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Archibald Garrod discovered AKU in 1902. It's time to #HelpCureAKU

Archibald Garrod discovered AKU in 1902. It's time to #HelpCureAKU

At the launch of AKU Society India, Dr Isaac and AKU patients #HelpCureAKU.

At the launch of AKU Society India, Dr Isaac and AKU patients #HelpCureAKU.

The whole team at the AKU Society, including two volunteers.   Join the #HelpCureAKU campaign today.

The whole team at the AKU Society, including two volunteers. Join the #HelpCureAKU campaign today.

Alkaptonuria patient Ann, joining the #HelpCureAKU campaign. Help find a cure for her and hundreds more by getting involved.

Alkaptonuria patient Ann, joining the #HelpCureAKU campaign. Help find a cure for her and hundreds more by getting involved.

Genetic Alliance UK's Chairman, joining the #HelpCureAKU campaign to raise awareness of the world's first genetic disease.

Genetic Alliance UK's Chairman, joining the #HelpCureAKU campaign to raise awareness of the world's first genetic disease.

This cute little chap is called Nate. He's a four-year old AKU patient in Australia, and he's joined the cause to #HelpCureAKU.

This cute little chap is called Nate. He's a four-year old AKU patient in Australia, and he's joined the cause to #HelpCureAKU.

Prof Jim Gallagher, from the University of Liverpool, with our RARE Champions of Hope Award for Collaborations in Science. He received this award on the 21st, in the middle of our campaign, recognising the #DevelopAKUre consortium's hard work for our clinical trials. #HelpCureAKU

Prof Jim Gallagher, from the University of Liverpool, with our RARE Champions of Hope Award for Collaborations in Science. He received this award on the 21st, in the middle of our campaign, recognising the #DevelopAKUre consortium's hard work for our clinical trials. #HelpCureAKU

Denise Higgins, AKU patient and President of AKU Society North America, with Ethan Perlstein - an 'Indie Scientist' who has been helping us with our #HelpCureAKU campaign.

Denise Higgins, AKU patient and President of AKU Society North America, with Ethan Perlstein - an 'Indie Scientist' who has been helping us with our #HelpCureAKU campaign.

Nick, the father of two boys with Black Bone Disease; Sylvia, President of the Italian patient group aimAKU; and Andrea, part of the clinical trial team curing Black Bone Disease.   Get involved with the #HelpCureAKU campaign now.

Nick, the father of two boys with Black Bone Disease; Sylvia, President of the Italian patient group aimAKU; and Andrea, part of the clinical trial team curing Black Bone Disease. Get involved with the #HelpCureAKU campaign now.

#HelpCureAKU goes multilingual! We're on a mission to get 'Help Us Cure Black Bone Disease' translated into as many languages as possible. Here's Hana and her parents holding up the slogan in Tamil, English and Malay.

#HelpCureAKU goes multilingual! We're on a mission to get 'Help Us Cure Black Bone Disease' translated into as many languages as possible. Here's Hana and her parents holding up the slogan in Tamil, English and Malay.

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