Because sickle cell disease affects millions of people around the world, we are totally committed. We take action every day to improve the lives of patients and their families.
Join us in this wave of solidarity and save lives with your donations!
In the face of the trials imposed by sickle cell disease, we believe in the inner strength of patients, their families and all those involved.Â
Informing, educating and raising awareness: we make transmission an essential pillar. By sharing medical knowledge, life experience and best practice.
Because everyone has the right to dignified and appropriate care, we are defending fair access to care, diagnosis and information, whatever the origin or social condition of the people concerned.
Listening without judging, understanding without detouring, supporting with kindness: our commitment is based on deep empathy for patients and their families. We put people at the heart of our approach.
We believe in the power of the collective. It is together, with families, healthcare professionals, volunteers and partners, that we carry our fight high. Solidarity is the driving force behind our day-to-day efforts.
"We often lack the resources to support sickle cell patients, especially young people from modest backgrounds. Donations from the Le Bien a dit association, particularly in the form of educational materials, healthcare products and food aid, have had a real impact on the quality of life of our patients. It's precious, humane and committed help.
"When you're young, ill and far from your family, you often feel alone. The Le Bien a dit charity reached out to me with a parcel of essential goods, and above all, with words of encouragement. It's not just supplies: it's a chain of solidarity that warms the heart."
"The children we look after live with chronic pain. Seeing their faces light up when the association came with games, books and gifts is priceless. This kind of initiative should exist everywhere. Thank you to Le Bien a dit for this breath of fresh air in our daily medical lives."
"My daughter is hospitalised regularly because of her sickle-cell anaemia. As well as the pain, there's the stress and isolation. The help provided by the Le Bien a dit association has made a huge difference to us: meals offered, listening, help with transport... It's the little things that change everything. We're no longer alone in this fight.
Aziliz talks about her battle with sickle cell anaemia, a genetic disease that turned her adolescence upside down and almost cost her her life. She recounts the intense pain, the repeated hospitalisations, the guilt linked to an invisible disease, and her journey of reconstruction after a bone marrow transplant thanks to her mother. Her story is a message of hope and courage for those who face silent trials.
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"Sickle cell anaemia is an invisible disease, but it makes me suffer every day. When the Le Bien a dit association gave me a well-being kit with food supplements, a heating blanket and suitable products, I was overwhelmed. It's rare to feel seen and supported. Thank you to them for thinking of us.