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Anne Toussaint
by Anne Toussaint
145€ raised
Goal 200 €
Le syndrome de Marfan est capricieux. Certaines personnes sont très malades et d’autres pas beaucoup ou pas du tout.
Des chercheurs en Belgique veulent découvrir ces gènes de super-heros qui protègent certaines personnes de la maladie. Ils espèrent ainsi pouvoir développer des traitement beaucoup plus efficaces pour toutes les personnes atteintes du syndrome de Marfan.
Les chercheurs ont besoin d’un outil bio-informatique qui n’existe pas encore, mais qui pourrait radicalement accélérer leurs recherches.
Je suis impatiente que cet outil soit mis en place et que les recherches avancent: plus vite, plus vite, plus vite !!!!
Je compte sur toi pour donner un coup d’accélérateur à la recherche. Ca va être géant.
— Anne
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 "Anne Toussaint"
5 €
Thomas
— 3 years ago
Test
35 €
Alisa
— 4 years ago
Joyeux Noël Anne! En espérant que notre effort collectif aide les chercheurs à mieux comprendre les maladies rares pour mieux les soigner.
15 €
Alisa
— 4 years ago
Le monde est meilleur avec toi. Merci Anne
75 €
Catherine
— 4 years ago
Merci Anne!
15 €
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 !
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