resources & thought-provoking ideas for flexible folk

Every season is nested into a context and has its own associations. What do you think about when you ponder winter season? Holidays, colder weather, the space in between fall and spring…? In my practice, about 80% of my EDS, MCAS, and/or POTS patients see winter through the lens of icy hands and feet

Astragalus… you may have heard of it. If you have EDS and/or MCAS and are familiar with the supplement options popular within the community, you probably have tried it too. Astragalus grows in China, Mongolia, and North Korea and is a beloved herb in Asian tradition. Its Chinese name is huángqi (alternate spelling: huáng

Self-care when you live with a complex disorder like EDS (especially if you have the usual add-ons like MCAS or POTS) is crucial…but what, for a person with chronic illness or pain, does this term actually mean? And how can a person create a meaningful program if they already dedicate considerable energy to making

Have you ever considered trying red light therapy (RLT) or were you wondering about whether or not a vibration plate might be beneficial? These are two popular tools used for mood support, skincare, wound healing, and pain reduction (RLT) and for lymphatic drainage, bone density support, and muscle stimulation (the plate). You can go

It seems unbelievable when I look at it, but the first blog post I wrote about tui na and EDS went live in September of 2017. At the time, I was already a certified practitioner. I had started treating patients in a shared office space and was in the process of completing my second

Acupuncture and other modalities of Chinese medicine can be an excellent resource for people with complex disorders, EDS and the common comorbidities included. But do you know how to get the most out of your treatment when you’re complicated? What happens when you are experiencing pain AND mast cells flares AND gastroparesis AND insomnia

***** Diagnosis. It should–at least in theory–be useful for treatment planning. Having an identified condition should also mean that the prognosis is reasonably clear, at least in theory. Not so fast. Anyone with EDS or MCAS or POTS (or MALS … or … or…) knows that diagnosis is rarely linear and you

Have you ever wondered about cosmetic acupuncture? Common questions from anyone, whether a normie or a zebra, relate to things like whether or not it’s safe and if it’s worth the investment. We all want to know about that before we plunk down our payment for services rendered. But being a member of the

Have you ever thought about the difference between mindful eating and intuitive eating? They are not the same thing, but both can be helpful approaches to nutrition when a person lives with EDS, MCAS, and/or POTS. Especially when a person is limited in what they can eat, an intentional view can soften the hard edges

I seriously almost titled this essay “girding your loins for the holidays when you have MCAS.” It kind of does feel like being thrown onto an obstacle course where you have to battle your way from point one (early November) to the finish line (the first week of January), doesn’t it?