Speaking in Cursive

Walking through this extraordinary life.



A Mother’s Hands

Lately, I have been fixated on my Mother’s hands.

Hands that held countless children, grandchildren and great grandchildren, neighbors and friends. Gently rocking them to sleep. Comforting them in sickness. Guiding them in their lives. Wiping tears away in sadness.

Hands that cared for my father through decades of illness. Preparing special foods for him. Cleaning and wrapping his wounds. Organizing his medicine and appointments.

Hands that took care of a home for over 66 years. Cleaning after 6 children, then their children, and their children. Cooking 3 square meals a day 7 days a week. Washing ,ironing and folding clothes for her family. Baking cookies and cakes.

Hands that sewed, and mended and darned. Making garters for homecoming, and costumes for plays, and flower girl dresses. Creating curtains and bedspreads and baby blankets for her family.

Hands that combed and brushed her 5 daughters hair. Learned how to give perms to them and their friends. Kept them from looking like “ragamuffins”.

Hands that cheered for her children in their activities. That rooted for her teams, The Packers, The Brewers, The Bucks and The Badgers.

Hands that disciplined. That grabbed our hands from crossing the road into traffic. Protected us from danger.

Hands that prayed. That took communion. Called others on her prayer chain from church to tell them who to pray for, or to ask for prayer for those she loved.

My mother doesn’t remember any of these things anymore. My last visit with her, she didn’t recognize me or my husband. I showed her a picture of myself with her and my dad, sitting next to her,she couldn’t recognize me in the picture either. But I am convinced while her head doesn’t remember, her hands do. Now, as she holds her beloved “Romeo” and rocks him like one of her babies, she takes her hands and pats him gently, speaking to him lovingly, and somehow I know he understands. He too feels all the love in my mother’s hands.

Bone for bone we are the same.

Bones get tired and can’t carry their own weight.

Mom don’t you worry, I will do the remembering.

Mom and Romeo.

I Miss You As Long As You Are.

It happened today. I know it won’t be the last time,and eventually there will be no going back from it. My mom didn’t recognize me on our weekly video call. She stared blankly at me when I said “Hi Mom.” I waited for the awareness to come to her eyes. It didn’t. The activity director, Jen, lovingly told her “It’s Mary.” Slowly I could see her coming back to me. But those few moments were and are heartbreaking.

Mom has been in a memory care facility for dementia for 2 years. With 1 year being during this pandemic. So the majority of my time with her is via video phone calls. While her recognition and memory of other relatives has faded, for the most part she has been able to remember her children. Until recently, I have noticed her mixing us up or thinking my brother is my father. So today was hard. But I knew it was coming eventually. When we talk, mom will fixate on one thing or time frame. With me it is 3 different events in my life between 25 and 35 years ago. When I was Jr Miss in 1987, when I took state boards to become a hairdresser, and when I had my twins. These 3 themes are on replay and repeat. But I do not care. I am happy to go back there with her. I sent her a photo of me with my Jr Miss sash on from 1987, and she has misplaced it( because I moved it from where she had it and now she can’t find it.) so every phone call, she asks about it. “Weren’t you “….. and her voice trails off, as I fill in the blanks, “Jr Miss” I say. And she is transported back there. The light comes back in her eyes. Or when she asks “didn’t you cut my hair?” I know she is referring to being my model for State boards. When we are chatting and one of her friends enters the area she will say “this is my daughter, she had twins.” These must be moments, memories embedded in her brain about me. I know she has these moments with my siblings too. We will meet her wherever she is. For as long as we can. But it doesn’t make it any easier.

There is this horrible meme that floats around Facebook, that people share thinking it is funny. You know the one…” Keep it up mom or I will put in Shady Pines Nursing home”…. or something along those lines. Listen, I am Not easily offended. I have all sons. But, when I see people so carelessly throwing that around it feels like a knife in the heart. Because when you are actually faced with that decision, there is absolutely Nothing funny about it. It tears you and your siblings apart. When the Dr. says ” Your mom can not come home anymore.” trust me, no one is laughing. I have already had this talk with my sons. That when that time comes, if it does, that I understand. That the mom I am now is telling them, it is ok, that I know how hard that decision is, but that I know it is made in love. The mom I will be then may yell at them, and cry and not understand, but the mom I am now does. And people will make comments not meaning to hurt, like, “I won’t ever do that,” or ” My mom will just stay with me.” Trust me, easier said than done. My siblings and I tried for years to keep my parents in their home. We did everything we could. And it killed us to have to sell their home, and place them in a facility. You don’t ever get over it or forgive yourself. I want my sons to know they have no reason to ever feel it. Furthermore, we have been absolutely Blessed with mom’s memory facility and team of caregivers. They have had to be her family this past year. They have stepped up gone above and beyond what their job description is. We are forever grateful to each one of them.

When we were about to hang up I said to mom ” I miss you mom.” She turned her head and looked off into the distance and quietly said, ” I think I miss you as long as you are.” I know it is a jumbled up sentence, that may not make sense, but to me, it has two meanings. I knew she was trying to tell me that she misses me a lot. That it has been a long time since we have all been together. I knew what she meant. But for me, that one sentence, “I miss you as long as you are.” summed up all I have felt since she has been living with dementia. I miss my mom, who she was, what she was, what we did together. I miss my daily phone calls to her, my visits with her at home. I remember after having my oldest son, I would walk over to her house, with him in a stroller. My mom and I would walk 3 miles everyday, and talk and solve all the worlds problems.I miss that. I miss going to lunch with her and my sisters, or going to plays, or baking cookies. You see, I have been slowly, grieving my mom for 2 years. It is a long goodbye. One day, maybe soon, she won’t remember me at all, or what I meant to her. But I will remember her. I will miss you as long as you are, Mom, and even after that.

Heaven sends Blue Jays too.

In Mourning For My Father.

It has been one year since you died. Yet, it seems as though time has stopped. The sun sets and it rises each day. The moon glows at night. For me, I seem to be stuck somewhere, a year ago, that weekend, that morning. Life goes on about and around me. You are missing. The gigantic presence you had ( for such a small German man) is no more. At least not earthly. I search for you, still. I am sure I always will. I am in mourning. This is what it feels like.

I had made you a Christmas shirt and filled a stocking with your favorite German candy. I had planned to come visit you and mom in the nursing home for Christmas. Instead, I saw you for the last time, in a hospital bed fighting off the infection that finally claimed your life. You were hooked up to tubes and wires, and you couldn’t speak. I whispered in your ear how much I loved you. I know you heard me. The family made the difficult decision to switch you to hospice care. A little over 24 hrs later you were gone. Freed from your earthly chains.While I am grateful for the first time in over 40 yrs you were pain free, I am forever hurting. An ever present aching in my heart and bones. I have hours and days of pure joy and happiness, but you are always there. This is constant mourning.

In some ways, a lot of ways, I lost mom that day too. The pandemic came right after your passing, (seems fitting) and changed Everything. Especially how and when I can see mom. I only can “see” her now via video chat with the help of her memory care activity director. I can’t just go visit her, I can’t make Christmas cookies with her this year, like I have for decades. Leaving slightly burned, unfrosted ones for you dad. I can’t bring her Christmas gifts or go to plays or dinner with her. So yes, in many ways I lost her too. However, I know she is safe and well cared for, and I know that makes you happy. She mentions you dad, when we do speak. She cries, gently. Her memory may be fading, requiring full time care, but she Knows she is missing you, and that she loved you. She may not understand, but she is mourning too dad. Last week when I spoke with her, she said ” I know your dad isn’t here anymore, but he came and told me his soul is.” And that was probably the most beautiful thing I have heard this year.

You have missed so much this year, dad. Most of it, I thank God everyday that you have. Still there have been things I so wish you could’ve been here for. Engagements, graduations, new jobs etc., but I believe somehow you do see it. The holidays were your favorite time of year. Last year, I was numb at your passing right at Christmas time, most of it is a blur. This year we are restricted to what we can and can’t do. I know you wouldn’t have liked it. You used to love people coming over for Christmas, or going by your kids. You loved surprising mom with gifts she didn’t know you bought her. Like the jacket you brought over to my house many years ago to wrap for her, to open Christmas morning. You loved decorating the outside of the house with lights and a cute penguin statue donning a hat and scarf. You loved watching gospel singers sing their Christmas songs. You dressed up as Santa for local parties. I am struggling this year, dad, trying to feel Christmas. Because of everything. Yet, Christmas always finds me, as I am sure it will this year, with help from you.

For a while now, I have been seeking out cardinals. Everyone says it means a visitor from heaven. Barb is getting cardinals , a couple even, by her. I put out the seed to attract them, and nothing. Nothing except for this blue jay, who makes a ruckus with his loud call. Like a horn. I can spot it a mile away it seems. Last week at work I could hear his unique call. I went outside to look and saw high in a tree, a hawk, perched on a branch, and a blue jay giving him a piece of his mind. Then more came to join in. I could see they must’ve been protecting a nest. I stood in awe and watched this blue jay make the hawk leave. It brought me back to the feeling I always had of protection from you. I felt safe when you were in the room.This morning at work, I could hear the blue jay, loudly speaking across the street. And then I remembered, Billy Blue Jay. How you always called for him, and left food out for him. I stood at the salon door, looking out the window, as Billy just sat there, on a wire. I whispered “I see you dad.” and he flew away. Maybe, for me, I won’t see Cardinals, maybe you will visit me in different less obvious ways. I have some of yours and moms things here, in storage for safe keeping. And I remembered, you had a stuffed blue jay. I searched through a few boxes, and I found him. I found your Billy the Blue Jay. Just like I know if I keep searching, I will “see” you in places or things I wouldn’t expect to. And maybe, that is what constant mourning is. Seeing or hearing or feeling you, when I least expect it. Where the grief swells up like a tidal wave, and eventually bursts, into a sea of tears. Only to repeat. Forever. If so, that is ok. Because you will still be here. In Trauer Um, Meinen Vater. Until we meet again.

Carried by Love


I have been spending a lot of quarantine time organizing old family photo’s. One thing seems to stand out to me. I was either in my mother’s arms, or in her hands. Never far from her touch or her sight. What comfort these pictures bring me now, of my dear sweet mother, and the love she showered upon me and my siblings. How BLESSED I am to have had that in my life. The gentle guidance and reassurance of a mother’s touch.

IMG_20200504_142642 (1)

As a small child, I was painfully shy. I remember needing to be near both my parents, but especially my mom. I recall hiding behind her, grabbing on to her leg, hoping no one would speak to me. And then she would say, “This is my baby.”  She never forced me to talk to them, or come out from hiding. Her gentle nudging helped me to outgrow my shyness, and become comfortable meeting and talking with people.


I can still hear my moms heartbeat, as I sat upon her lap with my head pressed into her chest. She would be on the phone, or watching her shows, but I was happy to hear her heart and breath. I was safe. I was calm. How grateful I am to have a mom who knew the importance of stillness, of quietness. I would listen to her voice echoing through her body as I drifted off to sleep. I still can hear it, and it beckons me home like a lighthouse on the shore.


I know how very fortunate I was to have a mom who was home with us. Who read to us, and played with us. She let  me put make up on her, and do her hair. She would spend hours cooking and cleaning, and like any child would, I took it all for granted. But as a mother myself, I so appreciate everything she sacrificed for us. She wanted to be a dancer, or a nurse. In a lot of ways, she still was. We would dance around the house for hours, she had her certain moves, she still does to this day. And she spent many a sleepless night up with a sick child. When I was very young, I would get a little too excited about Christmas. So excited I would break out in hives from head to toe and be sick to my stomach. For several years, my mother sat up with me on Christmas Eve, and then on Christmas morning, would help me open my presents. Never making me feel bad for being nervous or worried. Rather, comforting and caring for me, until it no longer happened.



Mother’s Day is so odd this year, for everyone. Most of us will not be with our Mother’s or our children. My mother now is in a nursing home memory care unit for dementia. I haven’t seen her in person in month’s. It breaks my heart, and I would give anything to snuggle up next to her, listening to her unmistakable laugh, hearing her heartbeat. To just share more of my life with her. But I can honestly say, I am who I am because of her. Because of the sacrifices she made to raise her children. To carry them with love.


“Bursting with empathy, I’m feeling everything
The weight of the world on my shoulders
Hope my tears don’t freak you out
They’re just kinda coming out
It’s the music in me and all of the colors
Wish we didn’t live, wish we didn’t live so far from each other
I’m just sitting here thinking ’bout the time that’s slipping
And missing my mother, mother”.
Happy Mother’s Day.

Grieving alone, with the world

IMG_20200415_093905This is how I picture you, in heaven. Standing high on a mountain, looking around and taking pictures, or shooting a video to show us.

I found this photo, shortly after you died. I keep in my bible, as a bookmark. I see it everyday. And everyday I imagine you this way. I miss you so much. I surround myself with things that are yours or remind me of you. Yet some days, no matter how hard I search for you, I can’t find you.

You left us right before the world went mad. Perfect timing on your part. I think of that daily, that I am so grateful you aren’t here right now. That this would be so hard and traumatic for you. With all the Dr. appointments you had, and lab tests, and being in the nursing home. Alone. And then I get mad at myself for being grateful you are gone. How can you being gone, bring me comfort? I can’t even grieve properly (is there such a thing?) because the earth is sick, and things are at a standstill. Life has literally turned upside down since you have been gone. I wonder, would it feel like that anyway, losing you, without a global pandemic? You have been gone 4 months, it feels like years. Maybe partly, because I, like everybody else, have no clue as to what day or month it is anymore. It doesn’t matter. I have been off work for a month now, so there is nothing to distract me like work did. In some  way, it makes sense the world is hurting too, because the world always revolved around you, to me.

I find myself searching for you everywhere. Trying to pick up signs from you.  When I see my dachshund, I see you with your doxie Fritz. When I make meatballs and gravy, or chicken and spaetzle soup I can see your face light up. But especially when I hear birds sing. I can clearly hear you imitating  every bird that flew into your yard. You could mimic them. And you named them. Billy Blue Jay for one. I was getting sad because everyone I knew was seeing cardinals, visiting them from heaven, they say. Not me. And cardinals used to fly into my yard all the time. I hadn’t seen any. Until this morning. I have a bird feeder right in front of my dining room window. Every day I check, multiple times for one to appear. I listen for their distinct call. I will run to the window, but nothing. Then this morning, in the quiet, sat a pretty little cardinal. And I just stared. And he stared back. I mean it. I didn’t have my phone to take a picture, and honestly, I didn’t want to. I wanted it to just be. To be etched into my memory.


Your 88th birthday would’ve been April 19th. I am anxious over it. And sad. Sad that, like in past years, I would take a picture of you and your twin grandsons who have a birthday a few days after you. It was our tradition. For years. I am mad that  it is over.  One of the many stages of grief I suppose. Anger. I just wish we could’ve had more. More birthdays with you, more Christmases and pool parties and weddings. It breaks my heart knowing you won’t see my sons get married or become dad’s themselves. I have to believe you Will see it though.


Mom misses you. Most days she remembers you aren’t here. “Your dad is gone you know.” she will say to me. As if to almost get confirmation. She, like everyone in a care facility, is on lock down. No visitors, and no leaving. It breaks our heart. We all call or facetime her as often as we can. Last night, when I called, her dementia had taken over, as it often does in the evening. She thought it was morning and Halloween. She was confused. But she said to me, “Your dad tells me everyday to get ready, to get dressed.” It made me scared and sad at first. But I had a different perspective this morning. I am sure she Does hear you. After 66 years of marriage, how could she not? Your voice must be filling her head. Heck, I can still hear you saying ” Mother, are you ready yet?”  You would chide her as she put her “warpaint” on, as you us to call it when she was applying her make up. She relied on you as much as you did her. Even though your last few months on earth were spent apart, you were still one. You always will be.


You would be happy to know, that most of your kids talk or text everyday. We are in constant communication. About you, mom, the mad world. We laugh and cry with each other. We support and comfort each other. We know family Is everything. We give each other a place to grieve and pray. You would be so proud. It is ALL you ever wanted. You are never far from any of us.


So much has changed since you left us. The world changed. Forever. All I can think is, while you were on the earth you were filled with pain, your life was never easy. And now, the world is suffering, every continent, every country, every community, and you are finally pain free and at peace. I hurt for the world and for all of us, down here missing you.

Lessons From My Father

My father passed away  December 16th at the age of 87. He left a legacy of lessons for his children to pass on for generations.

My dad was born to a German immigrant mother and a father who abandoned the family. Raised by his mother, grandmother and step father. He didn’t know that his step father wasn’t his birth father until he saw his birth certificate at age 15. This changed my father forever. And shaped who he was to become as a father himself. His youth, and the hardships he endured, molded the man, who never gave up or in. The man  who was determined, driven and strict. The stubborn, musically gifted, artistic and funny father he was. These are the lessons he left our family.


Be Punctual. Always.

My dad was never late. Ever. Not even once. And he made sure his children were the same, or at least while under his roof. If he said Thanksgiving dinner was to be at noon, you got there by 11. If you started work at 8 you got there by 7:30. To him it was a matter of showing respect, to your boss, your teacher or your family. It showed you cared enough to plan ahead for anything that could cause you to be late.  If we were going somewhere as a family, my dad would yell up to the bedrooms, “The bus is leaving in 15 minutes.”  We all knew it would really be 10. I believe there were a few times the bus left, with a few less passengers.  This punctuality obsession I now have my husband refers to as ” Jack time.” He will ask me if the time I say we have to be somewhere is the real time or am I telling him Jack time. No need to ask.


Wear Many Hats

Figuratively and Literally .

My dad was a Jack of all trades, But, a Master of them too. He could fix Anything. Anything. In his working years he was a welder, a painter, a maintenance man, and a butcher to name a few.And he was great at all of them. We didn’t go get new things if they broke, because dad could fix them.  He was known as Mr Fix It on our street. At any given time there would be a neighbors lawn mower in the garage for him to repair, another neighbors item to be welded.  He created beautiful lawn furniture, Swings and benches and picnic tables that many of us have in our yards. He was the Best at grilling out. Sticky Chicky was the favorite. A delicious barbequed chicken that he had convinced all of us, was a secret sauce he had concocted in our kitchen. He would empty out the cupboards to make us think he had mixed an elaborate recipe.He never told us, we will never know. But I can still taste it.

If you have been  blessed by many talents, share them, give them away


Eat The Foods You Love

My dad LOVED to eat. He loved Meatballs with Gravy ( extra gravy please). He loved Culver’s Cheeseburgers and McDonald’s chicken nuggets . He ate his hot dogs with peanut butter( don’t judge it until you try it) and sardines with peanut butter( feel free to judge this). He craved chocolate, especially German chocolate. Food made him happy, and sometimes was used to soothe him. Every single time my dad was hospitalized, we knew he was getting better, when he would request( or demand) for someone to bring him a cheeseburger. He would be on that phone by 8 a.m. calling one of my sisters to bring him Culver’s. He spent many years on dialysis, and had to watch everything that went into his body, so once he had the kidney transplant, food was once again a joyous experience. It really was the way to his heart.


Sing Sing Sing

Music was everything in our home growing up. Silly songs, Gospel songs, Polka’s. My dad sang them.   There wasn’t a child that sat on his lap that didn’t hear “”Kitties and Doggies” . My personal favorite was “I’m walking behind you because I can’t stand your face.”He would get out his harmonica, play You Are My Sunshine and we would dance around the living room. That tradition carried on 3 generations. My dad’s all time favorite song was Edelweiss . And his favorite way to hear it was when it was sung by his children. It made him tear up. Every single time.  If there was a party, a wedding, anything, and there was a microphone, my dad would get up, grab the mic and announce to his kids to come sing it. And we did. Every single time. It made him happy. And we have it on video and in our hearts .

Edelweiss, edelweiss
Every morning you greet me
Small and white
Clean and bright
You look happy to meet me
Blossom of snow
May you bloom and grow
Bloom and grow forever
Edelweiss, edelweiss
Bless my home-land forever
Small and white
Clean and bright
You look happy to meet me
Blossom of snow
May you bloom and grow
Bloom and grow forever
Edelweiss, edelweiss
Bless my home-land forever.

Be Prepared

Have a plan. Then have a plan B, and C…. My dad was nothing if not prepared in any and All situations. He was organized, and ready for whatever may come his way.  His garage was his castle. Every tool neatly in its place, cleaned and ready to go for it’s next use. There was never any ” where did I put that?” with dad. He could tell you where every single item in that garage was. Every year, when it would be time to Open or Close the pool, my dad would call for help. He would have Everything already out waiting for us. The cover to the pool had arrows and the initials N S E W printed on it, so we knew which way to put it on. If something was to be done, it was to be done Right , and the first time. Because of his readiness, it always was.  I will not lie, that had a tendency to drive us all nuts, but now, I understand. He taught us how to adapt to life by being prepared for anything. That life will throw you curve balls, but if you have your “tools” neatly in place, you won’t have to search to find them. And you will be able to handle it.


 Never Quit. Ever.

When I say my dad was stubborn, it is the understatement of the year. My mom always called him A Stubborn Old German. And he was. He wanted things his way. While that proved to be difficult at times for others, I firmly believe that is why he overcame so much time after time. All his surgeries, all the hospitalizations, dialysis. Diagnosis after horrible diagnosis, he just kept going. You couldn’t keep him down for long. There were so many times, we didn’t think he would survive a surgery, or make it through another night , and then, almost like clock work, that phone call asking for a cheeseburger would happen. He was Determined. He was Driven. And it taught all of us how to just keep going. To work hard. There was no lazing around. Many a morning, dad would wake us up, usually before 7, telling us not to sleep the day away. There was work to be done. That drive and determination in every fiber of his D.N.A. is what let him live probably two decades longer than someone else in his condition. While being stubborn can be a negative, it can also be an amazing blessing. He raised children who became hard workers, driven to succeed and get things done.


Laughter is Everything


My dad had a way of turning any situation into something to smile or laugh about. In sad times, trying times. And we had a lot of those, he would say or do something to make us laugh. I remember one time when I was little, maybe 9 years old. I had a friend sleeping over. There was this small hole in the carpet, and I was beyond mortified that my friend would see it . Dad had recently been disabled, so times were difficult. I am sure a hole in the carpet was the least of his worries, but He knew I was worried about it. So, he handed me his cane and a golf ball. We golfed for hours in that living room. That memory is etched into my brain. My sisters and I were cheerleaders, and sometimes dad would pick us up from practice or a game. But dad simply couldn’t just pick us up. Oh no, he would pull in, blaring his custom car horn programmed to play our school song. I remember wanting to crawl back into the school, but I saw how it made all our friends LAUGH and smile. Any time we had an issue with someone growing up, dad would say ” Did you tell them you know R.J. Bauman personally?”  It made us laugh, and it helped. He would spend hours singing funny songs, drawing Kilroy Was Here pictures or telling us jokes. He had a very inappropriate business card he would hand out to total strangers, the look on their faces was priceless. He faced every obstacle in his life with determination and humor. That gift also has been passed down 3 generations. The ability we have to laugh when times are hard, is the direct result of watching him do the same.


The Legacy a Father Leaves

My dad never knew his real dad. And that haunted him. He searched for years on his own. Then we joined in to help. We got close. We found an additional sister he never knew. His father left her family too. But that stopped with him. My dad never left. Ever. Times weren’t always easy. But he never walked away. His presence was everywhere. He was strict, which taught his children to be respectful. He was stubborn which taught us to be determined and go after our dreams. He sang and played his harmonica all the time and now his children, grandchildren and great grandchildren are talented singers and musicians and know every word to Edelweiss. His love of food taught his  family that simply just getting together to eat is all the Christmas present you need and now plenty of grandchildren enjoy a hotdog smothered in peanut butter. His undying love for our mother, his wife of 66 years, his comforter and care giver, was evident in his eyes. That showed his children, grandchildren and generations to come that True Love does exist. That times can be difficult and beautiful at the same time. The legacy my father leaves is this, a father Stays. He stays and raises his children and shows them how to carry on when he is called Home. Knowing he has prepared them for whatever happens in their life. That the tools they need are safely placed where we can find them. 10599133_10152290042475108_167294392677951294_nEnsuring they will sing and laugh through the good  days and the bad . And we will do it all on time, if not sooner. Jack time.








Even Here

My Faith was tested. It was pushed to the limits. I have never felt so helpless, overwhelmed and unprepared in my life. If it could go wrong, it had. 2019 was trying to kill me I was sure.It was trying to suck the life, Joy and Faith right out of me. Somehow, it didn’t. It made my Faith and my Joy stronger. Even Here, in the deepest, darkest days, Even here, I wasn’t alone.

Brett was admitted to the hospital August 4th. After a summer of sickness, and E.R. visits, we were prepping for his colonoscopy. My worst fears came true. As Brett began to vomit blood, I screamed for my husband to call 911. The tests confirmed Severe Crohn’s disease, a stricture blockage and ulcers in his esophagus. He was as sick as I had ever seen anyone. But it was different, he was MY Son, and I was helpless. I couldn’t fix him. He wouldn’t let me leave. So I stayed for almost all of his 14 days in the hospital. He wanted the room dark, blinds drawn, t.v. on E.S.P.N. ( he never watches sports) on mute, for 14 days. I had brought my bible and journal. So I spent time finding comfort in the Word. I was worried sick about Brett. They wanted to transfer him to a teaching hospital for possible surgery. I once again had to close my salon so I could be with him.( By the month of August I had shut the salon down a total of  almost 4 months. Two months for my broken arm, two weeks and a few days for when my parents were hospitalized and put into nursing homes and now this. ) Most days were spent quietly with Brett, while my husband worked.  My husband would come as soon as he could get off of work each day. But I felt so alone, in the muted darkened room. I had to reach up for help.


When the doctor names the pain you feel
And the air around you changes
When you don’t know what is coming next
You’re afraid to turn the pages
When the answers don’t give you relief
And they only bring more questions
When you wish that you could run away
But you don’t know what direction
There’s no waking up from this a bad dream
There’s no way to stop a slow motion emergency
Even here
In the unknown
Even now
You are not alone.   JJ Heller
 On the 8th day in the hospital, Brett was going to be transferred an hr away. I would go with him, in the ambulance, and Mark would join us when he could. That day also happened to be our 30th wedding anniversary. Earlier in the year we had booked a cute little cabin on the water for a get a way to celebrate it. As the summer went on we knew it wouldn’t happen, so we canceled it. I never thought I would end up spending it like this. The transfer was taking longer than expected. I was tired and weary and afraid for Brett.  My husband and I ended up saying some cross words to each other and in the midst of it he told me the company he had worked for 15 years would be closing their doors at the end of August. I felt the air leave my body.I stood still. How could this be happening. I know in that moment God took over. I felt a peace and calm, and I knew I needed to be there for Mark. I knew we would be okay. What I didn’t know, was that Mark had found  out about the job loss the day Brett was admitted to the hospital but wanted to spare me the stress. He knew I was beside myself over worry with Brett. So he took that burden away. I feel so badly he felt he had to. When the transfer was finally happening, I walked down one hallway with Brett on a stretcher and the paramedics and Mark walked the other way with the nurses. I turned, and quietly whispered “Happy Anniversary” to him as tears poured down my face. The nurses stopped in their tracks. These sweet women who had comforted Brett for 8 days were now comforting us. Mark came and gave me a quick hug and we said our goodbyes. I knew we were heading into so many unknowns, but I knew Who was going before me.
  Find me in the River
Find me on my knees
I’ve walked against the water
Now I’m waiting if you please
We didn’t count on suffering
We didn’t count on pain
But if there are blessings in the valley
Then in the River I will wait.   (Find me in the River by Delirious)
 Brett was transferred to one of the best hospitals in the country and got amazing care. We were close to family there for support, food and a place to rest our weary bones.  They ran more tests and confirmed the severity of Brett’s condition and even added more to it. Brett was diagnosed with Severe Fistulizing Crohn’s Disease. Which the Dr. said was good news bad news. The bad news was obvious, the good news was that it is almost a guarantee for insurance approval for Remicade. Remicade is a medication administered via infusion to try to bring on remission. I felt relief and fear all at once. But this is what I had spent all summer praying for. Answers and a plan. Just give me a plan. I live and die by a schedule, a calendar and a plan.  This year had thrown all of that to the wind. I knew God was teaching me, His schedule, His calendar, His plan. I need only be still. So after two weeks in the hospital we were going home. A bag full of prescriptions and a plan. He was quickly approved for the treatment and he started them 3 weeks later on my 50th birthday. Honestly the best present I ever could have.
I had been feeling sad about my birthday, but not for the typical reasons. I was sad because my mom couldn’t remember it. She has dementia, so I knew eventually it was coming, her forgetting important things, but I wasn’t prepared. I was born on their 16th wedding anniversary, so she always had a speech she gave to people about me. ” This is my baby daughter Mary, she is the 6th child, 6lbs 6 oz. on our 16th wedding anniversary.” She literally said this for years, to any friend of hers I was meeting for the first time. So when the days were drawing closer to our special day, I would ask her “Mom, do you know what day is coming? “No”. she would say. I would tell her it was her anniversary, then ask her what else happened on their 16th anniversary. ” I don’t know unless it was something special.”  Gut punch. Every time. But I kept asking, because I just needed my mom. I would quietly say, “It was me mom, I was born on your anniversary.” So to have the distraction of Brett beginning his treatment was exactly what I needed.

Exodus 14:14

14 The Lord will fight for you; you need only to be still.

As difficult as it was on us to have my husband lose his job, I also feel it was Gods perfect timing. I needed him home, we all did. We had been through so much this year, we were so overwhelmed, so we all needed the break. The lord is faithful and He provides. We had savings, and I was back at work. Mark was able to be home with Brett in the early days of his treatment. I could breathe easier knowing he was there. But then the rains came…the flooding rains. Our area was hit with over 7 inches, and we had a leak in our roof. Of course we did. I actually laughed, because, why not? I mean what else could happen, wait don’t answer that. So 13 grand later we are getting a new roof. ( Our second new roof this year as we had to put a new roof on the salon building after the tornado damaged it. No, I am not kidding). And God is still faithful. He never said we wouldn’t suffer, that wouldn’t have trials. He simply asked us to lean on Him. So I do. Every morning, with my coffee, I sit quietly with my bible, my journal and my devotional. And I thank God for getting us through. For the patience He is helping me learn when things don’t go my way on my time.I am learning I can’t and don’t control everything. Those were my lessons I needed to learn. My kids always tease me about how often I ask them if they are okay, if everything is alright. It is a habit. While Brett was so sick, I would probably ask him 40 times a day. I was so worried I would miss something. Every time the poor kid entered the room I would grill him. I am working hard to let that go too. Brett’s therapist mentioned that maybe I could try to only ask a few times a day. So I am trying. I bite my tongue, sometimes it works.


Consider it pure joy, my brothers and sisters,[a] whenever you face trials of many kinds, because you know that the testing of your faith produces perseverance. Let perseverance finish its work so that you may be mature and complete, not lacking anything. James 1:2


As I sit quietly here tonight, I am in awe of the work God has done for my family this year. This year filled with trials and tribulations. God is good. Brett is doing amazing, he has gained over 30 lbs back. He smiles and cracks jokes again. Mark starts his new job tomorrow. It was such a blessing having him home. He completed almost every honey do list I had. He was here for Brett when he needed him most. And for me. And I have a peace and calm I haven’t had in a long time. A clarity to see things how they really are. Each night when I lay my head to the pillow, I say “Help me Jesus.” He hears our prayers.

Even here.


Another New Normal.

Two years. We started this journey two years ago. Doctor appointments, tests, nurses. Two years of googling symptoms, of thinking I could cure him myself. Two damn years of worry, and fear. Today, I exhaled.

  My son Brett, started losing weight. Slowly at first. Enough to notice. Of my four sons, he was my “husky” one. So 20 lbs at first wasn’t alarming. It was more a wonder. Has he stopped just shoving food in his mouth, not caring what it is? Is he starting to control some of his oral fixations? Having autism, food for him is comfort. Certain foods, more than others. Anyone in the autism community knows all about  the chicken nuggets and bacon obsession. So could he be maturing?  Not wanting to miss anything, we made an appointment.

The Dr. Brett saw for years had passed away, so we would be seeing a new one. I was leery as Brett doesn’t do well with Dr.’s or lab work, or anything related. His old Dr. understood him. Knew how to talk to him, to get him to explain his symptoms. I was hopeful we would be lucky twice. As soon as we left his office, I had a gut feeling. That nagging feeling that this wasn’t the Dr. he needed. He seemed to blow us off, told us not to worry, his metabolism was probably changing. I so badly wanted to believe it. So I left the office, praying he was right. Brett also had a rash on his chest that wouldn’t clear up, he was not worried on that either. He said he would do some labs and get back to us.  When nothing showed up, I should’ve been happy. I wasn’t . I knew there was something wrong. But I did nothing. I let my fear of ruffling feathers, of making a scene, of using my voice stop me.

Over the next year we made multiple trips to the Dr. They ran more lab tests, but nothing further. Because he is on disability, and has long term care funding, he has a personal nurse, She would come often to monitor him, check his BMI. She had him drink ensure. He was now down 40 lbs. We were doing everything we could think of. Everything. I am so mad at myself. Furious. I should’ve marched in there, somewhere, and had a sit in. I should’ve been the mom in Terms of Endearment, when she demands they give her daughter the medicine. I should’ve screamed. I couldn’t find my voice. I will never forgive myself for that.

During all this time, my life was in a tailspin. My parents are elderly and failing. At the same time. So my siblings and I had to place them in a nursing home, sell their home and grieve all that was. My head was somewhere else. I stopped fixating on Brett, I had so many irons in the fire. I had fallen and broken my wrist so was off work for 2 months. I was worried about bills. I lost focus. It happens, I know. But as a special needs mom, there is this saying, ” I can’t die, like ever.”  It means that he will need me, us, forever. There is no moving out, no getting married. I dropped the ball.

On June 1st, Brett got sick. We thought it was a 24 hr bug. At least that is how it presented itself. He wanted me to sleep on the couch with him. To watch over him. Like I did when he was a child. As quickly as it came, it was gone.  Until Fathers Day morning at 4 a.m., when it came back. I asked if he was in pain. He said yes. I asked if he wanted to go to the hospital. Surprisingly, he said yes.  Thank God he did. He found his voice that day.

I am incredibly grateful for the NP he saw in the E.R. . As usual when we go into unfamiliar situations, I will whisper “he has autism” to whomever has to interact with him. It matters. It changes how he reacts to them, based on how they speak to him. She Listened to him, and to my husband and I. She showed concern and compassion. She immediately ordered a series of tests. Including a CT Scan and an ultrasound. For the first time in 2 years, I felt heard! After several hours, she came back in to tell us.  She sat down next to Brett, looked him in the eye, and said “I think we figured out why you’ve lost 60 lbs. You have Crohn’s Disease. I was simultaneously relieved and panicked.  Brett being Brett looked at her and asked ” Is it curable or is it like an STD?” Oh how we needed the levity. She laughed and then honestly told him ” It isn’t curable. Our goal is remission.” As hard as it was to hear, I was forever grateful. I looked at her and just smiled. I was crying inside. I was angry at myself. But I was happy we at least had the start of an answer.

Since June 17th, we have had many appointments. We have had many setbacks. We have made emergency calls to the specialists. There is more medication than I can keep track of. Today, we had a very big scare, and we ended back at the hospital. But in the end we were put at ease. He has more testing coming up in two weeks, where they will determine what medications will hopefully put him into remission, because right now he is in a flare, a serious one. My husband and I are stressed beyond limits. People tell me I look tired. I am. Not sleeping from regret and worry will do that to a gal. We truly live minute to minute. That is how quickly this disease acts on him. And we live in this new normal. A zombie like state. I hover over him, picking up his every signal only I can decipher.  We hope for good news with every new test they run. We pray what he eats stays down and gets absorbed. He is severely under weight, anemic and tired.  But he is still Brett. He still says highly inappropriate things, things that make us laugh.  He spends more time with us now, which is new, out of fear I suppose. He is scared, so we are his safe place to fall.

I have relied heavily on my faith in Jesus. For comfort for Brett, for peaceful nights rest for him as he struggles in pain or nausea. I have prayed for patience and grace for myself, so I don’t lash out at others around me, because there is a tornado inside me. Calm, I pray for calm. In my mind as it races and jumps ahead to years my husband and I are older, and beyond. We can’t die. I have cried countless tears, at home, or work. I have many  a

client grab me in their arms and hug me. They see the load  I carry.  I have been held up in prayer by our friends and family, and people I don’t know. I believe it is working. I am working on letting go of the anger I have at the Dr and Myself for not speaking up. Fool me once, that is what they say right? Never again. I am so impressed with his Dr and NP and nurse right now, I can not sing their praises enough.  His nurse today spent a half hr just going over his CT results with us. She knows how to talk to Brett, and understands his humor. At one point in the Dr’s office today Brett had enough, dropped an F bomb and stormed out. We looked at her as she laughed along with us.  “Welcome to the wonderful world of Brett “. we said.  Our new normal.

The House That Built Me

It is a horrible and odd feeling, packing up your parents lives while they are still alive. Putting their memories in boxes, and bags. Being back there, with some of my siblings, but without my parents felt wrong. But extremely necessary. We had to do what many adult children have had to do, face the horrible decision to place your elderly and ailing parents into a nursing home, and sell the house. You can never fully prepare for it or plan it. You simply grab on tight to your siblings and pray that the unthinkable decisions you all are making are the right ones.

My parents had lived in their home, just shy of 50 years. It was an extremely modest home, with a beautiful yard and pool. Enough bedrooms to sleep 6 children somewhat comfortably. The kind of street where all the neighborhood kids could play out on it until the street lights came on. A place where the friends you made on that street are still your friends today. A neighborhood where we referred to the adults as our Aunts and Uncles. Of course there were bad and difficult times, things we would like to forget, But all of it, the good and bad happened in that house on that street.

When mom fell and broke a hip for the second time, we knew we had to face the unavoidable. After her first fall and hip fracture, she was diagnosed with early stages of dementia. We felt okay with her coming back home, and so did the doctors. Mom had been dads primary caregiver as he suffers from a lengthy list of health issues, including arthritis,  a kidney transplant and has a colostomy bag. As a family, we had suggested to them that we felt maybe they should look into assisted living or something along those lines. Like most elderly people, they said no. They wanted to die in their home, no further discussion. If you have met my dad, no further discussion means Exactly that. Now, by no means does that mean that we left them all alone to fend for themselves. On the contrary, we all pitched in to help them stay home. The majority of the responsibilities falling on two of my sisters that live the closest. They took them to doctor appointments, and emergency room visits  and ran errands for them among other things. When my husband and I would come in we would bring groceries, and check off the list of things my dad needed us to do. We all checked on them daily. We all were anxious if the phone rang, knowing it could mean an emergency. Somehow we managed this routine for over a year. My siblings and I were actually more concerned with our dads health, as mom had recovered quite well, except for her repetitive questions. Then she fell, and everything as we knew it changed. It was out of our hands. Mom suffers from delirium after she has had surgery, and this time was no different. The confused state she was in was now permanent, as her dementia had progressed. One of the hardest and most heartbreaking things you will ever do as an adult child is to tell your mom that she can’t go home again.  It cuts you to the core, and changes you. We now refer to it as Ground Hog day, as we have to tell her over and over. Emotionally crippling for all in the room.

Mom is now permanently at a nursing home, while my dad is in the hospital, awaiting another surgery, then hopefully will be transferred to be with mom. They have been together since my mom was 17, and dad was 21. Their dynamic is typical of that era and generation. Mom stayed home and raised the kids and kept the house, while dad worked, hard, until he became disabled at the age of 47.  The term “waited on him hand and foot.” is actually how it was.  My mom took amazing care of my father, she kept him alive far longer than I think anyone ever thought she could. She kept track of all his medications, and appointments and special diets. She doted on him, making sure his

ice water, in his special glass, was always filled and always cold. And that was her one concern when I told her dad would be going into the nursing home too .”Will they be fixing him his food everyday?” she asked with tears rolling down her face. I assured her they would, that she had worked so hard all her life, it was her turn to have people care for her. And Dad, put my mom first, realizing She needed the care he couldn’t give her. That she needed to be safe. That is love. Their love.

The closing on the house will be final next week, so we are sifting through countless boxes of pictures and memories. Deciding what should be kept, what shouldn’t. I know, it is just a house. But it was my house, our house. My husbands childhood home sold several years ago, ( he originally lived on my same street until they moved 5 blocks over) and when we go back “home” he will drive by it and remember the good and the bad. I told him I don’t think I can.I don’t think I can go by the house without wanting to go in, without wanting to run into the back yard, the desire to jump in the pool on a hot day. That house is the house I learned to walk and talk in, where I fell down the stairs and busted my nose. The house that I had countless sleepovers, in tents made of blankets  hung over the clothes line. The house that I laughed and cried in with my sisters, where we told secrets, and healed each others broken hearts. The house where I came home to the smell of fresh baked cookies after school. The house I fell in love at. We are grieving so many loses at the same time. I can’t imagine wanting to go down my street and not stopping . My parents won’t be there. It won’t be our house anymore, so I want to remember it how it was when it was. It will be some other young families turn to make memories. I am okay with that. Or at least that is what I tell myself.

I thought if I could touch this place or feel it
This brokenness inside me might start healing.
Out here it’s like I’m someone else,
I thought that maybe I could find myself
If I could just come in I swear I’ll leave.
Won’t take nothing but a memory
From the house that built me.

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