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2 records where Véronique de Montchalin is listed as a sponsor, author, or other actor. Search with topics and years
Question· Question écrite17195open
France · National Assembly · 16 April 2024
Ms. Véronique de Montchalin questions the Minister Delegate to the Minister of Labor, Health and Solidarity, responsible for the elderly and disabled people, on the project to create a national resource center on brain injury. Indeed, this is a project carried out for several years by the National Union of Associations of Families of Head Traumatized and Brain Injured Persons with its two partners, France head trauma and the UGECAM health insurance group. To date, brain injury remains the leading cause of acquired disability among adults of working age. Highly awaited by the federation, as well as the injured and their families, this project was validated as an opportunity and included in the action plan of the national disability conference in April 2023 with an implementation schedule planned for 2024/2025. HAS To this end, she asks him if the provisional implementation schedule has been confirmed and what financing plan will be deployed, in order to bring greater visibility to the National Union of Associations of Families of Head Trauma and Brain Injured Persons.
Question· Question écrite17011open
France · National Assembly · 9 April 2024
Ms. Véronique de Montchalin draws the attention of the Minister of Labor, Health and Solidarity to the enrichment and diversification of the national register of official bone marrow donors. The biomedicine agency in France estimates that 2,000 people each year need to receive a bone marrow transplant to hope to be cured of their disease. If the national donor register counts nearly 385 000 people in France and the international donor registry more than 41 million people, finding a compatible donor with the same biological identity card as the patient is extremely rare. Indeed, the highest rate of compatibility remains within siblings. Estimated at 1 in 4, this ratio drops to 1 in 1 million outside the family circle (source: French blood agency). In this regard, the enrichment and diversification of the national register of official donors therefore seems essential in response to the low compatibility rate. On the one hand, it must be remembered that 80% of bone marrow donations consist of a blood sample and not a spinal cord donation, equated with pain and a higher risk. On the other hand, the biomedicine agency in France has lowered the maximum age for registering on the register of official donors of spinal cord at 35 years old. In fact, it is between the ages of 18 and 35 that stem cells offer the greatest chance of survival after transplantation. Therefore, she asks him if a future awareness and communication campaign in this area is planned in the coming months, in order to contribute to a change in the perception of this act and to a greater mobilization of donors aged between 18 and 35 years old.