You still have time to double your impact.

You still have time to double your impact.

Now’s the time to support the fight against Alzheimer’s disease. Your gift can go twice as far during this extraordinary Spring Matching Gift Challenge — but only until May 31.
A foundation, that wishes to remain anonymous, has agreed to give $600,000 to the Alzheimer’s Association if we can raise that same amount by May 31.

Your gift can go twice as far.
$35 ? $70
$60 ? $120
$120 ? $240


This foundation supports organizations that benefit and inspire local communities, and this generous gift will enhance local care and support services for those facing Alzheimer’s.
Your gift will move us toward our vision of a world without Alzheimer’s disease. Today, $35 can become $70, a gift of $60 can become $120 or your very generous gift of $120 can become $240. Any amount you give will help advance research and provide care and support for the millions living with Alzheimer’s and their families.
The May 31 deadline for this matching-gift opportunity is fast approaching, and those affected by Alzheimer’s need your help more than ever. Right now, one in every three seniors will die with Alzheimer’s or another dementia. That’s why we must act quickly to put a stop to this epidemic. Please give generously today.

Get the emotional support you need – Alzheimer’s Association

Get the emotional support you need – Alzheimer’s Association

Sometimes you just need to know that someone understands what you are going through. Attending a support group can provide that. They can have social, educational and/or support components and are facilitated by individuals who have received training from the Alzheimer’s Association. We have more than 90 support groups in the Greater Illinois Chapter area, at various times and locations.

Get the emotional support you need

A support group is a regularly scheduled in-person or virtual gathering of people with Alzheimer’s disease or another dementia, family, friends or caregivers who interact around issues relating to dementia. Groups can have social,
educational and/or support components and are facilitated by individuals who have received training from the Alzheimer’s Association. This information is provided as a resource but is
not intended as an endorsement of any one product or provider.
We have over 90 support groups in the Greater Illinois Chapter area, at various times and locations. Check to see if there is a group close to you that fits your needs. If you prefer, call our
24-hour Helpline – 800.272.3900

Support Groups

Statewide Early Stage Telephone Support Group >>

It may be difficult to tell depression and dementia symptoms apart

It may be difficult to tell depression and dementia symptoms apart

Depression is very common among people with Alzheimer’s disease, especially during the early and middle stages. Treatment is available and can make a significant difference in quality of life. Identifying depression in someone with Alzheimer’s can be difficult, since dementia can cause some of the same symptoms

Depression and Alzheimer’s

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Depression is very common among people with Alzheimer’s, especially during the early and middle stages. Treatment is available and can make a significant difference in quality of life.

Symptoms of depression

Experts estimate that up to 40 percent of people with Alzheimer’s disease suffer from significant depression.

Identifying depression in someone with Alzheimer’s can be difficult, since dementia can cause some of the same symptoms. Examples of symptoms common to both depression and dementia include:

  • Apathy
  • Loss of interest in activities and hobbies
  • Social withdrawal
  • Isolation
  • Trouble concentrating
  • Impaired thinking

In addition, the cognitive impairment experienced by people with Alzheimer’s often makes it difficult for them to articulate their sadness, hopelessness, guilt and other feelings associated with depression.

Depression in Alzheimer’s doesn’t always look like depression in people without Alzheimer’s. Here are some ways that depression in a person with Alzheimer’s may be different:

  • May be less severe
  • May not last as long and symptoms may come and go
  • The person with Alzheimer’s may be less likely to talk about or attempt suicide

As a caregiver, if you see signs of depression, discuss them with the primary doctor of the person with dementia. Proper diagnosis and treatment can improve sense of well-being and function.

Diagnosing depression with Alzheimer’s disease

There is no single test or questionnaire to detect depression. Diagnosis requires a thorough evaluation by a medical professional, especially since side effects of medications and some medical conditions can produce similar symptoms.
An evaluation for depression will include:

  • A review of the person’s medical history 
  • A physical and mental examination
  • Interviews with family members who know the person well

Because of the complexities involved in diagnosing depression in someone with Alzheimer’s, it may be helpful to consult a geriatric psychiatrist who specializes in recognizing and treating depression in older adults. Ask your doctor for a referral.

The National Institute of Mental Health established a formal set of guidelines for diagnosing the depression in people with Alzheimer’s. Although the criteria are similar to general diagnostic standards for major depression, they reduce emphasis on verbal expression and include irritability and social isolation.

For a person to be diagnosed with depression in Alzheimer’s, he or she must have either depressed mood (sad, hopeless, discouraged or tearful) or decreased pleasure in usual activities, along with two or more of the following symptoms for two weeks or longer:

  • Social isolation or withdrawal
  • Disruption in appetite that is not related to another medical condition
  • Disruption in sleep
  • Agitation or slowed behavior
  • Irritability
  • Fatigue or loss of energy
  • Feelings of worthlessness or hopelessness, or inappropriate or excessive guilt
  • Recurrent thoughts of death, suicide plans or a suicide attempt

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Treating depression

Getting appropriate treatment for depression can significantly improve quality of life.

The most common treatment for depression in Alzheimer’s involves a combination of medicine, counseling, and gradual reconnection to activities and people that bring happiness. Simply telling the person with Alzheimer’s to “cheer up,” “snap out of it” or “try harder” is seldom helpful. Depressed people with or without Alzheimer’s are rarely able to make themselves better by sheer will, or without lots of support, reassurance and professional help.

Map out a plan to approach Alzheimer’s

There are many questions you’ll need to answer as you plan for the future. Use Alzheimer’s Navigator – our free online tool – to guide you as you map out your plan.
Learn more:
Alzheimer’s Navigator

Non-drug approaches

  • Support groups can be very helpful, particularly an early-stage group for people with Alzheimer’s who are aware of their diagnosis and prefer to take an active role in seeking help or helping others; counseling is also an option, especially for those who aren’t comfortable in groups
  • Schedule a predictable daily routine, taking advantage of the person’s best time of day to undertake difficult tasks, such as bathing
  • Make a list of activities, people or places that the person enjoys and schedule these things more frequently
  • Help the person exercise regularly, particularly in the morning
  • Acknowledge the person’s frustration or sadness, while continuing to express hope that he or she will feel better soon
  • Celebrate small successes and occasions
  • Find ways that the person can contribute to family life and be sure to recognize his or her contributions
  • Provide reassurance that the person is loved, respected and appreciated as part of the family, and not just for what she or he can do now
  • Nurture the person with offers of favorite foods or soothing or inspirational activities
  • Reassure the person that he or she will not be abandoned

Medication to treat depression in Alzheimer’s

There are several types of antidepressants available to treat depression. Antidepressants called Selective Serotonin Reuptake Inhibitors (SSRIs) are often used for people with Alzheimer’s and depression because they have a lower risk than some other antidepressants of causing interactions with other medications.

As with any medication, make sure to ask about risks and benefits, as well as what type of monitoring and follow-up will be needed.

Take precautions when traveling with someone living with Alzheimer’s

Take precautions when traveling with someone living with Alzheimer’s

If a person is living with Alzheimer’s disease or other dementia, it doesn’t mean he or she can no longer participate in meaningful activities such as travel. However, it does require planning to ensure safety and enjoyment for everyone.

Traveling with Dementia

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If a person has Alzheimer’s or other dementia, it doesn’t mean he or she can no longer participate in meaningful activities such as travel; but it does require planning to ensure safety and enjoyment for everyone.

Deciding to travel

Whether taking a short trip to see friends and family or traveling a far distance for vacation, it’s important to consider the difficulties and benefits of travel for a person with dementia. In the early stages of dementia, a person may still enjoy traveling. As the disease progresses, travel may become too overwhelming.

When you take into account the needs, abilities, safety and preferences of the person with dementia, what’s the best mode of travel? Consider the following:

  • Go with the option that provides the most comfort and the least anxiety.
  • Stick with the familiar. Travel to known destinations that involve as few changes in daily routine as possible. Try to visit places that were familiar before the onset of dementia.
  • Keep in mind that there may come a time when traveling is too disorienting or stressful for the person with dementia.
Tips for a safe trip
  • Changes in environment can trigger wandering. Even for a person in the early stages, new environments may be more difficult to navigate. Keep the person safe by taking precautions, such as enrolling in MedicAlert® + Alzheimer’s Association Safe Return®, Comfort Zone® or Comfort Zone Check-In®.

    If you will be at a location for an extended period of time, consider contacting the local Alzheimer’s Association for resources and support.
    Find a chapter anywhere in the United States.

  • Have a bag of essentials with you at all times that includes medications, your travel itinerary, a comfortable change of clothes, water, snacks and activities.
  • Pack necessary medications, up-to-date medical information, a list of emergency contacts and photocopies of important legal documents.
  • Create an itinerary that includes details about each destination. Give copies to emergency contacts at home. Keep a copy of your itinerary with you at all times.
  • If you will be staying in a hotel, inform the staff ahead of time of your specific needs so they can be prepared to assist you.
  • Travel during the time of day that is best for the person with dementia.

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Documents to Take with You when Traveling

  • Doctors’ names and contact information
  • A list of current medications and dosages
  • Phone numbers and addresses of the local police and fire departments, hospitals and poison control
  • A list of food or drug allergies
  • Copies of legal papers (living will, advanced directives, power of attorney, etc.)
  • Names and contact information of friends and family members to call in case of an emergency
  • Insurance information (policy number, member name)
Air travel

From our Blog

The Love Story of a Football Wife Who Tackled Dementia
Sylvia Mackey was a caregiver for husband and football legend John Mackey, who had dementia. Here, she tells her story and details the obstacles she faced and overcame when traveling to the Super Bowl each year. Read more

Traveling in airports requires plenty of focus and attention. At times, the level of activity can be distracting, overwhelming or difficult to understand for someone with dementia. If you are traveling by plane, keep the following in mind:

  • Avoid scheduling flights that require tight connections. Ask about airport escort services that can help you get from place to place.
  • Inform the airline and airport medical service department ahead of time of your needs to make sure they can help you. Most airlines will work with you to accommodate special needs.
  • If appropriate, tell airport employees, screeners and in-flight crew members that you are traveling with someone who has dementia.
  • Even if walking is not difficult, consider requesting a wheelchair so that an airport employee is assigned to help you get from place to place.
  • Allow for extra time.

Erica Kubena’s crafty way to Longest Day

Erica Kubena’s crafty way to Longest Day

The Longest Day is a team event to raise funds and awareness for the Alzheimer’s Association. Held annually on the summer solstice, the duration of this sunrise-to-sunset event symbolizes the challenging journey of those living with the disease and their caregivers. In this article, we feature one of our Longest Day participants, Erica Kubena.

The Longest Day is a team event to raise funds and awareness for the Alzheimer’s Association. Held annually on the summer solstice, the duration of this sunrise-to-sunset event symbolizes the challenging journey of those living with the disease and their caregivers. Teams are encouraged to create their own experience as they fundraise and participate in an activity they love to honor someone facing the disease. In this article, we feature one of our Longest Day participants, Erica Kubena.

My name is Erica Kubena! A little bit about me…I will talk your ear off about anything and everything (came in handy when I worked in radio for about 8 years!) I love music of all kinds – from country to rock to pop. My choices of Counting Crows or Hootie & the Blowfish may not appeal to everyone, but stick around – it’s bound to change! I’m 38 years old and have lived in Elmwood Park, IL for the majority of my life. I also did some time out in Kansas and Quincy, IL. Sometimes a girl has to move around, but it’s good to have a place to call home. Speaking of home, I’m married to the most amazing (Australian!) man, Daniel Kubena, for the past 4 years (5 years in October!). I have worked at Steiner Electric Company for about 12 years – the majority of the time as the Service Coordinator in the Power Systems division. It can be stressful – but I seem to thrive under pressure. I mentioned radio and music already as interests/hobbies, but I also love to be creative through painting and other crafts and photography, and I also love to travel (I need a vacation!). I have a beautiful godchild, Melanie and some of the best friends and family ever!

How did you come to be involved with the The Longest Day?
My mother, Joanne Wieckert (or Mama W to my friends), was officially diagnosed with Alzheimer’s in October of 2010. I had no idea what was in store at the time and can definitely attribute earlier “incidents” to signs of the disease, especially now that I know more about it. My father passed away in July 2011, three months before my wedding, and I couldn’t imagine letting her go through this alone. So my husband and I put our house search on hold and we stayed with my mom. Since I became my mother’s POA, I started hearing about the Alzheimer’s Association more and more as a place to read about the stages of the disease, find support, resources, etc. So, I checked it out, signed up for newsletters and began following everything I could for more personal awareness of what the disease entails and what I could do about it. I heard about the Longest Day initially from my involvement with the Alzheimer’s Association website. I clicked the link and decided I wanted to do something – anything – to bring more awareness and funding to the disease, along with support for people who live with it, care for people who live with it or love people who live with it.

What activities will you do for the The Longest Day?
This is my first year participating in The Longest Day! I have a great group of friends who share my vision/passion for raising money and awareness for Alzheimer’s disease, and our team is called The Purple Winged Warriors! This year, we are exploring our crafty side and making a couple different paintings, mason jar lights and mason jar baseball team (Cubs/Sox) pen holders. We are also exploring the idea of creating t-shirts, hair clips and more! People can donate money and at a certain dollar amount ($30) and they can choose one of the crafts. Donate more, and you choose more! Then on The Longest Day, we will fill our orders and craft/paint all day. So far, we have raised $1,100 and still have a lot of time ahead of us to raise even more!

Why is The Longest day important to you?
It is important to me, not only because of my mom, but because of all of the people I know who have reached out to me and shared stories about losing loved ones to this disease. My teammates all have been affected in one way or another, and friends have reached out to tell me their stories — so many stories, so many people and it’s growing! This is NOT a club that people are trying to get into on purpose, rather it chooses you, and the member enrollment just keeps going up! I want people to be aware of what is going on, and I want more people to realize that there needs to be more funding for research, caregiver support, and hope for finding a cure. Living with this disease and all the care needed going through the different stages is expensive! There is a lot of awareness and support for other diseases like cancer, but now is the time to increase awareness for Alzheimer’s.

Why should others participate in The Longest Day?
Well, it’s a great reason to take off of work and hang out with friends! Also, because memories matter, and I want to remember every milestone in my life – every special moment with my mom, and all the fun times with my friends. I know other people want the same for themselves and their loved ones also! How fun, we get to raise money for a great cause and have fun at the same time! I’ve been reading about other team’s activities and literally, they’re doing everything and anything – from hiking to biking to outdoor barbecues and more!

I really love the work the Alzheimer’s Association does for caregivers as well as all those affected by this disease. I have enjoyed the support in every aspect for The Longest Day – from the great web design of the team page, to all of the resources, tips and suggestions for fundraising and activities to do. I have been building myself up emotionally to be strong enough to do The Longest Day and now that I’m doing it, I only see more in the future for The Purple Winged Warriors! #ENDALZ #TheLongestDay