The Anderson Family

Victoria, MN
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    Name
    Amy Anderson
    Injury/Illness
    Breast Cancer

    We are the Anderson family. Curt (husband), Amy (wife) and our two kids, Addie (16) and Asher (7), and our two dogs (Vizslas!) who are 14.5 and 13 and full members of our family! In February 2022, Amy was diagnosed with Stage 3 Triple-Negative Breast Cancer (Invasive ductal carcinoma—a highly aggressive, invasive breast cancer) that had spread to the axillary lymph. Care plan was identified as 1) treatment/chemotherapy; then 2) surgery; then 3) radiation. We wanted to “get at this” aggressive disease with everything we could. Amy already lived a healthy lifestyle and supported her body naturally, so we felt strongly compelled to follow an integrative plan (combining functional medicine with standard oncology) to support Amy’s body through treatment and manage pre-existing sensitivities and autoimmune disease. In June 2022, Amy completed 11 Paclitaxel+Carboplatin chemotherapy infusions, and though suffered significant peripheral neuropathy, Amy had an "incredible response."

    However, an ultrasound biopsy in July 2022 showed one remaining treatment-resistant tumor to be HER2+ disease. This presented a challenge, and perplexed every colleague our oncologist consulted. At that time, we also learned that our oncologist was moving out of state and would be unable to continue our care. He recommended an oncologist from his network, and also sent referrals to Mayo Clinic in Rochester, MN and the University of Minnesota Cancer Center for second opinions. During the next several weeks, we met with oncologists, surgeons, functional and medical doctors, seeking their advice on this new twist, while also searching for a good fit for a new oncologist that would support Amy's desire to continue integrating functional and standard care (especially since her body responded so well thus far to this approach). For every practitioner we met with, we had a different recommendation … the opinions varied wildly, and it felt a bit like starting over with a whole new cancer diagnosis. It took time to get second opinions and find a new team. During this time, we kept up the fight: Amy completed various functional therapies, including a series of antigen injections with RGCC (Research Genetics Cancer Center) aimed at revitalizing Amy's flatlined immune system and preparing for targeted HER2 treatments. In January 2023, after new baseline imaging, we established a new plan of (integrated) care with our new team.

    Amy completed four HER2+ standard targeted therapy infusions of Herceptin + Perjeta in early spring 2023 for the remaining HER2+ disease with “little to no” treatment response, and an increase in tumor size. A recheck biopsy showed additional HER2 neu expression, and targeted chemotherapy (Enhertu) was ordered with hopes of better treatment response.

    Amy’s strong desire is to continue to incorporate integrative therapies so long as resources are available, in order to maximize the effectiveness of treatment and help her body fight this disease well, while managing side effects. (All held loosely, based on risk of developing resistance, recurrence of the original Triple-Negative disease and risk of advancing neuropathy.)

    In December 2023, it was concluded after several reviews by our care team that the targeted HER2 neu therapy was not working. Early Jan 2024, amy completed a functional treatment through RGCC called SOT (Supportive Oligonucleotide Therapy). In Jan 2024 a repeat PET revealed mixed results, with some decrease in primary tumor and axilla, while some increase in axilla and one new node in the AP Window/Mediastinal area. This new node moved Amy from Stage 3 to a clinical Stage 4 disease.

    We continue to persevere, with hope. What began as a "five-month" journey has continued for more than two years of active treatment, taking one step at a time. We are grateful for the medical teams who have come alongside us to help us navigate our unique situation. We have weighed numerous mixed professional opinions, and we have relied heavily on our team, and ultimately our faith to help us know what is best for “us” and best for treating Amy individually and wholly as we walk this out one step at a time.

    As this journey has been much longer than we ever anticipated, we have finally found ourselves in a place of financial need. After a harder season of Curt’s business still impacted by the pandemic, and a critical job loss, we have found we can no longer keep up with our bills and some of our most critical care (Mayo Clinic, RGCC and all Functional therapies) have been out-of-network and out-of-pocket. Over the past year of this journey, we have exhausted our resources, including our entire savings, to carry us through to this point. We are grateful for the treatments we have been able to do so far, but very much appreciate any assistance to continue to receive the care that has been the most effective, and the best chance for Amy’s complete healing. We are so very grateful and absolutely could not walk this road without your help. Thank you for your support!

     

    July 10, 2023
    Enhertu Treatment #2

    On Friday, I got an IV treatment to prepare my body for my infusion #2 of enhertu today. This time, I opted out of premeds to help my liver focus on the drugs that are actually treating cancer, while I try alternative side-effect mgmt & comfort measures at home. So far today, I am managing well—there are far fewer side effects as last time, which affirms for me that some of the strange/neurologic side effects were due to premeds. I also think I experienced a bit of detox sickness (which is great—means treatment is killing cancer cells!) but also means giving my liver & kidneys less to deal with is a priority for me. So, trying no premeds this time, and we will see how the week goes.

    Thank you for the support. We literally could not be doing the things I need to do to heal without the help of community. It’s been humbling to be so “needy” but we are learning to appreciate community (not just being comfortable always being the “givers” but learning how to graciously need & receive help, too!) and we are growing as we are continually being stretched. We are grateful beyond words. Thank you so much for helping us “bounce.”

    For more details & updates, please visit our caring bridge. Thank you!!  

    June 30, 2023
    NEW Treatment #1 Completed!

    After my most recent pathology and a few switches in treatment plans, the oncology team unanimously chose Enhertu for my next treatment steps. this new chemotherapy-infused targeted therapy is effective for both HER2 amplified and HER2 low expressing disease. The possibility for remission is high, but it comes with a high risk of serious lung side effects and damage. This was a little unnerving for me. But it is where we felt led to go and so we walked the path laid out before us. The infusion went overall uneventfully. The following days were up-and-down, and aside from sleeping ALL DAY on Father's Day, I have maintained pretty good energy and nutrition. I am employing all the functional support I can reasonably do (for bio-terrain and cytotoxic benefits) in order to give my body the best chance to respond well to treatment and ultimately heal completely. Thank you so much for your support and prayers. We literally could not do this without you.

    June 14, 2023
    New Treatment Plan

    Biopsy shows heterogenity in the now-HER2 expressing disease, with added diagnosis of HER2 high and HER2 low. This is a newly-adopted diagnosis in oncology, differing from last year’s diagnosis of TNBC (even though some of the pathology is similar), and explains more clearly why, after an incredible TNBC response to chemotherapy, a resistant  HER2+ mass remained. This new diagnosis makes me a candidate for a new treatment, combining an antigen and “a good dose” of chemo. While it is great to have options, I will admit I am a little nervous about how new and less-tried this is. What they understand so far is a high risk for lung damage (1 in 10). But I am doing all I can to prepare my body to be strong and to mitigate any damage to my healthy cells. I am still working the (evolving!) plan, but will admit it feels (again) a bit like starting all over again, and it is a little wearisome, the thought of it, after what’s been a year already of a full-court-unrelenting-press in this battle! But, I’m here and I’m still fighting.  I would so appreciate your prayers for my continued perseverance, and for protection over my lungs, and for my husband Curt. This has been hard on him in all the things—taking care of me, our kids & dogs, working and managing our finances. We have not met our (high) annual medical deductible, and still paying out of pocket to keep treatment going. Oncology bills are crazy-high, and it’s has been crazy-humbling to continue to ask for help. Your help has been a giant blessing during this difficult season for our family. Thank you so, SO much for your prayers support!!

    May 27, 2023
    Biopsy and Labs complete

    Biopsy was yesterday. I am recovering well. We were able to get good samples of the breast lesion and the Level 3 Lymph (near the collarbone, under the pectoral muscle). We tried to get an additional sample of the Level 1 and/or Level 2 lymph underarm, but there were too many risk factors with those. I trust we got what we needed to, and Radiologist said, based on pathology of the acquired samples, we can go back if needed and retry those nodes. So we wait for pathology next week! Once we have that, we will meet with the functional doc to go over recent RGCC labs and biopsy results, then, meet with oncologist to discuss options. Thank you so much for your support. We have been able to continue my care without delay due to your generosity and prayer support. Thank you!!

    May 10, 2023
    Treatment Concerns & Next Steps!

    We had an ultrasound last week to check treatment progress. The results were NOT what we had been hoping and praying for. After three infusions of targeted HER2+ therapy, report is showing little to no change in the known areas in breast and axilla, and increased activity in the Level 3 lymph, near my collarbone (where there were three areas there are now seven). We had been noticing positive change by physical exam and so this was a little disheartening to hear. But my eyes are on the Lord, who leads every detail. Since the imaging reveals something vastly different than what we believed we were "feeling," we are also taking this time to gather some more data to check the overall state of things as best we can. 1) Getting a biopsy. Want to confirm we have a clear diagnosis. Based on our case history, and learning 4 months into treatment for Triple Negative disease that there was also a HER2+ component, we want to confirm the identity of what we are treating. 2) Getting labs. We are also working with our functional medicine team to get a clinical view of the state of my immune system and CTCs (circulating tumor cells) which will also help us discern the best next treatment steps. My plan is to get Herceptin+Perjeta #4 tomorrow! Though our oncologist is concerned that the H+P "may" not be working, I am tolerating side effects pretty well and I want to stay the course with what we can do now, while we wait and see what else we can do. Additionally, in the last couple weeks, my copper/zinc ratio "flipped" into a right balance (this shuts down the ability for cancer cells to evade treatment and spread), and puts my immune system in a better place to fight well. So I want to give treatment a good go with my copper in the right balance. I am also fasting, and doing MANY lymph- and detox-supportive therapies at home and in clinic to help move the lymphatics and help my body do what it was designed to do. THANK YOU for the support and prayers. We need them! I have been able to continue therapies without delay because of your extreme generosity!! Thank you!! 

    For more detailed update, please visit us at our Caring Bridge Site.

     

    April 28, 2023
    H+P Treatment #3!

    We were able to complete Herceptin + Perjeta treatment #3 last week! Thank you for all your support and prayers! We were able to pay an oncology bill when we showed up for infusion, and that felt great! THANK YOU!!!

    We were waiting to see if "now" was the right time to add the Taxol & Carboplatin chemotherapy back in to the mix (TCHP), and this past week, learned that we will stay the H+P course for another round. We are prayerfully awaiting the "next right thing" and whether we add the T+C in for infusion #4. We are very grateful that my copper levels went down after some hard work (detoxing and supplements!) and persistent prayer!! Still waiting to get US imaging in order to help us determine if/when we should resume the chemotherapy. Grateful for some progress! For more detailed updates, visit us at https://www.caringbridge.org/visit/ourstoryishis

    Thank you!!

    April 13, 2023
    Treatment Update!

    Thank you for your support and prayers!

    I have had two Herceptin + Perjeta infusions, and go back next week for #3. This week I had a DMSO IV to help with some treatment side effects and to help me fight this battle strong and well!! Can't say thank you enough for coming alongside us!! For detailed updates, please visit us at https://www.caringbridge.org/visit/ourstoryishis

     

    March 15, 2023
    Thank you for checking in on us!

    Follow us on CaringBridge to get the most current updates from our family. Thank you so much for your prayers and support!!

    https://www.caringbridge.org/visit/ourstoryishis

     

    March 8, 2023
    EBOO Treatmetn #2 Completed!

    THANK YOU so much for your support!! We were in Mankato yesterday and completed EBOO Treatment #2, in preparation for my first Herceptin + Perjeta treatment tomorrow! Thank you for your prayers and support!!

    February 24, 2023
    EBOO Treatment 2/21/23

    We made it through the snowstorm to get the first EBOO treatment this week!