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Kristina | Patient Advocate

@kppatientadvocate.bsky.social
89 followers 64 following 44 posts

📚 Board Certified Patient Advocate 🥴 SjD, dysautonomia, nr-axSpA 📖 Author of How to Be a Badass in a Broken Healthcare System and Chronically Ill, Wildly Capable (Amazon, Audible, and B&N) littleenginepatientadvocacy.com

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Reposted by Kristina | Patient Advocate
Chronic Illness Humor @chronicillness.bsky.social · 27/04/2026
No, he isn't my shitty doctor anymore. He used to be my shitty doctor 4 doctors ago. That makes him my great great great shitty doctor.
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Kristina | Patient Advocate @kppatientadvocate.bsky.social · 03/03/2026
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
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Kristina | Patient Advocate @kppatientadvocate.bsky.social · 17/02/2026
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...
littleenginepatientadvocacy.com
Building a Flexible Career with a Chronic Illness
I left “corporate America” to start my own business a couple of years before I got smacked over the head with multiple autoimmune diseases. I went from juggling four or five clients and…
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Kristina | Patient Advocate @kppatientadvocate.bsky.social · 11/02/2026
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...
littleenginepatientadvocacy.com
How to Build a Flexible Career With a Chronic Illness: Introducing Chronically Ill, Wildly Capable
I was running a successful digital marketing business before I got sick with multiple autoimmune diseases. Before fatigue knocked me to the ground. Before the pain was a gnawing distraction. Before…
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Kristina | Patient Advocate @kppatientadvocate.bsky.social · 27/12/2025
Could your lower back pain and stiffness be due to an autoimmune disease? littleenginepatientadvocacy.com/2025/12/27/1...
littleenginepatientadvocacy.com
12 Things I’ve Learned About Ankylosing Spondylitis (and Axial Spondyloarthritis)
While math and I are typically not friends, I’m going to throw some numbers at you: 4 years 4 providers 3 physical therapists 3 MRIs 2 referrals 1 hip x-ray 3 specific lab tests 1,272 gray ha…
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Kristina | Patient Advocate @kppatientadvocate.bsky.social · 06/12/2025
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
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Kristina | Patient Advocate @kppatientadvocate.bsky.social · 14/09/2025
Feeling grateful, and excited for my second book about building a custom career with a #chronicillness. First draft is 95% complete! ☺️
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Kristina | Patient Advocate @kppatientadvocate.bsky.social · 13/05/2025
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...
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Kristina | Patient Advocate @kppatientadvocate.bsky.social · 03/05/2025
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
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Kristina | Patient Advocate @kppatientadvocate.bsky.social · 27/04/2025
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...
dysautonomiainternational.org
Your dysautonomia may be caused by Sjogren’s disease. Here’s why that matters. | The Dysautonomia Dispatch
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Kristina | Patient Advocate @kppatientadvocate.bsky.social · 16/04/2025
Do you struggle with finding support or asking for support as someone with a chronic illness? littleenginepatientadvocacy.com/2025/04/16/c...
littleenginepatientadvocacy.com
Creating Your Chronic Illness Support Circle
When you’re living with chronic illness, the phrase “you’re not alone” is tossed around more than a football on a Friday night. But being surrounded by people doesn’t necessarily mean you feel supp…
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Kristina | Patient Advocate @kppatientadvocate.bsky.social · 09/04/2025
But it’s the 5/5⭐️s across all platforms that has me 😭 Available on Amazon, Audible and Barnes & Noble online.
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Kristina | Patient Advocate @kppatientadvocate.bsky.social · 08/04/2025
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
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Kristina | Patient Advocate @kppatientadvocate.bsky.social · 02/04/2025
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...
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Kristina | Patient Advocate @kppatientadvocate.bsky.social · 24/03/2025
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...
littleenginepatientadvocacy.com
Trusting Your Gut and Taking Control: A Story of Advocacy in the Face of Breast Implant Illness
The world needs to know that women’s health issues often get swept under the rug, and it’s high time we start listening, talking, and advocating for ourselves. This is why I’m so thankful to …
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Kristina | Patient Advocate @kppatientadvocate.bsky.social · 21/03/2025
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).
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Kristina | Patient Advocate @kppatientadvocate.bsky.social · 18/03/2025
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. ☺️
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Reposted by Kristina | Patient Advocate
Kara Wada MD FAAAAI, DiplABLM @immuneconfidentmd.bsky.social · 18/03/2025
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
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Kristina | Patient Advocate @kppatientadvocate.bsky.social · 16/03/2025
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
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Kristina | Patient Advocate @kppatientadvocate.bsky.social · 11/03/2025
One week to 🚀 #spoonies #chronicillness #zebras
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Kristina | Patient Advocate @kppatientadvocate.bsky.social · 08/03/2025
5 Reasons to Preorder "How to Be a Badass in a Broken Healthcare System" on Barnes & Noble! 📚
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Kristina | Patient Advocate @kppatientadvocate.bsky.social · 07/03/2025
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.
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Kristina | Patient Advocate @kppatientadvocate.bsky.social · 05/03/2025
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!
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Kristina | Patient Advocate @kppatientadvocate.bsky.social · 28/02/2025
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.
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Kristina | Patient Advocate @kppatientadvocate.bsky.social · 21/02/2025
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.
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Kristina | Patient Advocate @kppatientadvocate.bsky.social · 16/01/2025
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...
60% of patients say they forget key concerns during their appointment appointmentsA clear goal may improve your healthcare appointmentsPhoto of the patient, empowerment, workbook, tools, and tactics for powering up your appointments.
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Kristina | Patient Advocate @kppatientadvocate.bsky.social · 13/01/2025
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!
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Kristina | Patient Advocate @kppatientadvocate.bsky.social · 15/12/2024
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.
Printed book. Cover pages text says How to be a Badass in a Broken Healthcare System.
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Kristina | Patient Advocate @kppatientadvocate.bsky.social · 13/12/2024
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...
littleenginepatientadvocacy.com
MSing the Mark: Hypermobile Ehlers Danlos Syndrome Mimicking Multiple Sclerosis
Note: I am not a medical provider. Opinions in this article are based on my own research and personal experiences. Mission: Diagnosis After a particularly bad virus the month prior, I awoke to pins…
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Kristina | Patient Advocate @kppatientadvocate.bsky.social · 27/11/2024
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?
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Reposted by Kristina | Patient Advocate
ACR Journals @acr-journals.bsky.social · 25/11/2024
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
Summary of efficacy data at week 52 compared to week 24

Only patients with week 24 measurements and at least 1 measurement after week 24 were includedStimulated salivary flow rate over time up to week 48

Change from baseline for dose arms studied in treatment protocol 2 following the new treatment assignment at week 24. Baseline was defined as the last assessment performed on or prior to the date of administration of the first dose of the study treatment
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Kristina | Patient Advocate @kppatientadvocate.bsky.social · 20/11/2024
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.
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Reposted by Kristina | Patient Advocate
Sjogren’s Advocate @sarahschafermd.bsky.social · 17/11/2024
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...
sjogrensadvocate.com
New Self-Advocacy Tool – It’s Sjogren’s Disease
The official name change to Sjogren's disease can be used to encourage clinicians to address the serious, systemic nature of Sjogren's.
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