Couple affected by Alzheimer’s disease has a passion for compassion

Couple affected by Alzheimer’s disease has a passion for compassion

Nikki Dodson is care partner for her husband, Ken, who has younger-onset Alzheimer’s disease. Both only 37 years old, the couple has a huge passion for ending Alzheimer’s and are sharing their story to help raise awareness and uncover the truths about the disease.

Nikki Dodson is care partner for her husband Ken who has younger-onset Alzheimer’s disease. They are both 37 years old. We spoke to them about their reality of being a young family with a very unique story and a huge passion for ending Alzheimer’s.

Nikki

Ken received his Alzheimer’s diagnosis a week before his 30th birthday. Needless to say, it was a very difficult time. Even gaining access to some Alzheimer’s informative resources has been hard due to Ken’s young age. Grants have to follow specific guidelines related to the federal budget, and a lot of programs are senior-based. There are many programs to teach children about grandma and grandpa having Alzheimer’s, but not mom and dad. So many doors were closed to us, and we heard so many no’s.

Suddenly I was in the position of earning our primary income because Ken had to stop working. We didn’t live above our means, but we lived to our means. We are not materialistic people, but the things we had we worked very hard for. We have also made it a goal to teach our children that education and working hard is important. To provide for our family after Ken’s diagnosis, we had to sell our belongings piece by piece just to make house payment and put gas in the car. There was even a case worker that told us to get divorced so we could get more money.

Alzheimer’s is a grieving process throughout; you are losing a loved one daily. I have three kids, a husband and a petting zoo at home, so I just try to make the best of each day, even if I have to dig deep and then deeper to make it all work. I do that for my family.

Ken

The most important thing is to build a strong support group; it carries you. Nikki is by far my strongest supporter. At first I tried not talking about it, putting it out of the way, but it sunk in one day that if something isn’t done, my kids will be going through the same thing I am going through.

People need to know the truths about Alzheimer’s. They need to know that this is not an old person’s disease. They need to know that this is a fatal illness. If you don’t know the truth, you aren’t helping yourself or your family. I didn’t want to know, but if you don’t start talking about it, it’s never going to change. It can bankrupt the whole economy the way it is going. Something definitely has to be done.

Nikki

There is the stigma that it’s an old person’s disease which happens with age…that you expect it, or see it coming. That isn’t the case. This is not an elderly disease.  You watch some of the smartest people robbed of their dignity and independence. Ken notices the changes and sees where he is struggling, and that is why this middle part is the hardest.  He now has to second guess himself or look to me for guidance regarding things he has been doing on his own his whole life.  It not only affects the person with the disease; it affects the whole family dynamic. It has a ripple effect, but I refuse to let this disease win, even though I know what it’s doing.

It is hard and some days I want to give up. But I also have met some of the most amazing people. The Alzheimer’s Association knows us and our family, and it feels like an extended part of our family. Lauren Miller Rogen and Seth Rogen have done so much for us and helped us tell our story through the documentary film “This is Alzheimer’s.” I feel like I was a good person before Ken’s diagnosis, but my compassion truly came out with it. I realized that I could live in a personal hell of anger and frustration or I could make a difference. We have made it our focus to educate people, and I respond to hundreds of emails and social media contacts weekly.

Someone I know recently used the phrase “passion for compassion.” I love that. An ordinary person can do extraordinary things, and that is what we are trying to do. We are taking this negative and turning it into a positive. By sharing our story, we are helping to raise awareness and uncover the truths about Alzheimer’s.

Learn More:

Why I Walk… Ira’s Story

Why I Walk… Ira’s Story

My personal connection with Alzheimer’s stems from my mom who was first diagnosed with it in 1992, at the age of 72. My parents were both retired and living in Gainesville, Florida, where they were planning to live their golden years out. In fact, my dad purchased an RV for the both of them to travel around the country. Needless to say, after the diagnosis, the future for my parents changed.

My personal connection with Alzheimer’s stems from my mom who was first diagnosed with it back in 1992, at the age of 72. At that time, my parents were both retired and living in Gainesville, Florida, where they were planning to live their golden years out. In fact, my dad purchased an RV for the both of them to travel around the country. Needless to say, after the diagnosis, the future for my parents changed.

For the first four years my mom was going to a day care center for adults. These centers are great for both the person with Alzheimer’s and the caregiver. My dad was her caregiver, as both of them were alone in Florida, and their four children were living in Illinois and New Jersey at the time. My dad, who had a heart condition at the time of the diagnosis, was not in the best of health himself. My dad tried his best to keep my mom home, but at times she would wander outside looking for me in my baby stroller, or her mother. Her mother would have been in her 100’s at the time and I was in my 30’s. It got to the point that my dad finally had to put my mom in a nursing home as she needed more services and for safety reasons. Before he did all of this, though, my dad put together a celebration party for their 50th Wedding Anniversary, redoing their wedding vows to each other.

For the next six years, my dad would visit mom every day to make sure she was dressed right and that her hair was done. She had a standing appointment at the beauty parlor every week for her hair and nails to be done. My dad wanted my mom to live with dignity during all of this. He would always take her out to the mall or go for a bite to eat early on, but eventually she wasn’t able to go out anymore. My dad would conduct a singing session with the rest of the patients every day in the afternoon. Everyone looked forward to it. Keep in mind that this Nursing Home was near the University of Florida and Shands Teaching Hospital. A lot of the patients were once professors and doctors.

When I would visit the nursing home I would walk down the halls and be yelled at, but I never saw that type of behavior from my mom. My mom, even though at times she would remember you, and then sometimes not know who you were, was always so kind and loving. My mom finally passed away in August 18, 2002 at the age of 83. I always remember my mom telling me early on that she knew she had Alzheimer’s and that there is nothing she could do.

The hardest part of all of this was seeing this love affair between my parents coming to an end. Once my mom passed away, my dad moved up to Illinois where nine months later he ended up having a stroke and would eventually end up in a nursing home himself until he passed away in 2012.

So I walk in the McHenry County Walk to End Alzheimer’s because I do not want to see other families go through all of this. One day I am hopeful we can put an end to this.

– Ira Handelsman

House proposes critical Alzheimer’s disease research funding increase

House proposes critical Alzheimer’s disease research funding increase

Today, the House Labor-HHS Appropriations Subcommittee proposed a $350 million increase for Alzheimer’s disease research at the NIH. This bipartisan effort was led by Alzheimer’s champion Chairman Tom Cole (R-Okla.) and comes just weeks after the Senate Appropriations Committee proposed a historic $400 million increase.

House hears the call of Alzheimer’s Association advocates, proposes critical research funding increase

Today, the House Labor-HHS Appropriations Subcommittee proposed a $350 million increase for Alzheimer’s research at the NIH. This bipartisan effort was led by Alzheimer’s champion Chairman Tom Cole (R-Okla.) and comes just weeks after the Senate Appropriations Committee proposed a historic $400 million increase. The full House Appropriations Committee may take action on the House Appropriations bill as early as next week.

“On behalf of the millions of Americans impacted by this fatal disease, I thank Chairman Cole and other members of the subcommittee for their commitment to end the Alzheimer’s epidemic,” said Harry Johns, Alzheimer’s Association president and CEO. “Today, Alzheimer’s disease is the only leading cause of death without a way to prevent, cure or even slow its progression. Only research will change this.”

In 2012, the first-ever National Plan to Address Alzheimer’s Disease was released with a goal to prevent and effectively treat Alzheimer’s disease by 2025. Experts have determined that in order to reach this goal annual Alzheimer’s disease research funding at NIH must be at least $2 billion. Today, following last year’s historic $350 million increase, Alzheimer’s disease and related dementias receive $991 million each year.

“At a cost of $18.3 million an hour, Alzheimer’s is the most expensive disease in the country,” said Robert Egge, Alzheimer’s Association chief public policy officer. “Today’s announcement will provide important funding for research that will allow scientists to better address the gaps in our understanding about this devastating disease.”

Today, there are more than 5 million people living with Alzheimer’s disease and more than 15 million family and friends serving as unpaid caregivers in the United States. It is the most expensive disease in America at a cost of $236 billion annually. The Alzheimer’s Association’s relentless advocates have held thousands of meetings with their elected officials sharing their personal stories of how Alzheimer’s has affected them and calling on Congress to increase research funding at the NIH.

Alzheimer’s Association®
The Alzheimer’s Association is the leading voluntary health organization in Alzheimer’s care, support and research. Our mission is to eliminate Alzheimer’s disease through the advancement of research, to provide and enhance care and support for all affected, and to reduce the risk of dementia through the promotion of brain health. Our vision is a world without Alzheimer’s. For more information, visit alz.org.

Contact: Alzheimer’s Association
Media line: 312.335.4078
Email: media@alz.org

Early Bird Registration open for the 2016 Annual Research Symposium

Early Bird Registration open for the 2016 Annual Research Symposium

Join us on ?Tuesday, ?October 11 at the Chicago Botanic Garden? for our Annual Research Symposium. You will ??gain knowledge and insights on Alzheimer’s and other dementia-related research topics? plus? ?increase your ?awareness and enhance your skill sets?. A special focus ?will be given ?on translating research into care. Register now to take advantage of early bird prices.

Join us at Chicago Botanic Garden!

Gain knowledge and insights on Alzheimer’s and other dementia-related research topics designed to increase awareness and enhance skill sets, with a special focus on translating research into care.

Where is it?
This year’s Symposium is being held at the Chicago Botanic Garden, located in the heart of the North Shore and convenient to downtown Chicago. The Garden provides attendees a serene setting with peaceful lakes and native woodlands.

Who should attend?
Split into tracks, the symposium is designed for:

  • Attendee with early dementia or MCI
  • Family, friend, or care partner of person with dementia
  • Professional I (caregiver, direct care staff, administrator, non CEU/CME/CCMC)
  • Professional II (health and allied health professional with CEU/CME, or case manager (CCMC))

Continuing Medical Education (CME) and Continuing Education Units (CEU) will be provided for healthcare professionals.

Receive early bird prices by registering online or over the phone 847-933-2413 today!
Featured Family Session Speaker
Beverly Sanborn, MS, LCSW

Gerontologist
Vice President, Program Development Belmont Village Senior Living

Featured Keynote Speakers

 

Alireza Atri, M.D., Ph.D.

Ray Dolby Endowed Chair in Brain Health Research
California Pacific Medical Center

 

Dean Hartley, Ph.D.

Director of Science Initiatives
Medical and Scientific Relations
Alzheimer’s Association

New – Free Expo!
Attendees

New this year – visit the free public expo featuring vendors and consultants who provide dementia-related services and education.

Sponsors/Exhibitors

Directly engage with symposium attendees, healthcare providers, physicians, families and care partners to showcase your research, business, products or services. New this year – we are opening the Expo to the general public at no cost. View and sign up for available sponsorships and exhibiting opportunities.

Caregiver finds light amid the darkness of Alzheimer’s

Caregiver finds light amid the darkness of Alzheimer’s

Sara Gearheart is a caregiver for her father, who is living with Alzheimer’s. Throughout the family’s journey with the disease, Gearheart has learned to treasure every moment she spends with her dad, such as when he was able to attend her graduate school graduation ceremony.

My graduate school commencement ceremony was fast approaching, and I knew it would be next to impossible for my dad to attend.  My dad, who is in his 80s, is living with Alzheimer’s disease.

Just the drive to and from the school would be a challenge for him, so I made arrangements for the assisted living facility to live stream the ceremony. Little did I know, my family had other plans in mind. My mom had asked the assisted living health coordinator if my dad would be able to make it to Emory & Henry and back. She said, “Yes!” and the entire staff was let in on the plan. The big surprise was underway.

The day of graduation I got there early with my mom. We were able to save seats and still have a good view of the stage. As we were counting the seats, I noticed my mom had counted one extra. I asked her why, thinking maybe my cousin might be coming.  Mom fought back tears and replied, “Your father.”

After hearing those words I broke down.  I was so emotional, because I knew how difficult it was for him to make the trip. My brother Tim would drive him over so he could be there in person. That was the only graduation gift I wanted – for both parents to see me graduate.

When I met my classmates to line up, I broke down again as I shared my good news with them. A few of my friends joined me in shedding tears of happiness.

It wasn’t until I got to my seat that I saw my dad. He was wearing my school colors, including an ‘Emory & Henry Dad’ hat. He asked my mom why I was crying, and she told him I was so happy to see him. During the ceremony, I got up and walked over to him. I squeezed both his hands, smiled at him, gave him a kiss on the cheek and told him I was so glad to see him. His face lit up. I knew he was proud of me for what I had accomplished even if he had no idea what was going on.  God planned it perfectly.

Throughout the ceremony he was able to focus on me, his “punkin.” We looked at each other from the rows, smiling, waving, winking and mouthing “I love you.” Those were precious moments I will always treasure.

On the way back to the assisted living my dad was his old self. He even cracked a joke!  I was driving, dad was beside me in the passenger seat and my mom was behind me, when dad asked “Where’s mom?” “She is behind us,” I said. He gazed confusedly at the side view mirror, pretending to look for her and said “I don’t see her.”  The whole car broke into laughter. I laughed so hard that my body was shaking and no sound was coming out. For two minutes my dad was back. He was his jokester self.

Having him there with me was the perfect surprise and the best graduation gift.

As many of you know, Alzheimer’s is a very heartbreaking disease.  But throughout our “Alzheimer’s journey,” there has been light amid the darkness. I have learned to treasure every moment I spend with my dad, to laugh with him and to love him for being him. I thank God for blessing me with an amazing family and for making my graduation day one I will never forget.

Even though my dad doesn’t remember that day, I always will. It was a day of light.

About the Author: Sara Gearheart, 29, is a children’s director from Virginia. For the last five years, she has been the team captain for her Walk to End Alzheimer’s team “The Journey.” Sara is a caregiver for her dad who is living with Alzheimer’s.