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#AlexTLC #RareDiseaseDay #RareAware #EquityForRare

🌍 Rare diseases affect over 300 million people, yet access to diagnosis & treatment still depends on where you live.
💜 Equity for rare diseases means is access to suitable care, regardless of where you live.

Learn more 👉 https://go.rarediseaseday.org/equity
#RareDiseaseDay #EquityForRare

🌍 While 300 million people worldwide live with a rare disease, funding is limited.

💜 Equity for rare diseases means investing more where it’s needed most.

Learn more about equity: https://go.rarediseaseday.org/equity

#RareDiseaseDay #EquityForRare

🎗️ Rare cancers often receive less attention, leaving patients and families with fewer options and more uncertainty. Equal funding isn’t enough.

💜 Equity for rare diseases means fair funding, equal care & real hope for all.

#RareDiseaseDay #EquityForRare #RareCancers #WorldCancerDay

🦓 “Being rare shouldn’t mean being forgotten.” 💜

300M+ people live with a rare disease—many without a cure or proper diagnosis. Today, we amplify their voices.

🌍 Awareness drives research. Research saves lives. Let’s stand together!

#RareDiseaseDay #HopeForRare #EquityForRare

💜 For people living with a rare disease, equity means recognising unique needs & breaking down barriers — so everyone can fully participate in life, education & work.

⚖️ Equity ≠ equality. It’s fairness in action.

https://go.rarediseaseday.org/equity
#EquityForRare #RareDiseaseCommunity

👶 For children with genetic rare diseases, the rare disease journey often starts early.

💜 Equity for rare diseases means giving every child, everywhere, an equal start in life.

👉 Learn more:https://go.rarediseaseday.org/equity
#RareDiseaseDay #EquityForRare

HI Katie, a young adult with Hyperinsulinism shares her thoughts on fairer access to Continuous Glucose Monitors. She highlights their benefits & shares her experience of using a CGM at Great Ormond Street Hospital to help get her on the right medication dose.

#RareDiseaseDay #EquityForRare