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Fort comme un lion
by Geneviève Sonveaux
40€ raised
Goal 500 €
"Aurélien, ta 'Tati Ofi' m'a parlé de toi. Je ne te connais pas, je ne t'ai même jamais vu. Mais lorsque je ferme les yeux, je t'imagine papillon fragile mais tellement beau, je t'imagine dauphin, intelligent et attachant, je t'imagine lion, persévérant et courageux. Je pense que tu es tout cela à la fois et ça fait de toi quelqu'un d'unique. Tu vois, Aurélien, il y a même des personnes que tu ne connais pas qui pensent à toi et te soutiennent. Moi, je suis aussi maman et je crois au projet de tes parents. Tous ensemble, on sera fort comme un lion."
Soutenons ensemble la campagne de crowdfunding “impatients!” lié au projet de la Fondation 101 Génomes (F101G). Initiative pilotée par des patients pour faire avancer de 10 ans la recherche sur les maladies rares grâce à la création d'une base de données bio-informatique inédite.
— Geneviève
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.
Donation (1)
donation to "Fort comme un lion"
40 €
Anonymous
— 4 years ago
Pour une cause juste, pour So et sa famille.
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That's fantastic ! Your donation makes a difference !
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