Preparing for a disaster is important for everyone. But for people with vision loss, it requires some extra thought and planning. In this episode, we share some ideas on how you can prepare.
Hadley
Disaster Preparedness with Vision Loss
Presented by Ricky Enger
Ricky Enger: Contemplating what to do in an emergency is never easy, but it's a lot harder to figure things out while the situation is happening. Being prepared ahead of time can make all the difference. In this episode, Hadley's Chief Program Officer, Ed Haines, joins us as we discuss emergency preparedness. I'm Ricky Enger and this is Hadley Presents.
Before we continue with today’s episode, we want to acknowledge that we often record shows weeks in advance of their release. In this case, just days after recording the episode you’re about to hear, Hurricane Helene brought significant devastation to areas within the southeastern United States. And as this episode is set to air, another hurricane is expected to make landfall in Florida.
If you’re looking for ways to help or if you’re in the affected areas and you need assistance finding resources, please check our show notes for links, including disasterassistance.gov for information on available support. Or you can call Hadley at 800-323-4238 and we’ll do our best to connect you with the help you may need.
And now, we return to our originally recorded episode.
Welcome to the show, Ed.
Ed Haines: Thanks Ricky, it's a pleasure to be here.
Ricky Enger: Yeah, it's really good to have you. It always is, although we're not talking about warm and happy stuff today. I do actually think though that it does feel good, or there's a sense of relief at least, to have certain things figured out ahead of time to be able to mark off the list and say, you know, I may not know everything, but at least I have some ideas of what to do if this particular thing happens.
Ed Haines: Yeah, very true.
Ricky Enger: So yeah, that's what we're going to talk about today is emergency preparedness. So just thinking about what you will do when something unexpected happens. And it was interesting as we discussed this because at first it was like, well isn't this a universal thing? Like if you've watched the news or you've read articles about what to do in an emergency, you probably know what you need to. But I'm not so sure that's true. As we were discussing things, are there some extra logistics that vision loss brings to the table as you're thinking about how to prepare?
Ed Haines: Yeah, that's a great question, Ricky. And I should say that for many years, in my earlier days at Hadley, I taught a course called Safety in the Home. And it was about emergency preparedness. I know that emergency preparedness involves a lot of common knowledge and general knowledge. We think we know a lot about it. There is a facet of emergency preparedness that people with disabilities or people with vision loss particularly have to think about. In our everyday life, we have a reasonable expectation of accommodation in public places and services. Those expectations, as we know, are not always met, but we have an expectation of them. In an emergency, in a natural disaster, basically the ADA flies out the window, the Americans with Disabilities Act. Honestly won't have any reasonable expectation of accommodation in public places or services. People who are normally designated to help us out are going to be busy or non-existent. Places that normally provide accessible resources to us may not be either reachable or they just may be gone.
So it's incumbent on folks to be as knowledgeable as possible about what resources they're going to have in the event of a natural disaster and where to find them. So it's all about prior planning and knowledge is power. And that's especially true if you have vision loss.
Ricky Enger: Yeah, that makes sense. Because if you're in a situation where it's every person for themself, you have to know what you need and either where to find it or maybe how to ask very succinctly ask for it, right? Because if people are busy and they're overwhelmed, it helps if you can voice what your needs are and then figure out if they can get met.
Ed Haines: That's very true and as much as possible to be as independent and self-sufficient as you can for meeting those needs. You know, there's a couple of things you can do right off the bat that can make a huge difference. The first thing is, in a lot of places where we live, the risk level for natural disasters has changed in recent years. That's due to a number of environmental circumstances. But areas that previously weren't vulnerable to flooding or weren't vulnerable to fires, now are. So, you need to know your neighborhood and your area's risk level, it may have changed. Find out what that is. If your vision has changed recently and you've been comfortable with that risk level prior to vision loss, ask yourself honestly, “Okay, I live in an area that is prone to intermittent flooding, that was okay with me when my vision was typical because I knew I'd be able to cope. Well, now that I've lost some vision, is that still okay? Am I confident that I can still do what I need to do to survive in the case of the next flood?” So, know your area's risk level and then know your own capacity to be comfortable with that.
The second thing you can do right out of the gate, almost every municipality, every county in the United States has some sort of emergency management coordinator. So it doesn't hurt to know who that entity is, if it's a group or a single person, and to make yourself known to that entity and to ask them questions ahead of time. Like, what are your plans if my street floods, where are we in terms of priority for rescue, etc.
If you belong to a peer support group, a vision loss support group, if there's a local emergency management coordinator, in my experience, those individuals are more than happy to come to talk to your group and sort of educate you as a community. So it doesn't hurt to find out who that entity is and try to engage with them.
Ricky Enger: Yeah, that's a really good point and one that I hadn't really thought about. So that's going on my list as well. I've been in my neighborhood for a number of years and just hadn't considered it. It's hurricane season here so this has come up a lot right now. They always say make sure that you have your ‘go bag’ or your ‘bug out’ bag or whatever it is that you're calling it. Make sure you have that ready. I'm wondering if there are things beyond just the traditional stuff that you should have food, water, maybe a change of clothing, some hygiene items, stuff like that. What beyond those things should we think about with vision loss? Does that change how we prepare these go bags?
Ed Haines: You know, I think it might. People with vision loss often use adaptive aids to make sure that they can do whatever they need to do. I'm talking about magnifiers, canes, even mobile devices. So if you can afford to, or if you have the ability to, it doesn't hurt to have extras of some of those things, at least an extra cane or extra magnifiers if you're using them.
If you are someone with hearing loss and you have a hearing aid, they're often very expensive, but if you have a cheaper version, it doesn’t hurt to pack one of those. If you can have duplicates of some of those critical adaptive aids that you use to accommodate your vision, I would recommend packing those.
Ricky Enger: Yeah, like you said, it's hard enough to afford one of them. The approach I tend to take is for my cane, for example. I have an old beat up one that's still functional. I wouldn't use it for daily use, but it is still good enough for, well, in an emergency. I guess the same could be true for magnifiers. Maybe you've got that drawer full of stuff and you have the one that, “this doesn't work for me every day, but in a pinch, it's still going to give me what I need,” right?
Ed Haines: Exactly. In my experience, folks usually have a drawer full of magnifiers. Since we're talking about magnifiers, it also needs to be said that most of those have integrated lighting with them. They're lighted magnifiers, so batteries are going to be critical as well. If you have an old magnifier that you want to include in your go bag, it wouldn't hurt to keep some extra batteries for that, especially if those batteries have been sitting in there a long time. It's likely that they're going to be worn out.
Ricky Enger: Yeah. What about other technology? We talked about mobile phones, and I will be the first to say that I depend on my phone a lot. But are there things that we should be thinking through? If I'm depending on my iPhone for everything, is that going to be sufficient for me to grab during an emergency or are there some other things I should consider?
Ed Haines: Well, that's a good question because phones are only as good as cellular networks and data services, right? Now, if those are disrupted, if your power is out and your router's not working or cell towers are down and you're not getting a signal, a lot of the apps that you might use, particularly for navigation and communication, are no longer going to be sufficient. If you use a lot of tech to accommodate your vision loss and if you can think of workarounds for that tech, they may not be as convenient. They may not be as easy to use. It's not a bad idea to have a list of those in your head and if you haven't done that in a while to practice them. I'll just give you an example. If you're using your phone for navigation as a GPS for instance, can you use a braille compass or a talking compass? There’re other ways to make sure you know where north, south, east, and west are. That may be really critical when you hear on the radio, okay, everybody head south because the disaster is approaching from the north. If there are ways that you can do things without tech that you can have as a backup, that's not a bad idea to have those handy and have that knowledge handy.
Ricky Enger: Yeah, I think that's good advice no matter what, because, you know, tech is as good as its battery in a lot of cases, and it might not be an emergency, but being out and about and suddenly you're without it, like, hmm, do I have those backup skills? So yeah, that's important. What about things like figuring out what's in your go bag, maybe you've thrown a lot of stuff in there and now you're pulling things out and all these packages feel the same. What is going to help with that sort of thing?
Ed Haines: Organization really. You know, when someone loses vision, usually they find out pretty quickly that being organized is a big help in terms of just getting things done and getting things done as quickly as you used to. That's true for anything in your go bag, particularly if you have food items and different types of bandages or whatever you decide to put in there. And there are lots of lists out there, by the way, for what to put in a go bag.
But they should be labeled in a way that you can quickly, not just slowly, but quickly access them and get exactly what you need right away. So you need to label them in a way that you can identify them easily, either with large print or braille. You may be having to look through that bag in the dark, and if your vision is limited anyway and the light is not so good, you need to find a bandage really quick or an aspirin. Have them labeled in some way that you can find them or organized in some way that you can put your hands on them right away.
Ricky Enger: Yeah, that makes sense. I was talking to someone recently and she mentioned even having a roll of tape or something so if you are away for a little longer than a night or a day or whatever it is, having ways to mark things that you get that may not be in your go-bag. Maybe you're in a hotel or something like that and you need to label the shampoo and conditioner, just something that you can use to mark things that aren't marked already, whether that's a 20/20 pen or again a roll of tape or what have you. So yeah, there's a lot you can do. What about things like meds and eye drops and things like that? Are there any special things we should think about or just kind of knowing that you're going to need some on hand?
Ed Haines: Well, yes to both of those questions. If you've lost vision because of diabetes or glaucoma, then it's possible that you are taking medication for both of those conditions. You're going to want replacements for those. Particularly with regard to diabetes, if you are regularly using a blood sugar meter, test strips, things like that, you'll need to have replacements for those, or at least have a place in your go-bag for those things.
There are some medications that you might need to actually keep cold, so then you'll have to have a cooler on hand and a supply of ice or some kind of coolant to keep that stuff at the right temperature. There are some considerations if you've lost vision due to a medical condition that does require you to keep track of medication levels and sugar levels and that kind of thing.
Ricky Enger: A lot of what we've talked about so far is very physical, tangible stuff. So various items and various things that you can touch, mark, or see or whatever. But information is equally as important as the devices or items that you carry with you. I'm wondering if we can just talk about the kinds of info that you should have on hand and maybe how you go about doing that.
Ed Haines: Sure. We've all heard that we need to keep an emergency contact list, for instance. And for most of us that contact list, and I know mine is, it's on the phone, right? Okay, it's on my phone. But my phone is also locked. So if I've been injured in an emergency and I'm unable to unlock my phone for some reason, and someone who's assisting me needs to find out where my emergency contacts are, they're not going to be able to find them. So it's helpful to have a printed or braille version as well. Don’t just assume you can access your contact list on a mobile device. Other people need to access it too. And then it's helpful for someone else other than yourself to have a copy of that list. Maybe a relative or a friend who lives some distance from you because your list may not be secure. You may have lost it and in a hurry to leave. It doesn't matter. You're not going to remember all of those numbers. So if you have someone you can call or contact or go to that has a copy of your list, that's a big help too.
Ricky Enger: Yeah, that's a good point. And actually we do have a series of workshops at Hadley and it's the Safety Basics series. In that series, there is actually a contact list template. It is fully accessible, of course, and it gives you a nice place to start where you fill out that info and then you can print it, you can emboss it, you can do whatever. So maybe it's there on your device, but it's also available to someone else as well.
Talking about mobile phones, there is the medical ID and other stuff that's there on your phone. You know, theoretically the medical ID which has all of your meds info and such should be visible on the lock screen, but the problem can be if you are using certain types of accessibility options, if you have voiceover or talk back on that medical ID, you're not going to be able to tap on it. You have the gestures for double tapping for mobile screen readers and not everyone is going to know that. So just being aware of that, it's a good idea to have that filled out, but also know that if you're incapacitated, you might not be able to explain, here's what you need to do to unlock my phone or to view that stuff.
Ed Haines: That's absolutely true. And thank you for pointing out the Safety Basics series that we do have on our website. A series of workshops all about the subject today. I recommend anyone who's interested in further exploring the topic of emergency preparedness to go check those out.
Ricky Enger: It really is a good series of just basic stuff that you can do. There are some resource lists there as well. So, it’s really useful. We'll have that in the show notes. So let's think about if something is happening and you're not able to shelter in place. Maybe you have to evacuate for a fire or a hurricane or something where you have a little bit of time to then get out. What are some things we need to think about in terms of getting out safely?
Ed Haines: Good question and it really comes down again in my mind to self-sufficiency as a person with a vision impairment. Normally you'd want to have two places to go if you need to evacuate and one would be close by and that's where your local emergency management coordinator could help you out. Contact them to find out where the evacuation centers are and then another place would be some distance away like a friend or relative family member. If your entire community is in jeopardy, you’ll have somewhere where you know you can go. And here's the issue with self-sufficiency. I don't drive, for instance. So if you're not driving regularly, we sometimes tend to lose track of how to get where we need to go. We're letting other people do it, Uber drivers or taxi drivers or a paratransit, etc. But I think it's critical if we have our evacuation destinations in mind to actually know for ourselves the actual route, the roads, the turnings, the mileages, the landmarks, etc. to get us to where we want to go.
The point is you don't want to depend on someone else to find the way for you. You need to be able, as much as possible, to give them precise directions on how to get there. That means go two miles down this street, take a right on this street and really have it in your head, have that map in your head of how to get to your evacuation destination. Don't rely on anybody else. It's easy to do that. You get in a pattern of it. I know I do. So that's my advice there.
Ricky Enger: What about if you are in like a complex, maybe it's assisted living or an apartment complex or whatever, are there things that you should know, not just for yourself but perhaps the building has an emergency plan and a lot of times they're like, “Oh, yeah, didn't you see the signs? Well no, not so much.”
Ed Haines: That's right. Yeah, and this is classic, the emergency evacuation plans are in sort of a small little plaque somewhere at the end of a hallway. If you don't know what those plans are and you're not aware where the plaque is, you're not going to really be up to date. A lot of apartment buildings do have emergency plans and in fact in some housing units there might be a person even in your hall that's been designated to go door to door to alert fellow residents. So again, this is all about knowledge is power and self-sufficiency. Find out ahead of time what those emergency evacuation plans are in case of a fire or a flood, etc.
We all know we're told don't get in the elevator in case of a building fire. So if elevators aren't functional, it's really helpful for you to figure out if you can you navigate those stairs safely? Do you need to practice navigating the stairs? Do you need to find where the stairwell is and maybe do a couple dry runs to make sure that you've got it down? But you may also have to stay in your apartment and wait for assistance. And if that's the choice that you're going to have to make, what's the best way to do that? Do you hang an alert outside of your window to let people know you need assistance, how do you do that, etc. Again, this is all prior planning. But you're right, many of the cues for building plans are visual and they're obscure. You're going to have to be proactive to find out what those plans are.
Ricky Enger: Yeah, and you know, you said proactive and that made me think of something else as well. Again, it's hurricane season here and we often see on the news someone who has elected to stay behind, I want to stay with my stuff. I want to stay in my house. Then things go awry, and they need to be rescued. I feel like this is an individual choice, but do you think differently now about whether you would choose to shelter in place or whether maybe it is actually safe for me to get out ahead of time because I can't necessarily depend on other people to rescue me. I may have some additional logistics to think through. So, maybe I ought to just evacuate in the beginning before things get too bad.
Ed Haines: Personally, I air on the side of caution. But I will say, there will be notices if there’s a natural disaster or emergency and there's not enough time. There'll be notices from authorities about when it's time to evacuate. My advice would be not to ignore those notices. If you decide to shelter in place and you just don't want to leave your home and if the disaster occurs in your neighborhood or in your area, emergency personnel are going to be overwhelmed. So rescue may not always be quick, that's just something you're going to have to make a personal decision about.
Ricky Enger: Yeah, and I think as things are happening, you want to be able to keep up to date with what's going on. That in and of itself is a chore sometimes because if you watch the news, you are presented with an “as you can see here, you know, this is the trajectory of whatever this thing is heading your way.” And that may not be accessible to you anymore. So what are some ways to keep updated on what's going on in a way that is going to work for you?
Ed Haines: Good question. And you're right, you're watching the TV and they're pointing to a map. I have a weather radio, a NOAA, National Oceanographic and Atmospheric Administration weather radio on hand. It has a hand crank, so it'll power up without a battery. And I can monitor weather on that if I need to.
You can sign up for mobile phone alerts and warnings about severe weather in your area. And then there's the FEMA app, the Federal Emergency Management Agency. You can download that app on your phone and get alerts there as well. So there’s other places than just the television and local radio weather person who may or may not be giving you helpful information in a non-visual way.
The other thing I would say is if you are going to use a weather radio or use the FEMA app or whatever, practice using those first. You don't want to get familiar with that device or that app right in the middle of a disaster. You want to make sure that you're comfortable operating both. Again, it comes down to prior planning and it won't take long. It doesn't hurt to make sure that you can use those informational resources efficiently and quickly.
Ricky Enger: Yeah, and I'm kind of amazed at the features that are available on these weather radios now. It used to be it was just a radio and you might have access to some shortwave bands or whatever, but now they have flashlights on them. They have ways that you can flash SOS signals, and they have a power bank so you can charge your mobile phone for example. That can be really helpful. So, it's useful even just beyond being able to keep you up to date with what's going on, which I think is so helpful.
Once you make it through whatever the emergency, now it's time to think about what comes after. Are there other things that we should think about? Now that things are over, it's not immediately back to normal, right?
Ed Haines: Right, and a lot of this now comes down to just practical things that everyone's going to have to pay attention to. Your home may not be safe. Don't return to your neighborhood until authorities announce it's safe to do that and we can get that from a lot of sources. But you know, if you do have some vision loss, be aware that familiar landmarks and paths of travel might be damaged or obstructed. Don't expect to be able to just forge right ahead with your cane or without or with your guide dog in the same way you used to.
One thing I do want to mention in the aftermath of disasters is that mail can be halted for days or weeks. So, it might be helpful to think about how you get things like Social Security or federal benefits or any other kind of checks that come in that you depend on for your livelihood, are those all deposited electronically or are you dependent on the mail? If mail is disrupted, what are you going to do in the interim? So that's just one quick suggestion.
Ricky Enger: Yeah, even medications, a lot of people get mail order medications. So, knowing to contact your health care provider to figure out how am I going to get this emergency supply if my mail order stuff is not coming.
Ed Haines: Yeah, absolutely. There are lots of considerations. It depends on the disaster, and it depends on what the authorities are telling you to do. A lot of this is not vision specific at this point, but definitely pay attention to what your federal emergency management coordinator is telling everyone. Don't assume that your home or your neighborhood is going to be the same when you get back.
Ricky Enger: Well, I'm glad we had a chance to talk about a lot of this. Again, it's never comfortable to think about.
Ed Haines: No.
Ricky Enger: I feel like we all think that it's not going to happen to me. That's a thing that happens to other people. But if we are ready ahead of time, if we're prepared as much as we can be, then the things that we haven't thought about won't be piling on top of all the things that we could have done but didn't, right?
Ed Haines: Exactly, exactly.
Ricky Enger: This has been really good. In our show notes, we will have a link to our Safety Basics series, our video workshops. They will also have resources below the workshop that you can check out as well. There are things like what to put in your go bag and the contact list, a lot of the things that we've mentioned, you'll find there.
Of course, you can always call us to talk through some things as well. Ed, thank you so much for dropping by and going through some of this. It's been informative.
Ed Haines: Well, it was a pleasure, Ricky, and you're right, it is an important topic. I encourage people again to check out our Safety Basics series and then of course to call us at Hadley if they have any other questions.
Ricky Enger: Yeah, thanks so much.
Got something to say? Share your thoughts about this episode of Hadley Presents or make suggestions for future episodes, we'd love to hear from you. Send us an email at [email protected]. That's [email protected]. Or leave us a message at 847-784-2870. Thanks for listening.
Did you know that veterans are eligible for vision services and equipment through the Veterans Administration even if their vision loss developed many years later and was not as a result of service? Learn more as we chat with a representative of the Hines VA.
Voting can be tricky if you've lost some vision. In this episode, we discuss a variety of ways to cast your ballot, no matter your level of vision.
The Bright Focus Foundation funds research to find cures for macular degeneration and glaucoma, among other conditions. In this episode, we learn about their glaucoma and macular degeneration monthly chats. These sessions with scientists are open to the public and offer insights into the latest breakthroughs, treatments, and promising research on the horizon.
Artificial Intelligence (AI) has a lot to offer people with vision loss. Whether it's reading menus, describing pictures, or even narrating scenery, AI can make a big difference. This week we chat with Steven Scott, host of the Double Tap podcast, about some of the best AI-powered tools out there… so far. Link to Double Tap on Apple Podcasts.
When the doctor says, "there's nothing more I can do for you," what next? Who can help you make the most of your remaining vision and learn how to live more comfortably with vision loss? We break it down for you.
This week we talk to Dave Epstein, the visually impaired creator of the All Terrain Cane. He shares about his life with a progressive eye disease and his love of hiking. These two pieces of Dave lead him to develop his unconventional cane.
When you have vision loss, scams can be even more challenging to avoid. Listen in as we get some tips and tricks from Veronica Lewis who runs a low vision assistive technology website.
Be My Eyes CEO, Mike Buckley, joins us to talk about how this free, smart phone app merges technology and human kindness and how it's now using AI to describe the world in front of you.
Recently retired, David Tatel served for decades on the US Court of Appeals for the D.C. Circuit. He also happens to be visually impaired. In this episode, he and Ricky talk about his recently written memoir, a book about his life as a judge, a husband, a father, a grandfather, and how all of these roles intersect with his experience with vision loss.
This week we talk smartphone tools and when you might want to use the different options. Jennifer Shimon from the Wisconsin Office for the Blind and Visually Impaired joins Ricky.
Sometimes, navigating life with vision loss goes a bit sideways. Things don't always turn out exactly as we've planned, and it can help to just laugh at these strange situations.
We've shared several episodes of listeners' stories, what we're calling vision loss bloopers. Today, Ricky Enger and Doug Walker share some more of these bloopers along with a few of their own.
Prevent Blindness' patient advocacy program empowers people facing vision impairment. Patients learn how to promote change with their physicians, their families, drug companies, and even policy makers.
Ever thought about getting a guide dog? Listen in as we chat with members Jeff Flodin and Ed McDaniel about their experiences with guide dogs and some common misperceptions.
The National Library Service has a free talking book program for anyone in the US with vision loss. Tonia Bickford, an advisor from Michigan's talking books program, joins us to discuss how to get the most out of this free service.
This week we learn more about visual hallucinations that sometimes accompany vision loss, a condition called Charles Bonnet syndrome.
Sometimes vision loss can make us feel less secure. This week we talk about personal safety with Hadley's Chief Program Officer, Ed Haines.
For many living with vision loss, watching TV is less enjoyable as they can't see what's happening on the screen very well anymore.
Audio description fills the void by narrating key visual elements. Listen in as Ricky chats with Hadley member and avid audio description user, Judy Davis.
Listen in to our conversation with Dr. Mondal, a low vision optometrist and professor at the University of Wisconsin. We chat about what to expect from a visit to a low vision specialist and the kind of help they can offer.
Have you listened to Hadley's community-generated audio podcast yet? In this episode, Ricky and Marc Arneson, Hadley's Director of Community, share a few stories from Insights & Sound Bites and discuss how to contribute your own story. Insights & Sound Bites | Hadley
Listen in as artist Chloe Duplessis explains how a degenerative eye disease changed, and didn't change, her life and love of art. "I thought art required sight. I was wrong."
Dr. Judy Box, a Hadley member living with macular degeneration, shares her tips for managing those important conversations with your eye doctor.
In this episode, the Hadley team talks all things gifts. Giving them, getting them, what's on their wish lists, and how vision loss may, or may not, impact these activities.
Friendships often change when one has vision loss. Whether it's adaptations to the activities you enjoy together, asking for help, or turning that help down … there are conversations to be had. Let's tune in as two Hadley members, Eugenia DeReu and Tara Perry, share their experiences with what's changed for them — and what's stayed the same.
Losing some vision can make for shopping challenges. Here are a few mishaps that Hadley members have run into. Have your own to share? Email us at [email protected]
This week we chat with the chief technology officer from Envision as he shares how their free mobile app or camera-enabled glasses can help those with vision loss. It speaks aloud written information, describes surroundings and objects, and even tells you who's nearby.
Lots of questions, concerns, and stereotypes connected to use of the white cane. In this episode, we address several of them from past discussions on the topic.
Listen in as Hadley's Director of Community, Marc Arneson, chats with Hadley members Bill Massey and Gregory Peterson about their participation in Hadley's new Peer-to-Peer program.
To learn if getting a peer connection is for you, call us at 1-800-323-4238.
Listen in as we chat with Ed Haines about getting the most out of our magnifiers.
Listen in as we chat with animal lovers Debbie Worman and Sheri Robinson about the joys and challenges of caring for a pet when you have vision loss.
Listen in as Hadley member, Wendy Spencer Davis, shares why she decided to learn some braille and how it's helping her in everyday life.
Ed McDaniel, a psychologist with low vision, joins us to talk about common emotional triggers people with vision loss face and how to recognize and manage them.
Jessica Grogan from the American Diabetes Association joins us to talk about managing your blood sugar with vision loss.
Tune into our chat with Sarah Clark, a visually impaired marriage and family therapist, as she offers her unique insight into some common family dynamics that often make adjustment more challenging and how to navigate through them successfully.
Join us as we chat with Hadley member, Kris, about her experience living with vision loss in a senior community.
Listen in as Hadley staff share their real-life bloopers—times when things didn’t quite go as planned.
Join us as we take a dive into the features of the BlindShell cell phone.
Listen in as Pastor Scott Himel shares his advice for participating in religious services no matter your level of vision.
Join us to learn about how ScripTalk technology translates medication labels into speech and where you can find a participating pharmacy.
Join occupational therapist from Duke Eye Center, Fay Tripp, in a conversation about bioptic glasses—what they are and who can benefit from them.
Listen in as we chat with birding expert Freya McGregor who shares her tips on how you can enjoy this hobby, no matter your level of vision.
Listen in as Hadley's Doug Walker and Ricky Enger chat about how they use GPS in their daily lives. From walking directions to finding items or assisting a driver by navigating a trip, GPS can be a very handy tool.
Listen in as we chat with Dave Steele about his life, poetry, and vision loss.
Listen in as we discuss some common situations that can make us feel unsafe and share ideas on how to address them. We're joined today by Christy Ray and Ricky Jones of STRIVE4You.Org
Unfortunately, it's not uncommon for feelings of shame to creep in when we've lost some vision. Join social worker Jeff Flodin and psychologist Ed McDaniel, both visually impaired themselves, as they explore where these feelings come from and how they have worked through these emotions in their own lives.
Listen in as Dorrie Rush of OE Magazine shares how she resisted using a white cane for years, the stigma she feared, and the confidence and security she found once it was in her hand.
Learn how CVS pharmacy customers throughout the US can access a free service that reads aloud prescription medication information.
Join us as we chat with author Hannah Fairbairn about the tips and tricks she has learned to take some of the stress out of holiday get-togethers, no matter your vision.
We're joined by the creator of The Blind Life YouTube channel, Sam Seavey. Sam shares his personal journey with vision loss and advice he has for people who are newer to vision loss.
Whether you like to read for enjoyment or need to check your mail, reading is an essential part of your day. We're sharing tips and tricks for how to continue reading, the best low-tech and high-tech gadgets, and the benefits of learning braille.
Chief Innovation Officer Doug Walker chats with us about the launch of Hadley's newest podcast, Insights & Sound Bites. This new podcast will offer short stories shared by listeners. By tapping into the power of our community, we hope to share ideas, discoveries, and moments of inspiration along the journey through vision loss.
Jim Hoxie and Joanna Jones join us to discuss their children’s book, "Grandpa's White Cane." Jim shares how vision loss shaped his life and how he and Joanna, a retired teacher, began instructing children about the importance of white cane awareness and the do's and don'ts for helping people with visual impairment.
Blogger and social worker Jeff Flodin talks about his personal journey with vision loss and how his passion for helping people led him to blog about his experiences.
Hadley has partnered with the National Eye Institute (NEI) to offer a Spanish-language version of our popular cooking workshop series. Devina Fan, director of the National Eye Health Education Program at NEI, joins the podcast to talk more about this new initiative, NEI’s expanding Spanish content, and the importance of connecting Hispanic and Latino communities to important vision resources.
A change in your vision may make some parts of your job more challenging. But with a bit of help and some new skills, you may be able to stay in your job. Hadley Chief Program Officer Ed Haines and Learning Expert Steve Kelley join the podcast to talk about our new Working with Vision Loss workshops and to share tips for where to find support and how to ask for what you need.
Certified accessible travel advocate Melvin Reynolds joins the podcast to share tips for getting the most out of traveling, no matter your level of vision. Melvin gives advice on what to research ahead of a trip, considerations for traveling with a guide dog, and how a certified accessible travel advocate can help.
Karen and Dan Leonetti share how vision loss has changed their relationship and the advice they have for other couples.
Rabbi Lenny Sarko joins us to talk about how his vision loss journey led him to create a first-of-its-kind braille Sefer Torah that people around the country can access.
Actor and artist Bruce Horak talks about his personal journey with vision loss, how he got interested in painting, and his role in the new television series Star Trek: Strange New Worlds.
CEO of Eschenbach Optik of America Ken Bradley joins the podcast to discuss how Eschenbach has adapted through the pandemic to help people with visual impairment access low vision devices remotely. Through their "Telelowvision" program, you can try out magnification devices from the comfort of your home to find what works best for you before you buy.
Scottish radio broadcaster and podcaster Steven Scott loves finding and talking about tech stuff. He's especially fond of apps and gadgets that make life easier for him and others with vision loss.
NYT Columnist Frank Bruni returns to the podcast to talk about his new book. Frank describes his personal experiences with vision loss and how, with time, his perspective has grown.
IT professional and stand-up comedian Todd Blenkhorn talks about his personal journey with vision loss and how his passion for stand-up helped him find and share the humor in daily interactions.
In this episode, we're sharing highlights from previous interviews with a glaucoma specialist, retina specialist, and a low vision doctor. Listen in to learn more about common eye conditions, treatments, and what to expect at these specialist appointments.
Master Gardener Sue Brasel and Hadley's Chief Program Officer and gardener Ed Haines join us for a chat about gardening, no matter your level of vision or gardening experience. They share tips for how to get started, common challenges, and the many benefits of gardening.
We're joined by Carol Mackey, an avid discussion group participant, and co-host Debbie Worman to chat about what Hadley groups are, how to join, and what you can get out of them. With 10 groups on a variety of topics, there's something for everyone. Listen in or chime in – it’s up to you.
Bold Blind Beauty blogger Stephanae McCoy joins us for a chat on beauty, style and confidence. Stephanae talks about how vision loss shaped her life, and then shares some of her favorite fashion and beauty tips.
Hadley staff share their favorite kitchen gadgets and tips. Whether you're an experienced home chef or a total novice, you're bound to pick up a few ideas that fit your vision needs and make your time in the kitchen more productive (and fun).
We sat down with Kim Walker, co-director of research and development at Hadley, and Mark Andrews, one of the Hadley advisors who reviewed our exciting new approach for adults with vision loss to learn braille. From labeling items in your home to identifying buttons on an elevator, braille can be a wonderful tool for everyday use.
New York Times Best-Selling Author, Gretchen Rubin, chats about her research on how tapping into different senses can enrich our lives and connect us to each other in surprising ways.
Twin sisters Jenelle and Joy join the podcast to share their personal experiences with vision loss and adjusting to it emotionally. While they look identical, their perspectives and journeys differ, highlighting their mission to show that "there is no right way to go blind."
Hadley learner Sharon Noseworthy shares tips and tricks for hosting get-togethers of any type or size, no matter your vision. Sharon has always loved the role of hostess and has learned to adjust her approach now that her own vision has declined.
We're joined by Teepa Snow, occupational therapist and founder of Positive Approach to Care, to learn more about the challenges of having both vision loss and dementia. Teepa addresses common misconceptions about dementia and shares practical tips for supporting someone with both conditions.
We sat down with several Hadley staff members and asked them about their favorite tech tips, apps, and gadgets. Whether you consider yourself a tech expert or novice, the group recommends a variety of high-tech and low-tech options that fit your comfort level and interests.
Judge David Tatel has served on the second most powerful court in the country since 1994. He also happens to be blind. Judge Tatel joins us to share his story on building a law career and family while dealing with changing vision, the technology and resources he's found useful, and what made him consider getting a guide dog in recent years.
In honor of White Cane Safety Day today, we're joined by Hadley learner Larry Carlson and Orientation and Mobility Specialist Elijah Haines for a conversation about this important tool. Larry shares what made him decide to use a white cane, and Elijah shares tips for what to consider and how to adjust to using a white cane.
Supriya Raman, manager of the Disability and Multicultural branches of the TSA, shares tips on traveling among shifting COVID restrictions. Supriya covers what to expect at the airport and what resources are available for people with visual impairment.
Photographer Michael Nye chats with us about his latest art exhibit, "My Heart is Not Blind," a collection of photos and audio interviews of people with visual impairment. Through these stories, Michael provides a look into what he calls "our shared humanity and shared fragility," as well as common misunderstandings about blindness.
Champion blind golfer Chad NeSmith talks about how vision loss shaped his life, and how he shares his passion for golf with others with vision loss.
Doug Walker, Hadley co-director of R&D, and Ed Haines, Hadley Chief Program Officer, chat about the making of Hadley's "Adjusting to Vision Loss" workshop series. The series guides people through the emotional aspects of vision loss. Doug serves as the series' personal storyteller and narrator.
In this episode we chat with ophthalmologist Dr. Angela Elam from the University of Michigan. Dr. Elam addresses common questions and concerns, and shares her advice for returning to the eye doctor among shifting COVID restrictions.
Dorrie Rush, OE's Chief Content Officer, joins us for a chat about this wonderful online resource chock full of tips for living well with vision loss. You'll find great articles on using tech tools, tips for health and well-being, stories from others living with vision loss, a terrific podcast, and more.
Learn about a new service that’s just launched in 2020 called Accessible Pharmacy. Accessible packaging and labeling and personalized customer support all free of charge to the end consumer, and specifically designed for those with vision impairment.
Audio Describe the World! That’s the mantra of UniDescription: a free smartphone app that provides audio descriptions and navigation tips for US National Parks and other public places.
In this episode, we chat with low vision optometrist Dr. Mark Wilkinson from the University of Iowa. Dr. Wilkinson answers common questions and shares his advice for getting the most out of low vision optometry appointments.
Jan and Elgie Dow share how vision loss has changed their relationship and the advice they have for other couples.
Join Hadley advisor Eddie Becerra as he shares about losing his sight from diabetic retinopathy, and how he gained a new perspective on life.
Classically trained chef Regina Mitchell shares how vision loss shaped her life. Regina worked her way back into the kitchen and is now helping others cook with confidence, no matter their vision.
In this episode we sit down with the director of Well Connected, an organization that offers free, call-in groups for adults over 60 on a wide variety of interest areas: games, music, meditation and more.
Support groups can be a great way to connect with others who "get it." Listen in as as low vision support group leaders Lynndah Lahey and Judy Davis describe how their groups are run and what their members get out of them.
World-renowned artist John Bramblitt describes how vision loss has shaped his painting and his life.
In this episode, we chat with Dr. Tim Murray of the American Society of Retina Specialists. Dr. Murray treats eye diseases such as macular degeneration and diabetic retinopathy. He answers common questions and shares his insights into the future of treatments.
In this episode, we sit down with Dr. Jullia Rosdahl, a glaucoma specialist from the Duke Eye Center, and ask her some of the many questions we’ve heard about glaucoma, its risk factors, and how to treat the disease.
Hadley learning expert Jessica Smith shares her experience raising a puppy that may eventually become a guide dog. She covers what she’s learned and things to consider if you’d like to volunteer to help out a guide dog school.
October 15 is White Cane Safety Day, a day to recognize this important tool that empowers people with visual impairment to travel safely and independently. It also brings attention to the general public to be mindful of visually impaired neighbors, giving them additional consideration and right-of-way when needed. We sat down with Kellee Sanchez, an orientation and mobility specialist, to talk about the history of White Cane Safety Day, and how a white cane can help those with vision loss.
Be My Eyes is a free smartphone app that connects visually impaired users with sighted volunteers for help with visual tasks. We sat down with Will Butler from Be My Eyes to hear how the app started, tips for using it, and exciting new features that provide specialized assistance, including with Hadley.
Tracy Simon from Eye2Eye peer support program shares her story of vision loss, how her program works, and the benefits of connecting with and supporting each other.
Ophthalmologist Dr. Lori Provencher chats with us about how the coronavirus pandemic has changed doctor's visits. She shares tips for staying safe, questions to ask, and what to expect before, during and after your next office visit.
Mindfulness expert Tiffany Guske returns to the podcast to share tips and insights on how to cope with life's challenges, such as vision loss or an illness, building resilience and focusing on self-compassion instead of judgment.
Author of "When You Can't Believe Your Eyes," Hannah Fairbairn, chats with us about how to communicate in everyday situations when you can't rely on visual cues. Hear Hannah's own story about losing vision, her practical tips on adjusting to vision loss, and advice she has on regaining confidence in social situations.
In this episode, we continue the conversation on living during the COVID-19 pandemic with a visual impairment. Listen in as we share some experiences, tips, and strategies for coping during these difficult times.
The COVID-19 crisis has brought a wave of change and uncertainty to our everyday lives. Listen in as we share personal experiences, resources and some helpful tips...all from a blind or low vision perspective.
Assistive technology experts Ricky Enger and Steve Kelley review BlindShell, a mobile phone built for those with visual impairment. They discuss the basic features, how it differs from a traditional smartphone, and how to decide if it's right for you.
This week we sit down with Dan Roberts, author of "The First Year-Age-Related Macular Degeneration: An Essential Guide for the Newly Diagnosed" and founder of MDSupport website and support group. Hear Dan's own story about being diagnosed with macular degeneration and what prompted him to reach out to others facing similar circumstances.
Listen in as we explore the basics of using hand tools with a visual impairment. Gil Johnson, a visually impaired home repair expert, shares tips on everything from measuring, to leveling to hammering.
Elections are right around the corner. So we gathered a panel to talk about options for voting no matter your level of vision. Listen in as we explore everything you need to know, from registering to vote to the many ways you can cast your ballot.
Ricky sits down with Android Accessibility Product Manager Brian Kemler to discuss what is available on Android phones for those with visual impairment. From adjusting font size and color, or opting to listen with TalkBack instead, the commitment to making these powerful tools more useful to a wider audience is clear.
In this episode, we chat with Gil Johnson, an experienced home repair and woodworking enthusiast about things to consider when undertaking home repair with blindness or low vision.
Hadley's Debbie Good sits down to continue a conversation with author and visually impaired world traveler Dr. Wendy David. Together they explore a wide variety of helpful hints covering train, plane, and cruise travel as well as practical information on traveling internationally and navigating hotels.
In this episode, Ricky Enger chats with Joe Strechay, associate producer on the Apple TV+ series SEE. The show takes place in a future where, after a viral apocalypse, all humans are blind. Joe takes us behind the scenes of the show and his work to help build an inclusive set for the cast and crew, including those with low to no vision. From casting to costumes, scripting to scenery, hear how Joe helped create a science fiction world that strives to be authentic to life with vision loss.
Hadley's Debbie Good sits down with travel author Dr. Wendy David in this latest episode. In part one of this two-part interview, Debbie and Wendy discuss tips for traveling with confidence as a blind or low vision person, advice on picking destinations, considerations for traveling alone and in a group, and more!
Ricky Enger is joined by Hadley's Debbie Worman and mindfulness expert Tiffany Guske in this latest episode. Debbie and Tiffany talk about what mindfulness is and the specific benefits that mindfulness can offer for those living with vision loss. Tiffany then walks listeners through a short mindfulness exercise.
In this episode, Ricky Enger speaks with New York Times columnist Frank Bruni, who shares the story of his sudden vision loss from NAION. Bruni speaks candidly on his adjustment to the change, maintaining a realistic attitude towards his vision loss, and the failure of medical professionals to provide resources after diagnosis.
Listen in as we share practical tips on how to keep your handwriting readable. This resource-packed episode includes many useful techniques and solutions to common handwriting challenges. Hadley Learning Expert Jennifer Ottowitz chats with Sue Dalton, Certified Vision Rehabilitation Therapist.
In this episode, Hadley's Steve Kelley speaks with Kendra Farrow, from the National Research and Training Center on Blindness and Low Vision, located at Mississippi State. The episode serves as a guide for those new to vision rehabilitation, including determining who is eligible for services, key differences between the medical and social services models, and how to locate services in each state.
In this episode, Ricky Enger chats with Microsoft's Jeremy Curry, a Senior Program Manager with the Windows Accessibility team. New vision accessibility features are now available in Windows 10 for low vision and screen reader users.
In the inaugural episode of Hadley Presents, Ricky Enger and Jonathan Mosen of Aira chat about the ways in which a visual interpreter service, such as Aira, can be used to gain valuable visual information and enhance travel and leisure activities for blind and low vision users.