Services

Learn how in just one hour how to reclaim your life. Right now people are needing tools that will settle their minds, their nervous systems, heal their emotions, and restore a sense of creativity and hope. When people finally get to have an experience where they feel centered and creative, they feel empowered, and they want to know how they can continue their growth.

Go to YouTube to watch the free video https://bit.ly/Learn_to_stress_less

Join me monthly through the US Pain Foundation for mindfulness mediation support group sessions to learn tools and techniques to improve your overall wellbeing and reduce chronic pain. Registration required for sessions held the second Tuesday of every month at 7pmET. 
https://uspainfoundation.org/uspfevents/mindful-meditation-group/

We can in limited capacity provide individualized advocacy support that may include organizing complex medical histories, preparing patients for specialist consultations, supporting care coordination, and strengthening communication between patients and providers.

A key component of this work is the development of structured W.R.A.P.-style advocacy reports—comprehensive, research-informed summaries created through careful review of a patient’s history, symptoms, testing, and prior evaluations. These reports synthesize credible medical literature, current clinical guidance, and when appropriate, insight from recognized medical experts in connective tissue and related disorders. The goal is to provide patients with a clear, medically grounded roadmap they can use in their ongoing search for answers, accurate diagnosis, and effective treatment planning.

We also offer Disability Documentation support, helping translate diagnoses, symptoms, and real-world functional limitations into organized, clinician-ready narratives that may be reviewed, edited, and signed by treating providers for Social Security or long-term disability claims.

In collaboration with EDS-knowledgeable clinicians, including expert geneticists, she assists patients in preparing well-structured records and clinical summaries that support accurate recognition and documentation of Ehlers-Danlos syndrome and related conditions within the medical record—an essential step for appropriate treatment, accommodations, and disability determination. Her role remains educational, organizational, and advocacy-focused, ensuring patients are informed, prepared, and able to participate meaningfully in their care.

NOTE: Because Christie also lives with significant health limitations, her advocacy availability is intentionally limited. She accepts only a small number of cases at a time and works with clients as her health allows, prioritizing thoughtful, ethical, and sustainable support so that each individual she serves receives careful attention grounded in both professional standards and genuine lived understanding.

For much more information on dealing and healing from hypermobility and other complex condition, her book Holding It All Together When You're Hypermobile is available at all major retailers or more info at www.holdingitalltogether.com.  

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She is working on a new book due out July 2026.