August 12

Millions of people wear medical compression every day. Most of them hide it.
Compression Awareness Day is a new national observance created to change that.

On August 12, we’re asking people who wear compression garments to show them, however they feel most comfortable, and asking everyone else to wear purple in solidarity.

What Is Medical Compression?

Medical compression comes in many forms, worn on arms, legs, hands, feet, and torso, and supports a wide range of chronic illnesses. Lipedemama founder Kelly Schwartz uses it for lipedema, POTS, and hEDS. Other medical uses include lymphatic and venous conditions. Even pneumatic compression pumps fall into this category.

Why This Matters

Despite how common medical compression is, there’s no national day bringing awareness to it. Many people who wear it are hesitant to show it, covering it with long sleeves and long pants to hide their gear. We’ve been conditioned to hide it, even though it’s what helps us feel better. By sharing our compression, we hope to normalize it in the workplace, the grocery store, the waiting room, the hallway, and everywhere in between.

How to Participate

  • If you wear compression: Post a photo showing your compression garments, however you’re comfortable. Tag #CompressionAwarenessDay.
  • If you don’t wear compression: Wear purple on August 12 and tag us. You’re standing in solidarity with everyone who does.
  • Everyone: Share this page. Share the graphics. Talk about why compression matters, whether it’s part of your life or a loved one’s.

A Note From the Founder

August 12 is also my own lipedema diagnosis anniversary. In 2025, I found out what was actually going on in my body after years of not knowing. This year marks one year since that day, and I couldn’t think of a better way to honor it than by launching something that helps the next person feel less alone in theirs.

This day belongs to all of us. But I wanted you to know why this date, specifically, means so much to me.

— Kelly

Download the Kit (more coming soon!)

[Graphics for Instagram, TikTok, and Facebook] [Printable flyer]

Compression Awareness Day was founded by Kelly Schwartz of Lipedemama.

You’re Not Alone

If any part of my story sounds like yours, you’re in the right place.
Reach out directly, join our Wisconsin lipedema community, or just start reading. You don’t have to figure this out alone. 🩷