For every purchase, we donate $1 to organizations advancing research, education, advocacy, and patient support.
It adds up — and it goes directly toward communities that need it most.
Our Featured Cause
Understanding EDS
The Ehlers-Danlos syndromes are a group of heritable connective tissue disorders that affect the body's collagen — the "glue" that holds skin, joints, blood vessels, and organs together.
Because symptoms vary widely and awareness remains low — even within medicine — many patients spend years searching for answers, often being told their pain is normal, exaggerated, or imagined.
13
recognized subtypes of Ehlers-Danlos syndromes
10+ yrs
average time many patients wait for an accurate diagnosis
0
identified genetic markers for hypermobile EDS — the most common type
Why Donations Are Needed
It's Under-Recognized
EDS is often called an invisible illness. Many patients look healthy on the outside while managing chronic pain, joint instability, and fatigue every day. Low awareness — including among healthcare providers — leads to long diagnostic delays and missed care.
Research Is Underfunded
Hypermobile EDS — the most common form — still has no identified genetic marker. Without more research funding, diagnosis remains difficult and treatment options stay limited.
Patients Need Advocates
From education for providers to support networks for newly diagnosed patients, organizations like The Ehlers-Danlos Society give this community a voice — and every donation strengthens it.
How Your Purchase Helps
Place an Order
Shop Root Cost Meds — with or without a membership. Every purchase counts.
Your $1 Is Counted
Every time you place an order, $1 is set aside toward our giving fund.
We Donate
Funds go to The Ehlers-Danlos Society and other organizations advancing chronic illness research, education, advocacy, and patient support.
Our Commitment
"Healthcare should be transparent, accessible, and community-driven. Giving back is part of who we are — not an afterthought."