Daily Devotions for Caregivers

Sorry for the long absence. These hospital stays wear on me these days and take me longer to recover both emotionally and physically. I'm almost rested back up to the caregiver's normal!   lol. I'm still working on getting my little bookstore up online and last night I finished up another small study guide. I thought I would read back through some of the scriptures as I typed it all up. That is why this morning, I opened my Bible to Romans 5. This particular Bible study guide is called the Garden Connection .   It ties the fall and redemption together so we get a big picture of what the fall of Adam and Eve did to mankind. But then it ties it in with the New Testament and the impact of what Christ did, and how he reversed the chain reaction set in motion in the garden. Anyway, I opened Romans 5 this morning for a reread. I'm looking for the garden connection and the work of Christ but found myself stuck in the first few verses. Paul says, T herefore, being...

Every day is challenging for caregivers. Period. Even our better days are filled with things others may never even have to deal with or think about. I don't know the specifics of your daily drills - but mine include transfers, tube feedings, changings, dressing, range of motion, and feeding.. for starters. Of course, there are tons of other things that come up in the midst of the caregiver's norms. We do tend to adjust, don't we? And we just keep putting one foot in front of another. Other people might call these the "rough spots." But I call the extra bumps - like making decisions on behalf of another person or dealing with extra emotional baggage the rougher spots. What are we to do when things go from rough to rougher? Personally, I'm just sad lately. I'm sad Chris can't walk, talk, or do anything for himself. I think a lot about who he was - and all he did. That creates a rough spot emotionally. Sometimes there doesn't seem to be a way to t...

As caregivers, our emotions are often running on the edge. For me, it doesn't take much to tip me over into a huge downward spiral. For today I'm calling it the "big dipper." Just a single word, an honest question, a picture from the past - it doesn't take much to send me into the dip of depression. I have developed a few strategies that work for me and being able to identify it early on means I don't always dip as far or I can head it off at the pass. But not always. With so many things on our plate it doesn't take a lot, does it? This last week was full of dealing with a faulty internet provider which is enough frustration by itself when you work online and were without internet for two days! lol. Sometimes it's bigger things - but sometimes it's those little things that chip away at sanity and peace. How are we supposed to deal with this "big dipper?" It's going to come for us. Some day. Some time. We may feel broadsided by i...

Image via Pexels Losing a spouse is one of the most stressful events a person can go through. For seniors, that stress is even more dangerous. The depression and loneliness seniors feel after a big loss can put their health at risk. Grief also weakens the immune system, which makes them more susceptible to infection and other illnesses. Seniors dealing with dementia and related illnesses like Alzheimer’s have an even more difficult time with grief. Memory loss, emotional instability, and other symptoms of dementia make each day after a death a unique and challenging experience. Communicating about the loss and their emotions presents a difficult task you will likely have to go through multiple times.   There are many things you can do to help support a senior after the loss of a spouse. One of the most important things to do is to be there long after the death to listen and encourage healthy behaviors . However, if you want to help in a more immediate manner,...

Several things have occurred lately that remind me of the social isolation so many caregivers experience. Even in a crowd, many times we are alone. Even when people do talk to us on outings (if we can even get out!) they can't connect with us beyond the obvious. They only see us as a person behind the chair. I've done a few other blogs about being more than a caregiver and life behind the chair. But as we've been able to get out more frequently, it's come to light again - that invisible feeling. I'm starting to wonder if I'm just the invisible woman. lol It's not easy to do normal  things others take for granted. Things we really want to  do - but just are not feasible. Take going to church for example. Often, there's no fellowship - no one knows how to reach out because we stand out as so different. It's not their fault - they really don't know that they can still ask you out for coffee or lunch. Personally, I find myself in situations ...

Life is not "normal" for caregivers even though we find our own kind of normal to deal with our unique situations. We adjust. We proceed. We get through. But oftentimes, I find myself so on the edge emotionally that any little thing sends me flying off into the emotional pit of despair! lol (maybe that's just me......) This week has been more than enough for a normal life, let alone a caregiving life. I will spare you all the details, but the biggest problem by far was being without internet for nearly two days. I handled it well, I think. I painted, I learned some new chords on the ukulele and spent some great time with my grands. But I got behind on work, so now my frustration level is greater than it was before. That's just one  of the additional situations I'm dealing with on top of caregiving. Sometimes it feels like I am stretched tight like a rubber band and I'm going to pop with any more pressure. Life can feel really ugly sometimes, and I don...

As a caregiver do you ever feel like you live in a bubble? I sure do. For the most part, if I'm home I don't realize how un-normal my life is. Probably because it's become my new norm. It's a norm filled with lots of visits from case managers, nurses, doctors, and deliveries with a few surprise runs to the ER like yesterday. although each of our stories and days has differences, our norms include changes, dressing an adult, pureeing foods, tube feedings, spoon feedings, transfers, standing frames and range of motion exercises. Most of the time, we probably don't even think about those things - we just do. But when we get outside our comfortable norms, it can seem like we are in a bubble. Many times in public we are ignored. People cut in front of Chris' chair without a second thought. Others let doors go just as I am getting there - which is fine - I CAN do it myself - but it's just rude. Some of it, I'm sure, is my own awkwardness - conversations ar...