Resonate Massage Therapy

Screening for hypermobile characteristics is one of the first assessments I do in your first session.

I also scan your intake form looking for the symptoms listed in this post, and others, such as bruises easily and joint pain/ frequent dislocations.

It’s not in my scope of practice to diagnose hypermobile spectrum disorders (HSD) or hypermobile Ehlers Danlos Syndrome (hEDS), but I can help significantly improve many of the symptoms with myofascial trigger point therapy & FSM.

Reach out out you would like more info, I offer free phone consults. 📞

Hypermobile Ehlers-Danlos Syndrome (hEDS) is more than just hypermobile joints. 💙

Because connective tissue is found throughout the body, hEDS can affect multiple organ systems, leading to symptoms that extend far beyond musculoskeletal pain and joint instability.

Some people with hEDS may experience:
▫️ Lightheadedness or fainting
▫️ Rapid heart rate with minimal activity
▫️ Gastrointestinal symptoms
▫️ Nausea or vomiting
▫️ Stomach cramps
▫️ Constipation
▫️ Migraine headaches
▫️ Neuropathy
▫️ And many other symptoms

Every person's experience with hEDS is different. Symptoms can range from mild to severe and often overlap with related conditions such as dysautonomia and mast cell disorders.

💬 Which symptom has had the biggest impact on your daily life? Share your experience in the comments. 👇Your story may help someone else feel less alone.

If you're looking for a provider experienced in EDS, POTS, dysautonomia, MCAS, Chiari, and related complex neurological conditions, our practice is gradually accepting new patients.

As with all new patients, scheduling requires completion of the screening process and intake paperwork. Appointments are offered based on clinical review and availability.

🔗 Join the waitlist through our website using Klara. https://bit.ly/Learn_More_CCN

💙 Save this post for future reference.
📤 Share it with someone living with hEDS.
👍 Follow Center for Complex Neurology, EDS & POTS for more info on hEDS.

Most of the time that persistent pain between the shoulder blades is referral from the neck. 🦒

Releasing trigger points in neck muscles that refer to the upper back & adhesions in relevant tissues is often all it takes to relieve chronic muscle tension & related symptoms. 🎯

Often this is resolved in one session, like in this case. 💪

Myofascial trigger point therapy & FSM work by finding & treating the root cause, kind of like solving a mystery. 🔍

In this case, it was adhesions & trigger points caused by multiple head injuries & repetitive movements from a sport she played in high school. 🏋️‍♂️

When you treat the WHY, the WHERE often melts away. 👍

Reach out if you’ve been dealing with chronic pain, numbness, weakness, restricted movement, or other symptoms. These are signs of trigger points & adhesions/scarring.

By appointment only.
Call/text to schedule an appointment or a free phone consult. 📞

https://www.massagebook.com/biz/resonate

Foot restoration programs, foot-shaped footwear, & specialized myofascial trigger point therapy can help with stabilizing hypermobile joints, improving muscle tone, & managing chronic pain. 👣

The zebra is the symbol of the EDS community for a few reasons:

🦓 “When you hear hoofbeats, think horses, not zebras” is an old medical saying meaning to look for the most common diagnosis (horses) rather than a rare one (zebras). This leads to delayed diagnosis and often several misdiagnoses for people with EDS.

🦓 Just like no two zebras share the same stripes, no two people with EDS share the same set of symptoms.

EDS (Ehlers Danlos Syndromes) is a genetic condition that affects the body’s connective tissue. This tissue, which supports ALL of your body systems & structures, are weakened due to defects in collagen production, causing a variety of symptoms & conditions.

🦓 EDS is more than hypermobility.

Ehlers-Danlos syndromes are complex connective tissue disorders that can affect the joints, skin, blood vessels, organs, autonomic nervous system, and more.

For many patients, symptoms are chronic, life-altering, and often invisible to others.

This EDS Awareness Month, we stand with the community in raising awareness, encouraging earlier recognition, and helping patients feel seen and understood. 💙

EDS is...
REAL.
COMPLEX.
OFTEN INVISIBLE.

💬 Drop a 🦓 in the comments if you’re a zebra or supporting one
💜 Like to help raise awareness
🔁 Share this so more people understand what EDS really is

Let’s make sure zebras are seen this month 🦓