Hope for Hypermobility:
Live access to Rebecca. The validation, the answers... the next step you’ve been waiting for.
Twice a month. On Zoom. No appointment. No referral. No co-pay.
I'M READY TO JOIN →"Rebecca is truly amazing. Not only is she extremely knowledgeable in all things EDS, she also has EDS herself. When your provider can understand the same or similar symptoms you experience, it is so helpful. She gets it. Rebecca was able to provide a lot of "ah ha!" moments in regards to my health, and able to direct/refer me to EDS-knowledgeable specialists. Couldn't recommend her enough."
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– Sami L
Hi — I'm Rebecca.Â
I'm a Nurse Practitioner.
I'm also hypermobile, neurospicy, and someone who still remembers exactly how debilitating that pain and fatigue was — not just in my body, but in everything it touched. You don't have to convince me your symptoms are real. I already believe you.Â
What I remember most isn't just the pain and the bone-deep fatigue. It's the loneliness that settled in alongside it — being scared this was just how I'd feel forever, with no one around me who understood. I went looking for help online anyway. Most of what I found didn't give me hope. It took what little I had left.
I built this because I needed it, and it didn't exist...
I'M READY TO WORK WITH YOU!
I know what it costs emotionally, physically, and financially to book another appointment.
So I built something different...
Open Clinic Hours.Â
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Show up, get your answers from me, live. No prep required, no waiting a month for a consult.Â
Inside Hope for Hypermobility you get:
→ Twice-monthly Open Clinic Hours — live, on Zoom, with me.
→ A community of hypermobile humans who already get it.
→ The recorded library that took me years to build — yours to use as you need it.
→ Your H4H investment applies toward 1:1 work with me if you ever decide to go there. Â
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I'M READY TO JOIN →
What you actually get:
→ Ongoing access — not a one-time call. This continues as long as you’re a member.
→ Bring your current situation and receive immediate validation. We meet you right where you are.
→ You will get what you need just by showing up. No plan, no question, no script required. No appointment, no referral, no co-pay.
→ If you have a bad flare or low-energy week, definitely come. Off camera. Lying down. Just listen. I can turn a three-week flare into a three-day flare.
→ Neurodivergent-affirming design — for brains like yours
You don't have to try everything you know might help before you get help.
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You can come exactly as you are — imperfectly, unprepared, mid-flare, mid-question, mid-life. That’s the point.
"I feel so seen by Rebecca. She creates a very safe, supportive and uplifting environment. – whether that be in person, remotely or via emails/messaging.
I’m Non-Binary, Autistic and have c-ptsd. So to not only be in the care of someone who validates my gender, lived experiences and needs – but to also feel advocated for, encouraged and understood… it feels so empowering."
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– Elle J
This program is for you if:
✔ You want direct, real-time access to Rebecca
Open Clinic Hours are twice a month, live on Zoom. You bring the question — the new symptom, the lab result, the medication question, the flare you’re trying to make sense of — and you get an answer in the room. No appointment, no referral, no co-pay.
✔ You have been diagnosed with hEDS/HSD, POTS, MCAS
Or other related disorders and are seeking immediate, results-oriented symptom relief.
✔ You have not been diagnosed
But suspect you have hEDS/HSD, POTS, MCAS or other related symptoms. You don’t need to convince us–we already believe you. Our program can provide symptom relief bypassing the need for formal diagnosis.
✔ You’re desiring a supportive community
Of other hypermobile folks who get it and are just like you.
✔ You’re neurodivergent
And long for an empathetic, easy-to-follow program designed for brains like yours.Â
THIS WAS MADE FOR ME! I'M READY TO JOIN →Plus everything I’ve learned, built into a recorded library you can use as your body allows.Â
Open Clinic Hours is the heart of Hope for Hypermobility.
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The recorded library is the foundation underneath it — every piece of this took me years to research and learn. I want to save you the decade it took me, despite already being a medical professional.
Meet it where your body is. Watch in order, jump around, or just put it on to listen while you rest.
The course gives you the foundation. I give you the rest.
NEURODIVERGENT-AFFIRMING DESIGN — FOR BRAINS LIKE YOURS.Â
You’ll learn what neurodivergence really means and how it connects to chronic conditions like hypermobility and POTS. We’ll explore research showing that neurodivergent people are more likely to experience hypermobility, dizziness, and chronic pain — and how factors such as gender, race, and access shape who receives diagnosis and support. This section is about shifting perspective: understanding neurodivergence not as a deficit, but as a difference — and seeing how those differences intersect with your overall health.Â
UNDERSTAND YOUR BODY:
Hypermobility doesn’t just affect your joints — it influences how your whole body feels and functions day to day. In this section, you’ll explore how hypermobility can contribute to common issues such as a stiff neck, tight shoulders, recurring headaches, and hips that just don’t feel aligned.
You’ll gain a deeper understanding of why these patterns show up in hypermobile bodies and, most importantly, learn practical strategies to address them.
PAIN MANAGEMENT & REDUCTION:
Explore innovative approaches to being more comfortable in your body. This is not the boring or mainstream "go to PT, rest better, try this med" advice. You deserve so much better! By the end of this module, you’ll gain a deeper understanding of how pain shows up in the hypermobile body. You’ll also learn practical tips for reducing chronic pain, along with tools to support you during flare-ups (clients can see pain reduction of 25% in 60 days).Â
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SUPPLEMENTS & NUTRITION:
You’ll learn about my top three supplement recommendations that I share with almost everyone living with chronic illness or pain. You’ll also receive a link to my Full Script account, where you can purchase these supplements at a discount. In addition, you’ll gain a deeper understanding of nutrition — exploring the evolutionary biology of food, how to use nutrition for healing, and some of the most common nutritional triggers that exacerbate hypermobile pain.Â
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LABS FOR CHRONIC PAIN & FATIGUE:
You’ll learn about the top five lab tests I consider most important for people with hypermobility. These tests can reveal underlying factors that contribute to pain, fatigue, and inflammation, helping you gain a clearer understanding of what’s happening in your body.
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TALK SO YOUR DOCTOR LISTENS:
Master the art of talking to healthcare professionals to make those clinic visits effective. We know it is exhausting meeting yet another new person to ask for help. This course will help you know exactly what to say to your healthcare professionals minimizing frustration and back-and-forth with your medical team.
"My health stuff is radically more stable now and I feel so much better. Your partnership has been instrumental as I've navigated my bizarro health mysteries. Your validation of my experience and the realness of my strange symptoms took what was otherwise isolating, confusing, and at times scary – and reminded me that I'm not crazy, these things are indeed hard, and continuing to follow-up and explore leads is worth it…Thank you, thank you, thank you. I know it's your job, but it's been so much more than a job. It's changed my life, and the life of my family. We are all truly grateful."
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– Sarah M
Hi — I'm Rebecca.:
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I'm a Nurse Practitioner. I'm also hypermobile, neurospicy, and someone who spent years being told my symptoms weren't connected.
You don't have to earn your believability here. I already believe you.
I needed someone like who I am today so badly, earlier in my life. I went to clinician after clinician, hoping someone would finally believe me. Most didn't. And somewhere along the way, I started believing them instead — that I just wasn't trying hard enough, wasn't explaining it right, wasn't sick enough to deserve real help.
I was wrong about that. So are you, if you've ever thought it about yourself.Â
From 15 to 32, I was always either intermittently or intensely searching for an answer.
Seventeen years of that search, before I had a name for what I was living with: hypermobile Ehlers-Danlos Syndrome. Seventeen years of being told it was anxiety, or deconditioning, or nothing at all. I know that particular exhaustion — the kind that comes not from your body, but from constantly having to prove your body is real.
Here's the strange part: I didn't go into medicine to solve my own mystery. I went in because I loved mysteries themselves — I wanted to be Sherlock Holmes, the kind of mind that finds the one detail everyone else missed.
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I just couldn't stomach the dark side of that world. So that love of solving things turned into a desire to prevent suffering instead of just investigate it, and that's what led me to nursing. It took years before I saw it: the thing I was building a career around, and the thing I was quietly living with, were the same thing all along.
I built Hope for Hypermobility to be what I wish had existed back then. Not another clinician's appointment where you have to start from zero.
A place where the believing has already happened and the expertise is already there — so we can get straight to the part where you start feeling better.
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