Rare Disease Day is the globally-coordinated movement on rare diseases, working towards equity in social opportunity, healthcare, and access to diagnosis and therapies for people living with a rare disease.

Since its creation in 2008, Rare Disease Day has played a critical part in building an international rare disease community that is multi-disease, global, and diverse– but united in purpose.

Link – https://www.instagram.com/reel/CaiAqlyIjBZ/?utm_medium=copy_link

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Rare Disease Day is observed every year on 28 February (or 29 in leap years)—the rarest day of the year.

Link – https://youtu.be/vORB18tPwww

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#Collabration #NoActionNoPeace #EndDiscrimination #InvisibleDisabilities #YouthLead #LetsChangeTheNarrative #endcommodityeducation #NewVisionForEducation #NewVisionForWork #neurodiversityinbusiness #neurodiversity #changetheworld #changethenarrative #enddiscrimination #SENLIVESMATTER

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Please all also check out #TheClaudesSENLaw ~ (Link In Bio) for more information or even visit @a_claude_2020  @citymaas

Stay updated with next post in regards to The Claudes SEN Law Campaign. In the next coming days. ✍🏾✊🏾📢 #TheClaudesSENLaw