
A to Zebra Health
Diagnose, Stabilize, and Thrive:
An Integrative Approach to
Ehlers-Danlos syndrome (EDS)
and Complex Illness
Please don't try this at home
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*Hypermobile party tricks* discouraged
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Please don't try this at home 〰️ *Hypermobile party tricks* discouraged 〰️
“Show me your credentials!”
I have been a nurse practitioner for over twelve years but have lived in a body with faulty connective tissue my whole life! I think my diagnoses add to my credibility and make me a better practitioner. True, I am an advanced practice registered nurse (APRN) with board certification (BC) as an Adult Clinical Nurse Specialist (ACNS), but I am also a person who knows what it feels like to struggle with a chronic illness (or three!). Like many of you, I had decades of injuries and chronic pain and often felt dismissed by doctors. I was deeply entrenched in the conventional medical system working as an advanced practice provider for Neurosurgery at a level 1 trauma center, and even I couldn't find a nearby provider to pursue a more complete answer to my chronic nagging symptoms. I was fortunate that I had the means to travel to a specialist 4 hours away. Finally, at 42 years old, I was diagnosed with hypermobile Ehlers-Danlos syndrome and soon after, Thoracic Outlet syndrome.
With my symptoms validated, I knew that I was meant to reshape what it meant to care for complex, multi-system conditions like EDS. Admittedly, the official 2017 diagnostic criteria are nuanced and specific, but it's not brain surgery (and I would know, because I have assisted in that, too!). After nearly 10 years in Neurosurgery, I left the hospital for a smaller, integrative, and regenerative clinic for spine conditions. In 2024, as that clinic was closing, I was inspired to take the leap and build a new practice that would be quintessentially advanced practice nursing: heart-led and patient-focused. I pair heart and brain, conventional and integrative, but most of all, I believe my patients while holding space for a better, healthier future for all of us.
My goal is to build a clinical resource and networking hub for EDS and hypermobility care in Austin, TX (and beyond). Towards this goal, I am partnering with friends and colleagues that I have met along my journey. Christie Cox, now a board-certified Patient Advocate, is a champion for the under-recognized syndromes, and author of "Holding It All Together when You're Hypermobile: Achieve a Better Life Experience with EDS, POTS, and Joint Instability". I recruited her to work with my patients to help foster their own understanding of their medical story. Together, she works with patients to optimize the presentation of their symptoms and history to craft an easily digestible "one-pager" for providers. All of us have endured some form of medical trauma or gas-lighting, so I believe it is important to start with a clean slate and a positive reflection, while still honoring the odyssey we all travel.
Katie Volkers, APRN, ACNS-BC, hEDS, nTOS
Do you suffer with:
Tight muscles but loose joints
Clumsy with frequent injuries
Dizziness, palpitations, and fatigue
Migraines, headaches, and nerve pain
TMJ, cavities, and never getting numb
at the dentist
Bloating, nausea, and constipation
Increased pain when trying yoga, physical therapy,
or a new workout trendMystery hives, itchy rashes, and multiple food intolerances
If these sound familiar, I want to hear your story and carefully start putting the clues together. I chose to be out of network with insurance companies because it’s just not possible to be a medical detective in a 15-minute appointment. Let’s take back control of our healthcare and finally get the time you need with a provider to find the root cause.
Invest in your well-being, and let’s get back to
how medicine is supposed to be!

Hypermobile Integrative Care
Mast Cell Dysfunction
(MCAS)
New EDS Diagnosis
Migraine and Headaches
Dysautonomia and POTS
About Me
Katie has over a decade of experience as a neurosurgery advanced practice provider at our local Level 1 Trauma Center. Despite her long-held passion for neuroscience, she decided in 2020 to step back from conventional medicine to pursue a more holistic and integrative approach to neurosurgical problems and pain.
Ten+ years as an Advanced Practice Provider in Neurosurgery
Four years working in integrative and regenerative medicine
Lives in Austin, TX with her husband and two incredible kids (and puppy + 2 cats!)
Katie is a knowledgeable and compassionate provider. She quickly retrieves PubMed articles or scrolls through her Notion Infoverse to support her point and educate patients. When lecturing about neuroscience, she routinely got compared with Amy Farrah Fowler (AFF) so much that her boss gave her an AFF bobblehead figure. She is also relatable, witty, and empathetic, allowing her to hold space for our patients to feel truly cared for.
Outside of work, Katie enjoys spending time with her family (two children, husband, Aussie Doxie puppy, and two cats), volunteering with Cub Scouts, walking in nature, and pursuing her current creative hyper-fixation: watercolor painting and drawing with ink.

Why Zebras?
"When you hear hoofbeats, think horses, not zebras."
Healthcare providers are taught to expect the common conditions and ignore “rare” problems. In reality, hypermobility and EDS is NOT as rare as initially thought!
(Theodore E. Woodward, MD,
University of Maryland, 1950)
Sourced from the incredible
Ehlers-Danlos Society:
Why the Zebra?