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I have a family member who was declared "palliative". I think this is different that being declared "terminal" though, in that is just means that there will be no cure for the patient.
This patient has the typical symptoms of an untreated HIV infection, but he does not believe that HIV/AIDS is real. I do not think that theory makes sense, but no matter, he has symptoms of illness and each of those symptoms could be treated without declaring HIV/AIDS.
I do not know how to comfort his mother. She came and got her son and brought him home with her, apparently to die, but that could take awhile. I think they both believe he is going to die pretty soon, and so they are both comfortable with some kind of euthenasia or suicide.
On the other hand, from what I can tell, the patient is probably exaggerating his illness a bit. He might not die "naturally" for months or years, who knows. When he made some sort of feeble attempt at slashing his wrists he did it in front of his mom when I was on the phone to them - does that sound to anyone else like it was not a serious suicide attempt, and that he was just saying "save me"? Surely he knows that dying from bleeding takes awhile and is messy, and therefore you have to be somewhere private, not in the kitchen standing up, in front of your mom with me on the phone.
I am conflicted between being a bit angry at the patient for doing that, and sympathy for his mom. As for the patient, I have a strange lack of emotion about him. I thought he was being so brave to reject the HIV meds based on his beliefs, but he is not showing much courage now.
This is all very messy and strange, isn't it? I hope this is all anonymous.
What else can I help you with?
Why is a multidisciplinary team approach to palliative care recommended?
A multidisciplinary team approach to palliative care is recommended because it allows for comprehensive management of patients' physical, emotional, and spiritual needs. This collaborative model brings together professionals from various fields—such as medicine, nursing, social work, and counseling—to provide holistic support tailored to each patient's unique circumstances. By integrating diverse expertise, the team can address complex challenges more effectively, enhance communication, and improve overall patient and family satisfaction during the palliative care experience.
How does the practice of palliative care differ from acute care for nursing staff?
Absolutely, and I gave a lecture on this not long ago. Palliative care basically means care not aimed at curing or treatment of illness or malady, but rather providing comfort to the patient. The patient does not necessarily have to be diagnosed with a terminal illness to receive palliative care. Hospice care, on the other hand, encompasses palliative care with other types of care for the dying person and his family.
Family and friends of the geriatric patient in terms os availability to provide support?
Family and friends play a crucial role in providing emotional and physical support to geriatric patients. It's important to assess their availability, willingness, and ability to provide care, as this can greatly impact the well-being of the patient. Open communication and coordination between the healthcare team, patient, and their support system is key to ensure the best possible care for the geriatric patient.
Identify the concept of care that is focused on family support and comfort during life threatening illness?
palliative care
What is palliative care?
Palliative care (pronounced pal-lee-uh-tiv) is specialized medical care for people with serious illnesses. It focuses on providing patients with relief from the symptoms and stress of a serious illness. The goal is to improve quality of life for both the patient and the family. Palliative care is provided by a specially-trained team of doctors, nurses and other specialists who work together with a patient's other doctors to provide an extra layer of support. It is appropriate at any age and at any stage in a serious illness and can be provided along with curative treatment.
What type of care is given to a dying patient?
Dying patients typically receive palliative care, which focuses on providing relief from pain and other distressing symptoms, while also addressing emotional, spiritual, and psychological needs. This care aims to enhance the quality of life for both the patient and their family, often involving a multidisciplinary team including doctors, nurses, social workers, and chaplains. Additionally, hospice care may be provided when the patient is nearing the end of life, emphasizing comfort and support in a compassionate environment.
How does testicular cancer affect that person and their family?
Testicular cancer can profoundly impact both the individual diagnosed and their family. For the patient, it may lead to physical health challenges, emotional distress, and concerns about fertility and future family planning. Family members often experience anxiety and fear about the patient's prognosis, as well as potential changes in family dynamics and roles. Support is crucial, as navigating treatment and potential long-term effects can create a significant emotional burden on both the patient and their loved ones.
Why a multidisciplanary team approach to palliative care recommended?
A multidisciplinary team approach to palliative care is recommended because it ensures comprehensive support that addresses the complex physical, emotional, social, and spiritual needs of patients and their families. By integrating diverse expertise from healthcare professionals—such as doctors, nurses, social workers, and chaplains—this approach fosters holistic care tailored to individual patient circumstances. Additionally, it enhances communication and collaboration among team members, leading to more coordinated and effective treatment plans. Ultimately, this collaborative effort improves patient quality of life and supports family dynamics during challenging times.
What important information must a cardiac patient and his family have?
The patient and family should be fully educated on the physical limitations of the patient, his recommended diet and exercise plan, his emotional status, and the lifestyle changes required to improve the patient's overall health.
What special care is required for tay sachs disease?
Tay-Sachs disease requires special care focused on managing symptoms and providing supportive therapies, as there is currently no cure. Patients may benefit from physical therapy, occupational therapy, and speech therapy to help maintain as much function as possible. Nutritional support and pain management are also critical, along with emotional and psychological support for both the patient and their family. Palliative care is often an important aspect of managing the disease as it progresses.
Why do you all need a family?
Family is needed to have emotional support. It gives unconditional love and affection.
What a care giver needs to know when patients dying?
A caregiver needs to understand the physical, emotional, and spiritual aspects of dying to provide compassionate support to the patient and their family. It's essential to recognize signs of approaching death, manage pain and discomfort effectively, and facilitate open communication about end-of-life wishes. Additionally, caregivers should be prepared to offer empathetic presence, respect the patient's dignity, and provide resources for grief support for loved ones. Being knowledgeable about available palliative care options can also enhance the quality of care during this critical time.
