Thanks to the Beyond the Diagnosis art exhibit, an intimate window has been opened into the world of rare diseases, furthering education and faster diagnoses for a once near invisible community.

Beyond the physical, emotional and financial burden of living with — or supporting a loved one who lives with — one of 7,000 rare diseases recognized today, the rare disease community suffers from a crisis of visibility. “When you hear ‘rare disease,’ you think uncommon,” says Patricia Weltin, founder and CEO of the Rare Disease United Foundation. “People can't feel compassionate to our cause because it's unimaginable to them.”

The start of something big

In 2015 Weltin, whose two daughters live with hypermelanosis and Ehlers-Danlos syndrome, conceived of the Beyond the Diagnosis art exhibit in hopes of attracting the attention of the medical community. She recruited Rhode Island artists to paint local children living with rare diseases and hung the 17 portraits at Brown’s medical school.

Less than three years later, the grassroots effort has blossomed. “We now have some of the greatest research institutes in the world who are having symposiums and curriculums surrounding the exhibit,” she shares, adding, “Some days I have to pinch myself. I can't believe the extraordinary effect that this is having on the community.”

LIFE IN ART: Talynn (top left), Teagan (bottom left) and Brian (right), diagnosed with Opitz syndrome, schizencephaly and ataxiatelangiectasia.


Growing visibility

Now the exhibit travels across the country including annual stops at the National Institute of Health and the Food and Drug Administration. Thanks to word of mouth and a growing social media presence, hundreds of children have had their portraits painted, and there’s an international waiting list of artists that wish to donate their skills.

Tragically, since the exhibit began, five children painted have lost their battles. Weltin offered to return the portraits, but each family declined. "They want their child's life to continue to be the face of the disease... to raise awareness and to increase research.”

Beyond the Diagnosis is bridging the gap between the rare disease community and the wider world. “People have an appreciation for the arts,” Weltin reflects, “and that appreciation has become compassion for our children.”