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Finding Hope:  Jerry Wilma

11/26/2022

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 Jerry Wilma’s cancer journey started on Feb. 24, 2021, when he went to urgent care because his ankle was swollen. They discovered that Jerry had a blood clot and was taken by ambulance to Gundersen Hospital.
After many tests, it was determined that Jerry not only had a blood clot from his groin area to his ankle, but he also has Chronic Myeloid Leukemia (CML) in the blast phase, the most severe.

For 28 days, he had weekly chemo infusions at Gunderson Clinic in La Crosse and also needed blood and platelet transfusions depending on his daily labs. He had another bone marrow biopsy that showed the blast count was down but not enough.

Jerry went to the Madison Carbone Cancer Center at UW Madison, who said Jerry “might” be a candidate for an allogeneic transplant if they could get the blast counts down to around 0. Although Jerry’s three children were a 50% match, the doctors were set on finding an even better match.
For round two of chemo, Jerry was hospitalized to get the chemo infusions and be monitored 24/7 for any infections or fevers.

Soon after Jerry came home, they were notified by Madison that they found a donor that was about a 90% match. On July 8, 2021, Jerry received his stem cell transplant.

During his hospital stay, his blood counts were monitored throughout the day. He developed Graft vs Host Disease, was fighting fevers and had been given so many medications that they needed a spreadsheet to keep track of what he was taking.

After leaving the hospital, Jerry continued to go back to Madison every week for lab work, tests and doctor visits, and a bone marrow biopsy every three months. When a stem cell transplant is performed it not only wipes out some of the bad cells but also some of the good cells, so he had to start over with all of his childhood vaccinations.

The Wilmas knew Joe and Rachel Vogel and followed Joe’s journey with cancer, supporting Team Vogel events long before Jerry’s diagnosis. They were able to use the Team Vogel donation for gas, food and lodging for ongoing treatments, including travel to La Crosse and Madison. 

“I had heard of many people’s stories and how it helped them. I never dreamed that we would someday be those people, but I think that it gave me hope,” says Cheryl. “I think of how much Joe has helped so many people. I would tell people to please consider donating, there are so many families and individuals who have been helped. You never know when you might be that person.”

Jerry celebrated one year on July 8, 2022. The last bone marrow biopsy shows no evidence of the disease, but with Jerry’s type of leukemia, he will never be considered cancer free – just that the disease is not active right now.
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The Wilmas say they are thankful to God and their families and friends for all of the support they have given them. “We feel blessed to share our story to give others HOPE. We realize that life is not guaranteed for anyone. Any day our lives can change, and we have to have faith that God will help us through.”

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It's a Journey, One Day at a Time: Peter Berhow

10/23/2022

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 Written by Jody Berhow
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On May 5, 2020, Peter Berhow felt dizzy one day at work. He called his wife, Jody, for a ride to urgent care. Something was wrong. Once there, many blood tests were ordered and then the sudden realization that he immediately needed medical care with a cancer specialist. Following additional tests at Gunderson Medical Center in La Crosse, Peter was diagnosed with Acute Myeloid Leukemia at age 65. “You will need a STEM transplant,” said the specialist. “This is going to be life changing.”
 
At that moment, the process of cancer treatment began for Peter. So many tests, transfusions, drugs, chemotherapy treatments, insurance, etc. all wrapped inside, outside, twisted and knotted within a world pandemic and a frenzy to understand that as well. Once diagnosed and after many appointments, Peter and Jody chose to go to the Mayo Clinic in Rochester for treatment and a stem cell transplant. They lived at the transplant house in Rochester for what was assumed to be 100 days for recovery, from November to March. Fortunately, because of the closeness to Winona, they were able to come home on New Year’s Eve due to concerns of the pandemic and being safer at home with just the two of them. The transplant was successful, and Peter continues today to be so well with his donor’s stem cells (bone marrow) doing exactly what they need to do.
 
Through the years, Peter and Jody have supported Team Vogel through its many fundraisers, and Jody, an elementary art teacher for Cotter Schools in Winona, helps organize yearly school fundraisers to raise money for Team Vogel as well. Joe Vogel is an alumnus of Cotter Schools and was once a student in Jody’s art room. 
 
During the entire process of Peter's illness, Jody reflected on family and the full circle of life. Imagine, Joe, a young boy in her art room for seven years as a K-6 grade student moving on to offering his art teacher perhaps the most profound precious gift to receive, in his passing, a check of funds given to Peter and herself from Team Vogel to alleviate the stress of navigating the truly awful, painful and long, strange trip that cancer can be. The funds were used to pay for the transplant house rent and medicines too costly to afford. 
 
“God bless Team Vogel, all the doctors, Mayo Clinic, Gundersen Medical, donors, the givers, those that we meet, and those that we know, enjoy and call friends,” said Jody. “The group hug of family is resoundingly too large to wrap your arms around. But because of them, there are moments to rejoice, to smile, to remember Joe and to truly ‘Believe!’
 
Today Peter remains cancer free! He still goes to Mayo appointments for check-ups but is living life as well as can be. From words Jody posted to Facebook friends, “Living closer to our own God and wiser than we used to be!”
 


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From Applicant to Board Member...

9/16/2022

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​Christine Windsor
In 2014, Christine Windsor was diagnosed with breast cancer. Faced with numerous surgeries, ongoing treatment and expensive medications, she felt overwhelmed. As a single mother of a 13-year-old daughter and self-employed owner of a hair salon, Christine worried about how she would support herself and her daughter while battling cancer and traveling to and from Lacrosse and Rochester for treatment with no income coming in.
 
One of Christine’s clients nominated her to be a recipient of Team Vogel vs. Cancer funds, which goes directly to families to provide support for them during such a difficult time. Christine was able to use the funds she received toward her medical bills, medications, gas money to travel to her cancer treatments and food for her family.
 
“The Team Vogel donation impacted my life to provide food and gas for me and my daughter and provide basic living expenses at the time because I had no income,” said Christine. “It took a huge stress and weight off me not having to worry about those things.”
 
Wanting to pay it forward, Christine stepped up to become a Team Vogel vs. Cancer board member in 2015, organizing fundraising events and activities even while she was still going through treatment. Over the years, Christine coordinated numerous activities, including the Fall Frolic, Halloween Bash, Rollingstone parade participation, Pancake Breakfast and Joe’s Birthday Brew at Island City Brewing. 
 
Beyond the financial contribution, Christine said that Team Vogel vs. Cancer’s network of support between volunteers and families battling cancer is amazing. She loves connecting with the Team Vogel families, sharing her experiences and listening to them, so they know that they’re not alone.
 
“When we volunteer and donate, it’s such a blessing to see the wonderful impact it has on the lives of those struggling and fighting cancer,” Christine said. “Paying it forward is a blessing in itself.”

Today, Christine is five years cancer free. To celebrate this milestone, she is currently organizing a Chicken Q on Saturday, Oct. 15, at George’s Lounge to raise money for Team Vogel vs. Cancer. You can purchase tickets for $10 at Windsor Palace Salon and George’s Lounge. 

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...Liam's Journey

7/23/2018

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In August of 2017 Liam and his brother were wrestling when he stated that he couldn't walk. We took him into the ER and were sent home with what we believed was torticollis ( a pulled neck muscle). After six weeks, and 4 more appointments to the pediatrician we knew there was something more than a pulled neck muscle and we brought him to the ER at St. Mary's in Rochester. We were kept over night and the following day an MRI and MRA showed that there was a tumor the size of an orange on his brain stem. They quickly sent him to surgery to have a drain placed in his brain to relieve the hydrocephalus. After the drain was placed we were admitted to the PICU, and were told that his tumor was an anaplastic ependymoma which is a cancerous brain tumor. A few days later Liam had surgery to remove the tumor. The tumor was completely removed! Praise God!

We continued with therapy and hospitalizations until we started 7 weeks of proton beam radiation therapy, followed by chemotherapy. We started chemo in January and ended the beginning of March, of that time we were home for 14 days, the rest we were in the hospital. He was on oxygen, a feeding tube, and many other therapies.

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We are now done with therapy and will continue to monitor him every three months doing MRIs to make sure that that cancer does not come back. The reoccurrence rate for this cancer is 75%. We are believing that God is going to heal him and show a miracle through this! Whatever the outcome is, we know that God is in control and has been faithful through this. We have been really blessed to realize how precious life is!

​This summer we plan to use some of the funds from Team Vogel to help create a lot of memories and to also prepare financially if this were to come back. We are truly blessed to be part of such a great community in Winona!
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God bless! 
The Liam Schroeder family
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The Olson Family ~ Shared by Brian Olson

3/16/2017

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Brian Olson, the husband of Jenny Olson, along with their two children, Elise and Ben, were fortunate to be the recipients of Team Vogel’s 2013’s extraordinary efforts in assisting local families who are afflicted with cancer.

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The following was written by Jenny Olson, shortly after her cancer diagnosis:
“On August 1, 2012, a tumor was found in the back of my neck to the left of my spine.  We were assured it was 98-99% benign, as big as a lemon and it would need to be removed.  Surgery was set for August 6 (CHS Class of '96, important date, it gives me chills) and it was successfully removed.  However, the pathology tests came back positive for cancer.  I have a rarer cancer called synovial sarcoma.  Doctors set up radiation treatments and they were going to start September 19.  But, September 6, I found a lump in my neck.  After a CT scan, our worst fears were confirmed: the lump in my neck was a lymph node filled with the cancer, as well as the site in the back of my neck. The tumor had grown back that fast and is as big as before surgery in the back of my neck, so we have a new treatment plan.  I will start chemotherapy on September 25; three cycles over a course of 9 weeks. Then I will have chemotherapy and radiation every day for 5-6 weeks. That should take us to the beginning of January where I will have three weeks off.  Then in the beginning of February, I will have extensive surgery to remove the cancer from both areas.  It will involve reconstruction and plastic surgery.  Of course, this schedule is if there are no setbacks or big bumps in the road.  Let's just say it has been a long month and half and the hardest is yet to come. Thank you for your love and support.  I don't know what we would do without our fantastic family and friends.”
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During the entire battle with cancer, Jenny remained optimistic and upbeat as she was determined to beat the horrible disease, even though the cancer was overtaking her body.  The one thing that kept us going through the entire time was the love and support of family and friends.  Many people stepped up and helped us through the toughest of times.  It was a rough stretch of times.  Once you would think she would catch a break, another setback would be taking place.  When people surround you with their care, you can feel it and ultimately become a better, stronger person and family.  Jenny felt that the entire time from her diagnosis in August of 2012 until the day she passed away on January 25, 2014.  

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Jenny Olson was a classmate of Joe Vogel at Cotter High School.   One of those people/groups that supported us was Team Vogel.  We were in awe of the tremendous generosity and support we received from Team Vogel.  They supported us not only financially, but the people involved within the organization brought awareness to others about our family’s struggles which brought support from various parts of the community.  We are forever indebted to all that Team Vogel and so many others have done for us.

At the time of this writing, it has been a little over three years since Jenny has passed.  I would classify them as “adjustment” years.  We have been figuring out how to adapt to this new way of living.  It has had its fair share of bumps and hurdles to jump over, but we have been able to also experience many joys.  I would like to think that I have been laying a foundation to help get the three of us to where we need to be.  We are not where I would like us to be yet, but I have grown content with the progress that has been made.  I am convinced that we are set up for great things to come.  There will
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hopefully be some welcome changes in all of our lives involving many different aspects.  Jenny would not want us to be sitting around and feeling sorry for ourselves.  She would want us to live each day to the fullest and make a difference in this world in a great way.  I would like to think we are trying to do so.

Jenny and Joe would want us to “pay it forward” as much as we can and to “don’t stop believing.”
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New Year... New Blog

1/15/2017

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The journey that has a person's or family's path cross with Team Vogel is unique and individual. 

So this year we thought we'd try sharing stories from those who have joined the journey that is Team Vogel...

We invite our recipients, their families, those who volunteer time and talents, to tell their stories, and how they came to be part of Team Vogel vs Cancer.  Please email teamvogelvscancer@gmail.com if you would like to share on a future blog.

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    Team Vogel Journeys

    Team Vogel vs Cancer is a group of people, connected in a fight against cancer. We are dedicated to supporting families in the Winona area, and local cancer research.

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