Don't give up on future you.
I get it, you’ve tried everything and feel kind of lost in space with how to manage Complex Regional Pain Syndrome (formerly known as Reflex Sympathetic Dystrophy) or the culmination of multiple other chronic diagnosis…You’re doing your best to use your affected body parts as much as possible in the hopes of decreasing pain, but continue to feel stuck and hopeless with little guidance and support.
I know…I’ve been there.
But what if I told you it doesn’t have to be like that? That there are ways to take your power back to create more predictability and less pain?
And I can help.
I know finances are often difficult. Having to spend more on something that isn’t our fault is never fair. My goal is to help patients be more self-sufficient and taken advantage of less, not profit off pain myself. My methods, and what I have learned help people save a tremendous amount of money elsewhere.
Besides all my Instagram content, you can also join the free RWC community newsletter below, which I send out every week-ish with chronic pain tips, personal perspective and announcements around upcoming programs and partnerships.
PROGRAMS FOR PATIENTS
Need help decreasing pain enough to work out or creating an individualized workout plan?
Learn the MARSMethod and how to treat central sensitization with other awesome warriors.
DIY dude/dudette? I gotchu. Sometimes you don’t want/need high touch for impactful wins.
On-demand options to learn more about specific topics like breathing, movement, and sensitization.
How did I get here?
I was born and raised in sunny San Diego, CA, and always loved being active, competing at high school varsity & AAU level basketball for four years before college. 5 months after getting my B.A. in Marketing at Washington State University, I was in a car accident suffering a traumatic brain injury (TBI). Over the next 9 years, I went through a very slow and difficult recovery often in a cognitive haze, struggling through tolerating various severe treatments like electro convulsive therapy and tolerated over a hundred medication changes to combat the persistent insomnia, depression, chronic pain, and gastrointestinal issues. With the fortitude I developed as an athlete, I continued to persevere during this lengthy healing process and started regaining my independence cognitively and physically, developing the self care I’d lacked when so sick. As I got healthier, by June of 2019 I began running regularly. Unfortunately what began as a mild pain in my lower left leg turned into excruciating agony radiating from my shin. My left leg was covered in bruises and scalding hot, feeling as if my bones were freshly
shattered with an immense pulsating pressure. My skin from the knee down through my toes felt like there were bugs crawling on it and just the smallest bit of cycling at the beginning made it feel like my tibia was literally splitting and muscles were tearing. The spasms and contractures were relentless and constant limb guarding was the only way to survive. After months of not being able to put my foot on the ground, a bone scan in February 2020 finally confirmed the diagnosis of Complex Regional Pain Syndrome (CRPS). I was started on typical medications for neuropathic pain and received repeated lumbar sympathetic blocks with minimal improvement, finally making the decision to have a DRG Spinal cord stimulator (SCS) implanted in 2021. Although the SCS reduced symptoms, living with it while being as active as possible came with its own set of challenges, leaving me with the question, “How do chronic CRPS patients actually live with this disease once there are no more treatments to try?” That’s what I’ve learned to do, and have turned that experience into helping others do the same.
Let’s work together!
Or, you can also get free content on Instagram and join the no-cost RWC community newsletter, which I send out every week-ish for more chronic pain tips, personal perspective and announcements around upcoming programs and partnerships!