Cuando un ser querido necesita atención médica, tradicionalmente recurrimos a profesionales para despejar dudas, obtener un diagnóstico certero y opciones de tratamiento. En el pasado, los médicos eran la autoridad indiscutible que llevaba la voz cantante en las discusiones con sus pacientes sobre atención médica. Pero las cosas han cambiado, y la relación con el médico también.
Any time our loved ones need medical care we traditionally rely on professionals to answer our questions, diagnose properly, and recommend treatments. In the past, doctors were unquestioned authorities who took the lead in discussions with their patients on medical care. But things have changed; the relationship has shifted.
A trip to the hospital can be an intimidating event for patients and their families. As a caregiver, you are focused completely on your family memberʼs medical treatment, and so is the hospital staff. You might not be giving much thought to what happens when your relative leaves the hospital.
It is quite likely that you as the family caregiver have found yourself gradually assuming, month-by month, the role of taking care of your loved one as dementia or other disabling illness has taken hold, and a first encounter with the health care system has left you confused and with a feeling of the system being very impersonal.
When was the last time you left a doctor visit feeling satisfied that your concerns were heard and responded to? Successful communication with your doctor demands effective two-way communication. Here are a few tips to consider:
A legislative hearing before the Senate Subcommittee on Aging and Long-Term Care in Sacramento focused attention on strategies to support family caregivers in California. The session looked at future and current caregiver needs and the unique demographic trends that impact this important public health issue. Dr. Moira Fordyce was a key spokesperson. Below is her testimony.
Senator Alquist (now retired) and Members of the Subcommittee: