“Do You Have Parkinson’s Disease or a Parkinsonism?”

There’s a recent article in US News & World Report on how to tell if you have typical Parkinson’s Disease versus parkinsonism, a term that includes the four disorders in our support group (LBD, PSP, CBD, MSA).

The article notes that “An estimated 1 million people are diagnosed with Parkinson’s disease, but some are misdiagnosed.”  Brain donation studies show that 25-30% of those we say have PD actually don’t have PD.

Here’s a link to the article.  It’s rather basic for most of our group members but still a worthwhile overview.

health.usnews.com/health-news/patient-advice/articles/2014/10/27/do-you-have-parkinsons-disease-or-a-parkinsonism

Do You Have Parkinson’s Disease or a Parkinsonism?
How to know the difference – and get help.
US News & World Report
By Kristine Crane
Oct. 27, 2014 | 9:34 a.m. EDT

Robin

“Dad’s Not All There Anymore” – novel about LBD

LBD folks:

A short (28-page) novel was recently published in the UK about a family coping with LBD:  “Dad’s Not All There Anymore” by Alex Demetris.

A few months ago, I read this short review by an LBD caregiver on one of the LBD online support groups:

Alex…calls [his book] a comic; I call it a very short (28-page) graphic novel about a family coping with LBD. The book is beautifully done — a great job of explaining Lewy body disease for the layperson, compassionate, true to life, and astonishingly, almost eerily, close to our family’s own experience. I am so impressed by it that I’ve ordered copies for each of my children.  Alex lives in the UK and the book is not available in the US. I ordered it directly from him … It costs £5 (about $8.50USD) plus shipping. I’ve encouraged Alex to consider making [his novel] available as an e-book, and he’s thinking about it. But for now, I can’t recommend the book highly enough and wanted to let everyone know.

You can see a short excerpt on the LBDA website:

lbda.org/content/dads-not-all-there-anymore-alex-demetris-louie-what-pt3

If anyone gets a copy, please donate it to our BSN support group when you are finished reading it!

Thanks,
Robin

 

Adaptive equipment, personal hygiene, clothing, eating, communicating, etc. (Sharon Comden, 9-5-14)

This post may be of interest to those looking for tips for adaptive equipment, personal hygiene, clothing, eating at home and dining out, communication aids, touchscreens, and brain-training apps.

Sharon Comden, who lives in SoCal, attended our atypical parkinsonism symposium back in October 2012.  Many of us enjoyed meeting her.  She has a CBD diagnosis, and posts frequently to the CBD-related online support group at Yahoo!

She recently posted her “tips for dealing with hand apraxia” to the CBD online group. These tips aren’t limited to those with CBD or even those with hand apraxia.  Rather, they are tips for adaptive equipment, personal hygiene, clothing, eating at home and dining out, communication aids, touchscreens, and brain-training apps.

Robin

———————————————————————–

TIPS FOR LIVING WITH HAND APRAXIA
by Sharon Comden
9-5-14

Apraxia of the hands is a terrible burden, but there are solutions that will make it easier for you to function in your home or in public.  For ease of explanation in public places like grocery stores, I often say that I have had a stroke, that my hands don’t work too well, and I require some extra assistance and patience. Often, the person has a relative or friend who has had a stroke and they’re very accommodating.

Apraxia is a result of your neurons being destroyed or compromised by the tauopathy that is part of this disease. As time goes by, fewer neurons are available to sense pressure, coordinate muscles, and activate muscles when you direct them to do so. This accounts for the loss of strength and coordination so commonly seen in tauopathies. Loss of strength has implications where you sit too – – low couches, chairs, and toilets – – will not work for you anymore because your legs aren’t as strong as they were before you had this disease. Maintaining as much independence for as long as possible becomes our primary goal.  I offer these reality-based tips in an open and frank way because coping is paramount if we want to enjoy quality of life under challenging circumstances.

HOME IMPROVEMENTS

Door Handles/Knobs. One of the nicest home improvements my husband did for me, was to change out doorknobs for lever type handles.

Brondell Swash 900 Bidet Toilet Seat: a very good home improvement addition for personal hygiene when your hands don’t work well. Warm streams of water from adjustable jets cleanse you; this model has a wall-mounted push button control panel that adjusts the temperature and other features. It’s about $400 and my husband installed it himself, taking the electric service from the wall switch to create a separate ground fault interrupted circuit(GFI) and outlet.

Since we are talking about toilets, here is the information on proper height.

Comfort Height/ADA Compliant Toilets. Toilets that measure between 17 and 19 inches in height from the floor to the top of the seat are considered Comfort Height toilets, whereas traditional toilets measure below 17 inches in height. Many Comfort Height toilets are also ADA-compliant when installed per the applicable guidelines.

Handrails and Grab Bars. Stairs and steps need sturdy handrails that the person can grip easily. Decorative wrought iron handrails will not do because as the grip weakens, the fingers need a broad smooth surface to rest on and grip. Grab bars in the bathroom, next to the toilet and in the shower, are essential for safety as the balance and the grip changes. Likewise, around the bathtub too, so the person will not be tempted to use towel bars to steady themselves.

PERSONAL HYGIENE
Keeping clean is a high priority for a person with apraxia, but more difficult.

Method Foaming Hand Wash pump and refills: The container’s broad base makes it resistant to tipping over and the large and rounded pump handle makes it especially easy to use. Target and Walmart both carry this brand. The refills come in several different types–be sure to get the foaming type, not the gel..

Baby Wipes for cleaning face, hands and other parts.  Be sure your loved one is able to operate the lid on the package.

CLOTHING

Elastic Waist Pants, sometimes called “pull-ups.” These pants have no buttons or zippers and can be found listed as running pants or yoga pants. My favorite sources are Sierra Trading Post and Lands End, when they have good sales. Be sure to get the right size for ease putting on and taking off when you need to use the toilet.

Tops and shirts. Often, the first sign of apraxia is difficultly with buttons or zippers. Tops/shirts that have long sleeves and buttons are very difficult to deal with when you have advanced apraxia. If you want to remain independent for as long as possible, I recommend short sleeves and tops/shirts with loose collars. Tuck in shirts make it more difficult to pull your pants down when undressing or using the toilet. For that reason, tunics and long shirt tails are a no-no in my book. Guys can wear sports shirts.

Wallets and Purses. The simpler the better. I currently use a coin purse with slots for credit cards and the like. Some people will find zippers with large pull tags easier to use.

EATING AND DINING OUT

Eating utensils: there are many different versions of utensils. Your occupational therapist will have catalogs of things to make it easier to eat meals and snacks. Bowls are better than plates for people with poor hand coordination. My experience is that shallow bowls with sloping sides make it difficult to eat because you’re chasing your food all the time. That’s why I recommend round bowls with steep sides for eating.

Choice of food is a very personal matter. Often times, eating can become a chore for people with apraxia. They need their food cut up into small pieces. Soups and stews, chopped salads with bite-size pieces of meat/nuts/veggies/fruit/cheese, casseroles and egg dishes like quiche, are often welcomed. Many grocery stores carry bags of chopped salads in several different varieties. Crock pot recipes/cook books have a wealth of information and ideas for delicious meals.

Dining out. I try to remember to bring my round soup spoons with me. have found very kind waitresses more times than not. The same goes for chefs, who are often willing to cut your meat into bite size pieces in the kitchen. I order my salads chopped, with good results. When possible, I ask for a bowl instead of a plate and a short tumbler for my wine. Another alternative for the wineglass is a heavy bottomed cocktail glass with a straw.

Drinking Utensils. Grip and spillage potential are the driving factors in choosing beverage containers. For mugs, a rule of thumb is to look at the handle first. Conventional coffee cups with small loop handles, are not practical for a person with a advanced apraxia. Room for several fingers gives the drinker more control over the mug, important when hot beverages are consumed. The grip changes over time and gets weaker as neurons are destroyed. . Plastic glasses are best when your grip is uncertain. Sometimes it’s easier to grasp a small container than a large one. Restaurant supply places like Smart and Final or Cash and Carry are good sources of cheap, durable, dishwasher friendly, BPA free plastic glasses.

TERVIS Insulated Container. It’s easy to wash and snaps shut so it can’t spill. It has the round hole in the top makes it easy to secure. I got mine at Bed, Bath and Beyond. Suggestion from Cora Hoadley.

First-Year Brand Sippy Cups.  Walmart online has some that don’t have cartoons on them. This brand is easy to keep clean, durable, and doesn’t leak. They also come in blue and green as a set.

Pink

Bubba Brand Insulated Glasses and Mugs.  Durable, BPA free, and easy to wash in the dishwasher. Walmart has a selection of sizes and designs in their stores. The large drinking mug has a good handle on it and you can test it in the store for grip ability. I’ve dropped mine many times and so far, no broken ones.

COMMUNICATION AIDS
The ability to use the phone is essential for communication and safety. Push button desk speakerphones make using the phone possible for even advanced apraxia victims. Losing your keyboard skills is one step towards isolation from your friends, professional life, and family. Technology has much to offer us. I’ve been able to maintain my computer communication despite hand apraxia  and variable speech difficulties by using speech-to-text software.. If you have the patience, you can make it work for you. These are some tips that I can offer to similarly challenged victims of this disease.

Older Panasonic EASA-PHONE push button desk speaker phones.  Goodwill and other thrift stores are sources. Features to Look For: Good speakers and big buttons with auditory feedback if you don’t push the buttons hard enough – – a must have feature for people with apraxia of the hands. Cordless phones with small buttons are impossible to use if you have advanced apraxia. There may be push button speaker phones that will work as well the Panasonic, I confess to not shopping the phone market recently.

Dragon Naturally Speaking. This tool enables the user’s voice to both control the computer and develop and print documents. It is the best speech-to-text software on the market. Dragon Naturally Speaking software is the basis for most speech to text search engines as well. Basic computer commands are included. About seven to 10 commands will do most stuff on the computer and should generate text documents like emails and letters. Several different versions are available priced from $99 and up. The Home Edition@$99 will probably do well for most people.

Touchscreens on Tablets (IPad) and Computers, Laptops and Smartphones.  I use both iPad and a Dell all-in-one touchscreen computer with a 23 inch screen. The large-screen enables me to use the touchscreen with my limited mobility. Smaller screens don’t work for me, so be sure when buying a computer, to test them in the store, including touchpads on laptops. There are a number of adjustments in Windows 8 and earlier versions too, that are very handy. I asked my computer guru to type them up for future versions of this tip sheet.

Touchscreen Apps. These occupational therapist recommended apps are useful and sometimes even fun. They will help maintain your function in your hands and your hand – eye coordination.

•    Solitaire.   By MobilityWare. This is a classic card game that keeps track of your maximum scores, a handy feature. I use Solitaire scores to track responses to meds and therapies.

•    iOT Session.  iOT Session is an app that improves and addresses deficits in visual tracking, bilateral coordination, visual perception, fine motor/dexterity, visual scanning, and handwriting/correct letter formation.  By utilizing a game like format to address each area, iOT not only catches a child’s or patient’s attention through fun activities, but can increase his or her performance in all mentioned areas. With iOT parents, teachers, educators, and occupational therapists have the ability to automatically track and report a user’s progress through the user log-in feature. In addition, all progress is kept, can be reviewed, and emailed.

•    Review of Two Popular Brain Training Websites.

•    Fruit Ninja. Android or Apple. A great hand eye app with many variations. Using a swiping motion with your forefinger, you “slash” fruit moving across the screen. Easy one to start with is the Classic game.   Get the ultimate slicing experience on iPhone, iPad, Android, Windows Phone and Windows 8! Your success will please the wise ninja Sensei, who will reward you with new blades, backgrounds and more!

•    Finger fun fireworks.   Android or Apple. This is my favorite app for killing time and improving my hand eye coordination. Has cool sound effects too that you can turn off at will.  Fireworks Finger Fun is the perfect way to celebrate the 4th of July. The Star Spangled Banner plays in the background as you play this addicting action packed game. Slash the flying fireworks and watch them explode as you try and get the highest score. Try and slice as many fireworks as possible without hitting a flying bomb.

I hope these Tips make life easier, safer, and more enjoyable for people with apraxia.

Sharon Comden

Posterior cortical atrophy – short overview

One of Brain Support Network’s missions is to assist families with brain donation.  In the 200 or so brain donations we’ve helped with thus far, we’ve seen a few cases where the donor during life was diagnosed with Lewy Body Dementia but, upon brain donation, the confirmed diagnosis is posterior cortical atrophy (PCA).  Most people with PCA suffer from visual hallucinations or severe visual disturbances.

There is some dispute in the dementia community if PCA is a variant of Alzheimer’s Disease (AD) or whether it’s a separate disease.  The brain pathology is very similar; both typical AD and PCA have neurofibrillary tangles and amyloid plaques.  But the distribution of this pathology differs in the brain between PCA and AD.  In PCA, the pathology is in the back part of the cortex, where visual processing takes place.

The Alzheimer’s Association website has a good, short overview of PCA.  See:

www.alz.org/dementia/posterior-cortical-atrophy.asp

I’ve copied a short excerpt below.

Robin
________________________

From Alzheimer’s Association website

About Posterior Cortical Atrophy
Posterior cortical atrophy (PCA) refers to gradual and progressive degeneration of the outer layer of the brain (the cortex) in the part of the brain located in the back of the head (posterior). It is not known whether PCA is a unique disease or a possible variant form of Alzheimer’s disease. In many people with PCA, the affected part of the brain shows amyloid plaques and neurofibrillary tangles, similar to the changes that occur in Alzheimer’s disease but in a different part of the brain. In other people with PCA, however, the brain changes resemble other diseases such as Lewy body dementia or a form of Creutzfeld-Jacob disease. Most cases of Alzheimer’s disease occur in people age 65 or older, whereas the onset of PCA commonly occurs between ages 50 and 65.

 

“Tips for Healthy Living” Webinar (resilience, quality of life, occupational therapy)

The Parkinson’s Disease Foundation (PDF) is having another of its every-other-month one-hour webinars this coming Tuesday at 10am California time.  The title is:  Occupational Therapy and Parkinson’s: Tips for Healthy Living.  But this webinar is about lots more than what we normally think of with the term “occupational therapy (OT).”

If you don’t have web access at that time, you can listen in to the audio portion of the event.  Also note that the webinar recording is generally available one week after the live webinar.  If you register for the webinar, you will automatically receive an email alerting you to the webinar recording’s availability, whether you attended or not.

In general, I highly recommend these PDF webinars as they are typically great presentations and the speakers do a good job with audience questions at the end.  Even though they are focused on Parkinson’s Disease, they are still useful to those in our support group because they are often focused on symptoms that our group members also experience.

After taking a look at the two speakers’ slides, I’d really encourage you to participate in this Tuesday’s webinar.  The speakers start from research that shows that those with neurological diseases and their care partners have “highly compromised work and leisure lives” due to the disease.  In particular, those with Parkinson’s “had lower sense of feeling of control and consistency in their lives, fewer active coping strategies and lower well-being compared to people with chronic non-neurological disease.”

The speakers focus on resilience.  One of the speakers has published research showing that:

“People with Parkinson’s who learn strategies for how to maintain participation in valued life activities have a higher quality of life than those who do not learn these strategies.”

This reminds me of Janet Edmunson’s book titled “Finding Meaning with Charles.”  There’s a story about how she and her husband Charles (diagnosed with PSP during life and CBD upon brain donation) kept up the ritual of going out for frozen yogurt every week — despite the challenge and mess — because it had been an important part of their weekly routine.

This webinar will hopefully impart some self-management strategies for maintaining quality of life.  If you participate, let me know what helpful techniques you picked up that should be shared with others in our group.

The details are below.

Robin


Occupational Therapy and Parkinson’s: Tips for Healthy Living

PD ExpertBriefing
Webinar hosted by Parkinson’s Disease Foundation

Tuesday, September 9, 2014
1:00 PM – 2:00 PM ET
(The webinars are usually on the first Tuesday but are moved to the second Tuesday if the first Tuesday is close to a holiday.)

Speakers:
* Sue Berger, Ph.D., O.T.R/L., B.C.G., F.A.O.T.A., of Boston University College of Health and Rehabilitation Sciences: Sargent College
* Linda Tickle-Degnen, Ph.D., O.T.R/L., F.A.O.T.A., of Tufts University

Learning Objectives
* Understand how occupational therapy can help people with Parkinson’s disease and their families.
* Learn practical strategies for increasing satisfaction with daily activities such as self-care, leisure and work.
* Find tips for preparing for changes in life activities and roles on the road ahead after a diagnosis.

General info about this webinar:
http://www.pdf.org/en/parkinson_briefing_occupationaltherapy

Register:
event.netbriefings.com/event/pdeb/Live/therapy/register.html

Download slides:
www.pdf.org/pdf/parkinson_briefing_occupationaltherapy_090414.pdf

If you are only listening in by phone and not viewing the slides live, you can call in to this number to hear the audio:
(888) 272-8710
passcode 6323567#

Technical questions about how a webinar works?  Contact NetBriefings, www.netbriefings.com/support/, or at (651) 225-1532.