Category Archives: Research

If It Were Just the Memory Loss

Dear friends and family,

At a brainstorming meeting for Louisville Walk to End Alzheimer’s team captains last week, I talked with a woman who had just lost her husband at age 60 to Alzheimer’s disease. So much for the concept that Alzheimer’s is only about older people who will be dying soon anyway.

That sounds really harsh, and perhaps a bit bitter, I know. But that concept is one of the barriers we face in raising awareness and money for Alzheimer’s research and support services.  Here is my response:

1.  Early onset Alzheimer’s can affect people even in the 40s. The woman whose husband passed away in July said he was diagnosed at age 54. While our family was devastated at the loss of my mother-in-law who suffered 13 years with Alzheimer’s before her death at age 91 last week, I am grateful for the 20+ additional memory-intact years we had with her that my new friend was unable to have with her husband.

2. The memory loss is just one aspect of the disease.  Other symptoms of Alzheimer’s can include personality changes that make caring for your loved one incredible difficult.  Anger, aggressiveness and severe depression are just some of these symptoms.  There’s also the embarrassment of having to have assistance with eating, toileting and other personal care - these experiences can lead to uncharacteristic outbursts  of frustration that grow more and more common, and often more severe, as the patient continues to lose functionality.

There are medications that help slow some of Alzheimer’s disease’s symptoms, and they are  a huge blessing.  To date, however, there is not one drug that can slow the progression of the actual disease itself.  So, as of now, once the connections inside the brain of the Alzheimer’s patient are broken, they cannot be mended. Retraining eventually becomes impossible as more and more connections are destroyed.

3.  And then there are the dangers that become more and more serious as the person with Alzheimer’s continues through the later stages of the disease.  A dear friend of mine had to lock all of the exterior doors in her home so that her husband, who had been a nuclear physicist for NASA, wouldn’t wander away and get lost.  Imagine having to child-proof your home to protect your formerly brilliant spouse from going out to work in his garden.

4.  Alzheimer’s doesn’t just affect the person who has the disease. As with other diseases, it affects the whole family, including the spouse or child who is often the primary caregiver.  While more than 80,000 Kentuckians have Alzheimer’s today, there are nearly 265,000 family members and friends who are providing care for someone with Alzheimer’s in Kentucky, according to the Alzheimer’s Association.

If it were just the memory loss, that would be sad enough. But it’s the loss of dignity, the personality changes, the danger of wandering away or eating something bad for you or forgetting how to swallow that make Alzheimer’s so insidious. It is the inability to say goodbye. It’s the thousands of unpaid hours of care in a situation that, as of now, can only end in death.

The purpose of my blog is to help increase understanding of what Alzheimer’s is and how it really affects the individual who has been diagnosed, as well as his or her friends and family members.  I also hope to encourage more people to get involved. If you haven’t already, please visit www.alz.org to learn more. Thank you.

Sincerely,

Bonnie

Don’t Ever Think That Just Two People Can’t Make a Diffference

Dear Family and Friends,

Ten years ago, Cathy Nagy and Susan Oswald held the first Backyard Baseball event to raise funds for Alzheimer’s in honor of their mother.   It was literally a “backyard” baseball tournament, held in the empty lot behind Cathy’s backyard.  They signed up friends from the neighborhood and their children’s schools and raised $400 for their Walk to End Alzheimer’s team. That’s better than a lot of garage sales, and a whole lot more fun for the kids!

The event grew over time to include food, raffle items and a silent auction.  Every year, in the weeks before the event, Cathy’s living room would look like a warehouse facility for an “odds and ends” variety store. A few sponsors and donors became regulars they could count on year after year.  The kids grew into teenagers and looked forward every year to the event.  The neighbors, instead of complaining about the growing crowds and cars, joined in.

As they approached their seventh year, Cathy and Susan decided it would be their last, and they pulled out all the stops and set a goal: a total of $100,000 in funds raised for the Alzheimer’s Association over eight years.  Their loyal friends, colleagues and family members stepped up, as did sponsors, and in 2009, they reached their goal.  Over seven years, Cathy and Susan had raised $100,000 for the Alzheimer’s Association.

In 2010, Becky and Brent Beanblossom stepped up.  The event had too much name recognition, too many loyal participants and too much sponsor support to let it fade away.  Longtime supporters of the Alzheimer’s Association, Becky and Brent held a successful 9th Annual Backyard Baseball event at a new location, a local church, to accommodate the ever-growing crowd. Of course, Cathy and Susan continued to held tremendously, as they do today.

In the fall of 2010, I held  the last fundraising event for my younger daughter’s soccer team.  My specialty had been corn hole tournaments, an idea germinated by her Ballard High School soccer coach, Brooke Burd. I found that these were fun, family-friendly events that brought together multiple generations to enjoy an evening together for a good cause.

That’s why I agreed to begin chairing Backyard Baseball in 2011.  I relied a great deal on Cathy, Susan, Becky and their husbands, of course, and the name recognition that drew their dozens and dozens of friends, family and other supporters each year.

We are working to grow Backyard Baseball & Bar B Q into more of a community event. We’ve added live music — this year it was Muench (www.muenchband.com) — and scrumptious bar b q from Mark’s Feed Store.  The sponsors who have stayed with us over the years — Home Instead Senior Care, Byerly Ford/Nissan, First Capital Bank of Kentucky, Norton Brownsboro Hospital, YUM! Brands, LPL Financial, The Benefits Firm and WHAS AM 840 – have been joined by Guthrie/Mayes Public Relations, Christian Care Communities, WAMZ  97.5 FM, Q Country 103.1 FM, ESPN 680 AM, and Dr. Gary Reasor. Our generous donors continue to step up every year with wonderful gift baskets, gift cards, sports team logo wear and hand crafted items.

To date, Backyard Baseball & Bar B Q has raised more than $130,000 for Alzheimer’s (the numbers are still coming in for the 2012 event)!  This money funds workshops and services for people affected by Alzheimer’s in Kentucky as well as research to find a cure.

$130,000!  Don’t ever think that just two people can’t make a difference.

Sincerely,

Bonnie

National Alzheimer’s Plan Created

Obama administration presents national plan to fight Alzheimer’s disease

Health and Human Services Secretary Kathleen Sebelius today released an ambitious national plan to fight Alzheimer’s disease. The plan was called for in the National Alzheimer’s Project Act (NAPA), which President Obama signed into law in January 2011. The National Plan to Address Alzheimer’s Disease sets forth five goals, including the development of effective prevention and treatment approaches for Alzheimer’s disease and related dementias by 2025.

In February 2012, the administration announced that it would take immediate action to implement parts of the plan, including making additional funding available in fiscal year 2012 to support research, provider education and public awareness. Today, the Secretary announced additional specific actions, including the funding of two major clinical trials, jumpstarted by the National Institutes of Health’s (NIH) infusion of additional FY 2012 funds directed at Alzheimer’s disease; the development of new high-quality, up-to-date training and information for our nation’s clinicians; and a new public education campaign and website to help families and caregivers find the services and support they need.

To help accelerate this urgent work, the President’s proposed FY 2013 budget provides a $100 million increase for efforts to combat Alzheimer’s disease. These funds will support additional research ($80 million), improve public awareness of the disease ($4.2 million), support provider education programs ($4.0 million), invest in caregiver support ($10.5 million), and improve data collection ($1.3 million).

For the remainder of this news release, please visit: http://www.hhs.gov/news/press/2012pres/05/20120515a.html

 

Still a Long Way from a Cure

Dear Family and Friends,

Shivani Nandi , research manager at the Department of Neurology at the University of Louisville, recently returned from the 2012 Alzheimer’s Disease International  (ADI) Conference in London. She shared some thoughts – some stark, some poignant – with the members of the 2012 Louisville Walk to End Alzheimer’s committee, and I’d like to pass a few of these along.  To me, Shivani’s observations speak loudly and clearly to the continued and growing need for the Walk to End Alzheimer’s, as the disease affects more and more people.  We need a huge influx of funds for more research toward both treatments and a cure, and we also need national plan to ensure a coordinated approach to Alzheimer’s.

According to Shivani:

  • “It’s only too clear that there is not likely to be any end to this disease in the near future. There is not even an effective disease-modifying drug anywhere on the horizon to treat it, let alone cure it. So it’s going to be long process and we can only hope and pray that there will indeed be that one blockbuster drug that will put an end to this mind-destroying disease. “
  • “There were a lot of very exciting presentations on effective psychosocial interventions that involved modifications of the environment and other techniques to vastly improve the quality of life for persons with dementia.”
  • “I was very impressed that there was a parallel session where all the speakers were people living with dementia. See page 23 on this link  for a parallel session called “Living with Dementia: This is Me”. http://www.adi2012.org/Libraries/Documents/ADI_2012_Full_Scientific_Programme_v1_8.sflb.ashx
  • “It was truly an eye opening and yet and humbling experience to hear them speak; and what powerful emotions they had to share. A couple of the speakers already lived in care homes but for one of them her lifeline to the rest of the world was via her computer. Also, one of them was a former physician who lives in a care home but who spoke most wonderfully and without reading from any notes. I was particularly touched by an expression used by one of these speakers who said, ‘It’s not only our caregivers who give. We also have some capacity left to give back to the world.’”

Shivani also noted that two of the invited speakers have been diagnosed with dementia, Sir Terry Pratchett, an acclaimed author, and Helga Rohra, a translator in five languages, who shared their experiences with a packed international audience made up of medical professionals, researchers, caregivers, media, healthcare professionals and the general public. Shivani said she hopes more people with Alzheimer’s come forward to “share their lives and enrich our lives with their stories and also get media attention.” Here is a link to the list of speakers: http://www.adi2012.org/en/Scientific_programme/invited_speakers_copy1.asp

I am grateful to Shivani for sharing her thoughts.  Now, what are your thoughts?

Sincerely, Bonnie

One in Seven with Alzheimer’s Lives Alone

Kentucky Alzheimer’s Statistics 2012

Dear Family & Friends,

The Alzheimer’s Association released its annual “Facts and Figures” report today, and what I found most frightening is the fact that one in seven people with Alzheimer’s Disease lives alone. That means approximately 11,430  Kentuckians have a fatal disease with symptoms that make them more vulnerable to all kinds of dangers, and no one is right there by their side to be sure they don’t wander, or fall, or forget to eat or take their medicine.

Even scarier, up to half of these Alzheimer’s patients have no one who is identified as their caregiver. No one is regularly checking in to make sure they’re eating, taking showers, answering the door only for people they know. If someone with Alzheimer’s who is living alone takes a bad fall, and no one reguarly checks up on them … oh, I cannot imagine.  It could be days or even longer before someone comes to help.

Have you ever felt really alone?  My husband travelled on an extended business trip recently and there were several nights that I was home by myself and just plain lonesome. I am embarrassed to tell you how many times I re-watched the Twilight movies. But I was always safe, warm, and had everything I needed to take care of myself and entertain myself. If I had fallen, I knew there were people who checked in with me daily and that they’d figure out very quickly that something was wrong and head over to check on me.

But what if your brain wasn’t functioning correctly? What if something in your body hurt, but you couldn’t figure out why? What if you walked out your  door and got lost? What if the food in your home had gone bad, but you didn’t know? And what if no one paid attention?

The 2012 Facts & Figures report is another, very stark, reminder that we must find a cure for Alzheimer’s, and some treatment that slows it down. That’s what the 2012 Louisville Walk to End Alzheimer’s is all about – funding the research to find a cure, and providing resources to help those with the disease and their families.

But in the meantime, and at all times, we have to remember to check on our neighbors, friends and loved ones. Especially those living alone.  I’m going to make a more concerted effort to do that.

And maybe I’ll invite some of my neighbors to walk with me on Sept. 8.  Won’t you visit your neighbors and friends living alone and ask them to join you at the Walk to End Alzheimer’s as well?   Please visit www.alz.org/kyin and sign up today.

Thank you! Bonnie

Thank You Note from a Researcher

Researcher Dean Hartley, PhD, of Rush University Medical Center in Chicago, says National Institutes of Health funding for Alzheimer’s research is declining, so he is grateful for a research grant from the Alzheimer’s Association. Hartley’s research focuses on how the disease starts and spreads through the brain. Read Dr. Hartley’s full note here: http://act.alz.org/site/PageNavigator/FY12_Highlighting_a_researcher_page.html