Tuesday, May 29, 2012

Alzheimer's Disease and the Younger Generation

I've been with Alzheimer's Services for almost 4 months. Prior to becoming an employee, my knowledge of Alzheimer's Disease was quite limited. When I was in highschool, a friend's dad was diagnosed with Lou Gehrig's Disease and related dementia. I remember the toll his illness took on his family, and my friend, who, as a teenager, lost her dad.

It wasn't until I came to Alzheimer's Services, however, that I realized the true impact of Alzheimer's disease on younger individuals. Furthermore, I began to see how so many of us in our 20s and 30s are either unaware of the disease or just aren't interested because it doesn't really affect us right now. Many people think about the disease and immediately visualize the elderly. The stories we tell are about a grandmother or a great uncle. The reality is that in the next 10 years, the stories could become about our own parents.

Early-Onset Alzheimer's is on the rise. Those baby boomers are coming into their 60s and people are living longer, into the age of Alzheimer's. Statistics show that Alzheimer's affects 1 in 8 over the age of 65. To give a little perspective, my husband's parents will be over 65 in 10 years. If one of them developed Alzheimer's disease, we would become caregivers in our 30s.

Many people in their 20s and 30s don't think about Alzheimer's because they can't get it yet. That doesn't mean we won't be faced with caring for a loved one who does. It is my hope that my generation can begin to see that this disease can affect them sooner than they think and not shy away or brush the topic aside. Raising awareness now will better prepare us for what may come in the future.

For more information about Alzheimer's Disease and Alzheimer's Services, visit our website at www.BRhope.com.

Tuesday, May 22, 2012

SPIRITUAL SUPPORT AS COPING AMONG ALZHEIMER’S CAREGIVERS


Alzheimer’s disease can be a devastating condition for anyone experiencing the symptoms. This disease can also affect the family of the person who is experiencing the symptoms, particularly the primary caregiver. The symptoms of the Alzheimer’s disease are felt by the person who is suffering from the disease and witnessed by the caregiver. While observing a loved one experience the symptoms of the Alzheimer’s disease the caregiver may develop an overwhelming sense of burden.

This study examined the relationship between spiritual support and burden among Alzheimer’s caregivers. The collection of data was accomplished by a packet of surveys mailed to Alzheimer’s caregivers. We learned in this study, spiritual support is not the sole reason for perceived burden to be low; rather, spiritual support causes a more positive outlook on the burden, triggering the caregivers to report lower levels of perceived burden. We all must be confident in the knowledge of supports used in achieving the ability to cope with stress when caring for a loved one with Alzheimer’s disease.

To read more click on the link: http://etd.lsu.edu/docs/available/etd-04162012-152226/
 
Today is my first full day as a full time employee at Alzheimer’s Services of the Capital Area. I have recently graduated from Louisiana State University, Graduate School of Social Work. The above information is a small portion of my recently defended thesis which I found thoroughly interesting. As researching the topic I became more and more convinced coping with perceived burden cannot be done alone, whether a higher power is called upon and/or we receive a call here at Alzheimer’s Services. I am honored to be employed by such a wonderfully helpful organization and I look forward to many fantastic endeavors.

by Katherine Schillings, Program Coordinator

Friday, May 11, 2012

50 THINGS YOU SHOULD KNOW ABOUT ALZHEIMER’S DISEASE


  1. Alzheimer’s is a disease that affects a person’s brain.
  2. Alzheimer’s slowly makes it harder to think, learn, remember and make decisions.
  3. Alzheimer’s has no cure.
  4. There are medications that may help ease some of the symptoms.
  5. No one knows what causes Alzheimer’s disease.
  6. A family history of Alzheimer’s can be a risk factor for developing the disease.
  7. The biggest known risk factor for Alzheimer’s disease is aging itself.
  8. Nearly half of all people age 85 and older have the disease.
  9. There are two types of Alzheimer’s disease—early-onset and late-onset.
  10. Early-onset Alzheimer’s occurs in people younger than 60.  It is linked to a family history of Alzheimer’s.
  11. Late-onset Alzheimer’s may or may not be inherited.  It occurs in people 60 and older.
  12. Early symptoms of Alzheimer’s disease include getting lost in familiar places or having problems doing everyday tasks.
  13. Dementia is a term used to describe memory loss and confusion.
  14. Alzheimer’s is the most common cause of dementia, but other conditions can also cause it.
  15. Parkinson’s disease, stroke and brain injuries can all cause dementia.
  16. Dehydration, reactions to medications and head injuries can all cause temporary dementia.  This kind of dementia can be treated and often cured.
  17. Many people misplace items or forget people’s names.  This does not mean they have Alzheimer’s disease.
  18. If memory loss begins to interfere with daily living, Alzheimer’s could be the reason.
  19. The symptoms of Alzheimer’s disease can be different for different people.
  20. If you notice symptoms of dementia in yourself or someone you care for; consult a health care professional.
  21. Doctors diagnose Alzheimer’s disease by eliminating other causes of dementia.
  22. Early diagnosis of Alzheimer’s is important.
  23. Early diagnosis means you can take advantage of medications and treatments.
  24. An early diagnosis means a person can make medical and financial plans for their future care.
  25. People with Alzheimer’s will need a power of attorney for financial and medical decisions.
  26. They will also need a will and an advanced directive or living will.
  27. Alzheimer’s is progressive.  This means symptoms get worse over time.
  28. As the disease progresses, people often have trouble with the concept of time and numbers.
  29. Personality changes, such as an increase in anger, anxiety and depression, are common.
  30. A person in the later stages of Alzheimer’s may wander.
  31. A person in the later stages may no longer recognize loved ones.
  32. A person with Alzheimer’s may be unable to care for him or herself.
  33. The average length of Alzheimer’s disease varies.
  34. Scientists are learning more about the disease all the time.
  35. With more knowledge, new treatments may become available.
  36. Knowing that memory loss and confusion are due to a disease may help a person cope with these often scary changes.
  37. Understanding Alzheimer’s can help if you have a loved one with the disease.
  38. If you have a loved one with Alzheimer’s you will need to change what you expect from the person.
  39. Being flexible is key to coping with the changes caused by Alzheimer’s. 
  40. Having information about the disease can help you adapt.
  41. Most people with Alzheimer’s live at home with family and friends providing much of their care.
  42. Alzheimer’s affects family members and friends as well as those with the disease.
  43. Caring for someone with Alzheimer’s can be difficult.
  44. Caregiver support groups can help.
  45. It is important for caregivers to eat right, exercise and get enough rest.
  46. All caregivers need help.
  47. Caregivers can get help from other family members, friends or community organizations.
  48. Many communities offer support services such as meal delivery, in-home care, transportation, adult day care, or respite care.
  49. Alzheimer’s Services of the Capital Area is a good place to find resources.
  50. You don’t have to do it alone.  If Alzheimer’s disease is affecting your life, you can take steps to ease the suffering this disease can cause.
 For more information, contact us at Alzheimer’s Services of the Capital Area
(225) 334-7494 or our website: www.Brhope.com

Monday, April 30, 2012

The Dangers of Wandering


On April 25, the breaking news included an item about a Woodville, MS man, age 73, with Alzheimer’s who was missing. He was last seen driving his gray pick-up truck. Sadly, this gentleman may be hopelessly lost by the side of the road, may not have eaten and has become dehydrated, run out of gas and is wandering the streets or woods wherever he stopped. Wandering is a classic characteristic of Alzheimer’s disease and one we all need to be aware of to protect our loved ones with the disease.  

There are many strategies to assist caregivers with preventing wandering and the agony of not knowing where your loved one is. I can only imagine the fear of an Alzheimer’s affected individual who is lost and recognizes nothing around him or her. Often they don’t recognize their own belongings, clothes, and sometimes their own faces in everyday situations therefore the strange situation can be much worse.  

Six in ten Alzheimer’s affected individuals will wander in the course of their disease. Caregivers need to be proactive in preventing wandering. There are new electronic devices that can track individuals by GPS and the traditional Medic Alert Safe Return Identification program. The latest technology includes a GPS chip in shoes. Monitoring for some of the GPS devices can have monthly fees but also give caregivers peace of mind. Wristband transmitter can be used for tracking through Project Lifesaver. Regardless of what method caregivers use, preventing wandering is a necessary strategy to ensuring loved ones stay safe.  

For more information on wandering or free enrollment in the Medic Alert Safe Return program please check out our website at www.Brhope.com

Tuesday, April 17, 2012

TLC for Caregivers


Socialization is vitally important for the health and stability of caregivers to those with Alzheimer’s or similar dementia.  TLC for Caregivers provides wonderful occasions for caregivers to engage in creative, social interactions that are age, gender, and culturally diverse. 

TLC for Caregivers events are uniquely designed to give caregivers the much-needed break and opportunity to enjoy an activity or outing with others who share in their journey.  Oftentimes, dementia-affected loved ones are able to participate.  This provides caregivers with the priceless occasion of creating a beautiful and lasting memory with the ones they love, while eliminating stress and preventing caregiver burnout. 

Our most recent TLC for Caregivers event was an “Easter Brunch” held on Saturday, March 24th, at the Young Chefs Academy on Jefferson Hwy.  It was such a great time!  Caregivers and their loved ones enjoyed a fun and relaxing time making and eating a delectable lunch.  Guests were directed and pleasantly entertained by the dynamically witty chef, Chef M. J. 

The menu included:  Mini ham and cheese quiches, bird’s nests sugar cookies with colorful malted ball “eggs”, fresh fruit ambrosia salad, cinnamon bun “bee hives”, and orange juice spritzers as a beverage.  Guests also learned how to fold hot pink napkins into Easter bunnies.J
It was truly a memorable time for all who attended.

Calling all Current Caregivers:  If you are interested in receiving information about upcoming TLC for Caregivers events, contact Rashida Keith at 225-334-7494 or programs@alzbr.org. 
*** These events are sponsored for the memory impaired & their current caregivers. ***

Special thanks to:  The Junior League of Baton Rouge for supporting and funding TLC for Caregivers.
Special thanks to:  The staff of the Young Chefs Academy, along with the ladies of the TLC Committee, for being gracious, helpful hostesses. 

Rashida Keith,
Program Coordinator

Wednesday, April 11, 2012

Glimpses from D.C.


Leaving Baton Rouge and going to Washington, D.C. at the same time our 19th Annual Education Conference was scheduled didn’t seem like a good idea to me at first. After all, the Conference, though managed so well by Julie Darden, did fall underneath my responsibility umbrella, so I felt most obligated to be present for our Conference and for our extraordinary keynote speaker, Dr. Peter Rabins, along with the other lineup of well-respected presenters.

However, as Executive Director, Barbara Auten said, “Everything was ‘aligned’ to have me in D.C.” I am a Board Member of the National Adult Day Services Association and that meeting and Public Policy outing was at the beginning of the week. The Alzheimer’s Foundation of America offered a partial grant for attending its National Membership Conference, plus offered a discount to attend the one that followed, the American Society of Aging Conference. All in one week, back to back. Further, there were opportunities to meet legislators at Capitol Hill, to network with colleagues in the field and to attend a National Brain Forum with Dr. Paul Nussbaum, one of our education conference former keynote speakers.

And so the decision was made.  I traveled to D.C.

My all-day NADSA Board meeting centered on discussion for lobbying for more funding for adult day services, and members went to Capitol Hill the day I attended the AFA Conference. 

At the AFA Conference, I was pleased to meet the AFA Staff and CEO, Eric Hall and some AFA Board Members, including the newly appointed Chairman of the Board, Jeff Greener.   The two-day conference consisted of presentations about promoting organizations through Facebook and Twitter media, Music Therapy, the programs and services of AFA, Public Policy, and a “state of the union” [regarding the nation and Alzheimer’s]  address of AFA by President/CEO Eric Hall.   Special guest at the AFA Conference was MaryAlice Parks, Legislative Aide to Representative Ed Markey (D-MA).  Ms. Parks outlined the rigorous work Rep. Markey and his staff  forge in support of Alzheimer’s caregivers and patients.  Rep. Markey authored the National Alzheimer’s Project Act (NAPA).  She listed pending legislation, namely the HOPE Act (Help Outcomes Planning Education -Medicare reimbursement for diagnosis of AD); the Breakdown Act (National Institute of Health to jumpstart AD Research); the SPRINT Act (Spending Reductions through Innovations Therapies-$50 million for pharmaceutical grants); the National AD Supportive Services Grant and the Independence at Home Pilot Program.  Ms. Parks noted the tireless efforts from Rep. Markey’s office; however, urged attendees that AD needs to break from “aging issues to be more ‘attractive’ to lawmakers". “Alzheimer’s is still a stigma,” Ms. Parks said. “Celebrities say it’s not a sexy disease. The mold needs to be broken.” Agreeing, Eric Hall added, “There’s no language for aging similar to ‘children are our hope.’ Where’s the slogan for aging?”

In Eric Hall’s “state of the union” Alzheimer’s session, Eric noted that AFA is the second largest organization devoted to Alzheimer’s in the country. AFA is a diverse organization, with 1,600 members strong and growing.  Regarding the National Alzheimer’s Project Act, Mr. Hall shared with the group that 70% of the recommendations for NAPA came from AFA and its members, with the work of staff and conference calls with members across the country. NAPA has a long way to go, and Mr. Hall noted that as of right now, the discussion centers around finding a cure and researching non-pharmaceutical interventions. However, Mr. Hall, a member of the NAPA Advisory Committee, is trying to address more issues, such as education, respite care, and caregiver financial issues.

Eric Sokol, the AFA Vice-President of Public Policy, then presented an overview of protocol for meeting with legislators and gave handouts of key issues to address with them. For myself, I had scheduled a meeting with Rep. Bill Cassidy, M.D. (R-LA) and Mr. Sokol assisted me in that preparation.

So, on to Capitol Hill I went, starry-eyed and energetic, with my passion for Alzheimer’s care in one hand, and my hand-outs in the other. Rep. Cassidy’s staff members were warm and friendly, and Rep. Cassidy as well, put me at ease. I tried to encapsulate everything I needed to tell him in a short time, and felt both productive, yet discouraged. The reality is that our country is in a deficit, and there is really no guarantee how many dollars can get funded in the future for this devastating disease. However, eternally hopeful, I think our lawmakers are the key to begin the debate and discussion, considering that by 2050, the U.S. government will spend $600 billion a year out of Medicare and $200 billion a year in Medicaid on Alzheimer’s alone. In one generation, the Medicare costs of this one disease will be more than our entire federal defense budget is now.  As Rep. Markey puts it, Currently, the federal government spends a penny on Alzheimer’s research for every $3.50 it spends caring for our citizens with the disease. In the case of Alzheimer’s a ‘penny for prevention’ isn’t just worth ‘a pound of cure’, it is worth hundreds of billions of dollars.”

The three-day American Society of Aging Conference followed AFA. I attended an-all day pre-intensive,  the National Brain Forum, facilitated by Dr. Paul Nussbaum. Dr. Nussbaum illustrated his five critical factors of Brain Health (Diet, Exercise, Socialization, Mental Stimulation, and Spirituality), through five noted speakers. The next few days included sessions on Dementia Care and Activities, Early-Onset Alzheimer’s Programming, and LGBT Issues.

So, yes, the stars were aligned for me to be in Washington, D.C. for these conferences and activities and so much more.  I felt proud and privileged to represent Alzheimer’s Services.  I learned a great many things, a few of them to note:
  1. NADSA recognizes the need for more dementia-specific day and/or respite centers and funding needed to sustain them.
  2. The AFA Staff and Board members were truly impressed with the work of Alzheimer’s Services, noting that we had just been the nationwide recipients of the Brodsky grant, praising our “Faces of Alzheimer’s” Exhibit, appreciating the vision of educating law enforcement officers, and also, acknowledging our input with recommendations for NAPA.
  3. The Brain Health Forum validated our direction in providing “Brain Health” Education to our population as we have done recently with the LSU’s OLLI Lagniappe Class.
  4. Alzheimer’s Services seems to be on the leading edge of  Activities for Dementia, Early-onset Alzheimer’s programming and LGBT issues.  In fact, when I shared our new LGBT program with the presenter at the LGBT session, she remarked, “You make my heart swell.” 
  5. Regarding my meetings at Capitol Hill, Eric Sokol told me that watching laws being made is like watching sausage being made…not for the faint of heart….and that was so true.
  6. And, finally, the work of Alzheimer’s Services was affirmed and validated and we can truly say we are up with this country’s standards and more.  People were impressed.  I thought they would be.

 
Dana Territo, Director of Services

Wednesday, March 28, 2012

Reflections of a Past Caregiver


On the eve of my father’s passing in 2005, I reflect on how much joy and sadness were combined in caring for my dad after my mother suddenly passed away.  

My 82 year old father had Parkinson’s disease, a form of dementia.  

I was 30 years younger than my mother, who was 82 at the time of her death. I can only imagine how difficult the demands and struggles of caring for him must have been on her, his lifelong partner of 58 years. 

Statistics say that 70% of those affected by Alzheimer’s disease are being cared for at home by their loved ones, with the sole burden of care resting on their shoulders. I can only imagine how exhausted elderly caregivers, like my mother, who are often frail or suffering from other ailments and illnesses, must feel while caring for their loved ones or their lifelong partners. As with many couples who have been married for many years, Dad’s health declined rapidly after her death.

I did not know what caring for a person with dementia was like until I was thrust into it after Mother’s passing. It was a struggle to combine working full time, caring for my own 3 children and caring for my father. I often found myself wondering if I was doing enough and was torn between duties at home and duties caring for him at his home. At the same time, it was a joy to know that I was caring for him, the way he had always cared for me. It was a joy to know that I was doing the best I could, even though I always felt like I could or should do more.

It saddens me that I did not know a place like Alzheimer’s Services of the Capital Area or Charlie’s Place, our adult respite center, existed. What a relief it would have been to be able to bring my dad to Charlie’s Place while I was at work, or to have joined a support group to vent my frustrations and listen to others going through the journey, or to use the library to obtain information on how to better care for Dad, or just have the pleasure of walking through the doors to hear, “Your doing a great job.”  

I wouldn’t have been just a good caregiver; I would have been a “better” caregiver.   

It is my hope that all of you, who are caregivers of loved ones at home, seek knowledge, respite relief, and support by calling or visiting Alzheimer’s Services of the Capital Area at 334-7494 or by emailing info@alzbr.org. Please join us for Cause to Remember sessions. You can find dates listed on our website www.brhope.com.


Happy Easter!
Debbie Kidder Little – Development Director