Ask a Care Consultant: Holidays and dementia – Alzheimer’s – Optimum Senior Care – Chicago In Home Care


Ask a Care Consultant: Holidays and dementia – Alzheimer’s – Optimum Senior Care – Chicago In Home Carewww.OptimumSeniorCare.com

Holiday celebrations are often joyous occasions, but they can also be challenging and stressful. The Alzheimer’s Association Illinois Chapter tells caregivers and families that with some planning and adjusted expectations, the holidays can still be happy and memorable occasions for everyone.

Ask a Care Consultant: Holidays and dementia

The holidays can be a challenging time for families coping with dementia. Planning ahead and knowing what to expect can make this time less stressful. It’s also important to adjust your expectations—don’t try to put too much on yourself or on the person with dementia.

Planning ahead
Communication is key here. If you have people coming in from out of town you may need to clearly communicate with them regarding your caregiving situation, and what the person with dementia is and is not capable of. In the early stages of dementia, your loved one may seem to not have changed very much, but may have trouble with large groups or following a conversation. Telling visitors ahead of time that they can help by being patient, and not interrupting or correcting the person with dementia, will help prevent frustration and hurt feelings.

If the person with dementia is in the later or middle stages, there may be significant changes since the last time the visitors saw him or her. These changes can be difficult to accept, and it can be helpful to prepare the visitors in advance so that they know what to expect. For example, if the person with dementia might not recognize them it can be less hurtful if they understand in advance that this is a part of the disease process.

Don’t take on too much
Holidays can be stressful even without the added responsibility of being a caregiver. Do not be afraid of scaling back your celebration, and delegate, delegate, delegate. Clear communication is key here, as well. Consider scheduling a conference call with other family members to divide up responsibilities, and to set appropriate boundaries on what you can and cannot do. Consider scaling back to a smaller celebration to avoid overwhelming yourself and the person with dementia.

Focus on meaning
Look for ways to involve your loved one in meaningful activities that they can enjoy. Singing along with holiday songs can allow people even in the later stages to connect and feel part of the holiday. Looking through photo albums of past holidays and reminiscing with your loved one can be a soothing and meaningful way to spend time together. Perhaps they can help set the table or tie the ribbons on the gifts. Look for ways that your loved one can be a part of the celebration by scaling down activities to a level that is manageable for them.

Celebrating in a facility
When a family member is in a residential facility, people often want to know if it is a good idea to bring them home for the holidays. Consider carefully if this is wise for you and for the person with dementia. Sometimes changes in routine can be upsetting for the person with dementia, and they may not do well in a crowd of noisy people. Think about joining your loved one at the facility in their holiday celebration.

Take care of yourself
Be realistic about what you can and cannot do during this stressful time. Caregivers often feel guilty that they are not “doing enough” for the person with dementia and for their families. Holidays can make these feelings even harder to deal with when we have so many expectations about how things are supposed to be. Try to let go of these expectations, and give yourself some quiet time to grieve if you need to. As much as you can, focus on the moments of connection and happiness that you share with all your family members, and give yourself permission to not do it all.

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BOLD Infrastructure for Alzheimer’s Act passes Congress – Alzheimer’s – Optimum Senior Care – Chicago In Home Care

BOLD Infrastructure for Alzheimer’s Act passes Congress – Alzheimer’s – Optimum Senior Care – Chicago In Home Carewww.OptimumSeniorCare.com

The BOLD Infrastructure for Alzheimer’s Act, the Association’s priority legislation, has passed both the House of Representatives and the Senate and will soon be signed into law. Thank your members of Congress today for their support of this vital legislation that will combat the Alzheimer’s crisis and create a public health infrastructure to address the disease.

THANK CONGRESS FOR PASSING THE BOLD INFRASTRUCTURE FOR ALZHEIMER’S ACT

Alzheimer’s is an urgent public health crisis impacting our nation’s health care infrastructure. Investing in a nationwide public health response to this crisis will improve quality of life for those living with the disease and their caregivers, and reduce associated costs for individuals and the government. The Building Our Largest Dementia (BOLD) Infrastructure for Alzheimer’s Act (S. 2076/H.R. 4256) would combat this crisis and create an Alzheimer’s public health infrastructure to address Alzheimer’s.

Thank your members of Congress for passing this critical legislation.

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Under which roof? Residential placement vs. in-home care – Alzheimer’s – Optimum Senior Care – Chicago In Home Care

Under which roof? Residential placement vs. in-home care – Alzheimer’s – Optimum Senior Care – Chicago In Home Carewww.OptimumSeniorCare.com

As the roles transition from care partner to care giver, we find that there is no way one person can do it all alone. However, not every situation calls for a placement in a residential facility. Join us for a live webinar on Dec. 4 at 10 a.m. or 12 p.m. to learn about the different options and levels of in-home care that are available before a residential placement becomes necessary.

What Is A Webinar?

“Webinar” is short for “web-based seminar.”
The Alzheimer’s Association now offers these live, interactive programs conducted through the Internet. Participation is easy and is a great solution if you cannot easily attend a program in person. Instead, you attend via your computer, smart phone* or tablet*.
If you can open an email and click a link, you can join our webinars – it’s that easy!
We offer a variety of topics, professional speakers, and an opportunity to ask questions if you desire. Webinars are convenient and designed to meet the needs of busy caregivers and family members.
*With the Adobe Connect app installed on your mobile device. Available at Google Play & App Store.
Equipment You Need

You will need an internet connection AND a computer (PC or Mac) OR a mobile device with Adobe Connect app (Android or iOS).

How to Register & Join

Register online below by selecting the program(s) you are interested in. After registering, you will receive an email with a link to the webinar. On the day of the webinar, click on the link and launch the webinar.

Expert Speakers

Best-in-class experts who have extensive knowledge of the topic. All speakers are curated for their expertise.

Program Schedule

All Upcoming Programs

Dave Meyers
Care Partner

Understanding Alzheimer’s & Dementia
WED DEC 19, 2018

Alzheimer’s is not normal aging. It’s a disease of the brain that causes problems with memory, thinking and behavior. Join us to learn about the impact of Alzheimer’s, the difference between Alzheimer’s and dementia, Alzheimer’s disease stages and risk factors, current research and treatments available to address some symptoms and Alzheimer’s Association resources.

REGISTER » 11 AM-12 PM CST / 12-1 PM EST
REGISTER » 1-2 PM CST / 2-3 PM EST

View Past Webinars

Melanie Perry, MS, CDP, CADDCT
Director of Memory Care Support Services
Under Which Roof? Residential Placement vs. In-Home Care » 12.04.18

View

As the roles transition from care partner to care giver, we find that there is no way one person can do it all alone. However, not every situation calls for a placement in a residential facility. Join this webinar to learn about the different options and levels of in-home care that are available before a residential placement becomes necessary. Read more »

PROGRAM NOTES
Rebecca Freiman, MA, MT-BC
Board Certified Music Therapist
The Art & Science of Music & Dementia » 11.29.18

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Music has been shown to improve mood, behaviors and quality of life for people at all stages of Alzheimer’s disease. Log in to learn from a board certified music therapist about the science behind music therapy, and how you can employ music to help your loved one with dementia. Read more »

PROGRAM NOTES
Liana G. Apostolova, MD, MSc, FAAN
Alzheimer’s Researcher
Is it Time to See the Doctor? Alzheimer’s Symptoms vs. Normal Aging » 11.06.18

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If you or someone you know is experiencing changes in memory and cognition, how can you tell if it’s normal aging or something more serious? Join us as we speak to a board certified physician to learn about the symptoms of dementia and the diagnostic process. Read more »

PROGRAM NOTES
Lee Moriarty, CTRS/BS
Healthcare Consultant, IL Pioneer Coalition
How to Choose the Best Residential Care for Your Loved One » 10.24.18

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The move to a residential facility can be traumatic for all involved. Financial pressures, guilt, sadness and anxiety are all part of the process of transitioning to residential care. Learn how to select the best level of care for your situation. Once chosen, learn how to manage the process of choosing which option is best, from making the first phone call to making the most out of your first tour. Read more »

PROGRAM NOTES
Daryl Carlson
Mgr of Education & Outreach, Alzheimer’s Association IL Chapter
Sundowning, Sleeplessness & Alzheimer’s: How to Cope in the Evenings » 10.16.18

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Individuals with Alzheimer’s disease can not only have a tough time making it through the day, but the nights can be especially challenging. Day and night can become confused, and late afternoons can be difficult due to a variety of contributing factors. We will look at those factors and discuss effective strategies for dealing with late day confusion, lethargy and sleeplessness. Read more »

PROGRAM NOTES
Dr. Stephanie van Ulft
Medical Dir, Sr Behavioral Health Services, Decatur Memorial Hospital
Prescription Medications for Dementia: Pros, Cons & Watchouts » 9.26.18

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What medications are currently available to treat Alzheimer’s disease and other dementias? Are the benefits worth the side effects? Learn from a physician how these medications are prescribed, how they work and what you can expect from them. Read more »

PROGRAM NOTES

Meet the Experts

 

Dave Meyers
Care Partner

Dave Meyers lives in Normal, Illinois where he cares for his wife, Cheryl, along with working a full time job. Six years ago the Myers family entered the Alzheimer’s family when Cheryl received her diagnosis. Read more »

Wed Dec 19, 2018 – Understanding Alzheimer’s & Dementia

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Talking about an Alzheimer’s diagnosis is an important step – Alzheimer’s – Optimum Senior Care – Chicago In Home Care

Talking about an Alzheimer’s diagnosis is an important step – Alzheimer’s – Optimum Senior Care – Chicago In Home Carewww.OptimumSeniorCare.com

If you’ve been diagnosed with Alzheimer’s disease or another dementia, it’s normal to experience fear or discomfort about sharing your diagnosis. However, talking openly with those you trust can help educate those around you about the disease and engage their support.

Sharing Your Diagnosis

Sharing your diagnosis with others is an important step toward integrating Alzheimer’s disease into your life. You may be hesitant to share your diagnosis with some people, given the impact such a disclosure may have for you. Keep this mantra in mind: Alzheimer’s disease is not your fault.

Why tell others about your diagnosis

As the disease progresses, you will need the support of those who know and understand you. Concealing or denying your diagnosis will limit your ability to cope with the challenges ahead. While some relationships may be tested by what you are revealing, other relationships may be strengthened.

It is normal to experience fear or discomfort about sharing your diagnosis. However, talking openly with those you trust is a powerful way to educate those around you about the disease and to engage their support.

Deciding who to tell

Some individuals choose to share their diagnosis with just their closest family and friends, while others may be comfortable sharing their diagnosis with a broader group of people. Assess your personal comfort level before making this decision. You may feel more supported sharing your diagnosis with close friends and family first before telling others.

Consider the relationships in your life and determine who should be included in your disclosure:

  • Who are the people I feel closest to?
  • Who will continue to support me with this diagnosis?
  • Who I am responsible for telling (spouse, partner, friends)?

How to share your diagnosis

After deciding to share your diagnosis, consider when to tell your news. You may want to tell others about the diagnosis as soon as you get it. Or you may want to wait until you have had time to come to terms with your diagnosis.

It was hard for everyone to accept the diagnosis. While my family had to come to terms with this new situation, so did I. I needed to put it out there so that we could begin dealing with the new me.

LuPita G., Living with Alzheimer’s disease

To increase the likelihood of a comforting reaction when you tell your friends or family about the diagnosis, find a time when you can be alone and relaxed together. Give some thought to the conversation — what do you want to say? Consider writing your thoughts on paper and bringing that with you.

When you share your diagnosis, you may want to talk about planning for the future or about how family and friends can help; you also may wish to explain more about Alzheimer’s.

Help those closest to you come to terms with your new situation by considering these questions:

  • How do I think this person will react? If the reaction is something unexpected, how might I feel? What can I do in response?
  • How do I want this person to treat me? The diagnosis represents a big change, but it’s only gradually that my needs will change. What do I want from this person right now?
  • What does the person need from me now? What can I provide that will help?

Tips from individuals in the early stage

Go slowly.

You don’t need to talk about everything in one sitting if the person is having a reaction that is difficult for you.

Let the person know that both of you will be having different reactions about this over time.

You both can continue to talk about your thoughts and feelings throughout your relationship.

Provide educational brochures about the disease.

You can also direct him or her to alz.org for additional information.

Let the person know that you are still you.

Even though you are now living with this diagnosis, who you are and what has made you close to each other continues unchanged. Continuing your commitment to the relationship you have can be comforting to both of you.

Let people provide assistance when it makes your life easier.

Just like it helps you to feel useful and needed, helping may make them feel better, too. Accepting help is not an all-or-nothing proposition, and letting others help is not the same as being helpless. They are trying to make life easier for you, and it may help you to let them do that when it feels appropriate.

Responses to diagnosis

Consider how you felt after hearing your diagnosis for the first time. Just like you, the people with whom you share your diagnosis will likely experience similar reactions including fear, anger or relief that there is an explanation for symptoms. You may encounter unexpected or negative reactions. Family and friends may react with denial, or with comments or behavior that reflect their misconceptions about Alzheimer’s disease. Responses may include, “But you seem to be fine” or “You’re too young to have dementia.”

Denial is a common response to the disclosure of a serious illness; it provides distance from overwhelming feelings. Stigma or misconceptions about Alzheimer’s may exist due to a lack of information. These reactions reflect the person’s need for more time and/or education before they can respond to you in helpful ways. Allow your family or friends time to digest your news so everyone can move forward together in a positive way.

Your first conversation about your diagnosis may grow into an ongoing dialogue about your experience living with Alzheimer’s. Honest communication about your experience and your expectations of each other can help strengthen your connection. Learn ways you can help your family and friends adjust to your diagnosis.

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Tackling Alzheimer’s together – Alzheimer’s – Optimum Senior Care – Chicago In Home Care

Tackling Alzheimer’s together – Alzheimer’s – Optimum Senior Care – Chicago In Home Carewww.OptimumSeniorCare.com

Registration for the 2019 RivALZ Blondes vs. Brunettes Chicago flag football game is open, and now all we need is you! Help us tackle Alzheimer’s by raising funds and awareness on the field. Practices will begin in May and will help you prepare for the rivalry showdown on Saturday, July 20 – you won’t want to miss it. Want in on the action? Register today.

2019 RivALZ Blondes vs. Brunettes – Chicago, IL

Welcome to RivALZ, where two teams of women, divided to reflect traditional rivalries such as “Blondes vs. Brunettes”, compete in a flag football game to inspire fundraising, awareness and action in the fight against Alzheimer’s disease.
Looking to get involved? We need dedicated players, coaches and volunteers. Want to cheer from the stands? Donate to one of our players and join us on Game Day.It’s time to pick a side!
Together, we can tackle Alzheimer’s.

Date & Time:

July 20, 2019 Add to calendar

Location:

Lane Stadium – 2601 W Addison St, Chicago, IL 60618 Map it

Learn more

$105* RAISED TOWARDS THIS SEASON’S GOAL OF $75,000

TEAM BRUNETTE

$35.00

TEAM BLONDE

$70.00

*Total includes general donations and corporate sponsorships

DONATE NOW

Support your favorite team member.

TWO TEAMS, ONE GOAL #ENDALZ

Thank you to everyone who supported the
10th Annual RivALZ Blondes vs. Brunettes Chicago flag football game!
Our 2019 event will take place on Saturday, July 20th with kick off at 2:00 pm.
If you are new to the game and interested in learning more,
please contact Rebekah Marquez at rmarquez@alz.org or 847-779-6973.
Be sure to check out our 2018 Game Day photos here!

TOP FUNDRAISERS

RANKPLAYER NAMEFUNDS RAISED

Kelly Tresick

$70

Christine Whitemarsh

$35


NEWS & UPDATES

Recruitment Night – Join us on December 13th at Trophy Room in Chicago. Enjoy free pizza and get to know the team! 

Game Day – Saturday, July 20th

Be sure to check out our Facebook Page for further news and updates.



THANK YOU TO OUR SPONSORS

Become a sponsor >
View all sponsors >

TEAM BRUNETTE

Melissa Malejan

I have now lost both of my grandmothers to Alzheimer’s disease. While I do this first and foremost for them, I also do it for everyone else who has lost a loved one to Alzheimer’s or is currently fighting the battle. This disease not only affects the person with it, but everyone around them and I want to see a world without Alzheimer’s!

Visit my team page >

TEAM BLONDE

Jenn Bert

When it comes to Alzheimer’s, we’re all on the same side. This is a disease that must be defeated and we need your help to do it. Please help us tackle this disease – win or lose, our true goal is a world without Alzheimer’s! 

Visit my team page >

 

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