Advanced Planning with PSP

Advanced Planning with PSP

Advanced planning is an important consideration for individuals with PSP (progressive supranuclear palsy) and their families. PSP is a progressive and incurable disease, and as the disease progresses, it can lead to significant physical and cognitive challenges that may impact a person's ability to make decisions and communicate their wishes. Advanced planning can help ensure that a person's wishes are respected and their healthcare needs are met as their disease progresses.

Here are some advanced planning considerations for individuals with PSP and their families:

  1. Advance directives: Advance directives are legal documents that allow individuals to specify their healthcare wishes in the event they are unable to make decisions for themselves. This can include a living will, which outlines specific treatments or interventions a person does or does not want to receive, and a healthcare power of attorney, which designates someone to make healthcare decisions on their behalf.
  2. Financial planning: As PSP progresses, individuals may need increasing levels of care and support, which can result in significant expenses. Financial planning can help ensure that adequate resources are available to meet these needs.
  3. Caregiver support: As the disease progresses, caregivers may also need support and assistance. Advanced planning can include identifying potential caregivers, developing a care plan, and seeking support from community resources or organizations.
  4. End-of-life planning: End-of-life planning involves making decisions about end-of-life care, such as hospice care, palliative care, and funeral arrangements. This can be a difficult but important consideration for individuals with PSP and their families.

It's important for individuals with PSP and their families to discuss advanced planning with their healthcare providers and seek guidance from legal and financial professionals as needed. By proactively planning for the future, individuals with PSP and their families can have greater peace of mind and ensure that their healthcare needs and wishes are respected throughout the course of the disease.

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