Lindsay’s Story

Site created on February 3, 2024

Welcome to Lindsay's CaringBridge website. We are using it to keep family and friends updated in one place. We appreciate your support and words of hope and encouragement. 

Lindsay was diagnosed with Multiple Myeloma in January of this year.  This diagnosis was a complete surprise as she had gone to the doctor simply for a routine check-up. We are very grateful for the thoroughness of her primary care physician who chose to order additional tests and quickly scheduled her to see an oncologist as results came in. Lindsay underwent a bone marrow biopsy on Jan. 29th and followed up with her oncologist just 2 days later.  The biopsy and lab work have confirmed a diagnosis of Multiple Myeloma with 90% bone marrow involvement. Lindsay will begin an aggressive 4-drug chemotherapy regimen in the next few weeks with stem cell therapy to begin a few months later.  

We are very grateful for the incredible care and attentiveness that Lindsay has already received. The goal of treatment over the coming months is to get Lindsay into remission as there is no cure for Multiple Myeloma.  We are remaining optimistic though certainly still processing the information as this has all happened quite rapidly. If you know Lindsay, you know she is an inherently positive and outgoing person so it should come as no surprise that she is handling this news with an incredible amount of poise and only a few "well this f&%*ing sucks." 

Newest Update

Journal entry by Tatum Byhre

Hello! I’ve just completed my second infusion of the second cycle. It was actually the easiest one yet. Every infusion has caused challenges. They give me approximately 10 pills 30 minutes before the infusion to prevent reactions to the chemo. They help, but I wait 45 minutes after the infusions to watch and be certain I don’t have a reaction. The reactions have the potential to be quite dangerous so we want to ensure that I am safe before leaving the clinic. Today was the first day that I barely had a rash. A win for us! My body is adjusting and responding well to the chemo. My lab results are where they should be and this is great news. There will be a time that the results slow down and drugs may need to be adjusted to be more aggressive, but for now it’s good. 


Our family has found some odd ‘humor’ in my oncologists referring to me as ‘weird.’ We all already knew this, of course. This is a good and bad reference. They say this because of my Myeloma being a very rare variety. This a high risk type, which means it’s not a good ‘weird’. The other weird factor is good - It is very rare, if not barely heard of, for someone to find out they have Multiple Myeloma and not have symptoms present. Usually it’s found when a bone is broken, kidney and/or liver damage, or significant pain. Every time I go to the clinic, they first ask how my pain is. I don’t have any pain, again ‘weird’. This is when we pay attention to the blessings in this process. I am considered extremely healthy, which means I am able to respond well to the treatments since I’m not fighting other symptoms. This is where we sit with gratitude. All of this sucks, is scary, is infuriating, but it gives a new perspective of what we are grateful for and to take a win when we get one. 


Thank you for all your support, thoughts, prayers and love. It means the world to me and my family! 

Lindsay 

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