Michigan Assistive Technology (AT) Program Blog
A Feisty and NonCompliant View on AT!
The Michigan Primary Elections are taking place on August 7th and today is the final day to register to vote! Candidates for Governor, U.S. Congress, and state Senate and House members are among the important decisions on the ballot. If you haven’t registered already, you can still do so through the Secretary of State’s Voter Information Center.
Traditionally, people with disabilities as a group, have had a lower voter turnout rate than other groups. According to the AAPD’s Voter Statistics and Data, the voter turnout rate of people with disabilities was 6 percentage points lower than that of people without disabilities during the 2016 election. Does 6% make a big difference? Would higher rates of voting among people with disabilities make a difference? Absolutely! if people with disabilities voted at the same rate as people without disabilities who have the same demographic characteristics, there would be about 2.2 million more voters! It is important that our voices and choices are heard.
Part of the lower voter turnout rate may be due to a lack of information about your rights as a voter with a disability. Let’s address some of the major rights.
- Polling places must be accessible. Federal and state laws require polling places to remove or make accommodations for any barriers that prevent voters with disabilities from voting. For example, doors should not be blocked, alternatives to stairs such as ramps or elevators should be available, and lighting and seating should be adequate.
- At least one voting station should be adapted to allow a person to vote while seated. In addition, all voters, including voters with disabilities, have access to the AutoMARK Voter Assist Terminal. The AutoMARK features a touch screen, a keypad marked with Braille, and the opportunity for voters to use their personal sip-puff device, a stylus or a footpad to mark their ballots. The AutoMARK is wheelchair-accessible and is equipped with headphones so that voters may hear the ballot read aloud to them if they wish.
- ID is NOT required to vote. If you do not have identification or did not bring your ID to vote, you can still vote by signing an affidavit confirming your identity. Once signed to can cast your ballot.
- You have the right to take someone with you to assist you to vote. However, they cannot be your employer, your union representative, or a candidate. Poll workers can also help you vote, as long as there are two people representing at least two political parties.
- You can request an absentee ballot if you need assistance getting to your polling place or need assistance casting your ballot. To receive an absentee ballot you can contact your local county clerk or fill […]
By Jen Mullins, BS, CTRS, MATP Staff
The weather where I live in lower Michigan has been fairly hot lately (or at least, hotter than I would like!) Frozen treats seem to help with cooling down, but sometimes aren’t the easiest to access. Typical ice cream scoops require a good amount of upper body strength, cold temperature tolerance in hands, hand strength & grip, and muscle endurance. For someone who has a disability that impacts any of these areas, scooping hard, dense, frozen cream/sorbet/gelato/custard with a traditional scoop is not always possible. Thankfully, there are some great Assistive Technology supports available!
#1: The Ice Cream Scoop & Stack cuts slices of ice cream (instead of scoops): “Push the Ice Cream Scoop & Stack into firm ice cream. The beveled front edge of the scoop makes it easy to cut through even the hardest ice cream. Twist just a bit and then lift. Press the button on the top of the Ice Cream Scoop & Stack to release the ice cream.” No traditional scooping needed!
#2: “Beaked” ice cream scoops like the Oxo Good Grips I-Series offer a more precise solution: the large, aluminum beak of this ice cream scoop breaks into hard ice cream and the ejector or trigger button on the scoop handle helps to get the ice cream out of the scoop. I like that this scoop also has Oxo’s usual non slip coating; making it easier for my dry-skinned-hands to grip it while I’m scooping.
#3: Heated-conducting scoops & spades like ones from Zeroll have heat conductive fluid sealed within the handle. The scoop or spade uses the heat from the user’s hand to warm the fluid in the handle which transfers to the scoop and glides thru the frozen ice cream with less resistance. Something to note about this scoop is that it needs to be hand washed and can’t go in the dishwasher.
A low tech AT idea for scoops is to use a muffin tin. Let ice cream soften for a while and then scoop soft ice cream scoops into muffin tins (lined with plastic wrap) & refreeze. When you want a scoop, it’s ready and waiting without having to fight with the chilled cream.
by Aimee Sterk
Did you know that one out of three adults age 65 and older fall each year?
Disability.gov had such a great post about falls prevention, and safety, we wanted to share it here.
Falls are the number one cause of fractures, hospital admissions for trauma, loss of independence and injury or deaths for seniors. But you can take action! Learn how to prevent falls outdoors and at home or take a falls risk self-assessment. Visit the website of the Fall Prevention Center of Excellence to find information to keep you and your loved ones safe from falls. The site has resources for older adults and caregivers, including the three main strategies of fall prevention: balance training and physical activity, medical management and environmental or home modifications. Get answers to frequently asked questions about falls and aging adults from the National Institutes of Health’s SeniorHealth.gov. Learn about fall prevention programs and strategies from the National Falls Prevention Resource Center. For more information, read “6 Steps for Preventing Falls” for more information.
By Laura Hall, MATP Staff
A few weeks ago, I attended a training that was more intense and grueling than any other training I’ve given or received, but the reward was life-changing. For two weeks I attended “Team Training” through Canine Companions for Independence to receive my second service dog. After working with many dogs and learning a litany of commands, I was matched with Adler, a yellow lab/golden retriever cross. Adler, although he is not technically assistive technology, assists me in many ways. For example, he picks up dropped objects, helps get laundry out of the dryer, tugs the basket into my room, turns on light switches, opens doors, and can help me complete retail transactions at high counters, by giving the cashier money, taking the bag and delivering it to me. Having him has already helped me increase my independence greatly, yet, we still rely on assistive technology to help take care of each other.
Adler needs a few tools to help him do his job. One of the most important tools he uses is the tug rope. This can be an actual rope or just fabric braided together and knotted at the end. I can tie this to laundry baskets, doors, and drawers so he can tug them open. Upon returning to work, I was surprised that Adler could not find the power door button. When observing his behavior, it looked as though he didn’t know where to target his nose. I realized that he was used to pushing power door buttons that were circular, like the one at the training center. A co-worker had the idea to paste a cardboard cutout of a round button over our rectangular button, and immediately he recognized where he was supposed to push. During the course of the week, we cut the circular cutout smaller and smaller until he was able to target just the rectangular button. I suppose even the smartest of dogs can use some basic, low-tech AT.
While Adler can do many things, he cannot, unfortunately, feed himself, fully groom himself, or clean up after himself in the yard. This is where assistive technology comes into play for me. Before we even returned home, I purchased an elevated food and water dish, with storage space underneath for the dog food. This allows me to fill his bowls without attempting to reach them on the floor or missing the bowl by pouring from above. Elevated dishes are also better for dogs’ hips, back, and neck, and promote better digestion.
Contrary to popular belief, many dogs, and Adler in particular, love to be kenneled. It provides him with a safe, quiet place to relax and also prevents him […]
Memorial Day has been a time of taking stock since it was created. The holiday has the strength of being recreated every year in a form that reflects the personal histories and connections that veterans, their families, and their friends have with their lived experience, their social networks, and the larger society.
It seemed reasonable to me as a veteran to think about the ongoing importance of personal support in the crafting of freedom and choice in each of our lives on this Memorial Day, the 50th since I first entered Vietnam.
Over time, I have come to see Assistive Technology as far more than devices or single-purpose apps. To the extent that we focus on the small affordances that devices enable, as important as those affordances are, we miss out on the core purpose of AT, which is to facilitate universal access that allows each of us to forge the life we want and not just the life we have been dealt.
To me, that means that social connection enabled by technology is as much AT as an automatic can opener, and, to the extent that our vision of what AT can do extends to all who use it, and not just those of us who see ourselves as part of our common disability community, the use of AT builds inclusion and lasting social relationships throughout our society.
So, one of the values we need to remember on Memorial Day is the way our personal reflections and our personal struggles for choice and freedom must facilitate the building of all our futures together.
By Jen Mullins, BS, CTRS, MATP Staff
Earlier this year, I watched a very interesting video on the Pennsylvania Assistive Technology Foundation PATF’s facebook page. The woman featured in the video is a wheelchair user and shared that she uses a shower chair while showering. She said if there’s an emergency in the shower (such as if she starts to fall out of her chair) and she’s by herself, she can’t physically unlock her phone to call for help, but she can Amazon Alexa to call someone in her life for help. I recently met someone who uses a powerchair and he communicated that he can’t afford an Apple Watch or a newer iPhone, but wants to be safe in his home. His solution was to buy 2, Amazon Echo Dots (about $49.99 each vs an Apple watch that is about $329-$399). He shared that he knows that the two places in his home that he’s most likely to fall are his bathroom and his kitchen. By putting 1 Echo Dot in his bathroom and 1 Echo Dot in his kitchen, he knows he’ll be able to call someone if he falls.
More and more, traditional Personal Emergency Response Systems (PERS) are being replaced by Smart technology (like Apple watches, Amazon Echo’s, and others) and being used in even better/more helpful ways. Why the shift? I really think it comes down to cost and user interface. People who choose to use Smart tech to contact family/friends/neighbors/etc. in an emergency are:
- Talking to someone they know (who likely knows how to best help) versus strangers who are a part of a traditional PERS.
- Not paying any additional, monthly fees (other than what is included with the device in general such as an Amazon Prime membership or wifi or cellular data plan).
- Choosing how they get help (having more autonomy over their lives).
Writer and podcaster, Brant Huddleston, shares in his recent article why traditional PERS systems/fall detection systems didn’t work for his older mother, but why the Echo Dot definitely does. Huddleston writes, “My experience installing the Echo devices has been a sheer delight, and with their naturally intuitive voice interface (Alexa), my mom has taken to the technology like a duck to water. We are both continually surprised at the opportunities Alexa offers to engage her intellect, expand her world, reconnect her with friends and family, and generally improve her life. Voice first technology, like Alexa, is increasing the probability that my mom’s wish will come true, and barring a fall, that she can age in place with dignity […]
By MATP Staff Member Laura Hall
Earlier this month, I had the opportunity to represent the Michigan Assistive Technology Program at the National Symposium of AT Act Programs meeting and visit Capitol Hill to speak with legislators about the importance and benefits of assistive technology. Typically, I fly to this event, but due to some bad experiences in recent years, chose to travel by rail (an adventure all of its own that I will write about soon).
Photo Credit: Doug Davis, New Mobility Magazine
If you use a mobility device or other type of expensive AT, I’m sure you can understand why I made this choice, Taking a flight often means you’re taking the gamble of your equipment coming out in one piece. Since most mobility devices can’t be brought aboard, they are typically stored below with luggage, and just like luggage, they can be lost or damaged. I’ve had my power chairs arrive at my destination with broken armrests, headrests, joysticks, and in one situation, completely inoperable. Airlines are required to compensate for damaged wheelchairs, however, the process of getting payment and the repair itself can take many months. I am not alone – a United Spinal Association Survey of Wheelchair Damage and Air Travel found that on average, people with disabilities experience wheelchair damage aboard flights 1 to 3 times.
A few companies have marketed products to improve transferring and protect equipment in-flight. For example, the Comfort Carrier and Transfer Pants are portable products that claim to assist with transfers during travel. “The Flyer” Wheelchair Protection Case is a rigid box with a top and bottom piece that claims to be “armor for your wheelchair”. It should be noted that there are few reviews on these products and the MATP never promotes or endorses any particular piece of assistive technology.
Fortunately, there are disability advocacy groups working hard to require better standards related to passengers with disabilities and their mobility equipment. I recently participated in United Spinal Association’s webinar: How to Improve Air Travel for Wheelchair Users. In addition to discussing the problems that passengers with disabilities experience, the presenters also spoke of efforts that are being made to improve air travel. Specifically, they are working with lawmakers to pass the Air Carrier Access Amendments Act of 2017-2018. This legislation would increase penalties for damaged wheelchairs, and allow passengers with disabilities to sue in court. It would also require higher standards for accessibility, safety, and airline/airport employee training. Finally, it would help create a Passengers with Disabilities Bill of Rights and a federal advisory committee on the air travel needs of passengers with disabilities. If you would like to support this legislation, United Spinal urges you to contact your legislators to co-sponsor and support S. 1318 (Senate) and H.R. 5004 (House).
Have you experienced problems with air travel? Do you have tips or tricks for minimizing the […]
The Amazon Echo Dot
Many members of our community have learned to use specific Alexa Skills as AT to solve support problems in their lives. But how do we customize skills to exactly fit our needs? Developers have been able to create “skills” or programs for Amazon’s Alexa assistant for some time. What about those of us who don’t have coding chops?
In the Blueprints section of the Alexa development system , the templates (21 right now) are organized as a grid, and using them is as easy as:
- Pick a Blueprint.
- Fill in the Blanks.
- Use the skill you just created.
Many of the Blueprints are focused on family and friend activities. There is also a section of Blueprints for creating stories using various themes. I think that as the number of Blueprints expands, there will be ones that the disability community can use. For example:
There are two themes, one focused on creating information for a sitter, and one for creating information for a pet, that could be easily hijacked to:
- Create basic information for a personal assistant about your needs, red flags, locations of important resources, scheduling important tasks, emergency contact info, specific responses to your emergency reactions, and so on. The skill could be easily adjusted to deal with life changes or the unexpected.
- Create basic information about your service animal, so that their unique needs can be easily reviewed by anyone who has predictable interaction with the animal. When should the dog poop, how often, what food isn’t safe, what behavior is a red flag, and so on?
There is also a Houseguest Blueprint that could be used to orient care staff to where things are in your house, what to watch out for, how your neighborhood is laid out, where stores you use are located and local travel issues.
I would guess that the number of Blueprints will expand, but if you have an Echo and use Alexa for supporting your independence now, you might want to play around with one or more of the current Blueprints to get a feel for them. If you do, you’ll be ready to use Alexa as a more customized AT device when Amazon expands the repertoire of Blueprints.
There is a Help Page with a short video that outlines how to set up a Family Trivia Game. It also contains information about how to make better use of the huge library of existing skills.
Give one of the Blueprints a try, and let us know how it went!
This spring, it seems like winter is never going to let go! As I sit here using my lightbox, I wonder when can I start tapering off using it each morning? I use the light box to help keep my circadian rhythm in tune with the rest of the world. Otherwise, especially in Winter with my tendency toward Seasonal Affective Disorder (SAD) and Delayed Phase Sleep Disorder (i.e. extreme night person!), I would not sleep at night and be useless during the day.
With more natural light in the warm months along with more opportunities to be outside, I don’t need to use the lightbox every day. I usually taper off sometime in the spring, typically by the beginning of June and then start again in mid-September.
Spring usually brings more energy, you know, that feeling we used to call “run naked through the woods”. Not that we did, but it was a pretty good description of the feeling. [There used to be a TV show called Northern Exposure. One episode was about the annual spring “bull” run through town. Yes, could relate to the feeling!]. Maybe the feeling has a theme song like the song “Here comes the Sun” by the Beatles. The urge to get outside, to throw open the windows and clean out the dust of winter (see “AT for Spring Cleaning!)
Except one year when spring didn’t come. Well that is, outside the birds returned and flowers bloomed and the days got longer, but inside me, it was missing. Actually the lack of the “run naked through the woods” feeling made me even more depressed.
This was more than SAD. For those of you who have had major depression, you know. It’s hard to explain to people who haven’t been there. I’d get advice like “It’s a beautiful day, get outside, open the blinds, you’ll feel better.” So I’d try and the contrast between the Spring outside and the darkness inside me simply made me feel worse.
“April is the cruelest month, breeding lilacs out of the dead land, mixing memory and desire, stirring dull roots with spring rain.” – T.S. Elliot
Did you know, contrary to a common belief, suicide rates don’t peak during the winter holidays. They are highest in the spring and fall.
If you have SAD and use a lightbox and find you can’t taper off in the Spring as usual, please reach out and get some help. There’s apparently something called “reverse SAD”. However, it’s also possible that something more than SAD is going on. Depression is a life threatening condition and not to be taken lightly. Please take care of yourselves and of each other!
By Jen Mullins, BS, CTRS, MATP Staff
Earlier this year, I had an experience that I think many of us have had: I was home sick with a cold/virus/etc. and couldn’t get an appointment with my regular doctor (not that I really felt up to leaving my home to drive to the doctor & sit in the waiting room anyway). Thankfully, there was an accessible solution I hadn’t even considered: a co-worker informed me that telehealth is a part of our health insurance and I could have a video call with a doctor to get checked out & get medicine if they decided to prescribe it. Shortly after speaking with my co-worker, I had downloaded the app and was “on hold” waiting to video chat with a licensed physician; all from my phone!
When a telehealth doctor was available, they greeted me, asked a few questions, looked at the brief medical history I had typed into the app, and prescribed me an antibiotic (she said she thought I had strep throat, but of course couldn’t do the test for it over the phone). The telehealth doctor said that I should inform my regular physician if I didn’t get better within the next few days and book an appointment with them then. That’s it! The video portion took about 8 minutes and there was a prescription ready at my local pharmacy in about an hour. My credit card was charged the price of a traditional office visit co-pay. It was so easy & accessible to me, I remember feeling like I had cheated or something (but of course I hadn’t!) It got me thinking: why isn’t more healthcare more accessible? Assistive Technology can facilitate more accessible access to healthcare.
I’m an avid NPR/Michigan Radio listener and recently listened to a piece that talked about Telemedicine for Autism-related therapy. The therapy mentioned in the piece traditionally requires a therapist to come to the individual’s home to provide support/assistance to person and the caregivers. With Telemedicine, the therapist Skypes (does a video call) with the individual and their team/family to observe and provide those same ideas for support/assistance. The family highlighted in the radio piece lives in a rural area and it’s not always convenient or covered by insurance to have therapists come to them; a video call is a great solution and reportedly works well for their family.
While doing some household chores recently, I turned on one of my favorite podcasts, The No Sleep podcast. While I listened to the commercial introduction, I heard an advertisement […]