</p>
<div class="wp-block-image">
<figure class="aligncenter size-large"><img loading="lazy" decoding="async" width="768" height="1024" src="https://rarewithflair.com/wp-content/uploads/2025/01/IMG_0979-768x1024.jpeg" alt="Cass (left) and Case (right) enjoy an afternoon tea. They smile warmly and toast with delicate teacups in front of a tiered tray of sandwiches and pastries." class="wp-image-1381" srcset="https://rarewithflair.com/wp-content/uploads/2025/01/IMG_0979-768x1024.jpeg 768w, https://rarewithflair.com/wp-content/uploads/2025/01/IMG_0979-225x300.jpeg 225w, https://rarewithflair.com/wp-content/uploads/2025/01/IMG_0979-1152x1536.jpeg 1152w, https://rarewithflair.com/wp-content/uploads/2025/01/IMG_0979-1536x2048.jpeg 1536w, https://rarewithflair.com/wp-content/uploads/2025/01/IMG_0979-scaled.jpeg 1920w" sizes="auto, (max-width: 768px) 100vw, 768px" /><figcaption class="wp-element-caption">Case + Cass at tea, 2024</figcaption></figure>
</div>

111. lifting the burden: how we pay it forward

Casey + Cassandra are a pair of best friends with the same rare disease. Their goal is simple: sharing their lives to showcase the beauty and normalcy in disability, while having fun together. They’ll also touch on accessibility, friendships, style, and everything in between as they live their best, rare, lives! For show notes, go to rarewithflair.com

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111. lifting the burden: how we pay it forward

111. lifting the burden: how we pay it forward

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