June is here—and so is Scleroderma Awareness Month. We’re asking you to say it with us: #SayScleroderma. 📣
Scleroderma is complicated, often invisible, and still widely unknown. This leads to delays in diagnosis and treatment, and real harm to those living with the disease. Raising awareness is how we will change that.
This June, The Scleroderma Research Foundation, the Scleroderma Foundation of California, the Scleroderma Foundation of Greater Chicago, and Scleroderma Outreach Northwest are uniting forces–because when more voices join us to #SayScleroderma, we can get louder and reach farther than ever before.
We need YOU to join us! Here are just some of the ways you can make a difference this Scleroderma Awareness Month:
🖼️ Use our profile photo frame: Add the custom #SayScleroderma profile photo frame on your social media accounts to showcase your support for the cause all month long.
📹 Record a video: Share why you choose to #SayScleroderma and what this month means to you, whether you live with the disease, or care for someone who does.
💬 Have a conversation: #SayScleroderma in your community, whether at home, at work, or at a local event.
📣 Amplify: Re-share posts from across our coalition and help us reach beyond our existing audiences.
Every way that you #SayScleroderma brings us closer to a world where scleroderma is understood, treated, and one day cured.
