As you may have read in earlier blogs, I work at the Alzheimer's Association National Helpline. The title of this blog is laden with a caller's anxiety and feelings of resentment that this terrible thing has happened to their loved one and their family. Instead of quoting a bunch of stuff straight from the
http://www.alz.org/ website about what is Dementia versus Alzheimer's Disease, or what are the signs, in this blog I will attempt to speak of the a caller's reactions my words as a counselor when we discuss this issue.
I always ask why the person thinks their loved one has Alzheimer's Disease, so I can see where they are in the process of understanding the concept, and then I ask what they think may have caused the symptoms that they are observing to show up now. Sometimes, I hear a simple, "my mother hasn't been able to take care of herself since the surgery", or "well, her father had it at this age and we just had an argument", or "I was just reading about Alzheimer's on your website and it sounds a lot like me, and I take a lot of medications for my other illnesses".
Everyone has a different picture of what Alzheimer's Disease looks like in their head, most of the time it is of someone who is 80 years-old and so obviously demented that they need to be in the care of a nursing home. But what about the loved ones we know who are losing the ability to care for themselves at age 40 or 60? What then? Can we blame physical/mental decline on a biological change in the brain 100% of the time?

I usually ask the person to think about all the different things that may be contributing to the emergence of the Alzheimer's Disease other than age or genetics. To think about any major stressors that have impacted their lives recently, or any anniversaries of depressing events of years past. I'm not trying to dismiss the possibility of Alzheimer's Disease, but show the caller that there are many complex elements of a person's life that can be factors in causing someone to act Demented. I suggest writing down their newly refined thoeries and speaking with their loved one's doctor for further discussion of their symptoms.
However, even doctors have their own theories of what Alzheimer's Disease is. I've heard some doctors saying the most outrageous things, like Alzheimer's doesn't really exist or that there are no treatments for Alzheimer's symptoms so why diagnose it. I tell the caller that if they get these reactions from a health care professional to start looking for a second opinion. Go to a neurologist, or a geriontologist, or even a psychiatrist. I believe that if the family or the individual feels that there is something wrong, then there usually is, be it physical or mental.
The other important fact that I highlight to callers is that their loved one is at an un-determinded stage of Alzheimer's until they are thoroughly diagnosed. This means that your mother or father, sister or brother, friend or lover are still capable individuals until a doctor/court says otherwise, so let them know your concerns and encourage their participation in asking the doctor questions about the disease and the diagnosis process.
At the conclusion of the call, there is usually a sigh of relief that there is nothing set in stone yet about their loved one and that there are still things to be done, an action plan to talk to the doctor has been created.
Hmm... this could be an example of good ole social work empowerment?!