02/28/2026
🦓 We are so thankful to serve so many wonderful rare children at CS. We find it an honor to know them, learn all about their unique qualities, & seek out the treatments that give them the best quality of life.
To the families that war for their rare loved ones, keep fighting! Medical providers are listening, awareness is growing, & we pray for more accessibility to treatments. We’re in it with you!
🌍💜 Today we stand with the 300 million people living with a rare disease. We are united with their families, friends, caregivers, advocates, and the medical professionals, researchers and organisations that working tirelessly to build a more equitable future for our community.
Together, we’re showing our colours, raising awareness, and inspiring change by talking about what equity means to us.
Thank you to everyone who’s taken part, whether you’ve lit up your home, shared your story, joined an event, or supported someone you love. By standing together we’re proving that our community is strong, united, and truly more than anyone can imagine. ✨
👉 Learn more and discover ways you can still get involved: https://go.rarediseaseday.org/NEWS