Calling all scleroderma advocates—February is Rare Disease Awareness Month and Raynaud’s Awareness Month!
The SRF stands with the rare disease community because being rare does not mean being alone. And we continue to raise awareness of Raynaud’s phenomenon because it affects 90% of those living with scleroderma. Help us spread the word:
📣 Share information about what living with a rare disease is like using the hashtag #RareDiseaseDay.
📣 Tell people what Raynaud’s is, how you manage a Raynaud’s flare up, or how it impacts your life using the hashtag #RaynaudsAwareness.
📣 And use the hashtag #SayScleroderma while you do—because everyone should know what this disease is and does.
Looking for facts to share about scleroderma & Raynaud’s? Check out our resources. And stay tuned for more ways to help spread awareness. Your advocacy makes a difference in the lives of those living with scleroderma.
