Lindsay’s Story

Site created on December 5, 2019


Welcome to Lindsay's Caring Bridge website. We are using it to keep family and friends updated in one place. We appreciate your support and words of hope and encouragement.  If you are local and wondering how you can help, a meal train, and childcare schedule will be organized when the need arises. It can be accessed by clicking on the "Ways to Help" tab.  We literally have no idea what our needs are going to be at this point. 


Thank you for visiting.

From Lindsay (February 2024):
Well, here we go again. Thanks so much for supporting my family and I through this process. It is going to be a long haul with chemo, surgery, (maybe more chemo), radiation, and hormonal therapy. I will do my best to update this site with any news. The fact that this pesky cancer has found a way to still survive in my body is angering but I'm going at it with everything I've got. I'm confident that next year at this time, my hair will be growing back, I'll be adjusting to new medications, and I will settling into a life of survivorship. Thanks again for all the love and support! 

From Lindsay (December 2019):

In the weeks since my diagnosis I find myself being more grateful than angry, and more touched than sad. However, I am gearing up for a surgery I never wanted and a life that will never be the same. I am also preparing myself to live a very long, cancer-free life. I'm focused on my amazingly supportive family and friends. and being here to annoy them for as long as possible. 

If you are here on this site, I imagine you are a family member, a friend, and/or a coworker of mine or Justin's...or even of our extended family. Thank you for your concern. I welcome your messages, positive thoughts, love, and of course, prayers (that was for you, Mom). I didn't pick this fight but your support gives me strength. Much love to you and thanks for following me through this journey.

Newest Update

Journal entry by Lindsay McAllister

I had a great (but quick) weekend seeing friends and family at the annual Pig Roast (shout out to all our Santa Cruz peeps who overflowed my cup with love and laughs)! I felt rejuvenated moving into the start of my new treatment today. 
Erin was here again for this treatment and she and Justin tag teamed since I can only have one person in the infusion suite with me.
For this drug, Taxol, there is a possibility of allergic reactions so they pumped me full of antihistamines which made for a sleepy afternoon but for the first time I felt good enough to drive myself to acupuncture. 
There is also a risk of neuropathy with Taxol so I wore ice packs on my hands and feet. There is some research showing it could help decrease neuropathy. Same idea as cold capping in hopes of not losing your hair. I must say, it was pretty uncomfortable having frozen fingers and toes for an hour and a half. I was a total wuss but eventually got in a groove. As always, Erin was a good distraction with her humor - reminding me not to worry, because I only have to do this 11 more times. I have decided that cold plunging is not something I ever need to try.
I’ve promised my oncologist that I will not over do it tomorrow but right now, I’m feeling much better than I anticipated. I know this will be the easiest of the 12 but I’m pretty confident that it will be easier than AC.
Thanks again for all the love and support. Xo




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