FAQs

Providing care for the unique needs of persons with dementia is a specialty of Hospice of the Valley. We believe our comfort-focused approach represents the best in end-of-life care for your loved one. We also care for the family, friends and caregivers-offering services such as respite care (breaks from caregiving) and spiritual support. We offer information to help you create opportunities for meaningful interactions with your loved one, using music, massage techniques and aromatherapy.

Frequently Asked Questions

  1. How do I know if my loved one with dementia is ready for hospice care?

    Persons suffering from dementia are generally ready for hospice care when they experience steady weight loss, and/or need help for all activities of daily living, are incontinent, speak few intelligible words and need help to sit up.
  2. How do I choose a hospice that will meet the unique needs of my loved one with dementia?

    The hospice you select should have a clear understanding of the unique needs of persons with dementia, how to meet their care needs, and how to determine proper medication. They should care about your family member's quality of life.
  3. What if I want my loved one to remain with me at home?

    Hospice of the Valley provides the same caring services whether the patient resides in their home, a skilled nursing facility or other location. All members of the team, including physicians, make home visits.
  4. What if I can no longer care for my loved one with dementia at home?

    Hospice of the Valley cares for patients wherever they reside. As dementia progresses, there may be a point when home care is no longer an option. We can help you understand what to look for in a care facility as you make your decision.
  5. I don't understand why my loved one behaves so differently - what's happening? What can I do?

    As the disease progresses through the brain, day-to-day living may become increasingly challenging and frustrating. Behavioral problems are common in persons with dementia. What was once done independently will eventually require total assistance from a caregiver. Because of increasing confusion and paranoia, the person may misinterpret the caregiver's help, and strike out verbally or physically.

    Agitated behavior is often the person's way to communicate that something is wrong. Remember, if the person could tell you what was wrong, he or she would. Caregivers should begin responding to behaviors by considering and anticipating what the person may need.