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AIDEZ LES PARENTS IMPATIENTS
by AURORE VERMUE
100€ raised
Goal 500 €
J’ai connu la Fondation par l’intermédiaire de nos amis Ludivine et Romain dont le petit garcon souffre du syndrome de Marfan.
C’est à cette maladie qu’est dédié ce projet pilote.
Cela leur donne beaucoup d’espoir dans l’avancée de la recherche qui permettrait de réduire les impacts négatifs de la maladie sur leur fils.
Pour mettre a la disposition des chercheurs une base de données inedite la F101G a besoin d’aide.
J’ai décidé de soutenir ce projet et je vous propose d’en faire autant.
La F101G est hébergée par la Fondation Roi Baudouin et a reçu le Prix Edelweiss 2018 décerné par l’Alliance Belge pour les Maladies Rares : RaDiOrg.
Soutenons-les dans leur combat.
Aurore Henry-Vermue
— AURORE
The Fondation 101 Génomes (F101G) is a patient-led initiative that aims to boost groundbreaking research in the field of rare diseases. F101G is hosted by the Fondation Roi Baudoin.
Our goal is to advance the understanding of the human genome to better treat rare diseases affecting children. We want to accelerate discoveries into new diagnostics tools and more efficient treatments.
To this aim, F101G is set to create a unique bioinformatic database that will unleash the full potential of genomics and artificial intelligence.
Our crowdfunding campaign “Impatient” wants to accelerate funding for research. We are “Impatient” because, when it comes to saving lives and improving the quality of life of people with a rare disease, there is no time to waste.
Gifts worth over 40 EUR are fiscally deductible.
Your money will help to support F101G’s pilot project, focused on Marfan Syndrome. Marfan Syndrome is a rare genetic connective tissue disorder affecting 1 in 5000 people. It’s a serious condition, which can be potentially life-threatening without an early diagnosis and medical treatment.
The pilot project aims to create a bioinformatic database crossing genotypic (Whole Genome Sequencing) data and detailed phenotypic (clinical) data from a cohort of patients holding the exact same mutation in FBN-1 gene. The ultimate aim is to understand the extreme variability in the symptoms of Marfan patients.
World-class medical scientists will have open access to this database. They will be able to launch algorithms designed to understand why some people display severe symptoms while others are only mildly affected by the mutation causing Marfan Syndrome. This discovery will allow scientists to develop accurate diagnostic tools and personalised treatments and cures for Marfan patients.
The project has galvinized support from the international scientific community. F101G’s scientific committee is formed by scientists from Antwerp University, UZ Gent, Erasme Hospital, Nijmegen, and Bichat Hospital.
Donations (2)
2 magic donors are supporting "AIDEZ LES PARENTS IMPATIENTS"
50 €
Marie
— 4 years ago
50 €
Anonymous
— 4 years ago
Bravo Aurore!
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That's fantastic ! Your donation makes a difference !
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