Even if you suspect you may have Alzheimer’s, it can be difficult to hear the diagnosis. However, you can still take control of certain aspects of your care by knowing as much as possible. This means you need to ask even more questions, including:
- Who will treat me?
- What changes can I expect in the future?
- Are there treatments that could help slow the disease?
- Am I entitled to the treatments?
- Are there treatment options for my symptoms?
- Are there any clinical trials I might qualify for?
- Should I make any changes in my lifestyle such as: B. Diet and exercise that will support my overall health while potentially helping to slow the progression of the disease?
- What resources are available to me and those who care for me?
- What decisions should I make now, such as advance directives or powers of attorney?
- Is it safe for me to continue driving?
- What kind of support do I need if I want to continue living at home?
- What are my next steps?
Some people may find it difficult to receive dementia care due to cost, insurance status, language, and location. If you encounter obstacles, ask your doctor if there are support systems for you, such as: E.g. low-cost services, transportation options, interpreting services or local support programs.
If you are alone and do not have family or friends to care for you, it is especially important to research what types of resources are available and how you can access them. Initially this could be a social worker or a care manager.
You may be eligible for community services, such as those found at the Eldercare Locator, part of the HHS Administration for Community Living. The Alzheimer’s Association’s 24-hour hotline (1-800-272-3900) may also be helpful.
