It’s my book birthday! 🎉 Chronically Ill, Wildly Capable is ready to help you build a flexible and sustainable career. Available on Amazon and Barnes & Noble. a.co/d/03rsY0Fu

Cover reveal of my next book! Find out what a busted ladder and vines represent for those of us working with a chronic illness: littleenginepatientadvocacy.com/2026/02/17/b...

Exciting news 🎉 My next book, Chronically Ill, Wildly Capable, comes out March 3rd! Packed with relatable and humorous stories, heartfelt interviews, and easy to implement strategies to start planning your flexible, sustainable career. Read the blurb ⬇️ littleenginepatientadvocacy.com/2026/01/21/h...

Could your lower back pain and stiffness be due to an autoimmune disease? littleenginepatientadvocacy.com/2025/12/27/1...

If you want to start the new year with more confidence on your health path, these 2 resources are on sale thru 12/31/25: 🎁 Streamlining Sjogren’s course: 20% off with code HEALTHYHOLIDAY 🎁 Patient Empowerment Workbook: 15% off with code POWERUP15 resources.littleenginepatientadvocacy.com

Feeling grateful, and excited for my second book about building a custom career with a #chronicillness. First draft is 95% complete! ☺️

I was honored to be invited on the Uncompany CMDQ Podcast, which explores what it’s like to leave things behind. Through sharing my story, I talked about quitting being a passenger in your healthcare journey and how to stay in the driver's seat. www.weareuncompany.com/podcasts/cmd...

Honored to be in @sarahschafermd.bsky.social recent newsletter. Her kind words about my book have me smiling from ear to ear! #autoimmunelife #sjogrens #patientadvocate

Understanding dysautonomia played a significant role in advocating for my Sjogren’s diagnosis. Excellent article that dispels myths around this autoimmune disease. dysautonomiainternational.org/blog/wordpre...

Do you struggle with finding support or asking for support as someone with a chronic illness? littleenginepatientadvocacy.com/2025/04/16/c...

But it’s the 5/5⭐️s across all platforms that has me 😭 Available on Amazon, Audible and Barnes & Noble online.

I’m at 99 books sold in less than 3 weeks! Snag the 100th copy…for you, a friend, a neighbor, or a loved one. 5/5 ⭐️ across ebook, paperback and audible. Giddy & grateful. 🥰 🛒 Amazon, Audible and Barnes & Nobles online 📷: Buddy the Foxhound

Shared with permission: “I cannot thank Kristina enough. That book is a game changer for me. I've been sitting here blaming God. Blaming myself. Thinking it was just me -that nobody cared about me and that's why no one was helping me because it was what I deserved...

I never heard about Breast Implant Illness (with no leakage) until this brave woman shared her story. She knew what was wrong, but doctors wouldn’t listen. This is true self-advocacy work on her part. littleenginepatientadvocacy.com/2025/03/24/t...

Knowing how many people buy a book and never finish it (guilty myself), I had a goal of how many books I wanted to sell my 1st year. My book has been out for 4 days and I’m 60% to goal. If I didn’t have Sjogren’s, I would have tears of joy 🥹 I hope it empowers readers & gives them hope (& a laugh).

It is my book birthday! 🎉 As a chronically ill patient and board certified patient advocate, I wanted to create a self-help book that provided patients with validation through relatable stories and proven strategies on how to battle through common healthcare challenges. On Amazon & B&N online. ☺️

Double duty: patient with Sjögren's & dysautonomia AND a physician. Just finished "Being a Badass in a Broken Healthcare System" by @kppatientadvocate.bsky.social 🤯 It's like she wrote my life story... but also gave me a manual for how to be a better doc. 😅 🧵1/4

3 more days until 🚀! I poured my heart and spoons into this book for the past 13 months. I wrote it for anyone who feels alone, scared, frustrated, and abandoned in their chronic illness journey. Get your copy Tuesday, March 18th on Amazon and Barnes & Noble online. ☺️ #spoonies #zebras #healthcare

One week to 🚀 #spoonies #chronicillness #zebras

5 Reasons to Preorder "How to Be a Badass in a Broken Healthcare System" on Barnes & Noble! 📚

The audiobook version of my book is live! Available on Audible and iTunes. It’s a mix of relatable stories and proven strategies for my fellow chronic illness warriors or caregivers. Ebook & paperback will be available Tuesday, March 18th on Amazon and B&N online.

My debut book, How to Be a Badass in a Broken Healthcare System, is #1 and #2 in new releases in two categories 🥰 for Kindle preorder. Thank you for the early support. All formats come out Tuesday, March 18th on Amazon and Barnes & Noble online. Let’s feel better together!

It’s Rare Disease Day. As someone navigating a rare disease, I know how challenging it can be to get that elusive diagnosis, find a care team you can truly trust, and then figure out what actually works for your body. It’s like trying to solve a puzzle that doesn’t even have all the pieces.

Only a few spots remain for advanced copy readers (ARC) for my new book. Free ebook for an honest review. It’s a mix of stories (told with sass & humor) and strategies from a board certified patient advocate to empower chronically ill patients. Reach out if interested & I’ll send more details.

Do your doctors appointments leave you feeling dismissed, hopeless, angry & confused? We can’t control how providers show up, but we can control how we show up. The Patient Empowerment Workbook teaches effective communication & goal setting. resources.littleenginepatientadvocacy.com/patient-empo...

Getting excited for my book, How to be a Badass in a Broken System! It was written for chronically ill patients who want to go from overwhelmed to empowered. Coming out in March!

Coming in March! A complete guide for being your own best advocate. Perfect for chronic illness patients struggling to be seen and heard in the healthcare system. Help get the care you deserve! Still same spots available for ARC readers. Let me know if you’re interested.

MS got all the attention before I was correctly diagnosed with hEDS (and later Sjogrens & myasthenia gravis) because the symptoms can mimic each other. littleenginepatientadvocacy.com/2024/12/04/m...

If you struggled to get diagnosed with your chronic illness, would you have joined a program / bought a course that provided tips & tactics to help reduce time to diagnosis & care?

Week 52 efficacy results and up to 2-year safety follow-up of ianalumab in patients with Sjögren’s disease from a phase 2b dose-finding study In A&R acr.tw/3CEmaUJ #Medsky Figures (1) Summary of efficacy data at week 52 compared to week 24 (2) Stimulated salivary flow rate over time up to week 48

Excited to be on this platform and off of x. After battling symptoms & dismissive doctors for years, I found my way to answers & treatment. As a result, I went back to school & just passed my board exam as a patient advocate. I’ll be specializing in #autoimmune and #connectivetissue conditions.

It's Official: Sjogren's DISEASE, not syndrome, has been accepted by the international community. This better reflects the serious systemic nature of the disease, which is never limited to sicca. Learn more: www.sjogrensadvocate.com/post/new-sel...