A Christmas reset

Check. The last gift is ordered. Check. The uniform is clean for the basketball tournament. Check. The baseball-playing son is registered for camp. Check. The laundry is done, and I am ready to pack for a clinical trial. Check. The Christmas menu is planned. 

Check. Check. Check. I’ve been treating this Christmas season like a checklist. Items that need to be completed are not like the holy season it truly is. 

The first days of Advent flew by. I went to Saturday Mass with some of my family for the first Sunday of Advent. A telling sign is that I don’t remember the homily or even which of my kids were with me. I do remember the bulletin and seeing Mass Times for Immaculate Conception Holy Day Mass. I knew it would be easy to forget as I was going to be traveling out of state with my three sons with Duchenne Muscular Dystrophy (DMD).  

My sons had an opportunity to screen for a new clinical trial for a medicine that has the potential to help them by slowing down the progression of the muscle deterioration caused by their disease.  We would get home the day before the holy day, but I knew that my boys would be exhausted and potentially me. So, I made sure to remember the date and times. 

We traveled the five-hour drive to and from our appointments in Denver.  We stayed for three days, and I was right; we got home exhausted late after a full day of appointments, three cardiac MRIs, three physical therapy appointments, and so much paperwork my head was mush.  In fact, I left our suitcase in the parking lot of the hotel right next to our parking spot and didn’t realize it for hours until one of my sons asked for a water bottle, and I realized the case of water bottles was sitting on top of the said suite case in the parking lot. 

I again attended a Saturday evening mass, and when I was in the church, I realized I had missed the holy day.  I was upset. I felt terrible. And then I realized I forgot my holy hour of perpetual adoration as well.  I was rough on myself for not making Advent the focus of Christmas.  

I knew I would be distracted with the clinical trial (we made it in the trial and will travel back to Denver next week for all three boys to have an infusion). So, I made a list of gifts, menus, dates of travel, etc. And I checked everything off that list and thought I was ready for Christmas.  But my heart was not prepared.  I had not given Jesus any time in my schedule. 

On Monday, I went to confession before my next scheduled hour of adoration. And it was divine. Father told me it was good of me to be in confession during Christmas time, that it would help fill my heart with the right things, and that those things would overflow into my family for the rest of Christmas.  

My eyes filled with tears.  The grace and forgiveness I received in the confessional that day touched my heart.  I had been so harsh on myself for all that I wasn’t doing well. 

 Forgiveness was a reset. I believe in what the priest said, that what is in my heart will flow into my family.  That gives me the courage to keep trying, the motivation to do better, and the peace that I am doing my best. 

When Holidays are Tinted with Grief

It has been a long time since I posted here. I’ve been writing regularly for MuscularDystrophyNews.com and CatholicMom.com. Both are a dream come true. For those that have been here from the beginning know I never believed I could be a writer. But now I am paid to submit columns and can see name in a byline. I will never, not be thankful for that.

This is an article I wrote to submit but holiday articles can’t be submitted after the holidays. However, I think this is something worth getting out there because I don’t think I am the only mother/parent/caregiver that feels this sentiment during and after the holidays. I hope you enjoy, and I hope to write here more often. Thank you for sticking with me.

Small victories are my favorite thing to celebrate. But I also like to celebrate my children, my husband, our home, and our life. The holidays are a wonderful reason to celebrate too.

This time of year, outside our house, is strung with dozens of strands of colored lights. You’ll find a blow mold of Santa and Frosty, too. Once through the front door decorated with a swag of fresh pine, the walls are decorated with natural greenery and twinkly white lights. Several Christmas trees of all shapes and sizes are placed in every room, the biggest and best trimmed in the living room. Collections of old Santas and Mrs. Clauses can be found at every turn.

Food enough to feed ten or more people is almost always in a constant state of preparation. The smells of baked cookies and pumpkin pies linger long enough for another batch to go in the oven. Prime rib and soups are served on Christmas and Christmas Eve and reheated for days as leftovers.

This year gifts were put under the tree Christmas Eve to save them from being unwrapped and tossed around our youngest, an 11-month-old girl named Callie.

We had a wonderful Christmas. All seven of our children, ages 11 months to 21 years old, were home together for an entire week. We had the kids’ boyfriends and girlfriends here, too, and even an extra dog for a couple of days. We had an ugly sweater party with cousins, made gingerbread houses, and celebrated a family friend’s wedding.

I have no reason to feel sad, yet a piece of me is hurting. I think this way every holiday season. I watch my children, taking snapshots of them in my memory, wishing I could freeze the beautiful moments in time so I never forget.

My three sons with Duchenne Muscular Dystrophy (DMD), especially so, because time with them is a thief. Their rare disease doesn’t take a Christmas break. Instead, as they happily eat a cookie or laugh at their baby sister, DMD is at work, progressing through bodies where the disease has already wreaked havoc.

In the last several weeks, many young men and boys with DMD, some of whom I know and others I am familiar with because of social media, have been very sick. Some fought for their lives for weeks and made it back home, while others fought and didn’t make it home. Last Christmas was their last Christmas.

My heart must have holidays confused because that last line haunts me. And although I try very hard not to think about it and focus on the joys of here and now, it never goes away, like a ghost living in the closet of my heart. So I anticipate grief but don’t know how not to either.

I feel it in little waves of anxiety, a stirring in my stomach that sometimes leaves me nauseous. A voice says, “this could be their last Christmas. They could get sick.” My oldest son with Duchenne, 17-year-old Max, is home today with the symptoms of Influenza. We are managing it for now, but what if he gets worse? What if there are complications? It’s hard to so often be in a state of balancing logic, reality, and fear.

And I ignored it and continued with our holiday as planned. But because I can’t tell the voice that it’s not true, because I don’t know that it isn’t, can’t prove it wrong, I can’t forget the voice either.

And so it remains like an uninvited guest. Instead, it becomes part of the celebration, creating a holiday tinted with grief.

Looking Back and Ahead: Reflecting on My Words for 2020 and 2021

Resilience was the word God put on my heart for the year 2020. When I chose the word I thought the year would be about healing some past hurts. It did, but in ways I did not expect, but even more unexpected was the worldwide pandemic that literally changed almost everything. My life, the world, my family…none of them look the same. Resilience was what I experienced, what my kids experienced, what I think the world experienced.

At home learning for the kids. Isolation and social distancing beyond what most of their peers were and are experiencing. My oldest had her freshman year of college and life in the dorms cut short and never experienced an entire freshman season of husker track. She had to move home early. A very sick and hospitalized mom and tayta (grandma). A broken bone for Rowen and our first major set back with any of the boys with DMD.

Periods of pure stir crazy from being shut in and away from everything we knew up until this year. Grief for what we were losing and how the world was changing. Two periods of quarantine, an intensive home remodel that we lived in. My full-time employed husband suddenly acting head coach for a varsity football team he had played for decades before. An election unlike any before. Rioting and tension and unrest.

Before that my husband’s short journey with skin cancer, a season ending injury for Chance and our first hospitalization because of Duchenne for Rowen.

We made it through all of that and regardless if 2021 will resemble that in some way, we were resilient in 2020. I learned so much about my own heart, the broken hidden little areas that needed access to the light. Visiting those areas, acknowledging those areas and finally giving them up was resilience.

I’ve spent several years chronically my joy in this journey of life. In 2019 I fell behind. I was so sad about the changes in Rowen’s disease progression that I forgot to look for the joy. In 2020, in the midst of pandemic, God helped me find my way back. Overall, our year has been joyful. I am counting the joys and blessings again.

Jason is home now; for a long time before the pandemic he was dreaming of a home office and now he has one permanently. He is happier. He is here for everything. When I need extra help with the boys he can come out of his office and help. He knows the kids better and he and I know each other better. I can honestly say we are more in love now that we have ever been. As we prepare to celebrate our 20th year of marriage in 2021, it feels like a pretty good place to be.

When everything else in the world shut down and things stopped my family experienced kindness that did not. In the middle of a pandemic we were given $70,000 to buy an new handicap accessible van that will hold 3 power chairs. Another $10,000 to purchase and install a ceiling lift system. Our boys are so loved. It is a humbling and beautiful and tear-producing and amazing gift to experience a love like that.

Rowen did fall and break his leg and he does walk less; but he does so much more!!!! His quality of life has improved.

I was brave enough to listen to an answer to a prayer I wasn’t sure was right. It was and my son is happier than he has been in years! I also learned that if you are going to ask God to help you where you are, you better be ready to say yes to what he asks! The thing he has planned is so much better than you can imagine will go wrong. Perhaps the best lesson I learned for 2020!

Lexi moved out permanently and I was so sad about that. But, as much as I thought she would not be here enough, she has come for several visits and stays and humbly shares the bunk bed with a 6 year old. Even more though, she has grown into such an adult. She balances school, work, and the demands of being a college athlete and pays her own rent. As parents, we could not ask for more. We are so proud of her and love seeing the woman she is going to be start to take bloom!

The kids have been fighting since Thanksgiving. The colder weather has basically forced them to live on top of each other as we avoid going out and crowds during the pandemic. It’s not been the most joyous part of the year; but they are happy and healthy!

Another positive thing this year brought was a pool! With everything closed last summer we finally did what we’ve dreamed of for years and the kids benefited so much from it! And finally, after years of talking about finding a neuromuscular clinic closer to home, the pandemic forced us to take that step and we could not be happier about the change. We are even going to be able to switch our clinical trial site to Denver so that we don’t have to take separate trips to Kansas City in the future. It could not have worked out better.

That’s 2020 for you. The word God gave me was perfect and so I’m trusting God. My word of the year 2021 is trust.

It’s not the word I wanted. I wanted love. If someone were to ask me what I want people to remember about me once I’m gone I would tell them that I want to leave a legacy of love behind. That is my goal, that is what I want out of this life.

God said the word this year is trust. I knew it was the right word the moment it landed on my heart. I heard someone say recently that if you think you are not loving Jesus enough, it is not a love problem, it is a trust problem. When the word trust fell I knew it was exactly right. I need to learn to trust Jesus more with my life, with my family, with my future. If I want to love better, I need to trust better and so I pray that 2021 is a fruitful year for trust in my life and I pray that sooner than later I can love like he does. I’ll be back to share my journey with this word. I know already that his first challenge to me has been issued and I will work to love me like he loves me and trust myself with what he trusts me with.

Happy New Year friends! I’m sending my love and prayers for all of you.

Distance

My word of the year for 2020 is resilient.  I picked this word long before I was concerned about a worldwide pandemic, before we isolated ourselves for months, before there was a health recommendation to distance yourself.

2020 is proving resilient was a great word.  It keeps popping up, too. In fact, tonight I am a panelist at a virtual conference.  The topic: resiliency. I’ll maybe share more about that later, but today I wanted to talk about distance.

I’m was reading about charisms the other day.  God given gifts or strengths, if you may.  Writing is my gift.  I was reading about using charisms as intended.  Thinking about my strengths got me started thinking about my weaknesses.  I’ve always faulted myself for being distant.  Outside of my immediate family of husband and children, I find closeness is not a natural feeling for me, sometimes it is even uncomfortable.

I’ve always wanted to me more social, more like my husband and my children. I wanted social interactions to be as natural as breathing to me. I wanted conversation to come easy.  I wanted to be able to small talk, that for sure is not my gift.  I’m sure others must feel awkward with my awkwardness, but that is me.

Then I started to think about it differently.  Perhaps my distance is necessary.  If I wasn’t quiet, if I didn’t take that step back and observe, if I didn’t respond to my inner need for quiet I’m not sure I could write.

I do not think distance is my fault, not anymore.  I think distance helps me observe my world and that same distance gives me a space to write and a space to share.

I have started praying that God use my distance, meet me in my distance, and most importantly, fill up the distance.

Running the Race in Front of Me

I went for a run this morning. At one point in my life I was an enthusiastic 1/2 marathon runner. I would run 5-6 miles daily. For various reasons, I haven’t run regularly for 3 years.

Maybe, this will be a positive I chalk up to the Covid-19 pandemic. We are still practicing strict social distancing. The world is starting to open back up again. I see friends on Facebook doing things like fast food drive through. I’m jealous.

We just finished week 11 of strict social distancing, As the US starts to open up again, Jason and I have decided it’s a risk we are not ready to take yet. Max, Rowen, and Charlie take a medicine that suppresses their immune system. We don’t know how their bodies would react to an illness like this. Maybe they would tolerate it well, maybe it would kill them. The last time Rowen had Influenza, he also developed pneumonia and was hospitalized. We are not willing to risk it. I’m hopeful that summer will go well and we can return to normal activities in the fall. Until then, we will play it safe.

This makes me sad. I miss baseball games, pool days, the library, the movie theatre. I miss not being worried about exposure to a disease the boys may not be able to fight.

We spent two weeks in quarantine in April. We had been exposed, even when being very careful. We were tested and had to report our temperatures daily to the health department. We lived in fear that the boys would get sick. It was awful. We did not have Covid-19, but that fear will not leave me.

The days we go to a store or to drop off something at the kids’ school, I find it difficult to sleep, wondering if we did everything right or did we just put ourselves at risk. I constantly think we are not doing enough, but I have a college daughter that reminds me how much we are doing.

It’s hard for her to be here. We are practicing at a level not right for her. She wants to go back to her college town and move into a house with teammates. It’s the right thing for her and for us; but that is excruciating to me. I will miss her and I’m not sure I would ever have been ready to know she was moving out for (most likely) the last time. It also means we may not see her for a couple months while the pandemic settles down, that hurts a mama’s heart.

We’ve been making the most of this. We’ve had more s’mores, more family dinners, movie nights family walks, and game nights. The boys have had more energy, not exerting so much at school. Sleep has improved for a child that struggles with anxiety. Jason and I are as close as ever.

Then two days ago Rowen fell and broke his leg. His bones are weak because of daily steroids (the same reason his immune system is suppressed). We have lived in fear of a moment like that since diagnosis. We know it could mean he may never walk again. He was slowly losing the ability anyway, but to lose it because of a break doesn’t seem fair.

Moments after the break, I was holding him. Tears were falling down his face, he started to shake out of fear and shock, and he cried a question, “will this make me stop waking?” I didn’t cry, but I didn’t answer either. I just told him I was going to be there no matter what.

He hasn’t been able to bare weight since it happened. I’m thanking God it happened while Jason is working from home. We are lifting him in and out of his chair, bed, the toilet. We are using a urinal because our bathroom is not accessible.

I was able to do all of that before the break, but he was helping during transitions. Now, I’ve done it 3 times and I know I can’t do it much more. He is heavy for me. Jason has had to do almost all of it. We whispered to each other that we need to find out about a hospital bed and hoyer lift. We will call the contractor for the bathroom Monday and figure out how to protect the boys’ immune system while also having a bathroom they have to have, built.

We are very hopeful that he will walk again. This however, has been an eye opener. As much as we thought we knew, you simply don’t know until you do.

Sleep has been restless. The first night after his break, I laid awake with my hands on him, praying that God would protect him from FES, a terrible, fatal reaction to bone breaks known to happen in DMD. Each time he moved, I would startle awake and start to pray again.

That same night, I told myself, “you need to run; wake up tomorrow and you go run that mile loop you take the dogs on.” I woke up that morning exhausted and stressed and that run never happened.

This morning I was more rested, but I wasn’t in a great mood, I snapped at the same child two times. I just looked at Jason and said, “I’m going for a run.”

It felt great. I smiled most of the rest of the day. A lot was going on inside my head. There was fear and stress and sadness. It was bubbling and the only way I knew how to relieve all that was running. It’s why I started running after the boys’ diagnosis.

It gives me a bit of control in a time when I have so little, in a time when there is so much uncertainty. I choose how fast to run, how far to run, where to run, when to stop, what to listen to during the run. The pounding of my heart, the heavy breathing, the sweat dripping…all of it was stress and fear leaving. It isn’t magic, it doesn’t last forever, but if I can string together 4-5 a week, it will sure make me feel better.

My One Thing

This lent I have been using an idea I learned from my favorite podcast, Abiding Together. At the end of every episode the three women will all give their one thing, sometimes something spiritual and sometimes not. The one thing is something that has helped them grow in faith or in some other way.

Last year was one of the hard ones for me and I needed to focus on all the positives in my life and find my joy in the journey again. Basically, I am using my one things as a gratitude journal. I’m using this lenten season to grow in my ability to live out 1 Thessalonians 5:18, “In Everything Give Thanks.” I want this. I want this heart. I want, even in times of sorrow and suffering to say, “thank you Lord, for allowing this so that I may grow closer to you.” blog 1 (2)

I have been using social media each day to post my one thing, on instagram and facebook, both accounts are under my name if you are interested in following the rest of my days this Lent. Today, my one thing is being mom to my three sons with Duchenne Muscular Dystrophy. I’ve been writing this one in my head for the last several days. It is long and deserving of a blog.

We were on a family walk. We’ve been going two miles everyday of quarantine to get out of the house and for change of scenery. My two children that were walking turned to take a different route home. My three children on wheels were ahead of us, driving too fast for my husband and I to keep up. I watched them for awhile. They were driving side by side by side. They were laughing and joking and being brothers. The beauty of it struck me. I tried to verbalize it to my husband, but I failed to use the right words to truly get across the inflated feeling I had in my heart. It was so full I thought it might burst. I felt special, blessed, in on a secret.blog

I’ve thought about the moment over and over the past few days. How do I express what it means to me to be their mother?

I love all of my children with every fiber of my being. I remember the first moment of motherhood. Extremely young and honestly, unprepared for the amount of love that would rush my body when I felt the weight of her little body in my arms.

Those that know me well have heard me say and many of you may have read me write that I was scared to be a mother. I really didn’t even know what the word meant. I was convinced all the months of my pregnancy that I wouldn’t know what to do. Having been removed from my own mother several times, it was a real fear for me that I might also have my child removed from me.

Was I experiencing extreme anxiety? Yes. I didn’t know it then. I didn’t know how unrealistic it was that I was assuming that was part of motherhood I would inherit.

The moment I held her, everything in my world felt right. It felt as though I had found the thing I was meant to be. The fears left me as fast as my love for her rushed through my body.

I was very fortunate that my first job after college and as a young, inexperienced mother was as director of an Early Head Start program. A program designed for mothers, many of them just like me, young and inexperienced. A program that included parenting classes, home visits, vast amounts of information on how to help your child learn, lessons on how to become your child’s first teacher. I guarantee I learned as much from that program as director as any mother enrolled in the program. I worked with mothers from all over the world, Mexico, the United States, Sudan, Guatemala, Cuba, etc. I was teaching a class about child care in Grand Island to a group of Sudanese refugees when I learned the art of the bounce-and-rock-and-pat-the-baby-to-sleep secret, watching a woman from Sudan magically put her very screaming baby down for a nap in record time. I used that method on my next five children; dare I say, conquered it.

I was also very fortunate to marry a man that brought me into the Catholic church. A church that believes motherhood is a vocation. A faith that sees Mary, Jesus’ mother, as our mother. A mother Jesus shared with all of us to help us grow closer to her son.

It was as a young Catholic mom that I first learned about the sorrows that pierced Mary’s heart. It was from Mary I learned that you can know a sorrow before you experience it. Mary knew sorrow before she ever watched her son crucify. It never stopped her from being the mother that her son needed, or the mother that the whole world needed. Little did I know then, that I would someday share with her the feeling of sorrow before it was experienced.

I watched other moms, gleaning from their already established abilities. I read every parenting book and listened intently to my daughter’s childcare providers that would give me suggestions. I would, like everything else in my life up to that point, study how to do it. I would study how to be a mom.

I learned how to be a mom. When we were blessed with each of our other five children, I felt as ready as you can ever feel about adding children to your family. Then, our second child was diagnosed with Duchenne Muscular Dystrophy. A disease I learned in just a matter of minutes would take my son from me, would kill him. As the first two years of diagnosis passed, another two sons were diagnosed.

There was not a book to study to tell me how I was supposed to be the mom they needed me to be, there is still no book with all of that information in it. Instead, I had to rely on the things I had already learned and I had to learn to trust my instinct. I found an amazing group of mothers that were already rocking motherhood in this world of motherhood that didn’t have a book. I watched them and I learned from them.

I leaned heavier on my faith and started to learn the stories of the saints, so many of whom owned stories that seemed impossible but who left lessons and directions on how to do it. Lessons as important as how to die.

An example. I saw this just yesterday on twitter. Someone retweeted a tweet. I can’t take credit for it, but apologize for not being able to give it to the right person either. It was a lesson from one of the newest saints, Pope Saint John Paul II.

At the end of his life, suffering greatly from the affects of Parkinson’s disease, he still addressed massive audiences. He didn’t want people to look away, he wanted them to see him. He wanted the world that he taught how to live, to also know how to die. He wanted us to know that the saints were there for us and brought us hope, not because they conquered the world, but because they allowed Christ to conquer them. There is no one like a saint, that will teach you how to live with joy, how to suffer with thanksgiving, or how to die with hope. These are the lessons I need to study and learn to be the mother my sons will need me to be.blog3

It’s been 10 years since diagnosis. I cared for each of my sons as newborns and infants and toddlers. I changed them and cleaned them. I took care of them just as all the mothers reading this cared for their newborns and babies. They learned to become independent as we celebrated those milestones. Then, almost as quickly, they started to lose their independence. As the years led up to this, I dreaded it. I was again very afraid I would fail at being the mom my children needed me to be. It is here now, but it is not a feeling of dread that consumes me.

I have been so blessed. Blessed by the experiences at Early Head Start, blessed with a God fearing man that brought me into the church so full of goodness and teaching that it fuels my heart, and blessed with these beautiful boys.

I worry about the boy’s dignity. As they grow older and disease progresses, we will continue to face experiences and circumstances that could threaten that, but I know it will also be respected. I feel privileged that they have a trust in me to both care for them and protect their dignity. We have conversations I never thought I would have to be had. They may be uncomfortable at times, but we grow so much closer because of them.

I share my boys pretty openly with the world. They are contagious. Their smiles, laughs, fearlessness, perseverance, and joy even in the face of obstacles and suffering attracts people with a magnetism I find rare in this world. It’s a pull to be part of something very special; so very special, that it is rare for a parent to experience this kind of love. It’s not just for the three with Duchenne either. My other children have been privy to these same experiences and as parents we are privy to share a special love with them also.

It doesn’t escape me that these words have been put on my heart during the Covid-19 isolation, when the ones sacrificing the greatest are caregivers, the nurses and doctors and other healthcare professionals. Caregiving is a gift. I hear so often, that so and so is so lucky to have a mother, father, daughter, spouse like that to take care of them. The truth is that it is us mothers, fathers, daughters, and spouses that are most blessed.

It is heartbreaking at times to watch the ones I love suffer? YES. Is it exhausting at times? YES. Do I have bad days? YES. Do I love my job? Yes. Would I do it again to get to be their mom again? YES. Do I celebrate the successes? Yes. Do I count being their mom amongst my greatest blessings? Yes!

These boys have changed my life.  Knowing the little details of their life, walking next to them on their journey, and being their caregiver hold more beauty than even the grandest of sunsets, the biggest of cathedrals, or the fullest of moons. It will never set, it will never fade. It is everlasting.

Today, my one thing is getting to be their mom. 

 

Word of the Year Update: Resilient

It’s really only two months into the new year and it has become obvious why God put the word resilient on my heart. Like so many other areas of my life, he is asking me to live it out.

I definitely started the new year in a place of woundedness. Wounds that had been lying dormant for most of my adult life were reopened. My two worlds crashed into each other like waves from a massive storm at sea. My lack of control over my children’s health made me feel useless and like I was failing. The harder I tried to be more perfect, the harder I tried to be more in control, the more broken I felt. It opened old wounds. There were several situation in my young life that I had no control of and that often left me feeling like I had done something wrong or I wasn’t good enough.

It became glaringly apparent that my pain although completely warranted at watching my children suffer, was connected to old pain that resurfaced. I’m in the process of healing from all of those wounds. I’m learning to be gentle with myself. Those of you that know me best know that I am not kind to myself. I hold myself to unrealistic expectations, and when I fail at those unrealistic expectations I am cruel to myself with my words and beliefs in myself. There have been tearful days as I wrestle with old habits and beliefs and the truth. The truth that I am loved and I am good. It seems like it shouldn’t be so hard to know that, but it has been difficult for me.

As I started this healing process several other things in our family just kind of went haywire. My husband has long had an area on his face that would get irritated when he shaved. Sometimes it would bleed and scab over. In the last year it became enough of a nuisance that I asked him to go to the dermatologist when our son had an appointment and ask about it. I’m so glad he did. The area was skin cancer. It is the only area and it has been completely removed. It happened quickly and other than 12 stitches, pretty painless. The stitches are out and the doctor did a very good job placing them just along the smile lines and as it heals I think the scar will be hidden when he smiles. He smiles a lot! We are feeling blessed that it was only that. But, wow, it really shocked us and you better believe when I’m putting sunscreen on all the kids at baseball games, I will totally be the wife to walk out the the field where he is coaching and put more on him too!

As he was getting his stitches, an appointment I had hoped to attend with him, I was actually home with a sick boy. Our son Rowen got Influenza B twice this year. The second time he also had pneumonia. It did require him to stay a night in the hospital for extra fluids and meds and then several days at home as he regained strength and we waited out a bout of Influenza going around his school. It was the first time one of our boys needed hospitalized and we realized how underprepared we were. It worked out because Jason’s mom and several other people showed up big time when we needed them. But we now know we need to have a plan and need to have another person or two that can give the boys medicine if we are both at the hospital or an out of town hospital is required.

Towards the end of January our son Chance sprained his MCL at basketball practice. At first we thought it might even need surgery, but thankfully a couple weeks of crutches, a knee brace, and physical therapy was all that was required. It was tough on him, he loves playing sports and this ended his basketball season and delayed the start of his baseball season. He handled it as well as could be expected and has been rather mature about the process. Let me tell you though, that he has been jubilant the past week because he was cleared to practice.

I know how much Chance helps with his brothers and around the house, but his injury really showed us what a helpful and giving young man he is. It was also good for the entire family to come together to help him when he was not allowed to put weight on his knee. Maybe I’m just wishfully thinking, but I think his brothers even realized how much he helps them and seem to be more thoughtful about asking him for help, instead of demanding it.

Resilient seems to be a good word for me and my family this year and in this season of healing. I always think the next thing is the one that will do us in. But that next thing never stops us. Sometimes it slows us down and we have to find new footing, but we keep going. In this, all of what I just shared, we have done a lot of giving it up. We alone cannot do this, any of this, but when we let God do the heavy lifting, it’s possible. I think that it’s not been realization, because I knew this is how it is supposed to work, but I’ve come to a place where I figured out how to actually do it. I’m not perfect at it by any means, I stumble nearly every step and there are going to me places I fall. I’m sure I will spend the rest of my earthy life working at it. I’m learning how to give up control; learning to wait on his timing, not mine; and I’m learning how to ask him to meet me where I am, especially in the hard places.

Thursday Morning Thoughts

Thursday morning thoughts…

I am working through a really thought provoking bible study right now with a mother’s prayer group. We met as a group this morning and had great, thought provoking discussion and now I’m sitting here, chewing on all those thoughts.

We are studying women of the Bible. This week we focused on Sarah and we discussed waiting, as Sarah waited a long time for motherhood. We discussed her handmaid Hagar, how she got mixed up in Sarah trying to do things on her own; and how God saw Hagar, even as she felt insignificant. He saw her and he saved her.

Yesterday, I listened to a podcast that talked about letting your light shine. It’s a podcast by Danielle Bean, the girlfriends podcast, it’s worth a listen! Anyways, she talked about figuring out the things that you are good at, your gifts, and using them for good. She discussed how you find what those things are and let them shine.

As I was walking the dogs and listening to the podcast, I named two gifts out loud that God gave me, writing and public speaking. I thought, I can use these gifts; I need to quit hiding them.

Hours later I got an email, asking that I speak. It’s for a conference at Georgetown University in Washington, DC. It will be one of biggest engagements where I have been asked to speak.

I felt a little like God had been waiting for my yes. As soon as I even thought it, he was like, “finally, I’ve been waiting; I have places where I need your voice!”

I felt like Hagar. Like in all my insignificance, he saw me.

It never ceases to amaze me how at work
He is in my life and how he even uses the very books I read and podcasts I listen to to guide me.

Turning 40

Before the weekend begins I will have turned 40. In the past few weeks I’ve thought about this new age, this new decade, this new beginning.

I thought back to my 30th birthday. I had 4 kids when I turned 30, the youngest had just celebrated his 1st birthday. My goal, the entire year leading up to my 30th birthday was to wear a bikini. I reached my goal and we celebrated at hotel with a waterpark attached. The kids had fun and I have fond memories of them going down the waterslides together and their soaking smiles!

Ten years later I can’t believe there was a time and yearn again for a time when the hardest thing was fitting into a bikini. Ten years is the amount of time it took our family to grow from six to eight; for 3 of our children to be diagnosed with a fatal and progressive disorder; for us to experience a miscarriage; for my husband and I to each lose a parent; and to experience the loss of a sibling. Ten years seems like a blink of the eye and it seems like an eternity.

I’ve grown and changed in 10 years. In some ways, I am the same and in others it is like that younger version of me never existed. I’m thankful for every experience because each one of them has shaped me into a person I am learning to accept, love, and be proud of. It took each of those experiences and many many others to get me closer to the person God is calling me to be. It reminds me of the quote by Saint Catherine of Siena, “Be who God meant you to be and you will set the world on fire.”

I have struggled always with accepting who God is calling me to be; to see my value. I swallowed lies and I made them my truths. I grew up around church and with faith my entire life, but somehow along the way, I either never learned or swallowed another lie. I never believed that there was nothing I could do to earn more favor with God and that there was nothing I could do to fall out of favor with God. I am just now internalizing the love of our Father. It had always been there, but because I thought I was unworthy I wouldn’t accept it. Many experiences in my life were so lonely for me because I could not believe I was worthy of love.

Discovering the truth is changing me. I feel it kindling in my heart. I feel the chains of fear and self-loathing breaking and beginning to fall. I feel myself in the beginning of a warm embrace with my true and authentic self. I am going to let God put all my broken pieces back together and make something beautiful them with them. I am going to let the light shine through my cracks.

I am learning to accept who God is calling me to be. I accept that I will not be perfect and that God already knows when I’m going to mess up. I accept that he will love me still. I am learning to love God’s daughter, just as he always has. That kindle is going to spark as I answer God’s call and I will soon be warmed by the fire Saint Catherine of Siena talks about.

I am excited to turn 40! I am doing something I’ve never done before. I’m going to let people celebrate me. I am going to accept it and soak it all in. For the first time in 40 years I’m going to smile (hopefully without too many tears of gratitude leaking from my eyes), I’m going to hug my family and friends, and I am going to embrace the strong and gentle, open and sensitive loving person that I am not afraid to be.

Resilient

Recently, someone told me I was resilient.

For days before that, I was praying for God to put a word on my heart. I wanted to practice a word for the year.

I was thinking of words and considering many that I thought would be good, that could help me grow spiritually. But, once I heard the word resilient, it settled deep into my heart and I knew it was my word for 2020.

Recently someone told me I was resilient. I shook my head in disagreement.

I struggle to accept a compliment. I struggle to believe the good others see in me. Long ago, years before I was an adult, I adopted this coping mechanism. If I could tell myself and believe all the worst things, then it wouldn’t hurt as much when someone would say them to me.

I think focusing on resiliency this year is going to do a lot in my life.

I have been resilient.

I’ve been able to get through some difficult situations. This year, I think God is challenging me to think of resiliency in a different light. God is calling me to be more gentle with myself. I think God is calling me to be a person that loves herself and sees herself for what she is, His beloved daughter.

If I can be resilient to the one who attacks my heart and doesn’t want me to believe I’m God’s beloved daughter…

If my heart can be softer and more malleable…

If I give it all to God….

Then the crosses I will bear today, tomorrow, and later in my life will be as God’s Beloved daughter and through Him I will be able to pick up those crosses and follow Him.

I think focusing on resiliency is going to do a lot in the life of my family. Things I can’t even imagine.

My children, overhearing me talk to my husband about the word of the year idea asked me about resilient. After an explanation, one of my boys, my 10 year old who is currently transitioning to a power chair because disease progression is taking from him his ability to walk; Rowen said he wanted to be resilient, too.

He is already one of the most resilient people I know, this year going through more change and loss that anyone his age should have to and is making it out stronger and more independent. But to see Him and all of my children and my husband grow in this area will truly be the work of God in our lives.

I’m excited to see where this year leads us. I will continue to use this blog for many topic areas, but promise to update you here about the things we learn and experience on this journey with this word God has put on my heart.