Day: May 17, 2024

  • Baby Steps

    It was a much different experience than I expected during my period of “Learning to Live Again” after being a caretaker for so long. I titled this article “baby steps,” because sometimes it feels like that is what we are taking to get ourselves back to normal. There are many small, new adjustments we must make after going through any sort of caretaking journey, because it is almost impossible to approach life the same way as you did before. 

    There are certainly things you may have once enjoyed doing, but in the midst of many life changes, you had to put them aside for a while. In my own experience, I know that many things that were once part of my daily or weekly routine weren’t as easy to jump back into as I had expected them to be.

    Pacing yourself back into life is a good thing to do. You might find that some of those hobbies you used to enjoy don’t seem quite as appealing now. It is kind of like a process of “out with the old and in the new!” Find your joy in something that you want to do, something that you desire to spend your time and energy doing. You may have a newfound perspective on life and how you want to live it.

     Being careful to ease back into things can help you both emotionally and physically. You don’t want to have to work too hard at things right away.If you find you are becoming too exhausted, then pull back and give it a rest. When making a schedule or list of priorities, be sure to put yourself and something you enjoy doing on there. Just focus on making progress to find that new normal, whatever that may look like for you.

    I can remember having that feeling of guilt as I took those baby steps to try and get back into the mainstream of life, but those little steps can turn out to be very big steps towards continuing to heal. Before you know it you will be running!

    (originally published on Shannon Miller

     “No one can go back and make a brand new start. Anyone can start from now and make a brand new ending.” – Unknown

  • Can You Really Be Guilt Free?

    Can You Really Be Guilt Free?

    Out of the articles I have written and continue to write, the biggest request I get is to share about the guilt that is involved in being a caretaker. There isn’t a caretaker I have met who doesn’t tell me how they feel some sort of guilt.

    When thinking back I always considered it a privilege to be able to take care of my husband. I loved every minute that I could share with him. Believe me, I was that person who did it all and still felt like I couldn’t do enough. Sometimes, I wondered if I was just feeling helpless in my caretaking role instead of guilty. What I came to learn is that my sweet husband felt guilty too. He didn’t want to see me exhausted, worried, or anxious. In hindsight I wish we would have talked more about the feeling of guilt that I know we both shared. 

    I bet if you were to talk to your loved one about the guilt you are feeling, they would tell you they want you to be happy and rested. It will probably even bring them joy for you to do something for yourself and be able to find release from some of that guilt you are experiencing. If you feel like you are in a situation that you cannot express how you feel, I encourage you to try and come to terms with knowing that you are doing everything you can for this person that you love and take care of. It is okay to turn guilt into peace and it’s okay to reach out to for help. This is why I do what I do..so other caregivers have someone to turn to when they need help. https://ltlagriefcoaching.com/caregiver-guide-services/

    Caretaking is the hardest, yet most rewarding thing you can do. I know there is guilt that comes with watching someone suffer day in and day out and you have to be able to find that place of peace in knowing that you have comforted and provided for your loved one to the best of your ability. I remember I would have days where I felt relaxed, rested, and so assured of things (yes, those days did exist!). I used to say those were the days I was floating in God’s “peace bubble”. I was safe in there, no one could get to me, and I felt guilt free for a while. Find your “peace bubble.”

    I cannot talk you out of your guilt, and no one could do it for me either. What I can do is offer you hope and encouragement. Chances are, if that person you are taking care of knows you love them and knows the sacrifices you are making for them, they will understand if you cannot be there every minute of every day. I used to say to my husband, “Honey, I do not need a break from you, just the situation.” He completely understood that.

    Find a place of encouragement you can go to when you feel overwhelmed by guilt (church, friends, family, support group, grief coach).  We all need encouragement, especially when we are taking care of someone who is ill. You are doing a great job, you are an amazing caretaker, and you will get through this. You will realize you have become a much stronger, confident person in the process.

    “If you find it in your heart to care for somebody else, you will have succeeded.” – Maya Angelo

    (originally published on Shannon Miller)

     

  • Feeling Scared

    Feeling Scared

    In my last couple of articles, I have tried to touch on some of the emotional effects of caretaking.

    I don’t know what your situation is right now. Maybe you are taking care of an elderly parent, a sick child, or a terminally ill spouse. Plainly and simply, there is usually fear that comes with taking care of another person who is ill, no matter what the circumstances are. You often find yourself asking, “Am I doing this right? Am I doing enough?”

    I would say next to guilt, fear was one of the most frequent emotions I felt during my husband’s illness.  I’m sure you have a list of things that your fear stems from. As a caregiver to a terminally ill patient, I often found that my fear came from the “unknowns” and the “what-ifs” in regards to finances, my husband’s prognosis, the effect of it all on the kids, and the changes in day-to-day life. Fear is natural, but it can be severely limiting.

    I think we can become afraid to the point that we are unable to enjoy the time we have with our loved ones. Looking back, there were moments I would let fear take over. I started to realize the value of dealing with my fear and uncertainties in a healthy way.

    There’s an old saying that “having a good day is sometimes as easy as choosing to have one.” There’s such great truth in that when it comes to fear. Ask yourself the tough questions: Do you want to base your day on a diagnosis, a pain level, or a distant bill? Or do you want to choose to have a good day with your family and friends in spite of the circumstances?

    Attack it from all sides: physically, mentally, and most importantly for me, spiritually. I found great peace in my prayers, and great laughter in some of the more offbeat “adventures” at the hospital or doctor’s office. Fear evaporates in the face of joy. Think about it…when was the last time you laughed and felt entirely afraid at the same time?

    As caregivers, we will almost certainly face scary moments and realizations. If you find that these times truly are paralyzing you, I encourage you to seek out coaching or counseling in person and/or place where you are comfortable.  

    You will become a survivor in this as well!! You will find the confidence to do and ask things that you could not see yourself doing or asking before. You will hopefully start to realize that you are feeling that fear a lot less, and that you are able to take control of what once seemed like the uncontrollable.

    Courage doesn’t always roar.  Sometimes courage is the little voice at the end of the day that says I’ll try again tomorrow.  ~Mary Anne Radmacher

    (originally published on Shannon Miller

     

  • Finding Your Joy

    Finding Your Joy

    Being a caretaker is an emotional roller coaster for sure. Personally, I felt the emotional fatigue was much more draining than the physical.

    At the end of some days I could not even put a thought together. My mind was flooded with the well-being of my loved one, our future, and the kids. While this is normal in the process of everyday caretaking, it can become unhealthy and often times lead to depression and anxiety if you let these thoughts consume you. You will have to find some ways to occasionally release the thoughts and relax your mind.

    What I learned through my own journey is that it was okay and also very therapeutic to cry. I would usually let go of the tears in the evening hours when everyone was already in bed asleep. Sometimes I would cry with my friends, but for some reason I felt like I had to stay stoic and strong in front of my husband and son. I know a lot of caretakers feel that same way. It is important to be able to find your time and place, where you can let go and let the tears flow freely. Many times I would feel a sense of relief after a good cry.

    As with any challenge you face in your life, there are good and bad days. On the bad days, I used to try and find what I would call my “nuggets” of joy. Sometimes they would be as big as receiving unexpected, good news from a doctor’s visit and sometimes they would be as small as five minutes of quietness while the sun was shining down on my face.  It didn’t matter what form they came in; I was on the daily hunt for my nuggets. I became determined to find some joy because I knew this would eventually help me and those around me.

    I encourage you to look for and find your own “nuggets,” particularly on the bad days. Find some good stable, emotional support. Surround yourself with people that want to lift you up and encourage you daily. I easily became very guarded with my time, and I had to be careful not to isolate myself too much. Share your joyful daily finds with your loved ones, and it will bring them some much needed encouragement as well. You never know, they may have a few of their own to share with you too!  The times that my son and I were most joyful and content were the times that my husband’s smile was the biggest.  I hope you will share some of your “nugget” stories with me.

    “Joy is the holy fire that keeps our purpose warm and our intelligence aglow.”- Helen Keller

    Originally published on Shannon Miller.

  • Getting Organized at Home

    Getting Organized at Home

    I will admit I have a little “June Cleaver” in me!  We had lived in our home for close to twelve years, and for most of that time, you would have found my house spotless with everything in its rightful place. It seemed so important to me at the time, but that quickly changed. Don’t get me wrong I like having my house in order, but spotless became a thing of the past, and the best part is that was okay. It didn’t take long for me to find that it was more important to have medications in order than to have a clean kitchen sink. Don’t feel guilty if priorities at home start to change.

    If Nick was in the hospital, home was a place that I would go just for some sleep, a shower, an occasionally mindless TV show, and to spend some sweet time with our son. There was no cleaning or cooking, just a short reprieve in a place that was filled with so many memories and brought me great peace. It was almost like a time for me to try and regroup. My home became the place that I “visited.”

    When Nick was home from the hospital, things ran much differently. I wanted home to be that peaceful environment it had always been before my husband got sick. I loved him being home, but honestly these were the times I was in full-on adrenaline mode. I was a wife, mother, caretaker, and nurse 24/7. There had to be schedules of medicines, home healthcare, showers, and so on. I found it helpful to have a big desk calendar that I could write everything down on and review daily. I felt so responsible for taking care of him, and I always felt the need to get it all right.

    One of the strangest feelings I encountered during this experience was the way in which my feelings about being at home changed. In many ways, home becomes just as much of a workplace as it is a resting place. Your loved one (depending upon the severity and effects of their illness) may be unable to do many of the practical tasks they were once able to, and these responsibilities are suddenly yours, from getting them out of bed to getting them dressed. Tasks will quickly be overshadowed by daily necessities, but setting up an organized system at home is the best way to help you get it all done to the best of your ability.

    You have to find the system that works best for you and your family in your home. For us organization and structure was key to making things work. I would have telephone numbers of doctors, the hospital, and pharmacy out and accessible, with medicines lined up across the counter. I would get familiar with the appointments that we had to be at each week, and often times the hospital would call and add more. If you’re frequently on the go, set up your cell phone to alert you of upcoming appointments. There is no right or wrong way to do this…..find your way!

    As far as food goes, you can have someone set up a meal chain for you. If you are not up for visitors or won’t be home, ask a neighbor or a friend if people can deliver food to their home for you to pick up at your convenience. There is a lot of great information at www.lotsahelpinghands.com that can help you get organized with meals and other practical things.

    I do not know if this will make sense, caregivers, but you will begin to forget about “you” for a while. This is why it is so important to get some rest and have a good laugh or a good cry whenever you can.

    (originally published on Shannon Miller)

     

  • Getting Through

    In several articles of my articles, I’ve talked about many things that can hopefully help you if you are taking care of a terminally ill loved one. As I reached the end of chronicling this part of the journey as a caregiver I thought about many things that I know you are facing daily. For some of you as you reach the end of your caretaking journey it may coincide with grief.

    Grieving can be a different process for everyone. Some may experience delayed grief, while others begin grieving before even losing their loved one who has been sick for so long. It is said that there are five stages of grief:

    • denial
    • anger
    • bargaining
    • depression
    • acceptance

    Many people will go through all of these emotions in order to heal, while others may experience very few.

    During my own personal journey, I have experienced several stages of the grieving process and in no particular order. Depression was a much more prevalent part of my healing process than bargaining or anger. For others, however, such stages are necessary steps to acceptance. There is no handbook to grief, and nobody should ever feel the pressure to grieve in a certain way. The healing process is just as personal as the rest of your journey to that place of acceptance.

    I encourage you to find peace in knowing that when you reach this place of acceptance, it doesn’t mean you forget about or stop grieving for your loved one. It simply means you are getting to a point where you are able to take in and process your grief, and that maybe you are ready to take those first steps to finding the “new normal” in your life.

    It has been seven months since I lost my husband, and of course I still have those somber days. We cannot predict how long we will grieve when we lose someone that we love so much, but the pain and sorrow begins to fade a little each day and that opens up some space in our hearts for all those good memories to start pouring in.

    I can never stress enough to cling to the things that are most important. Faith, family, and friends can pull you from any pit, and before you know it, you are standing on your own again…and maybe even smiling a bit!

    Originally published on Shannon Miller.

  • Giving Encouragement

    Giving Encouragement

    As I’ve journeyed through life, one of the most valuable lessons I’ve learned is that you never truly know what someone else is going through. The world around us is filled with challenges, and it’s easy to see how tough times have become for so many. Yet, in the midst of these struggles, there lies a simple but profound truth: offering encouragement can make a world of difference.

    When you take the time to encourage someone, you give them a priceless gift—hope. You remind them that they are loved, that someone cares, and that they are not alone in their journey. Think back to the moments in your own life when someone extended a kind word or gesture to you. Remember how it lifted your spirits, how it made you feel seen, valued, and understood. I can personally attest to the incredible impact that encouragement has had on my life. It has been a source of strength, helping me to navigate through some of my darkest days, and it continues to be a guiding light even now.

    The power of an encouraging word should never be underestimated. In today’s world, reaching out to someone has never been easier. A simple text message, an email, or even a handwritten note can bring warmth to someone’s heart. One of my personal favorites is offering to pray for or with someone. There’s a unique comfort in knowing that someone is lifting you up in prayer, holding you close in their thoughts and intentions.

    Encouragement is about more than just words; it’s about recognizing someone’s needs and connecting with them on a deeper, personal level. Sometimes, you might wonder, “Is there really anything I can say that will help?” The answer is almost always yes. Rarely does anyone turn away from a kind word, especially when it’s spoken with sincerity and love. Over the years, I’ve had the privilege of forming some incredible relationships that began with nothing more than an encouraging word.

    I recently came across a passage that beautifully encapsulates this idea. In his second volume of the leadership book “Habitudes,” Dr. Tim Elmore compares a person’s spirit to a hot air balloon. He writes, “We fill other people’s balloons by affirming them, meeting their emotional needs, and giving them hope.”

    So, who will you encourage today? Whose balloon will you fill with hope? Remember, as Dr. Tim Elmore wisely said, “Encouragement is the oxygen of the soul.” Your words have the power to uplift, inspire, and breathe life into someone’s weary spirit. Don’t miss the chance to make a difference in someone’s life today.

     

     

  • Caregivers and Palliative Care

    Caregivers and Palliative Care

    Believe it or not, we did run into some unexpected blessings along the way, one of which was “palliative care.” At first, however, we had no idea what palliative care was. We heard about it from our oncologist, and I am so grateful that we did. This care came at a time for us when Nick had emotionally hit rock bottom. He had been through a revolving door of bad news for a while, and his pain was increasing.

    One of the biggest blessings during our journey came when we met Dr. Shannon, a wonderful, caring, and compassionate palliative care doctor. Immediately after we had our first appointment with him, I can remember feeling a little bitter. In my mind I had been thinking that he would be yet another doctor to add to the list. I wondered if he was going to be able to help my husband at all.

    To be honest, a lot of my doubts came from the fact that I had never even heard of “palliative care.” So, what exactly is it?

    The Palliative Care Program at the California Pacific Medical Center (CPMC) describes palliative care like this:

    • Palliation means relief of symptoms, easing pain, and offering support.
    • Palliative care helps patients and families find assistance in their community when they need it.
    • Palliative care strives to relieve suffering.
    • Palliative care provides support for a comfortable and compassionate dying process.

    (Source: CMPC.org)

    It provided all of this for us, and more. We could not believe the amount of support and compassion we received. Dr. Shannon knew how to ask the difficult questions in a way that we could digest and actually answer them. Palliative care really helped us with the quality of life versus the quantity. I will never forget the role that this played in our lives.

    One of the common misconceptions about palliative care is that it is only for cancer patients. As I researched this topic a little more closely, I found that CPMC suggests palliative care for a wide range of terminal illnesses from Alzheimer’s to heart disease, and that palliative care can be sought at any point during a “chronic” or “life-threatening disease,” or even after for the loved ones left behind. (Source: CPMC)

    If you feel like you are in need of this service please don’t hesitate to check with your healthcare provider about finding a physician who specializes in palliative care.

    At the heart of this compassionate approach are the 7 C’s of palliative care. These principles serve as the pillars of palliative care, ensuring that care is holistic, patient-centered, and respectful of the individual’s wishes and needs. https://wcc.ca/blog/what-are-the-7-cs-of-palliative-care/
    • Communication.
    • Coordination.
    • Compassion.
    • Collaboration.
    • Continuity of care.
    • Continued Learning.
    • Care in the Dying Phase.

    Family caregivers are truly the heart and soul of palliative care. They don’t just handle the practical tasks like managing medications or tending to daily needs—they provide something much deeper. They offer emotional support, comfort, and love in ways that only someone truly close can.

    Caregivers, palliative care is there for you, too. It’s not just about supporting the patient—it’s about making sure you have the strength, knowledge, and resources to continue caring for your loved one. I remember so many times walking out of those appointments, hand in hand with my husband, both of us smiling. Palliative care gave us both the comfort of knowing we weren’t alone in this journey. It provided moments of peace, relief, and sometimes even joy, knowing that we were doing everything we could together. So, don’t hesitate to lean on the care team for yourself as well. You deserve support just as much as the person you’re caring for.

     “Three keys to more abundant living: caring about others, daring for others, sharing with others.” – William Arthur Ward

    (originally published on Shannon Miller)

     

  • Prioritizing Your New Life

    Prioritizing Your New Life

    Living life as a widow is more than just carrying an extra set of responsibilities; it is a journey through profound emotional and physical challenges that shape every moment. The absence of a partner to share decisions, provide comfort, and lighten the load magnifies the difficulty of day-to-day tasks. Facing these moments alone can feel overwhelming, but finding practical ways to manage them helps carve a path toward healing and balance.

    Creating a system to prioritize responsibilities is not just helpful—it’s essential. When I found myself navigating these waters, I discovered that breaking tasks into lists brought a sense of order amidst chaos. Initially, I focused on urgent matters, separating those I could handle by myself from those that required the support of friends or family. Completing even the simplest tasks on my own brought a sense of accomplishment, fueling the confidence to face the next step. Each small success was a gentle reminder that I was capable of handling what life had set before me, one day at a time.

    Beyond the immediate to-dos, there were bigger, more daunting tasks that required time, patience, and energy. These were the ones that tested my resilience most. I learned to be gentle with myself, recognizing that tackling these challenges would take more than just time—it required emotional pacing and the courage to ask for help when needed.

    For those also raising children, involving them in the process can turn moments of challenge into valuable life lessons. Teaching kids to write their own lists and celebrate each completed task not only gives them a sense of agency but also builds a shared understanding that working together is key to navigating difficult days.

    In the beginning, the lists may seem endless, but little by little, tackling one thing at a time adds up. The mountain of responsibilities starts to shrink, replaced by milestones that mark both progress and healing. Looking back, I remember how impossible it all seemed at first, but with each task completed, my faith in myself grew stronger. Every step was a testament to resilience, a reminder that while the journey is hard, it is also full of growth, strength, and pride in overcoming the seemingly insurmountable.

    If you are not sure where to start I am here to help you. I may not know the way your particular path will lead, but I know what it takes to survive in this place. That’s where we can begin together. As a certified grief coach, my commitment is to offer you the utmost support and guidance.

    Originally published on Shannon Miller.

  • Quality vs. Quantity

    Take a moment to consider how you would spend your time if you were given just one more year here on this earth.

    I remember before my husband became ill that, as a family, we always seemed to be going and doing while never really slowing down. We had a lot of good times and made some amazing memories. That all quickly changed, however, as Nick’s illness began to get worse. Over the last couple of years, holidays and summers were primarily spent at the hospital.

    That was certainly a difficult adjustment.

    What I began to realize was how important those times around the dinner table, a short walk, or  just sitting on our back porch (my favorite!) having sweet family talks would become. Those are and always will be some very fond memories.

    As a spouse or a parent, you understand and enjoy the value of that quality time with each other. As a caregiver, that special time to you can become your peace and joy throughout the day.  We simply couldn’t plan the types of family “adventures” we were used to. It was more than enough, however, to watch a movie with my husband and son in our home. Those times allowed me to relax both physically and mentally, and I was very grateful for that.

    You do not have to be sick or taking care of someone who is, to enjoy the most life has to offer. What a blessing we found in knowing we did not even have to leave our home to make the best of memories!  Be encouraged by the fact that true quality time provides you with both a sense of joy and greater control over how your time together is spent.

    Let me challenge you with this thought: When we knew our quantity of time was going to be limited together, we found out how important this quality time would need to be. Why does “quality of life” seem to have a new meaning to it when you are ill? It shouldn’t.

    (originally published on Shannon Miller)

    “The more sand that has escaped from the hourglass of our life, the clearer we should see through it.” – Jean-Paul Sartre