Tag: blog

New website = new offers

I’m really excited because…  I’m moving away from one-time trainings and spending more time on what I really enjoy doing: consulting projects. I now offer a calendar on my site where you can book a phone call with me. This means zero back-and-forth emails about when we’re both available. Step One of my new consulting package is my EVALUATE & ESCALATE offer. It’s normally $1,500, but you can book it for only $975 through the end of May. This offer includes:  A detailed evaluation of your current dementia care program with proposed solutions you can implement, including interior design concepts to make your building more dementia-friendly  3 staff webinars  1-month access to my online “Everything You Need to Know About Dementia” course for anyone who wishes to take it (maybe your residents’ or clients’ family members!)  25 signed copies of my book www.rachaelwonderlin.com

The 10 most important things about dementia caregiving

Are you enjoying my blog posts? Grab a free download of one chapter from my audiobook here and also receive any future helpful tips and posts right to your inbox! Communicating with people living with dementia can be challenging. Understand that their world may be different from our world, and that’s okay. We want to EMBRACE THEIR REALITY rather than trying to convince them of things that are true in our reality. Just because their reality is a different shape, it doesn’t make it wrong.   Don’t get hung up on the word, “lying”: realize that if you are telling them the facts of their reality, you are doing the best thing for both of you. Here are 3 questions you want to use when talking to people with dementia: “Where do you think they are?” when someone asks you about loved one “Can you help me?” when getting them to do something with you “What do you think about this?” when introducing a baby doll or animal Get to know them on a personal level, and this will help you live in their reality. Ask, “What did you used to like to do?” instead of, “What do you like to do?” Offer them 2-3 choices instead of asking open-ended questions like, “What do you want to eat for breakfast?” or, “What did you do today?” TIMELINE CONFUSION is the concept that time isn’t linear in dementia. If the individual cannot identify their loved ones, it isn’t because they don’t know them or love them, it’s because these people don’t fit on their timeline. Never try to “convince” someone living with dementia of something. Don’t use “logic” to try to help them understand. No weddings, no funerals, no cemeteries.  Not everything is Alzheimer disease! The phrase “Altttttheimer’s and dementia” sounds ridiculous. Recognize that their timeline and reality may change, and that we can learn to be flexible and change with it. Dementia caregiving is an art form that takes practice and patience to learn.

Only 3 Questions You Need in Dementia Caregiving

Are you enjoying my blog posts? Grab a free download of one chapter from my audiobook here and also receive any future helpful tips and posts right to your inbox! These are my best 3 tried-and-true questions that you need in dementia caregiving. Are you ready? 1. “Where do you think they are?” This is the question that you’re going to use with someone who has dementia when they are talking about a loved one who has passed away. For example, perhaps your mom is saying, “Hey, where’s my dad?” You know that her father (your grandfather) died years ago, but saying, “Don’t you remember? He’s been dead for years!” is a terrible answer. Let’s figure out where her reality is so that we can embrace it! Ask her, “Where do you think he is?” and then repeat that answer back to her. For example, it may go like this: “Where’s my dad?” / “Where do you think he is?” / “I think he’s at work.” / “That sounds right, he must be at work.” The great thing about this answer is that it takes you completely off the hook: you don’t have to come up with anything, and you won’t accidentally give them the wrong answer! I spoke to a staff member at a local SNF recently who told me about the wrong answer she gave one of her residents. “Uhh…I think your husband is at work,” she offered. “My husband is on disability, so he doesn’t work!” the resident called back, annoyed. If the person you are caring for believes that their loved one is dead, you can also confirm this. The trick is to always repeat their answer back to them. You can also reuse their answer, without re-asking the question, multiple times in a row! 2. “What do you think about this?” This is the question that you’re going to use when introducing a stuffed animal or baby doll to a person with dementia. Just like in the first question, we give the person with dementia the opportunity to tell us what THEIR reality is! We don’t want to introduce a stuffed dog and say, “Look at this real dog!” because they may say, “That’s not a real dog.” Let them guide you to what their reality is, and then do that. 3. “Can you help me?” If you ask someone with dementia if they “want” to do something, what will they probably tell you? They’ll probably tell you, “no,” even if they may have been interested in the thing you were asking about. If you ask someone “for help,” you’re actually asking a completely different question! I’ve done this many, many times with people who have dementia. The phrase, “Do you want to help me?” or, “Do you want to…” is very different from, “CAN you help me?” “Can you” inspires a sense that you are the one needing assistance, and everyone wants to feel helpful and needed! Like this article? Follow me here Love this list? Buy it in poster form on my website!

Don’t ask if they “remember your name”

If I can, I always opt to ditch my name tag in a dementia care environment. I let my friends with dementia decide what my name is: I’ve been Susan, Gwendolyn, and various peoples’ kids. I’ve been so many identities to my residents, too: a coworker, a boss, a student, a sibling, a friend from home, and more. Don’t ask your friend with dementia if they “remember your name” — especially if that person is your parent, spouse, or other family member. It’s quite likely to embarrass them if they can’t place you, and, frankly, it doesn’t really matter what your name is. What matters is how they feel about you. Here’s my absolute favorite story about what I call, “Timeline Confusion”: Alicia danced down the hallway, both hands steadily on her walker. She moved her hips from side to side, singing a little song, and smiled at everyone she passed. Her son, Nick, was walking next to her. Nick was probably one of the best caregivers I’d ever met. It wasn’t just that he visited his mother often, it was how he visited her. He was patient and kind—really, he just understood dementia care. He got it. Alicia was what I like to call, “pleasantly confused.” She thought it was a different year than it was, liked to sing and dance, and generally enjoyed her life. One day, I approached the pair as they walked quietly down the hall. Alicia smiled and nodded at everyone she passed, sometimes whispering a, “How do you do!” “Hey, Alicia,” I said. “We’re having a piano player come in to sing and play music for us. Would you like to come listen?” “Ah, yes!” she smiled back. “My husband is a great singer,” she said, motioning to her son. Nick smiled and did not correct her. He put his hand gently on her shoulder and said to me, “We’ll be over there soon.” I saw Nick again a few minutes later while his mom was occupied with some other residents. “Nick,” I said. “Does your mom usually think that you’re her husband?” Nick said something that I’ll never forget. “Sometimes I’m me, sometimes I’m my brother, sometimes I’m my dad, and sometimes I’m just a friend. But she always knows that she loves me,” he smiled. Nick had nailed it. He understood that, because his mom thought it was 1960, she would have trouble placing him on a timeline. He knew that his mom recognized him and he knew that she loved him. However, because of her dementia, she thought it was a different year. And, in that year, he would’ve been a teenager. Using context clues (however mixed up the clues were) Alicia had determined that Nick was her husband: he was the right age, he sure sounded and looked like her husband, and she believed that her son was a young man. This is the concept that I like to call timeline confusion. It’s not that your loved one doesn’t recognize you, it’s that they can’t place you on a timeline. What matters is how they feel about you. Not your name or your exact identity. Are you receiving my emails? Sign up now!

The BEST communication tip I have

Are you enjoying my blog posts? Grab a free download of one chapter from my audiobook here and also receive any future helpful tips and posts right to your inbox! Here it is, the best dementia care communication tip I have for you. Although I’ve been using it (and tweaking it) for a long time now, I didn’t really “name” it until very recently. Ellen had a problem. “Dad wants to go out walking around the neighborhood, like he used to do…but he’s so confused! I’m terrified that he’s going to get lost or hit by a car or something awful. How do I convince him he can’t walk around the block anymore?” I paused and thought for a minute. “You can’t convince him that he can’t walk by himself,” I said. “So you need to ask him if you can go with him.” CAN vs. WANT If Ellen were to ask her father if he “wanted” her to go with him, he’d almost definitely say no. No, he’d think. This was his walk, this was his thing—he didn’t need or want help! Instead, I suggested she rephrase her question: “Dad, CAN I go with you? I’d love some exercise!” It’s a totally different question, even though the goal is the same: she wants someone to go with him so he doesn’t get lost. Now, though, it’s hisidea if he takes her along. He’s also very unlikely to turn her offer down, because she’s asking for his acceptance and assistance. Use “CAN” statements in dementia care, instead of WANT statements. For example, check out these comparisons: Do you want to paint this birdhouse with me? vs. Can you help me paint this birdhouse? Do you want to take a shower now? vs. Can you take a shower now, we are getting ready to go out? I want you to help me set the table for dinner! vs. Can you help me set the table for dinner? The doctor wants you to move to assisted living because of your dementia vs. Can you help me pick a great place for you to stay during your rehab? The beauty of this phrasing is that you can really use it in any part of your life, dementia care or not! People are much more willing to do things if they feel like it was their idea to begin with. Have you signed up for my blog yet?

How one woman got her husband to agree to attend adult day care

She knew that she’d have a hard time getting her husband, Ben, into adult day care. Ben loved working, and now that he was retired and had dementia, he still liked to find projects to do. Convincing him that he could benefit from adult day care certainly wasn’t going to work (and doing this with anyone with dementia is not advisable.) Instead of arguing with him, she spent a couple weeks getting Ben excited about the opportunity. Each morning at breakfast, she’d begin talking about the adult day program, but reframing it. “There’s this new program,” she told him. “They need more people to work there, but it’s really tough to get in.” A couple weeks into repeating this idea, she finally announced to him that she’d gotten good news. “It turns out they have an opening!” she told Ben. Ben was excited: he’d gotten into this new program. At first, Ben just went a couple days a week. He seemed as though he enjoyed “working” there, but didn’t really want to take on more days. “Here’s the thing,” she told him. “They love your work and they want you to put in a few more hours…do you think you’re up for the task?” Of course, he was up for the task. Ben was thrilled to be needed like this. “When will I see my paycheck?” Ben asked his wife.  “Well, you see, it goes right back into the program, that’s how their non-profit status works,” she explained. Ben goes to day care every weekday now. Both of them are very happy with how it’s worked out. By embracing his reality, she was able to make this new arrangement work for both of them. Have you signed up for my blog?

HOW TO: 3 tips for keeping them engaged while you get other tasks done

Are you enjoying my blog posts? Grab a free download of one chapter from my audiobook here and also receive any future helpful tips and posts right to your inbox! “It sounds bad, but I can’t get anything done with my wife around,” Walter sighed. “She wants to ‘help,’ but I end up having to re-do her task or just stand over her shoulder the whole time, helping her do whatever it is.” I’ve heard this story many, many times over. You want your loved one with dementia to be engaged and active, but you also don’t want to be doing 99% of the task yourself. And, more than anything, you want to get your own chores and errands done…but it’s tough when you have someone needing your attention 24/7. The holidays are an especially challenging time when it comes to providing care for someone living with dementia.  Let’s review my best 3 tips for getting someone out of your hair (in the nicest way possible!) while still keeping them happy and feeling successful: Set them up for success. This takes a little more time for you on the “front end,” but provides a lot of extra time saved on the back end. Find a task that is easy, repetitive, and doesn’t require any special or particular outcome. A good example would be folding towels or making a salad. When it’s done, it’s done, and it doesn’t need to look a particular way as long as the towels can fit in the cabinet and the salad has the ingredients in the bowl.  Ask them for help, and then let them do the task by stepping away. “Can you help me with…?” you ask. When they begin, step away. Encourage them. It may take a few tries to make this work so that they feel comfortable and confident. Your loved one may feel, at the start, that they “don’t know how” or are afraid to make a mistake. Don’t worry about the outcome. It’s all about the experience of doing the thing and the opportunity for you to have a break. Praise your loved one’s finished project, no matter what it looks like.  Then, repeat. It could take a few tries to perfect this. Don’t give up. Sign up for my blog emails here!

Hospital Kindness Cart

[youtube https://www.youtube.com/watch?v=4ItWgP9rly0?feature=oembed&enablejsapi=1&origin=https://safe.txmblr.com&wmode=opaque&w=540&h=405] Memorable Pets is my favorite company to work with. I’m currently working in my third community, and this is also the third community where I’ve brought Memorable Pets to work. (See example below) My residents love playing with and cuddling the Pets. Currently, Memorable Pets are being featured in a Connecticut hospital. This is a really amazing thing, considering the challenges that I know come with hospital administrations. The fact that a “Kindness Cart” is really making a difference is wonderful.  Volunteers take the Cart from room to room, visiting the patients with dementia. Each is offered something special from the cart: combs, books, floss, crayons, or other useful items. Many of the patients, it seems, choose a Memorable Pet instead.  From my own experience, I have seen the impact that these realistic-looking pets have made on my residents. They have the same impact as the baby dolls often do. Sometimes, the impact is even greater, I think because of the kind of joy real pets brought to people in their younger lives.

An Imaginary Marriage

“Henry! Get your keys, we gotta go!” “I can’t find my keys, Irene! Where did you put them!” “I didn’t put your keys anywhere! Where did you lose them!” They argued like a married couple, but they were not actually married. Jeff and Ellen were two of my residents who believed that they had been married for years. In fact, they usually called each other by their actual spouse’s names (Henry and Irene) instead of their real names. Still, they each responded to the other’s call. “Henry! Get your shoes on, we gotta go,” Ellen would call. “Irene! Help me with my shoes!” Jeff would yell back. I happily found that, instead of being distraught, Ellen and Jeff’s adult children were agreeable about the “union” between the two. The relationship between Ellen and Jeff consisted mostly of trying to convince the other person to “drive” them home. This was actually a helpful union for the staff because the pair would bug each other about “going home” instead of getting other residents worked up. I have found that many adult children become uncomfortable when relationships develop between their parents with dementia. Sometimes, when the actual spouses are still alive–like in this case–the adult children suggest that it’s “unfair” to the living spouse. But, that’s dementia. It’s not a “fair” group of diseases. And, sometimes, a little bit of confusion provides a person with a partner–and that can be for the best.

Special Offer: FREE Poster

Rachael wrote "16 Things I'd Want If I Got Dementia" in 2014 and it's circulated the globe many times over. Download your free copy here!