Vertaling van "caring for their loved " (Nederlands → Frans) :

55 percent of AD caregivers surveyed said caring for their loved one has taken a toll on their own health
· 55 percent of AD caregivers surveyed said caring for their loved one has taken a toll on their own health

“AD caregivers are typically the first to notice when their loved one’s symptoms are becoming worse and whether the disease may be progressing to the next stage, which is why caregivers are essential partners in disease management discussions,” said Barry W. Rovner, M.D., director of the Division of Geriatric Psychiatry and professor in the departments of Neurology and Psychiatry at Thomas Jefferson University, Philadelphia.
“AD caregivers are typically the first to notice when their loved one’s symptoms are becoming worse and whether the disease may be progressing to the next stage, which is why caregivers are essential partners in disease management discussions,” said Barry W. Rovner, M.D., director of the Division of Geriatric Psychiatry and professor in the departments of Neurology and Psychiatry at Thomas Jefferson University , Philadelphia .

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The three greatest caregiver concerns about the progression of their loved one’s AD were memory loss (41 percent), personal safety (33 percent) and confusion (27 percent)
· The three greatest caregiver concerns about the progression of their loved one’s AD were memory loss (41 percent), personal safety (33 percent) and confusion (27 percent)

67 percent of AD caregivers surveyed named at least one change in cognitive symptoms as a main concern about the progression of their loved one’s AD
· 67 percent of AD caregivers surveyed named at least one change in cognitive symptoms as a main concern about the progression of their loved one’s AD

It takes only one unhappy event (the loss of a dear person, the loss of a job, the end of a love affair, a conflict with their parents, some marital dispute, an illness…), which adds to the existing problems and unsolved difficulties, for those concerned to slip into an anxiety crisis that can lead to suicide, which seems to them to be the best manner of putting an end to a state that has become unbearable.
Il suffit qu’un événement malheureux – disparition d’un être cher, perte d’emploi, rupture amoureuse, conflit avec les parents, dispute conjugale, maladie… – vienne s’ajouter aux problèmes préexistants et aux difficultés non résolues pour que cet individu se trouve précipité dans une angoisse pouvant le conduire au suicide, lequel lui apparaît comme le moyen de mettre fin à un état devenu insupportable.

53 percent of AD caregivers surveyed who said they were not very involved (somewhat or not at all involved) in these interactions were dissatisfied with their loved one’s treatment, as compared with 31 percent who said they were engaged
· 53 percent of AD caregivers surveyed who sa id they were not very involved (somewhat or not at all involved) in these interactions were dissatisfied with their loved one’s treatment, as compared with 31 percent who said they were engaged

The progress made in treating depression: this makes it possible to help those suffering from depression to give meaning to their suffering and suicidal thoughts, to suggest that they should take part in a project that provides appropriate care in order to contain their determination to commit the lethal act.
Les progrès dans les traitements de la dépression: ils permettent d’aider le dépressif à donner un sens à sa souffrance et à l’idée suicidaire, lui proposer de s’investir dans un projet de soins adapté pour contenir sa détermination à passer à l’acte.

This calls for a guideline on optimal care that groups together the necessary indicators to assess the follow-up of the quality of care, as well as an inventory of the different persons involved and their specific skills, a distribution of the tasks, including a communication strategy and a co-ordination task, a precise list of the health professionals and other organisations involved, and adequate means to support the completion of these tasks.
Ceci requiert une directive de soins optimaux, reprenant des indicateurs nécessaires pour évaluer le suivi de la qualité des soins, un inventaire des différentes personnes impliquées et leurs compétences spécifiques, une répartition des tâches, y compris une stratégie de communication et une mission de coordination, une liste précise des professionnels de la santé et des organisations concernés, et les moyens adéquats pour soutenir la finalisation des tâches.