From February 9 to March 9, 2025, the Moulin de Colagne is launching a solidarity campaign in support of the SCN8A France association, which is dedicated to raising awareness, supporting families, and funding research on the mutation of the SCN8A gene, a rare genetic disorder.
A Month of Mobilization to Raise Awareness and Support Research
The month of February is a key time for raising awareness about rare diseases, with the World SCN8A Awareness Day taking place each year on February 9. It is within this context that the Moulin de Colagne has decided to launch a support campaign for the SCN8A France Association, which will run from February 9 to March 9, 2025.
Through this initiative, for every bag of our “Julia” flour sold, 1€ will be donated to the association. These funds will help finance scientific research to better understand and treat the disease, as well as support families affected by this rare condition.
By choosing “Julia” flour, you are not only selecting a high-quality product, but you are also participating in a solidarity-driven action.
The Story Behind Our “Julia” Flour
The “Julia” flour is named after the granddaughter of Mrs. Rech, co-manager of the Moulin de Colagne, who is affected by the rare SCN8A disease. The name was chosen by the company’s employees to create an exceptional product while conveying a message of solidarity.
By naming the flour in this way, the Moulin de Colagne is not just offering an exceptional product. It is, above all, a message of solidarity, a strong commitment to raise awareness about this rare genetic disease, and to encourage scientific research.
Through this, the company hopes to provide significant support to the association and actively contribute to scientific advancements.
What is the SCN8A Gene Mutation?
The SCN8A gene mutation is a rare genetic disease, considered “de novo,” meaning it is not hereditary but occurs spontaneously.
Discovered in 2012 by Michael Hammer in the United States, it is estimated that there are only 700 to 800 cases worldwide.
This gene plays a crucial role in transmitting electrical signals between neurons by regulating the passage of sodium ions in nerve cells. A mutation can disrupt this mechanism and lead to severe consequences:
- Severe epilepsy
- Global developmental delay
- Neuromotor and neurodevelopmental disorders
- Coordination and motor difficulties (ataxia)
- Muscle weakness (hypotonia)
The rarity of this disease makes medical research essential to improve patient care and support the affected families.
A Commitment to Support Research and Families
This support campaign will allow the SCN8A France Association to continue its essential missions:
- Inform and raise public awareness about SCN8A disease
- Provide support to families dealing with this condition
- Contribute to funding research for better patient care
We hope that the support from Moulin de Colagne will help amplify these actions and advance research to offer new prospects for patients’ futures.
Join the mobilization and support research by choosing “Julia” flour!
