A Grit Story: A Journey of Determination

Inspired by “Grit” by Angela Duckworth, as recommended my VP at Land O’Lakes

Growing up, no one read to me or helped with homework—math facts were my responsibility alone. From first through third grade, I was labeled “behind average,” not because I lacked effort, but because of circumstances at home. My mother worked the second shift as a nurse, picking up extra hours whenever she could. My father, on the other hand, squandered what little we had on ill-fated “get rich quick schemes.” Paying the electricity bill and filling the tank in the yard for heat was a struggle.  My dad called himself a farmer but we had a large garden and some chicken and turkeys then never turned a profit. You are looking at the only employee, along with my brother and sister. 

My siblings and I were raised in a wild, unstructured environment—no rules, no routine, just the shifting demands of whatever our father was yelling about that day, the random times his loud truck was home. Living on eggshells barely describes it; it was more like running barefoot across razor-thin glass, or squeezed into pink cowboy boots two sizes too small. I desperately wanted to make him proud, even as I wrestled with fear and resentment. Those feelings can coexist, though as a child you don’t recognize their names. You simply keep pushing, striving to be the best kid you can be.

I picked the most beans in the garden, cleaned up endless piles of junk he dragged home, shovel chicken crap and volunteered—over and over—to feed those mean, towering turkeys. My father belittled and insulted my mother and the three of us kids constantly. From the start, I was determined to prove him wrong. I wasn’t the “worthless female” he so often called me, nor any of the other cruel names he hurled in anger.

Looking back, I suspect my father suffered from undiagnosed Ankylosing Spondylitis (AS) and depression—pains I now understand, having managed my own diagnosis with the help of doctors and a pain clinic. AS is incurable, and even with treatment, it’s one of the most painful diseases to endure. Depression, too, runs in families. I’ve been blessed to avoid any mental health issues, thank God but others in my family have not been so lucky. Knowing this provides context, not justification, for his actions. Was there kindness? Yes—there were days he took us swimming at the lake after work, or brought us candy bars from the gas station. He never locked us in the basement or anything so cruel. But the years of emotional abuse left a mark, fueling my drive to achieve.

I became fiercely focused, determined to excel at whatever I did. I needed to prove—perhaps to him, mostly to myself—that I could be the best.

The turning point came in fourth grade. I remember thinking, “This is ridiculous. I’m done letting other kids outperform me. I’ll figure this out, push my teacher to teach me, sneak books home if I have to. I will be the best.” And that’s what I did. I hid textbooks in my backpack, stayed up late re-reading lessons, and moved from “special needs” to “gifted” by the end of the year.

There was a reading challenge in our class: for every book we finished, we earned a paper scoop on the wall, building an ice cream cone. My cone stretched up past the ceiling. I questioned everything—asked, learned, persisted—until I understood, even the most difficult topics. I wasn’t the smartest in the class; I never have been. But no one would out work me.

My progress amazed my teacher so much she called both my parents in. I was terrified—I’d just completed the second half the handwriting book in a single night, against the rules. But instead of reprimanding me, she showed them my work: the improvement from the start of the year to now. She told them, in all her career, she’d never been prouder of a student’s growth in such a short time. She looked at me and asked, “What are you working toward?” Without hesitation, I answered, “I want to go to college and get a great job.” She smiled and said, “Keep working like this, and you will. People who work hard and never give up always succeed.” My parents beamed—no words of praise, then or anytime later but I caught the look. Maybe that silent pride drove me more than any compliment ever could.

Yes, old man—sit back and watch what this “worthless female” will accomplish. I remained polite and kind to him all his life, until his death at age 69, I’m not even sure why.

This is what grit means to me: the relentless pursuit of better, the refusal to be limited by circumstance or anyone’s opinion. My story is proof that determination can coexist with pain and that hard work, above all else, can change the course of a life.

 And yeah, this is me after being first in either side of my family to get a 4 year degree, then Masters. 8 or 9 promotions in corporate Ag, I lost count because I stopped doing things for my dad decades ago, thank goodness. But the grit remains.

13 yr olds view… on poverty

I came across this today, James wrote this when we got back from a mission trip three years ago. It’s powerful.

This trip carved the path he wants the follow the rest of his life but more on that later. First his reflection statement:

Written by James Velde in 2022:

Jesus stood for helping the poor and disenfranchised. He stood to help people in places we don’t typically think about. When I went on a trip to Guatemala I got to see first hand for the first time the need and suffering that that Jesus asks us to aid. 

       I went on a mission trip to Guatemala in January of 2022. When I was there I helped to build a 3 room brick house for a family living in a house with corn stalks for walls and dirt floors. The family had only one income because the wife had to stay home to take care of their 4 kids. And their dad earned only $4 a day working in the corn fields. 

The realization that 100’s of millions of people are condemned to living off of first world pocket change, and then seeing that for relatively low cost, it doesn’t have to be like that, has led me to stand strongly with Jesus’s believes that as well off people we have an obligation to help those without. 

         One thing that really stuck with me when I went to Guatemala was the hearing the parable of the starfish for the first time. It goes like this, an old man walks along the beach everyday and throws all of the washed up starfish into the ocean. A young man comes up to him and asks “what difference can you make throwing them? It doesn’t matter if you throw the starfish into the ocean because they will continue to wash ashore”. And so the old man picked up a starfish and he threw it as far as he could into the ocean and he said “it mattered to that one.”.

        This story stuck with me because it really helped me get over some of my nihilist thinking patterns. Even though I couldn’t help all of the homeless I was still able to make the lives of one family much easier. Even if I couldn’t fix all the problems of that one family, that one village, or the whole country, I could still fix one problem for a family in need and I realized that that was enough.

      I couldn’t spend 100s of thousands to feed everyone but we could donate a relatively small amount of $200 to build a kitchen for the family and make their lives significantly easier. 

       This kind of personal community based aid it the exact kind of thing that Jesus always speaks of. I am early in my faith journey but I think that helping others is a way to get closer to God and to carry out his work here on earth as Jesus would have wanted.

 

James building a kitchen in Guatemala 🇬🇹

 I’m back! Upon returning from this trip he was focused to become a doctor so he could do Doctors Without Borders. That’s the program where doctors provide medical care to people in need. Because he was 13 at the time, I supported him but did not think much of it. However, he thought about it a lot. He got straight ‘A’s, joined a couple of sports just to build a resume for college (even though he dislikes sports), national honors society, just got his ACT scores back at 97% level. He registered today to do First Aid and CPR certification so he can work in healthcare for summer jobs before in Senior in high school. He really wants to make his goal to help people a reality.

What I’m most proud is he’s figuring most of this out on his own. If he asks me questions I answer them but he digs in and owns his dreams. That is a key. Parents can’t own kids dreams. I repeatedly remind him that he can change his mind. He also has a real passion around plant 🌱 science. But he tells me that’s a hobby. Ok buddy.

Parenting has ups and downs. This element with James is certainly an up. To be fair and balanced I should a post on Victoria’s journey on getting diagnosed with ADHD and autism. Wow, that’s been a rat race. It’s to a point Nick and I get an email from the teacher when it’s a good day. Yup. It’s that bad. A couple times she’s raised a chair over her head when she gets real sad or mad. Not good. She is funny, sassy, smart, sad, silly, and vert challenging sometimes.

Friends of young ones, in case it helps- James has ADHD and had issues in school in early grades. He was not always a high performer. Sometimes kids just adjust at different rates and ways. We just love them. We expose them to the world as parents we desire to do so. Pray for them. And try our best not to stress.

God has a plan for all of us, that includes each of our children.

 

James handing out Toying in Guatemala 🇬🇹

Guatemala Mission Take Two

This is my second mission trip to Guatemala. On this visit, we were helping build a classroom onto the school, but let’s be real: our physical labor is not the real value we bring. The true value all happens many months before back at home with fundraising at our church. This entire classroom build only costs around $5,000 USD because we work closely with the local town to get labor donated and all supplies purchased locally and at the best price, as they know it’s for a low-income mountain village school. This village is about 7,000 feet up the mountain. 🏔️ You can see active volcanoes 🌋 in the distance. It’s just breathtaking.

A local Minnesota couple, Woody and Lety, make this all happen. They work with multiple churches, taking groups to Guatemala, showing them where the greatest need is, how to get the best prices, and how to serve the people. This couple is 82 and 78 and are still working hand in hand with each group as they bring them. What a testament to being God’s serving hands on Earth! They have been married for 58 years.

It does not matter what church you go to or what language you speak: if there is a need, you can do something. That is the message I am passionate about teaching my kids.

The world needs more people like Woody and Lety! They are walking testaments to God’s love. ❤️

Follow Up Lymphatic Arm Surgery

I had surgery on Tuesday at Mayo Clinic. Checked at 5:30 am and left about 8 pm. It was a long surgery as Dr. Tran carefully reviewed the veins in my left arm and remapped them in such a way that hopefully lymph fluid will be able to start draining in the future. This will prevent the classic “tree trunk” arm many breast cancer survivors before me were told was incurable. The power of Mayo Clinic.

The good news is he found so many viable options that he did not have time to do any de-bulking of the upper arm. Aka liposuction so that was a bummer but hopefully some elements that have not solidified can still be removed naturally by the veins. The remainder will stay but is no big deal.

Healing has been ok so far certainly a lot easier than Diep Flap surgery but still painful. I’m going to try to go back to work Monday AM full time but be gentle with the left arm for two more additional weeks. He does not want me using it to mess up his work.

I get stitches removed at the two and three week marks. And the three week mark I can stop wearing the daily ace bandage wraps.

Minutes before going into surgery

I am blessed to get access to this surgery when so many others struggle life long. I’m going to try to remember that as dealing with recovery from yet another surgery. I am so grateful to be cancer free and on the other side of the very long road.

I could not have had a better community to love me. I gained strength from sharing my story and value so much the kindness you have given to me along the way. I promise to pay it forward.

Mayo Clinic Magic

Waiting for Dr. Tran for Pre-0p

I’m hanging out at the Mayo Clinic. Three appointments to prepare for surgery next week. One week from today I am getting surgery to hopefully fix my cancer caused Lymphedema. On one hand 🤚 (did you see what I did there) I’m excited for a fix; on the other I’m so over pain and healing. ❤️‍🩹

This surgery connects tiny vessels to veins in the affected arm so fluid can begin to flush out again. Only two places in the U.S. do this surgery and one of the is right here in MN. We are so lucky.

All pre-checks done and approved. I am ready to move ahead with no my Lymphatic drain issues in my left arm after next week!

Tram Flap

I’ve attempted to start this post multiple times but it’s been a hard week so just getting back to it. Here it goes. June 11 at Piper Breast Institute I was hoping to have a Diep Flap surgery but ended up with a Tram. What’s the difference? Muscle. They had to use some muscle, about the size of a tennis ball 🎾 to complete the surgery. That is not ideal and shed some tears when I learned this. Granted I was drugged up so anything different would make me cry but I was bummed about that news.

But the good news the tummy tuck made for nice left boob side. The doctor did a beautiful job. It’s painful and swollen now but that is expected for weeks to come. But surgery was a success. All blood vessels took to the new home. A big win. And stomach looks better than before kids, heck yes. Just need to handle a painful recovery. I am missing those muscles right now and this hip to hip incision is no joke.

Waking up at the hospital they told me that my labs were off so they thought I should leave my catheter in for a day. Hmm ok. Turns out I lost a bunch of blood so I opted to get a blood transfusion on day 2. It’s a humbling experience peeing in bed when you are fully awake. Wow! The things we do for a new boob. 😉

I’ve been through a number of surgeries life long probably 7-8 total and this is far the most painful to recover from. Tops. Not sure if it’s because of how many wound areas there are or because of the AS flare on top that is the causes the internal back pain but it’s intense. The first time I needed to force myself to sit up I almost pass out from the pain but did not. However it is a little better each day so that is such a positive bright light.

I was released from the hospital on Saturday. So surgery Tuesday. Released on Saturday. It feels good to be back home.

Blood transfusions- my first one ever

I’m crossing fingers for no infections and improvements everyday.

Happy Father’s Day to all the Dads!!

ER Visit Leads to Treatment Change

Hi Friends! So I’ve been on a chemo pill for 3.5 weeks now and it’s been challenging. I was expecting the fatigue, nausea and diarrhea but in the past three days I’ve been increasingly struggling with shortness of breath, mild dizziness when I change positions, and my heart was beating fast if I did just mild physical activity like walked around the house to make a sandwich. 🥪 Not cool.

I wanted to wait until my big appointment with my Oncologist but after I got super dizzy yesterday at lunch time while simply trying to get a glass of ice tea, I decided to call the nurse line at the Oncologist office. Apparently, this medicine can cause blood clots so they said I needed to go in immediately for a CT to rule that out. Ugh.

Yesterday was a big day at work for me. Huge accomplishment day actually. We were meeting with all our teams to explain a regional model that would impact reporting strategy. For the first time in my career all teams in Purina CS would report me which is exciting and new and I’m bailing to have a CT scan. Super annoying and frankly embarrassing!

Nick drove me. CT showed crap in my lungs so walking pneumonia and they gave me IV Antibiotics. Labs showed low white blood cells count but not as low as it was when I was on IV chemo in the summer. They let me go home and gave me pill antibiotics. They gave me the option to stay at the hospital, no thank you. 😉

Today my Oncologist explained that she’s confident that this chemo pill is not treating me well at all. She wants me to stop immediately. I did not argue. She is going start me on something else in August. June 11 I have reconstruction surgery. I get to heal now until surgery. Then focus on surgery. I will stay on Tamoxifen and monthly estrogen shots. I’ve been handling both of those well. very well actually. Today was a shot day, all was fine.

Perhaps I should feel like a failure for having to quit the chemo pill but honestly but im just excited, that chemo pill sucked! Now I can focus on my new expanded role at work that I’m so excited about without worry of nausea, diarrhea, and shortness of breath. Yes! A big win. Plus I can now let myself get excited for the surgery coming up – can we say tummy tuck and boob job? Ok so it’s a little different but it’s as close as I’m gonna get so I’ll take it.

Love you all and blessings to you! Here’s to getting this crap out of my system and feeling better soon!

Next Step Chemo Pill

I’ve been enjoying the relative calm of no active treatments over the last couple of months. I take daily Tamoxifen to reduce Estrogen. And go into the Doctor to do an injection to further suppress reproductive elements of my body.

This past week it was time to up the game and add a Chemo pill into the mix. The one I’ve been put on is called Verzenio. It’s a twice a day pill. One in the morning and one at night. The side effects are nausea, diarrhea, fatigue, some hair loss, muscle pain. They are starting me at 100 mg and wanting to increase if I tolerate it well. I’m not sure on the definition of that. I have not vomited but sure feel yucky. Zero fun. I’m hoping that it’s just a new drug situation and it’ll get better. I can’t imagine walking around feeling like I have the flu for two years. No thank you. But it’s just week one. The jury is still out.

Plus I’m dealing with a flare of Ankylosis Spondylitis (AS). So my neck, joints are in a bunch of pain. Fatigue is high so AS is likely not helping matters.

But overall I super grateful to be in a place that I’m in remission and two months away from having reconstructive surgery. I have access to great doctors to help me navigate decisions. Overall, everything is going smoothly and with a little luck with a few weeks my body will adjust to this new medicine. Crossing fingers!

Most days working full time is going smoothly but I will be taking 6 weeks off to heal for surgery starting June 11, surgery day.

Thanks for reading my little update!

Out to lunch with the family and enjoying the weather!

Hormone Therapy- Be Careful;)

I’m so glad to be back to work full time and back to most of my previous volunteer commitments and just loving life again! Very short hair and one boob, don’t care! It’s all good!

The main thing I need to deal with now is hormone therapy. I’m on taxol and get monthly injections to further shut down my female system. The hormones levels are changing very quickly so the cancer stays away. The main side effect is mood crankiness. And OMG it can be bad. I really should just not say anything to anyone for like 3 months.

For example, the other night after a long day I decided to go to bed early. Nick decided to stay up later and watch Judge Judy (his fav). When he came to bed he decided to wake me up and ask me where his pillow went. I literally thought I might just kill him. Buddy- We made it 20 years but if you don’t roll over and let me sleep you will have hell to pay. I don’t care if your head rests on rusted nails. He was a little scared. 😳

When I find my eye twitching, I need to take a deep breath 😮‍💨 and remember it’s the hormones and not anything else. All is good….

Hair is growing back!
I think I’m getting curls! That’s fun!

Bye bye Active Treatment!

Today I met with my Oncologist that walked through what to expect during survivorship. The medicines, blood checks, scans, etc. It sounds like music to my ears after these last 10 months of active treatment. Bring it on!

Wednesday next week I’ll have my last daily radiation so just 3 more to go. Radiation has gone very smoothly for me. I’ve used this clear plastic film over the entire area that reduces burning in half. Go Mayo Clinic to this technology! That combined with an amazing team at work that is so flexible I was able to work 60% time from home throughout radiation without it being stressful.

Additionally, FINALLY my AS is under control. The joint and back pain is down to a dull roar. I do have a bunch of appointments coming up- EKG to check how my heart is doing after Chemo, MRI of the brain, a couple AS follow up appointments but all in all things are going to get much closer to “normal” in February and I’m so grateful.

I started Tamoxifen a week ago and my body is handling well. A little nausea but not bad. I don’t think I’ve been too cranky (it changes hormone levels) but perhaps the hubby would disagree. Radiation is causing some fatigue but not bad. All is going in the right direction!

The first week in February Nick and I are taking the kids and going on a road trip to the Gulf Coast. We’ll spend a week in an Airbnb in Long Beach, Mississippi and celebrate having a cancer free family. My favorite activity we have planned is a boat ride through the swamps of Louisiana to see gators 🐊.

I want to thank you from the bottom of heart for your love and kindness to our family this past year. I’m so grateful to my co-workers at Land O’Lakes, my church community at Roseville Lutheran Church, my sisters at Beta of Clovia sorority, board members on the FFA Foundation, and everyone that has prayed, sent positive vibes and in anyway helped make this crappy journey easier. You are a blessing.

God is good! I don’t know what next year might bring or five years from now but none of us do. The now is good and the now is a blessing.