Kimberly’s Story

Site created on November 16, 2021

" Being a mom and wife, raising 4 kids is a marathon, but today this momma needs to stop and tie her shoes.  "
  This pause in our race is brought to you by Stage 3 Myxoid Round Cell Liposarcoma.  


You may be asking yourself did you miss something over these past few months- but no you did not- I did not really make any of this public knowledge as every week the treatment plan changed and I have reached the point after biopsies, surgery, MRI's and PET scans to where there is a definite plan in place.


To go back it all started in September when I had Dr. Rothrock take a look at t lump on my inner thigh. I had noticed it for some time but it seemed to be getting bigger and causing some pain when the kids would sit on my lap.  So MRI's , Biopsy, CT and Surgery filled the rest of the month. I had the tumor removed on October 1st, and it was the biopsy of the tumor itself that indicated this soft tissue sarcoma was more aggressive than earlier the preliminary biopsy indicated. I consulted with Avera Medical and Radiation Oncology at the end of October, both of whom recommended this cancer still needed to be treated further with both chemo and radiation therapy protocols. Fast forward to Nov. 16 and today I  just had my first chemo infusion and radiation treatment.

Soft -Tissue Sarcomas are pretty rare and not a lot is researched about them. And what research there is, isn't always specific to the type of tumor you are diagnosed with. Given my age, it is not advised to watch and wait even though every MRI, CT, and PET-CT done over the past month indicates there is no sign of spread/metastasis. 
The possibility of it showing up somewhere else is too high, so I will have radiation therapy treatments 5 days a week for a total of 30 treatments. This will have me going to Sioux Falls every day for these treatments till about the end of December.  During this time I will have 3 chemo infusions, the first one is done, the 2nd will be on Dec. 7, and the 3rd around Dec. 28-29. 
I hope to keep this updated but will have my mom and sisters help me out too. 
Don't be afraid to reach out if you have any questions. 
Love you all!



Newest Update

Journal entry by Scott and Kimberly Van Beek

Yesterday was a good day! Not only was it World Down Syndrome Day, a day we get to celebrate Jameson and all our friends across the country and increase awareness and acceptance for Down syndrome, but it was also the day of labs and scans to see if the radiation/chemo I have undergone the past 6 months was successful at keeping me clear of any spread or reoccurance.  I had both a CT of my Chest/Abd/Pelvis and MRI of my Rt. Femur (the tumor/surgical site). I am happy to report that the results of both the CT and MRI are clear and continue to show no evidence of metastatic disease or recurrence at the tumor site. I can now say that I am officially done with treatment.  I do not need to do any maintenance or oral chemotherapy that is prescribed for some cancers. I will have to repeat the CT and MRI every 6 months for the next 3 years.  The thing about sarcoma is it is such a rare cancer, that there is not a lot of information out there to give specific follow-up treatment plans. But Dr. Solomon is encouraged by the fact that there was no evidence of spread at the time of diagnosis and also that the size of tumor was much smaller than most sarcomas are when they are found.  So my prognosis is very good, but it is something that will just need routine scanning. I can handle that!

So I may not be posting a whole lot anymore as things will start to go back to normal. I want to thank you all for the prayers, words of encouragement, and support provided in so many ways by so many. It is an experience that has changed our family and shows us not take anything for granted. Our family will be forever grateful and know that someday if the same support is needed by someone else in our "village", we can and will offer the same generosity to that individual/family that was shown to us. 
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