/pictures/picture%2F74f6639ebb0f7c6d79a7e2e99c7ada54_Beau+gosse.jpeg)
IMPATIENT D'AIDER LA RECHERCHE
by Sebastien Henry
500€ raised
Goal 600 €
Je connais bien le petit Aurélien, fils de Romain et Ludivine.
C'est un chouette bonhomme, très attachant et très courageux.
Courageux? Curieux adjectif pour un jeune garçon de 4 ans.
Pourquoi Aurélien est-il si vaillant?
Parce que, comme ses parents, il se bat au quotidien contre cette maladie qui le touche.
Romain et Ludivine se sont creusés la tête et ont fait énormément de recherches.
Leur Fondation (F101G) cherche a faire avancer la recherche sur les maladies rares.
L'objectif étant d’améliorer la compréhension du génome pour mieux prendre en charge les enfants souffrants d’une maladie rare.
La F101G cherche à créer une base de données bio-informatique inédite qui permettra de libérer l’énorme potentiel de la génomique et de l’intelligence artificielle.
Cette campagne de crowdfunding “impatients!” a pour ambition d'accélérer le financement de la recherche.
Sachez que les dons de plus de 40 EUR bénéficient d’une déductibilité fiscale.
La recherche avance à grands pas.
Soyez fiers de participer à cette révolution!
Rejoignez-nous et apportez-lui tout votre soutien.
L'union fait la force.
Sébastien
— Sebastien
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 (5)
5 magic donors are supporting "IMPATIENT D'AIDER LA RECHERCHE"
150 €
Martine
— 4 years ago
Grosses bises a Aurelien et sa famille. "IMPATIENT" est une Excellente initiative! Nous vous soutenons a 100% !!!
150 €
Diego
— 4 years ago
Merci de ton initiative Seb !
50 €
Anonymous
— 4 years ago
50 €
Jacques
— 4 years ago
100 €
Anonymous
— 4 years ago
The beneficiary of your donation is 101 Génomes, who will establish your tax return document. The transaction is managed by Stripe - payment solutions, implemented by Raise & Shine SCRL — developer and host of the website you are visiting right now.
That's fantastic ! Your donation makes a difference !
Ooops... Failed payment... Sorry about that
Our payment provider encountered a problem, don't hesitate to try again later. Please write us to info@f101g.org for more information