds of women. But by now, she must be 10 years post diagnosis. I think it must be exhausting to keep cancer at the center of your life for that long.
If you’re the friend or family member of a cancer patient, try to accept whatever response your loved one has. They’re just trying to get through treatment. It may seem that your loved one has lost their mind, or changed personality. It may make you feel confused. Just remember they’re in the fight of their lives right now, and they just need understanding and huge helping of forbearance.
If you’re a cancer patient, remember that however you respond to your cancer, your way is okay. We’re all just trying to cope.
Heather Millar is an award-winning freelance writer and author. In her blog My Left Breast, she details her treatment for breast cancer as well as the science, history, and ethics of the disease.
 
 


Wednesday, September 30, 2015

What A Difference A Year Makes!

I can hardly believe that a year ago today, September 30, 2014, I was still struggling to rebuild my blood weeks after chemo was done. I was also trying to build up strength. I had just had my fourth radiation treatment that morning. 
 
This September 30th, I am feeling almost fully recovered. My strength and stamina are very near back to normal! I have been thanking God all summer and fall for the wonderful times that we have been blessed to share with family and friends at the lake. It has been at the lake that I have done a lot of my physical and mental healing.

 
I have been so fortunate to spend time at the lake, not only on weekends as we have done in the past, but also days during the week. Most of the weekdays, Arland is at the lake with me but on some days he has to be in Fargo for meetings.

A few days ago, Arland had to be in Fargo so I spent a leisurely day reading, walking and enjoying the beauty of the lake...my flowers, the water, the clouds floating across the bright blue sky.




As evening approached, I sat in a chair on our dock watching the glorious sunset and thought about these past 18 months.



I looked out over the lake and watched as the breeze made gentle ripples across the water. As I gazed over the lake, a fish jumped out of the water near me, making a little "blip" sound as it reentered the water.

As I sat there thinking, I realized during those moments of serenity, solitude, and reflection that cancer was like that little fish. Just like that small fish made a little "blip" of ripples in the large lake, so too had cancer made a little "blip" of ripples in my life. Eventually, the ripples the little fish had made on the water smoothed out. In due time, my cancer "blip" will smooth out too.

My "blip" has started to smooth over. Now my prayers are for that little cancer "blip" to be the only I will ever have to encounter.



 
 
 

Tuesday, August 25, 2015

The Tug

It's happened twice this past week. I've run into someone and they'll say, "How are you doing? I haven't been to your website lately."
 
Sadly, I think to myself, "Neither have I!"
 
Life has been going smoothly since my last checkup with Dr. Terstriep, about a month ago. Arland and I have been at the lake every weekend and several week days this summer. The week day stays give us more time to "get things done" so we can enjoy our family and friends when they are at the lake on the weekends...and we've had lots of people at the lake this summer. It's been fun! We feel summer is passing us by very quickly though and there are still a lot of people we'd like to have spend time with us at the lake.
  
Each year, as August rolls around, I feel a tug to go in to school to start getting things ready for the upcoming school year. This year is no different. I began to feel that tug, that pull to be doing "school things" a few weeks ago.
 
Since I no longer need to get a classroom ready, I justify my need by taking our grandsons, Brody and Logan, out for a day of school shopping. It's a perfect way to spend one-on-one time with each of them separately doing something that we both enjoy. Of course, there is always ice cream and other treats involved for both of them.

A grandmas gotta do what a grandmas gotta do!!!

Brody, age 8, enjoys his "Scoops" ice cream.
 

 
Logan, who is 5, decided the bubble gum ice cream was the yummiest!!
 
 
 
Life is good...
 
Maybe that's why I haven't been to my website lately.
 
 
 

Tuesday, July 14, 2015

And All Was Well

 
As the title says, all was well!!!

After my last post, I thought I would let you know that I am breathing easier. My doctor appointment with my oncologist, Dr. Terstriep, went just fine! She found nothing new and for that I am grateful!
 
Arland and I decided to head for the lake for a few days after my
appointment. This is what we saw as we enjoyed the lake Monday evening. What a glorious sunset!!!
 


 

And "All is calm and well!"



Sunday, July 12, 2015

The Storm




 
Thoughts are rumbling through my brain mirroring the
thunderstorm outside.
 
My thoughts are reflective of the weather. Half my thoughts are preoccupied by dark, stormy thunderheads while the other half smiles in the gloriously brilliant sunshine.
 
My heart quickens every time I think about tomorrow. This will be my first appointment with my oncologist since my treatment ended nine weeks ago. The big question rumbles and looms...
 
 
What if she finds something new?
 
 
This is just a routine visit. All will be well.
 
Then I remember that this all started 16 months ago with
"just a routine visit" during which I fully expected that "all would be well".
 
My cloudy, tumbling side booms with doubt.
 
My bright, sunshiny side whispers that all WILL be well.
 
The dazzling blue sky that is now peeking out from behind the thunderclouds tells me to be calm. Breath deeply. Be calm. The storm will pass and all will be well...
 
And calm!