Since January, the Cystinosis Research Foundation has awarded $1,023,953 in research grant payments across 7 countries — fueling innovation and accelerating the path to better treatments and a cure. From Canada to Italy, and the U.S. to Switzerland, our global network of scientists is pushing boundaries every day in the fight against cystinosis. 🔬 Explore our full impact and areas of research focus: 👉 cystinosisresearch.org/impact #CRF #CystinosisResearch #RareDiseaseAwarreness #RareDiseaseResearch #HopeForACure #BetterTogether" #BackToSchoolTips #CystinosisCommunity #RareDiseaseParenting #CystinosisAwareness #ChronicIllnessSupport (fb)

New grade. New goals. Same unstoppable spirit. 💙 Heading back to school while managing cystinosis can feel overwhelming, but with a little planning, your student can step into the year with confidence. Here are 5 quick tips from the CRF community. Parents, caregivers, and students: What helps you feel prepared for the school year? Drop your advice below to help another family out. 💬📚 #BackToSchoolTips #CystinosisCommunity #RareDiseaseParenting #CystinosisAwareness #ChronicIllnessSupport (fb)