• Unfit for Publication

    “I blush to add that when the bird
    Took in the situation
    He said one brief, emphatic word,
    Unfit for publication.”
    (~Guy Wetmore Carryl)

    My Bear is memorizing The Sycophantic Fox and the Gullible Raven for his literature class. When he recited this stanza to me, I thought to myself, “How fitting for today.” (Although to be quite honest, I’ve heard no words unfit for publication from myself or my hubby today.)

    This may be a bit of a grumbly post… a rambling post… an honest post… and an overwhelming “Seriously?” kind of post.

    You see, everything around us seems to be falling apart. Our downstairs bathroom is under renovation due to a leaking shower, and the chaos and clutter of our home is a bit, well… chaotic and cluttery. Bri is having a hard time finding time to work on the renovation because he’s in a busy season with work and the kids have track and softball and I have chemo and well, we have a life to try to live, too. In the midst of the renovation, our water heater blew. So Bri replaced that, but it’s larger than the old one which meant ripping out shelves and my pantry, so my pantry is now my dining room. But we have hot water!

    The water pump on my car is getting fixed tomorrow. Our washing machine broke two weeks ago. We ordered the part, and my dad (who is MacGyver in the flesh) spent Thursday tearing apart the washer to put the new part in for us, only when he got the new part ready to put in, he found a crack that happened during shipping. So we are returning the part and getting another one, only now they are out of stock, and I am without a washer indefinitely (and now we have washer parts strewn all over our only working bathroom; however, they’re strewn neatly because that’s the kind of man Daddy is). My mom took a bunch of laundry home with her, but I’m hand washing our unmentionables and the children are learning to not just throw things in the dirty clothes that they’ve had on for five minutes. *grin*

    Tomorrow, a guy is coming to look at our house’s foundation, because we’ve found a spot or two that look rather crumbly and inside our 120 year old house, you can see it’s leaning a bit more. *sigh*

    I keep telling myself, this will all be over in a few months. That it’s the normal wear and tear of life. Things happen. And praise God, we have a life together that has normal things that happen.

    Then today happened.

    Bri and the kids went with friends for the last day of skiing season on the mountain. And about two hours after they left, I got a call from Tim. “Have you heard from Brian?” Ummmm… no. Turns out he fell snowboarding and his finger was injured, like immediately swollen and twisted, either broken or dislocated. Tim had all the kids. Milt was taking him to the ER. Seriously?

    When I talked to Bri he was a bit incoherent, and I was really okay until he told me they had to cut off his wedding ring. Tears, y’all, tears. I put that ring on his finger almost 20 years ago…
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    He has a spiral fracture and sees an orthopedic doctor tomorrow to talk possible surgery.

    It could’ve been a lot worse. I keep telling myself that. It could’ve been an arm or a leg or a concussion or an even worse injury. I won’t go there. It could’ve been one of the kids. Bri is a rock star when it comes to sickness and injury. He really is. I know the stereotype of whiny men. I don’t have one of those. His pain threshold is very high, and he pushes far past a normal person’s breaking point. Honestly, y’all, I’m the sissy in our family. After today, I’d have popped a very potent pain pill and curled up in bed expecting everyone to cater to my needs. Not Bri. He got home from the ER and showed up at our church’s talent show tonight, huge bandage on his arm, couple of ibuprofen and, “I’m fine as long as I don’t move it.”

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    I keep asking, “How are we supposed to do this?” If he has surgery… how am I supposed to take care of him and have chemo at the same time? And what about all. this. stuff.? How do we add all this in? Will we even be able to take our spring break trip now?

    Sigh.

    Friends, I know all the right answers. Perspective, for one thing. Yes. I know this all stinks, but just one week ago, we were celebrating some of the best news we could have heard about my cancer. None of this is life-threatening. It’s just life.

    And as for how we’ll get through it all. I know how. I’ve written about our community so many times… I know we’ll be carried and cared for. I know we’ll be loved and prayed for. I know it will all work out for our good. It always has. It always will.

    And in five months, Lord willing, we’ll celebrate our anniversary with or without his ring. It has our life verse engraved inside. Joshua 24:15–as for me and my house, we will serve the Lord. We’re still together weathering all the brokenness life brings and thankful for the good gifts God has given us… a home with two bathrooms, a washing machine, a firm foundation for our family, a community who rallies to encourage and provide, and the love of 20 years.

    Living through this brings the sweetest kind of love.

  • A Resounding Yes

    This past year and a half has been a drain on our family… on Brian’s and my marriage, on the children, on my parents. It is exhausting to be constantly fighting for survival–survival of us, of our hearts. Sometimes it seems survival of our very faith, even though I know that He Who began a good work will complete it…

    Years ago, I wrote of how my sweet Bear was struggling as his fear turned physical for him, and almost every night we found him coming to us or running to the bathroom with nausea and feeling as if he might throw up. Every time, he cried and begged us to pray for him, to ask God that he wouldn’t throw up because he hated it so much.

    One time my mom was with him during one of his episodes. He said to her as he shook and swayed, his little body clammy and weak, “Oh, Grandma, I hope God answers yes and not no to our prayer.”

    As heart-breaking as this all was for me, for him, for us to go through, I marveled at the wisdom of a 7-year-old boy. He got it. God doesn’t just answer our prayer when we get what we want, when the yes comes.

    Even a no is an answer…

    God chose yes that night for Bear and chose yes subsequent nights, although Bear’s misery was obvious. And each time we thanked God for His mercy that He would choose yes. But if the answer were no, we would thank Him as well. We would thank Him for strength to get through it and for hearing our prayers even when we didn’t like the answer.

    God always… always answers prayer.

    He is no less good and no less loving and no less God when the answer is no.

    But, y’all, this week…this week has been a resounding YES.

    My oncologist called me this week. “Your PET crossed my desk, and I know Brian often takes time from work to come with you to your appointments. I didn’t want him to have to miss time, so I thought I’d call you with the news.” (Can I just interject again how awesome she is?!) And y’all the news was good. This morning I met with her and we went over the scan.

    Are y’all sitting down? If not, please do.

    There is NO activity. NO hot spots. Nothing that would indicate active disease. My abdomen is clear. My chest and neck are clear.

    Because of the nature of my cancer, there will never be a time when she will look at me and say that I am cancer free, because there could always be residual disease lurking that is too small for the scan to pick up, but for today, she said, “This is the best possible PET we could have asked for.”

    Oh, y’all. OH, Y’ALL!

    We are so overcome, so thankful, and yet still cautiously optimistic.

    There are two spots on my bones (one one my hip and another in my spine) they are watching, but she cannot confirm one way or the other that it’s cancer. They’re are too small to be active on a PET.

    So, where do we go from here?

    I continue on the current course of treatment. I started my new chemo a week ago, and I have had minimal side effects so far. This is the week where I should start to anticipate more. My blood counts are lowering, so fatigue is hitting, and I have to be careful of infection. I’ll stay on my diet and supplement regimen. They will see how I tolerate this new chemo, do another PET in a few months to see if the cancer is still being suppressed, and then we will make decisions from there.

    There are days where I question why I am doing this… feeling so miserable in order to live. When I know it’s working, it makes it a whole lot easier.

    In staff meeting this week, we discussed Acts 27 and Paul’s shipwreck on his way to Rome. He knew he would make it to Rome. God had told him so. And as the ship shuddered and the men feared for their lives, Paul tells them in verse 25, “Therefore, keep up your courage, men, for I believe God that it will turn out exactly as I have been told.” It struck a deep chord with me and I shared it with them. We know. We know how it ends. We’ve been told in His Word, and it’s a glorious telling.

    A co-worker spoke up, “Yes, and look at vs. 26,” she said, “Nevertheless, we must run aground…” Nevertheless. We know how it ends. We don’t know what life will look like in between. We will run aground here on earth, but we know it will turn out exactly as we have been told.

    I do not understand God’s ways. I do not understand why I have been given a yes for now and other friends have been given a no. I beg God for them, that they will still receive a yes… but for all of us, I pray for grace to accept His will no matter what that will may be. And I know that it is the glory of God to conceal a matter. (Proverbs 25:2)

    He is not unfaithful. He cannot be.

    And His final answer, whether my cancer explodes again or not, is and will be yes for us. As I have studied the Psalms and Isaiah, I am struck by how many times God says, “I will…”

    I will.

    I will.

    I will.

    My final hour on this earth, whenever that may be is a final “I will.” I will bring you to glory… to no more pain, no more tears, no more sin, no more cancer. I will bring you to perfection, to ultimate peace and joy and love, to Christ, to HOME.

    His promises are true, and one day I will hear it…

    The final yes to all my prayers and longings…

    Until then, may I have faith like my Bear, who asks God for anything and hopes for yeses and not noes, who accepts His will no matter what, and utters thanksgiving for either answer.

    “When life is sweet, say thank you and celebrate. And when life is bitter, say thank you and grow.” (~Shauna Niequist)

  • Heavy Lifting

    As I enter our church’s sanctuary this Sunday, a man whom I knew but had only spoken to a handful of times stops me with a gentle smile. “Angie,” he says, looking intently, “We are praying. Over and over and over we are praying for you.” I bow my head, already weepy from the truths we had sung earlier in the service. “Thank you.” I choke out, humbled.

    Christmas Eve Brian runs into a family after our service. “Is Angie here?” Yes. “Oh, good. We were hoping she would be, but if not we were going to stop by and sing carols for her. We have these.” and they hand him bags of apples, banana bread, spiced pecans and hot chocolate.

    “Oh, my dear.” a dear elderly lady sees me each week at church and kisses my cheek and fusses with my hair. “I love you so MUCH. I just want you to stop that nasty old chemo!”

    The text pops up a few days after she delivers a meal. I saw your meals ended on Monday. Would you let my family and me bring you dinner Tuesday, Wednesday and Thursday? Again, the tears spring, and my thumbs hesitate over my keyboard. Do I really neeeeeeeed them? Yes. I responded. What a blessing! I had just told my mom I wasn’t sure what meal needs I’d have with my new chemo. She replies, Thank you for letting us serve you.

    My friend comes to visit last weekend and brings with her a note from someone I only know by name. She had written truth and love and prayers on a paper towel at a restaurant for me when she heard Donna was coming down to see me. Her words could not have been more perfect for my weary heart that day.

    Another text today. I’m at Costco. Can I pick up anything for you?

    Y’all, I could share story after story after story… the phone calls, the emails, the hugs, the letters, the texts. Not to make it about me. Not to make it about you. But to make it about God and His glory.

    I struggle often with how little I have to give these days… with how much I am receiving and taking (and rarely finding the time to write the notes of thanks I long to express). But the truth of the matter is that when I say, “Yes.” to those people who offer their help, I am helping them, too. I’m helping them serve as they have been led. It’s a hard lesson to learn.

    This post isn’t much, really. Just another opportunity for me to share how you’ve blessed me and humbled me.

    In His book, Side by Side (which is by far the best book on community and what it looks like to care for one another I’ve ever read), Ed Welch writes in the introduction, “Along the way we will find that God is pleased to use ordinary people, ordinary conversations and extraordinary and wise love to do most of the heavy lifting in His kingdom. The basic idea is that those who help best are the ones who both need help and give help. A healthy community is dependent on all of us being both…We were meant to walk side by side, an interdependent body of weak people.”

    Thank you.

    Thank you for being the ordinary people who are doing some extraordinary heavy lifting for our family and His kingdom.

    We are grateful.

  • Twists and Turns

    “The world is indeed full of peril…”

    The last week has been a roller coaster with as many twists and turns as it has had ups and downs. I have reeled afresh with the struggle that cancer brings, the unknowns, the changes to what had become normalcy, the physical suffering. I have had several phone conversations with staff from the cancer center as they work toward my new regimen. We have had encouraging news and we have had frustrating news, and I have good days and bad days.

    I will begin a new chemo this week, only this will be an oral chemo. No more hours spent in the infusion center. Instead I’ll be dosing myself at home twice a day for two weeks, then a week break. Every few weeks, I’ll receive a shipment of pills in the mail, and I have a daily schedule for eating and dosing that I must keep. Even that seems overwhelming to me… how cancer runs my schedule. And I have fought against this kicking and screaming. It seems so silly, I know, to writhe against this small change, but I want to be in charge of my schedule!

    On Friday, the oncology nurse from the company that ships my chemo called and spent 45 minutes on the phone with me going over expectations and regimen and dose and side effects, and I walked away completely and utterly overwhelmed. How? How am I going to do this all over again? I cried for a while, then realized how often through this I have been doing the “small things” in my own strength and living like only the big things are in God’s hands. But no. I need Him for every breath, every dose, every minute of my schedule.

    “May Your mercy come quickly to meet us, for we are in desperate need.” (Psalm 79:8)

    This has been my heart cry once again as I realize how self-sufficient I have become and how desperately I need my Jesus.

    And His mercy is great. New every morning.

    Today I saw my oncologist and brought pages of notes and questions with me. I know I’ve said this before, but she is amazing. She handled every question with a smile and made sure to fully answer not just what seemed like my intense interrogation of her, but she alleviated many of my fears as well. She helped me grasp what my chemo schedule will look like and how to give myself grace with approximations. As a person who tends to live in black and white, the gray of approximations was a lovely color today!

    Her integrated medicine approach is encouraging, and I can bring my list of supplements and diet changes to her, and she says, “Go for it. No interactions. Keep your body strong.”

    After my appointment, I went into the infusion center for blood work, and the oncology pharmacist came over to spend some time preparing me for the new chemo, too. He is a wonderful man and went over to-dos and what-not-to-dos in great detail. “Don’t be a hero.” he told me. “Call us anytime for anything that seems wrong or unmanageable.” Then he smiled gently, “God has placed you on my heart,” he said. “I’ve been praying for you, and I prayed over these pills, that God would use them to heal your body.” Yes, my friends, tears.

    The new chemo will take some adjusting, and it may require some dosage changes as my body metabolizes it. I have lost even more weight, and she is concerned that the common dose may be too high for me. If I show severe side effects, we will revisit how much and how often I take them. It’s all an unknown still, but sounds somewhat manageable.

    Unknowns. *sigh*

    This morning I texted a dear friend these words from Charles Spurgeon’s Morning and Evening that I read today: “Be thou bold to believe for He has said, ‘I will never leave you nor forsake you.’ In this promise God gives His people everything. ‘I’ will never leave you…” She is walking through a fiery trial, too. One that has fostered many phone calls, weeping together, and sleepless nights of prayer for us both. There are so many unknowns…

    But the truth is, no matter what any of this brings, He is with us. And truth doesn’t change.

    Yes, “the world is indeed full of peril…”

    “…and in it there are many dark places; but still there is much that is fair, and though in all lands love is now mingled with grief, it grows perhaps the greater. (~J.R.R. Tolkien)”

    This weekend I was able to go out to eat with my family and then a square dance at my church (and even danced a couple times!). A dear college friend came down for Saturday and Sunday, and we watched my Ash play basketball, then went to a JMU game while my younger two went skiing with friends. We shared hearts and struggles, and she didn’t balk at the chaos of a home undergoing renovation. It was a much needed weekend.

    Tonight I am curled up with my boys. Ash-man has been home from school with a high fever and deep cough. Bear is battling a sore throat and cold, and we are hoping it won’t turn into more. My Bella-girl is out with her daddy. We have worked on homework and flash cards and maps and memorization. A friend brought us chili and fruit and corn bread. The fire warms. Texts and phone calls have reminded me of the truth above… that love is mingled with grief, but that love grows greater.

    Your love. His love.

    Yes, His mercy has been poured out in so many ways.

    (I have a PET scan on Thursday morning and will begin taking the new chemo Thursday night. Will you pray for us? And pray for protection from so much sickness? Your love and prayers are a gift.)

  • What Has Been Given

    Lately life has seemed like just a chaos of holding on to hope and making it through each day. I realize there are many of us out there who feel this way, no matter what the cause may be. We have been learning the new normal of treatment, response, recovery and then chemo again, and life feels like a it has gotten into a rut.

    At the end of the day my exhaustion and pain often overwhelm, and it is rare for me to find time to write anymore. I hate this feeling. My words seem stolen from me, and the catharsis they once were is gone. It is one more thing the struggle of life has taken from me, and I ache with the longing for words to come.

    But I am writing now… full of gratefulness for a clear brain MRI and yet shuddering at some disappointing news with my heart and a new chemo we must now try.

    Yes.

    I was sent this past week for an MRI of my brain to make sure there is no spread there. My neurologist ordered this for me to see if they could find a source for my continued headaches. Thankfully it was clear, but what this means is we don’t know why I’m still having so much pain, although they are leaning towards it being chemo side effect related .

    On Tuesday I had a routine echocardiogram to monitor how my heart is doing through this process. This last one showed heart damage, so I am going to have to be pulled off the current chemo. I may experience some shortness of breath and trouble with weakness, but I haven’t so far. And the good news is that this can reverse itself over time, so we are hopeful.

    In the meantime, my oncologist is ordering a PET scan to see where we are with things and to set a baseline for the new chemo (if insurance will approve). I will start my new chemo in a couple weeks and we will adjust to another “new normal” for us. Although I’m learning there really is no normal in our home.

    Every day is different.

    I fatigue easily, and I find chemo brain to still be extremely frustrating. There are so many things I know I should know, but my brain just. won’t. work. My head aches constantly and for the first two weeks after treatment I ache like I have the flu as well as deal with nausea. Then things start to rebound and I am able to function somewhat well… until another treatment. We’ll see what this new one holds.

    This up and down has been really hard on the children and last night I held my Bella-girl for well over 20 minutes while she cried and cried. “It’s all so scary,” she said, “Never knowing how you will feel. And I am just so afraid my mommy is going to die.” Oh my heart, y’all. This hurts it far worse than chemo.

    Thankfully, my Bri stepped in to help comfort and calm and the protection he offered in his arms and words to her were life-giving to all of us.

    As our friend, Joe, tells me, “He’s a good man, Ang.” Yes. Yes he is. I’m so thankful he’s mine.

    We are learning that the new normal that we keep waiting for will probably never come, and we are learning to be okay with that. Normal will change for us on a consistent basis, and as hard as that might be for someone who doesn’t do well with change, I’m learning to accept it.

    Learning to accept.

    Thankful for what’s given and choosing to move forward.

    There’s a scene in the movie, The Voyage of the Dawn Treader, where King Caspian has reached the edge of Aslan’s Country and is given the chance to enter. He has longed to be with his father again, and now is his opportunity. He reaches out and touches the wall of water then turns back to his friends, to Aslan, to his life. When asked why he didn’t enter, he responds with something along the lines of, “I’ve spent too long focusing on what was taken from me and not enough on what was given.”

    Grieving is a hard place to be. It will always be a part of me, a part of this, of us. But I am taking steps forward… away from grief and tasting grace.

    It is a struggle. Daily I see and feel the effects of so many surgeries and cancers and lupus and fatigue and pain and scars and the inability to be and do what I have been and done for years. There is all the time my family and I have lost together and the moments we haven’t had were our life a “normal” one. I struggle with all the sacrifices my husband and children have made for me. It is a hard place to be. But I don’t want to be stuck here either.

    There is a place to grieve all of this, I know, and there will be moments when it all hits like a tsunami and takes my breath away. This past week was one of many, many tears.

    But, oh y’all, look how much I have been given!

    There will be so many moments where God’s grace will steal my breath away… so many moments where He already has.

    His grace fills me.

    Look. how. much. I. have!

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    Yes. So much has been taken.

    But look what has been given.

    I could not ask for more.

    It is the nature of grace to fill the spaces that have been empty…

    ~ Goethe

  • Fourteen

    It was just Wednesday evening that I realized it. We were chatting with one of your teachers in the kitchen. She had brought us supper, and you came down to say, “Hello.” Chatting and laughing, I turned to look at you and your eyes met mine in exactly the same place. “Wait!” I cried, and pulled you over. Standing next to each other, I looked directly into those big brown eyes with lashes for days. “How did you…? When did you…?” and you threw your head back to laugh but not before I saw the sparkle in them.

    You’re as tall as me now. Strong and handsome with a deepening voice and a bit more assurance in the way you carry yourself.

    Fourteen tomorrow.

    Has it really been fourteen years since this happened?

    …the nurse finally placed him in my arms. I was mesmerized. It had nothing to do with the fact that I had been carrying him for nine months, but it had everything to do with the realization that he was a wonder, a gift, and–as trite as it may sound–a miracle. I loved him instantly, and I was deeply, profoundly humbled by the realization that as much as I loved [him] in that moment, it was just an infinitesimal fraction of how much God loves us. It was an instantaneous, profound, life-altering shift in perspective.
    (~Sophie Hudson, A Little Salty to Cut the Sweet)

    You, my son, have always been such a gift, studying the world around you with intensity and leaping into life with exuberance. Your love for laughter and your friends pours out of you, yet you hold worlds of pain inside you with quiet strength. Strong-willed and resolved, you are your father’s boy, and as I watch you grow and become more like him, it makes my heart happy.

    Of my three gifts, you are the one who remembers me before cancer came, before life shipwrecked us into a new world of survival and chaos. And yesterday when I melted down over failed lasagna I was making for your birthday, over feeling miserable and not able to play outside, over the continuous cycle of chemo, pain, and recovery, you came to me and put your arm around me. “I’m sorry, Ash,” I cried.

    “Oh, Mom, it’s okay. There’s nothing to be sorry about.”

    And I lost it. I cried while you held me close, and you know what I realized?

    That spot? Under the chin? I’ve written about it so many times before… how no matter how big you get, your head still fits just perfectly under my chin.

    That spot? You have one, too. And my head fit just perfectly into it yesterday and you held your mama while she cried.

    Your heart is a gift, dear boy, and I love imagining where God will take you and use you.

    Dad and I often talk about the teenage years with excitement… so much you will learn and do and ways you will change and grow. We long to walk through those days with wisdom for you and watch you grow in that wisdom. And we pray. May you never lose that heart, that faith, that love for your friends, and that delight in life around you. Wise and strong and brave and true… these are the words that pour from my lips each time I pray for you. Wise and strong and brave and true.

    Happy fourteen, buddy.

    You came into this world, Ash-man, and you changed everything for us.

    In all the best ways.

    Version 2

  • Cries in the Dark (A Repost)

    Because even with the good news, the heaviness of chemo threatens to overwhelm and five days of weakness and headache and body ache and throwing up pull me down into darkness… I need to be reminded that He comes.

    ~~~~~
    When I woke in the morning it was dark, and our house was still and quiet. As I began moving down the stairs I heard a rustling sound, and I knew my Bella was awake. I popped my head in her room and saw her silhouette illuminated by her nightlight. “Hey, Bella girl,” I whispered. “You coming down with me?”

    She jumped out of bed and I helped her into her robe. We started walking together in the dimly lit room, then suddenly she turned and ran back across her room to her new nightlight. Excited to have something new, she switched it off not thinking about what would happen, and the room was plunged into darkness.

    All I heard was sheer terror in her voice as she cried out, “Mommy! MOMMY!”

    I heard the panic. I knew she was afraid of the dark. I knew even more so, she was afraid I was gone out the door and she was alone in that dark room.

    I knew because I know her.

    And I went to her, finding her hand in the darkness, I pulled her close and wiped her face–a face saturated by tears in just a few short moments. I picked her up, hugging her, soothing her and letting her know it’s all right. I knew she needed to hear those whisperings.

    I knew because I know her.

    I carried her down the stairs and we began working on breakfast and packing lunches together, and she sang as she worked, “Saviuh, he can move the mountains! My God is mighty to save. He is mighty to save!” All fear was gone.

    That’s a bit how life has been for me these past couple of months. Since my surgery, my body has been slow to recover, but more than that, because all of my cancers and the surgery are hormone related, everything is off kilter. I am on different meds that I must adjust to. My replacement thyroid medication is imbalanced. My body is worn and weary and my sleep patterns are off as I wake 5-10 times a night. All of it causes physical imbalance and depression that is overwhelming.

    Like my little girl, plunged into darkness, I feel that terror rising up in me every single day. The sadness, the darkness. And there is “no reason why” to my reasonable mind. And like my little girl, I find myself unable to do much more than cry, “Father! FATHER!” to my God. He knows everything I am going through… He’s known all along.

    He knows because He knows me.

    He comes to me. Sometimes I don’t hear Him or see Him in the darkness, the apathy. But He comes anyway. And over time, I see Him. He shows me Himself in the big things and the small things (and there have been both big things and small things hitting us these past few months.) He whispers truth from His Word or from the mouths of my friends who are walking through this with me. He carries me into the light because He knows I need to see.

    He knows because He knows me.

    And it is good to be known.

    (Written just after my fourth cancer in 2011.)

  • Quiet Celebration

    Today I should be at work, but I am curled up under blankets next to a roaring fire… splitting headache, achy body, nausea, fatigue. Chemo.

    Y’all, I don’t even know how to describe the wretchedness of chemo.

    On Monday as I walked into the cancer center with my dad (best chemo buddy ever!), I told him how hard it was to enter those doors. Every time I go in, I know what awaits me when I leave. Days of misery, of curling up, of watching life happen around me, of stressing over things I think need to get done that I cannot do. I read some, write some, watch some tv, and sleep. My children spend time in my room, snuggling, sharing of their days, getting instructions for chores to take care of the home while I’m unable. Some days it’s really hard to see the gifts in this misery.

    And then…

    The phone rings late, and I see it’s the cancer center and my heart does a flip-flop.

    “Angie, it’s Dr. U.” she sounded almost giddy, “Your lab work just crossed my desk and I had to call right away.”

    Y’all, my tumor markers have dropped again. In fact, they’ve almost halved again!

    I will have more details and answers to lots of questions that I have after I see the doctor again for my next treatment, but in the meantime, we are thankful for this gift for this day.

    Chemo continues. It is hard. It is miserable.

    Diet and supplements continue. It is hard. But it is wholesome.

    And it is working!

    Quiet celebration resounds in my heart… there will be time for noisy celebration when I feel better.

    Thank y’all for walking this road with us… for encouraging us, for gritting your teeth in the pain with us, for praying for us, for not giving up on us, for weeping when we weep and rejoicing when we rejoice. It takes a village, and you are a wonderful village to “live” with.

  • Dreams

    Oh, my Bear.

    I remember those days of knowing you were a life inside me and dreaming of who you would be, of holding my hands on my belly and whispering my dreams with you.

    I remember those days when I first held you, wrapped in all the wonder of your quietness and your sweet, snug softness, and praying over you with dreams your future.

    I remember those days of silliness and laughter and sharing dreams of things you’d do and be as you “gwew up to be oldah.”

    I remember those days of adventure and travel and sports and hearing dreams of all the things you would do and places you would go.

    I remember those days of holding you close and crying together over life’s hard days and fearing for dreams we might not share.

    And I remember yesterday where we snuggled together still on the couch watching flowered parade floats and talking of birthdays and school days and sharing dreams of the days to come.

    Some days I wonder how my heart doesn’t explode for love of you and all you bring to this life, this world.

    You’re so much better than those dreams, you know.

    Happy birthday, my son.

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  • Christmas Magic

    No…there is no Santa Claus. At least not in the way [we] have been led to believe. Usually the truth hurts, but in this case it is much more wonderful. We’re all Santas, you see. We all have magic. The pretend Santa gets to work only one day a year. But we, the real ones, we get to work every day.

    We get to spread joy. We get to give gifts. We get to help those who need help and plant smiles where there are frowns.

    There is magic in this world, I will say. God is the magician. And we are His hands.
    (~Billy Coffey)

    May we all be blessed to spread magic in the year to come.

    Merry Christmas and Happy New Year!

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