Japanese fabrics. Quilt made for my son.
Quilt
french doors
Do you struggle with movement? Moving with Ehlers-Danlos syndromes (EDS) or hypermobility spectrum disorders (HSD) requires extra care and attention, but it's critically important! Many people with EDS or HSD struggle with pain, fatigue, and joint instability, which can make moving a daunting task. However, with the right approach, you can be active and mobile while minimizing the risk of injury. #PainManagement #ChronicPain #ChronicIllness #movingtips #chronicillnesswarrior #movingsafely
This Lanyards & Badge Holders item is sold by IDMedCard. Ships from Brooksville, FL. Listed on Feb 12, 2024
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Morgan Shaw shares a list of things she wishes she knew after her diagnosis with Ehlers-Danlos syndrome.
If you're one of the many people living with a chronic illness, you know that packing your chronic illness travel essentials is key to having a successful trip, regardless of where you're going.
The Mighty's Ehlers-Danlos syndrome community shares the funny, frustrating, sad and positive aspects of EDS only those with the condition understand.
One of the most common questions is how to manage dislocations and subluxations. Here is a description of what happens, and some suggestions on what to do when they happen.
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EDS resources, printables, freebies, awareness products, etc.
The Mighty collaborates with The Ehlers-Danlos Syndrome Society for Ehlers-Danlos Syndrome Awareness Month to ask their communities to share a photo of one symptom of EDS others often don't see.
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#FactualThursday - The different types of EDS How much do you know about the different types of EDS? There are several forms of EDS. Looking through the list of types might seem a little daunting, but for the majority of individuals the diagnosis is most likely to be the Hypermobile type (hEDS), followed by the Classical (cEDS), then the Vascular type (vEDS). You can find more information on the website: http://hypermobility.org/help-advice/hypermobility-syndromes/what-is-eds/
The Mighty's Ehlers-Danlos community shares little-known symptoms of EDS that aren't talked about as much.
