Posted in Abundance, Christian music, Community, Jesus, Uncategorized

Our Stories

I preached this at Point Hope UMC this morning.  They were very gracious to me and we had a delicious lunch after church that Mike and the kids have raved about all afternoon.  Thanks for being with me on this crazy journey called life.  I want you to share your stories  with me too!  ‘Cause we’re not meant to do this life alone.  Amen?

Psalm 77

1I cry aloud to God, aloud to God, that he may hear me.

2In the day of my trouble I seek the Lord; in the night my hand is stretched out without wearying; my soul refuses to be comforted.

3I think of God, and I moan; I meditate, and my spirit faints. Selah

4You keep my eyelids from closing; I am so troubled that I cannot speak.

5I consider the days of old, and remember the years of long ago.

6I commune with my heart in the night; I meditate and search my spirit:

7“Will the Lord spurn forever, and never again be favorable?

8Has his steadfast love ceased forever? Are his promises at an end for all time?

9Has God forgotten to be gracious? Has he in anger shut up his compassion?”

10And I say, “It is my grief that the right hand of the Most High has changed.”

11I will call to mind the deeds of the Lord; I will remember your wonders of old.

12I will meditate on all your work, and muse on your mighty deeds.

13Your way, O God, is holy. What god is so great as our God?

14You are the God who works wonders; you have displayed your might among the peoples.

15With your strong arm you redeemed your people, the descendants of Jacob and Joseph. Selah

16When the waters saw you, O God, when the waters saw you, they were afraid; the very deep trembled.

17The clouds poured out water; the skies thundered; your arrows flashed on every side.

18The crash of your thunder was in the whirlwind; your lightnings lit up the world; the earth trembled and shook.

19Your way was through the sea, your path, through the mighty waters; yet your footprints were unseen.

20You led your people like a flock by the hand of Moses and Aaron.

Some of you may be wondering what on earth is this preacher doing using a Psalm as her text on her first Sunday.  The Psalms get to the heart speak.  They get down deep, to the nitty gritty.  They’re full of real people celebrating their Good Shepherd and crying out desperately to God.  Both the mountaintops and valleys, the fullness of the human experience, is captured in the Psalms.

Let me tell you a story.  In my previous appointment I went to Costa Rica for a Spring Break mission trip in 2013 with Pura Vida Ministries.  Listen to their mission statement: “We exist to transform lives by providing Christ-centered, life-changing mission adventures.  We believe that following Jesus is Not an Event, but a Life!”  Not an event, but a life.  Not an event, but a life.  I believe that.  You will hear in my messages and hopefully see in my life a fervent desire to live our faith out loud, no matter the storms or challenges.  They had different merchandise you could buy with “Not an event, but a life” so I brought back a mousepad for my office, not knowing then that I would have my second brain surgery later that May.

At a conference in Winchester, VA I had my first seizure.  It was 2010 and I was 30 at the time.  I was diagnosed with a brain tumor that they removed most of two weeks later.  My tumor has a Harry Potter spell-like pronunciation to it – an oligodendroglioma. I had no complications or deficits after surgery.  I mean I had a tube coming out of my head with a blood bulb that I would put in the pocket of my hospital gown when I went to the bathroom but you go through what you have to.  I had the surgery on Friday and I was out on Sunday.  My son Enoch had just turned 3 and Evy was 1;58969_656598733737_2486331_n

so I recuperated at my brother Josh’s house.  I was back home and at work the next Thursday, less than a week later, easy, peasy, lemon squeezy.

I remember writing on the prayer request card from Pura Vida at the end of the trip that I would have an MRI the following Monday.  The MRI unfortunately showed the tumor had grown and so I began sharing with people that I would have a second surgery.  I thought it would be like the first surgery, so I agreed to do a wedding 3 weeks later and was set to do a workshop in Chicago that June and set to preach at camp for a week in July.  Unlike the first surgery where I had no complications, when I woke up I could understand everything the nurses, doctors, and my family were saying but I had lost my ability to speak.  The doctors and speech therapists call it apraxia.  Apraxia is the inability to execute learned purposeful movements, despite having the desire and the physical capacity to perform the movements. Oh, I had the desire in spades.  In other words, the words were still there but the ability to form sentences was broken, non-existent.

The tumor is on the motor cortex, that’s why they didn’t get it all the first time, so I had no feeling in my right arm or hand, and I’m right-handed.  I texted these words to my husband, Mike, with my left hand over two weeks later, “The quickness with which I speak comes back?”  It took me 45 minutes to text that.  I did 30 radiation treatments, 6 months of chemo, physical, occupational, and speech therapy over that year and then I went to the Ukraine to speak at a conference, but that is another sermon.

I’ve learned to rely on God because I HAVE to.  I am an independent, non-conformist person mixed with a perfectionistic people pleaser and I ALWAYS relied heavily on my communication skills.  I didn’t know how much until I couldn’t rattle off a prayer or answer a theological question or explain simple things to my kids or preach without a manuscript, or even the little things.  I used to carry around a small calendar in my purse to jot stuff down in, I used to type x number of words a minute, I used to love to send handwritten notes to people.  The ease and what came naturally to me before was lost and I still sometimes grieve that loss.  It’s okay to grieve.  God is with us when we mourn.  God promises to bring joy in the morning, so I went back to preaching in June.  I could read things and I reused every sermon that I had full manuscripts for that summer.  My oncologist, who I met with more frequently that first year and now at least every 3-4 months, was an older man who was all business and had a wry sense of humor.  Dr. Stahl always asked me if I was still preaching every week and I would always say yes.  He doesn’t know, by him asking me that question every time that I’m just stubborn, bull-headed and tenacious enough to see that as a challenge and with God’s strength, to make it happen!  He wrote this to me when he found out as I was moving, “It has been a privilege and a pleasure to have you as a patient-You have remarkable courage and determination-both of which have you served you well.”

We at the time had services every Sunday at 11 and every Wednesday night at 8:30 and shared in communion each time and it was a challenge to say the least.  A number of things helped me get through that time great students and other church members, Gator Wesley had been a local church and our older members sent me cards of encouragement almost every day, my speech therapist being patient and pushing me and saying your brain will rewire itself, songs like “Lord I Need You,” movies like “Rise of the Guardians” talking about what is your center and having faith even when you cannot see and “The Legend of Bagger Vance” talking about each of us has one, true, authentic swing, when I didn’t feel confident in my own voice, and y’all’s prayers, cards, and prayer shawls from around the United Methodist connection.  When I didn’t have the strength or the words or even the desire, on the dark nights of the soul, God was faithful.  When my primary care doctor said to me that September, I don’t think this brain tumor’s going to kill you, let’s get you healthy and strong, God was working through her to give me the hope that I needed to keep putting one foot in front of the other.  God can and does use us to be lights in a world full of darkness.  I knew then and I know now that God is with me every step of the way, continuing to strengthen me for the journey.  How do I know?  God gives us proof.   The little reassurances along the way – the person that says something and God’s speaking to me through their voice, the song that happens to come on the radio or the itunes shuffle at just the right time, the passage of scripture I happen to read that morning…it doesn’t just “happen.”  It’s a God thing.  Claim it.  Know it.  Trust it.  Be the person that Mother Teresa emulated as she said, “I’m a little pencil in the hand of a writing God, who is sending a love letter to the world.”

God is ever present reminding me I am enough even when I don’t have the words.  I am worthy even when I don’t have the answers.  I can claim my inheritance by simply resting in the surety that I am a child of God.  We all can.  We are all worthy and enough.  If I have learned anything over the past 6 years is it’s not enough to just merely have these quick fix Jesus highs, these Psalms of praise alone – no matter how great they are – because they won’t sustain you when the ship hits the sand or when the rubber hits the road and you’re left bereft.  Developing a real, in depth relationship with Jesus will.  Developing a faith that lasts and is rooted and grounded in scripture will.  A verse, a song lyric, a prayer….When the storms of life are raging, I know where my hope is and that is in Christ alone.  We sang the hymn, “In Christ Alone” at Annual Conference in 2011, one year after the first surgery, and we sang it just now before the sermon.  It’s a song that means very much to me, especially the last verse.

No guilt in life, no fear in death,
This is the power of Christ in me;
From life’s first cry to final breath.
Jesus commands my destiny.
No power of hell, no scheme of man,
Can ever pluck me from His hand;
Till He returns or calls me home,
Here in the power of Christ I’ll stand.

At a retreat a year after the second surgery, the facilitator asked us to write questions on 3 cards.  They were to be questions where we needed the Holy Spirit to intercede, questions that were rolling around our heads but we had never articulated.  Then we were to paint and cut out pictures from magazines for each card without seeing what questions were on the back.  So I went to a place by myself and I invited the Holy Spirit to come by lighting a candle and I wrote these questions:

1.  What do I need more of in my life?
What do I need to embrace? 
Question 1

2.  What obstacles of the joy God wants for me do I consciously or subconsciously allow to hinder me from experiencing that joy? Question 2

3.  What do I need to let go?  Why am I so afraid to share my story?  Question 3

I went through the cards and picked colors and themes as I felt the Spirit leading me to.  Despite my skepticism, this activity ended being one of the most powerful practices that I have ever experienced.  I had gotten so caught up in my designs and cutting anything out that struck me that I had completely forgotten the original questions.

The answer to the first question was this: written in pencil “In Christ Alone, cancer, and colors.   I needed to embrace my cancer.  I was a cancer survivor.  And I need to place my trust “in Christ alone.”  Even the part about the skin was pointing to me embracing myself.  I had the dot tattoo so they could line me up to do my radiation and I had the scars from both the surgeries, but in the back of my mind I was still hiding.Image 1

We had been singing “In Christ Alone” during this retreat and when I shared that piece of my story later when all of us were sharing, we sang that as a closing song, which brought me to healing, relieving tears, like I let go of a burden.  The second question was this picture.  I look at this picture, I feel peace and beauty, and I needed more of that in my life after the year I had so I made a commitment to make room for beauty and positive and calming messages, so that’s why my office and home are decorated in such ways.Image 2

The last question of “What do I need to let go?” was the safe question.  God was leading me to ask what I really needed.  And the Holy Spirit was so loud in me, that I scribbled down the last question. It was surprising to me because I try to be real and authentic in all aspects of my life.  That’s why I created the blog in 2010. I didn’t want to actually talk about my blog or anything that I wrote.  And it was self-preservation and a bit of laziness to be sure because it was a  way to share with my family, friends, students and the communities that raised me and fed me and are praying with me something I couldn’t say out loud.  It was to share authentically with the world what was going on with me.  It was a way to update everyone at once with what was going on inside my head.  I rarely re-read and edit.  So this question was surprising to me.  But Proverbs 3:5-6 says “Trust in the Lord with all your heart, and do not rely on your own insight. In all your ways acknowledge him, and he will make straight your paths.”  It struck me as I was writing this sermon that I use “afraid.”  And I think that is telling.  I admit now I was afraid and I am afraid of being misunderstood, of losing my words, of not being in control…but as 1 Timothy 1:7 says God does not give us a spirit of fear, but rather a spirit of power and love.  God doesn’t call us to be silent, God calls to be bold and step out in faith and God will give us the words to speak. Image 3

Everything.  I needed to let go of everything.  And I felt safe in the arms of Mike in it all, but more than that I felt like God had and is protecting me from the storm.  God was creating the perfect shelter, an eye in the hurricane.  God was also giving me a clear message with these cards.  I needed to share my story, integrating the cancer, no matter how hard, personal, and vulnerable.

 I’ve claimed the words of Isaiah 41:8-10 (NRSV) But you, Israel, my servant, Jacob, whom I have chosen, the offspring of Abraham, my friend; you whom I took from the ends of the earth, and called from its farthest corners, saying to you, “You are my servant, I have chosen you and not cast you off”; 10 do not fear, for I am with you, do not be afraid, for I am your God; I will strengthen you, I will help you, I will uphold you with my victorious right hand.”

Bob Goff in his book Love Does says, “I once heard somebody say that God had closed a door on an opportunity that they hoped for.  But I’ve always wondered if, when we want to do something that we know is right and good, God places that desire deep in our hearts because He wants it for us and it honors Him.  Maybe there are times when we think a door has been closed and, instead of misinterpreting the circumstances, God wants us to kick it down.  Or perhaps just sit outside of it long enough until somebody tells us we can come in.”

God wants us to dream large God-sized dreams.  God wants us to sometimes kick doors down.  God wants to give us a future with hope.  As Jeremiah 29:11-14 says, “11 For surely I know the plans I have for you, says the Lord, plans for your welfare and not for harm, to give you a future with hope. 12 Then when you call upon me and come and pray to me, I will hear you. 13 When you search for me, you will find me; if you seek me with all your heart, 14 I will let you find me, says the Lord, and I will restore your fortunes and gather you from all the nations and all the places where I have driven you, says the Lord, and I will bring you back to the place from which I sent you into exile.”  Or as it is in 1 Corinthians 2:9, “What no eye has seen, nor ear heard, nor the human heart conceived, what God has prepared for those who love him.”  Or as it is in Ephesians 3:20, “Now to him who by the power at work within us is able to accomplish abundantly far more than all we can ask or imagine.”

We’re not meant to walk this road alone.  I want to walk with you and hear your stories so that in the mountain tops and the valleys, we can share with one another, come alongside one another, praying for each other, being church with one another.  It’s a crazy cool relay race in the United Methodist Church’s system of itineracy.  Joe passed Walter the torch. Walter passed me the torch and I am ever grateful for that torch and the care in which he handed it off.  In 1 Corinthians 3:6, “Paul wrote, “I planted the seed, Apollos watered it, but God has been making it grow.”   The earth is fertile here at Point Hope and God is indeed in your midst making things grow and making all things new.  I trust God to rock our socks off!  That’s the beautiful and crazy gift of having life in Christ.  You follow where God has called you, no matter that you’re too old to have kids, like Abraham, no matter if you’re a prostitute, like Rahab, no matter the speech impediment like Moses, no matter if you don’t want to, like Jonah, no matter if you’re left in a foreign land with your mother in law, like Ruth…and that’s just the Old Testament.  The Bible is chock full of stories about God doing extraordinary things with ordinary people.  God didn’t stop writing stories two thousand years ago.  I’m reminded of the Big Daddy Weave song that weaves in the hymn “This is my story, this is my song.”  The lines are

 If I told you my story
You would hear hope that wouldn’t let go
If I told you my story
You would hear love that never gave up
If I told you my story
You would hear life but it wasn’t mine

If I should speak then let it be

Of the grace that is greater than all my sin
Of when justice was served and where mercy wins
Of the kindness of Jesus that draws me in
To tell you my story is to tell of Him

We all have a story and when we take a moment in our busy lives to catch our breath and let the God that came and dwelt among us have room in our lives, we create room for God to share with us.  If you’re thinking you don’t have a story, ask God and God will reveal your story.  Or if the problem is not you not knowing, but getting it out or just not telling it, than Marianne Williamson says it this way, “Our deepest fear is not that we are inadequate.  Our deepest fear is that we are powerful beyond measure.  It is our light, not our darkness that most frightens us.  We ask ourselves, Who am I to be brilliant, gorgeous, talented, fabulous?  Actually, who are you not to be.  You are a child of God.  Your playing small does not serve the world.  There is nothing enlightened about shrinking so that other people won’t feel insecure around you.  We are all meant to shine, as children do.  We were born to make manifest the glory of God that is within us.  It is not just in some of us; it is in everyone.  And as we let our own light shine, we unconsciously give other people permission to do the same.  As we are liberated from our own fear, our presence automatically liberates others.”  Let your light shine that the world may see and know.  If we all share our lights together – we will – with God’s strength – rock their socks off!

I had no idea before the age of 30 that my story would include a brain tumor, but I know I have life, indeed abundant life in Christ.  Not just surviving but thriving. Too often I hear that we’ve just got to get through high school or college or grad school or we have to get our first job or get married or have children or retire to figure out what in the heck to do with our lives, but God doesn’t want us to let life pass us by so that we’re only barely surviving. God wants us to thrive.  Jesus didn’t come so we could have a complacent life.  He came for us to have abundant life.

I want each of us to be a part of God’s larger. Broader story, in our own particular way, with our own spiritual gifts, strengths or weaknesses that God works for good.  Look under your chair, some of you might have peeked already, and that’s perfectly okay.  This is to basically sum up my sermon and it was made by one of my favorite artists Suzanne Vinson.  Here’s the full quote from Frederich Buechner.

“The grace of God means something like: Here is your life. You might never have been, but you are because the party wouldn’t have been complete without you. Here is the world. Beautiful and terrible things will happen. Don’t be afraid. I am with you. Nothing can ever separate us. It’s for you I created the universe. I love you. There’s only one catch. Like any other gift, the gift of grace can be yours only if you’ll reach out and take it. Maybe being able to reach out and take it is a gift too.”

I would like you to take this with you.  Keep it in your wallet or in your dashboard or on your bathroom mirror.  Let it be a reminder that nothing can separate you from the love of God and God’s abundant grace, and though beautiful and terrible things will inevitably happen, we are not to fear, because we know the One who spoke things into existence, who is our Creator, Redeemer and Sustainer.  Amen.  Let us pray.

*  Music that I was listening to while I wrote this sermon.  TobyMac “Move” Hawk Nelson  “Drops in the Ocean” “Lord I Need You”  Lauren Daigle “Trust In You” Sidewalk Prophets “Prodigal” Ryan Stevenson “The Eye of the Storm” Aaron Shust“Ever Be” Hollyn “Alone”

 

 

 

 

 

Posted in Brain Tumor, Cancer, Health, Helpless

Survival Mode

I had coffee with a friend last Thursday night, and we both intentionally want the friendship to go deeper than just our kids play together, so that’s why we made it a no kid time coffee date. Two-thirds of the way through the conversation she asked me, and I’m paraphrasing here, if I had processed the surgery? I stopped before answering because I want to be honest in our burgeoning friendship, and I said no. Not entirely. That stayed with me throughout the entire weekend. I was shocked at the strong, protective feelings her initial question evoked and there was a definite shift in the conversation.

Mike and I celebrated a long overdue date night. We had received a gift card for Mark’s Prime, a fancy place in Gainesville (thanks Brittany and Brian!) and we splurged ordering appetizers, steak, and dessert. (See Mom I do make an effort to eat red meat the week before chemo!) Then we watched a movie just right for us. Saturday was spent in typical fashion, Evy talking to Mr. Sun on our way to Krispy Kreme, Enoch threatening to put Mommy and Daddy in time out if we yelled any louder at the football game. Then Sunday it was a full day at Gator Wesley.

I didn’t consciously think about my friend’s question until they started my IV for the contrast in the MRI this morning.

Then left with no phone or book or students or laundry or things that need cleaning or ways to procrastinate, I was left alone and perfectly still with my thoughts for a whole 45 minutes. I’ve had longer MRI’s, but this FELT longer. I was trying to pray. To be present. To make this time somehow “productive.” To fight off the occasional panic attack. But the question remained.

And then fast forward to the doctor’s appointment. The oncologist’s resident came in first to ask me a few questions. I was struck by two things. The first the only person to have cancer in my family was my paternal grandfather (prostate cancer). After my grandmother died of a heart attack, the results came back the next day that she had leukemia. Now, don’t get me wrong, it’s not that we don’t have our fair share of health problems, diabetes to the extreme on Dad’s side and cholesterol and extreme heart disease on my mom’s. But growing up, cancer was never something we worried about. My grandfather was given 6 months to live when Dad was a little boy and then he lived until I was a junior in college.

The second was how different this recovery was to my first surgery. They were DRAMATICALLY different. In 2010, I came out of surgery completely normal (or as normal as I could be…). The surgery in 2010 I had no deficits, except recalling some names. I woke up in ICU talking and thinking clearly, and I went back to work a week later, ready to be back. I experienced the same pre-op that I had before, but waking up in the recovery room unable to speak but fully understanding all that was happening around me and to me….(what I was experiencing was apraxia, which I define below)…and the nurse(s) wondering aloud what was wrong with me, they had never seen someone come out of brain surgery like this…and my people pleasing nature coming out for sure…me wondering how to communicate to them about my pain needs…wondering all the time if this was permanent…the doctor checking in because the nurses apparently called him…me trying to communicate with my eyes the helplessness I felt…and sobbing when I couldn’t communicate with the doctor. That’s the last time I cried in the hospital. I guess I flipped a switch. Moving into survival mode.

I was reading back through my “notes” before the MRI. Iphones have these things called “notes” that are an app where you can type directly into it. At the end of May/beginning of June this was my preferred method of conversing because it was still hard for me to speak at that time. Somehow it was easier for me to order the words if I typed them. In the midst of “notes” of song lyrics, movies to watch, quotes from speakers at the UMCMA conference, benedictions/prayers that I had to type up to say them, notes from our staff retreat in NYC, was this hidden gem. May 24, 2013, exactly two weeks after the surgery, I typed, “The quickness with which I speak comes back?” I imagine this was thrust in the face of Mike at some point, as I gathered the courage for days to ask that question.

I ended the work day with a meeting of a newly formed clergywomen’s covenant group. I could barely articulate to them the events of the day. They had seen the facebook post so they knew the results of the MRI. A fellow clergywoman, I had not met before today, at the end of our conversation, called me a beautiful person and I answered honestly that I don’t feel that way now. I repeated my answer, but I was unable to add or articulate the words that would disguise my bruised soul. So it was left hanging out there.

So on my way I called Mike debating if I should go home or back to Wesley before freshman small group. And he said that he had been feeling the same way. He didn’t understand it either. He said he had walked around the neighborhood with the kids and that made him feel better, to get out the excess energy. And he encouraged me to do a blog, because that’s the way I process. Why are we not feeling relief/excitement/joy at the good news of the MRI results? I don’t know. Maybe we never turned off survival mode. Maybe during “recovery” we never quite recovered. Maybe it takes time. My mom texted me tonight, “Ask Jesus to show you where he was” in the post-op. And that may lead to an entirely different blog post.

I’m glad for the friend who asked the question. Because she, without her knowing, set me off on a journey towards healing….

*** Apraxia (from Greek praxis, an act, work, or deed[1]) is characterized by loss of the ability to execute or carry out learned purposeful movements,[2] despite having the desire and the physical ability to perform the movements. It is a disorder of motor planning, which may be acquired or developmental, but is not caused by incoordination, sensory loss, or failure to comprehend simple commands (which can be tested by asking the person to recognize the correct movement from a series). It is caused by damage to specific areas of the cerebrum.

Posted in Death, Dreams, Future, God, Health, Impossible, Romans 4, Tired, Trust, Tumor

A little too much…

I don’t know why but it’s been a hard couple of days in thinking about brain tumor land. Don’t worry nothing new – no change. This sounds so morbid, but on Saturday night I dreamed that I died – literally – and then went to heaven. Let’s just say in my dream, heaven was not what I expected. The pros – my three cats greeted me at the entrance. Who knows what that means…could be because two weeks ago I found out that the oldest cat Pug is in the beginning stages of kidney and renal failure or then again it could be because they greet me at the door all the time and any time they have thrown up a hair ball somewhere or made another mess Mike likes to threaten them. =0)

I don’t remember a ton about the dream or how things were laid out or anything and I am not at all saying that this is what it’s like or any sort of premonition at all (is that enough disclaimers there?), but I spent the dream waiting for people to get there. Now I know that heaven is heaven and duh we’re not going to be miserable sitting around swinging our legs back and forth waiting for the rest of our family to get there, but that was the dream. It sucked. Royally.

I didn’t really tell anyone about it until yesterday primarily because I had been thinking about it a lot and I know that if I say something out loud or if I write about it, in some crazy way, that helps me to process and make sense of things.

And then brain tumor stuff has just been popping up everywhere – wonderful friends checking in, a minister on the conference prayer list that we should be praying for, on everyone’s cancer statuses yesterday which was great, me still trying to get hair gel to smooth down the little hairs from the scar that are now long enough to look a little ridiculous, and the sometimes headaches and tingling that I often ignore but sometimes in one of these moods, wonder about. It is so stinking frustrating sometimes. On Sunday at the South Carolina delegation meeting we listened to a presentation on Benefits and Pension for close to two hours hearing about possible changes at the upcoming General Conference. When talking about life insurance and death benefits and spouses and pensions and insurance and disability for that long there is a large part of me that wants to just think of this as a tiny bump in the road and things are going to be fine and I’ll make it to the mandatory retirement age of 70. It could happen. I know that it could. And there’s another part of me that wants to figure out ways to provide and care for my family no matter what will happen and looking at all scenarios have as much of a plan as I can.

For the most part, I don’t even like bringing it up because I know if I talk to Josh about it while playing basketball or Mike about it when we get home from Wesley or to whoever in some ways, especially for my family, it stresses them out too. They don’t know what’s going to happen any more than I do.

It’s scary. And there’s still a part of me that is angry and frustrated that this is even part of our lives. There’s enough to worry about with kids and bills and living out one’s calling and vocational discernment to actually deal with all of this.

So that’s where I am. Saying to God it may just be a little too much and that I’m a little tired of battling in so many areas.

Are pastors “supposed” to say that? Who knows. But if I don’t keep it real and have my integrity than to me I’m nothing but a hypocrite and someone in denial.

The irony of this is that last night I preached during our sermon series on the book of Romans about God making impossible things possible. We were specifically looking at Romans 4 where it talks about Abraham and his faith. We then had some time of silence at the end where we could have a chance to think about some things that we would see or do or figure out or try or find if only we didn’t have doubts or fears or even sometimes “reality” holding us back. What would you do with your life if you could do absolutely anything and money nor education nor baggage nor what people would think were obstacles for you? What are some of your hopes and dreams for your family, your friends, your community, your church, your work? If we threw all of the “buts” out the window what would we grasp hold of and pursue?

What are the things that get in the way of that? What are some things we need to let go of in order to move forward and try to make our dreams into a reality?

These aren’t questions that you wrestle with for five minutes and than you’re good to go. Or maybe that works for you. I find that I have to intentionally pray and meditate and think and actually force myself to look and open my eyes and heart to the possibilities while telling my fears and frustration and failures to “shut it” for a few minutes so that I can see the light.

Because sometimes it feels like it’s a little too much. Actually sometimes it feels like it’s a lot too much. As excited as I was to move from 3 months to 6 months in the amount of MRI checks, there is a scared part of me that is nervous about that. What if that’s 3 months of something growing and us not doing something about it? I know that my doctors would never have let me go longer if I wasn’t ready to, but that’s what fears do…they somehow make it where even the things you want, you’re nervous about because you’re still feeling a way into a “new normal” or any kind of normal for that matter.

Then you go down the list of all of the people that have it so much worse than you and that things could be a million times more terrible….but that’s not comforting. I don’t want anyone to be going through anything like tumors or cancer or sickness and uncertainty of any kind. Does it mean that you’re thankful for all that God has done, is doing and will do? Sure. I have no idea what I would do without that. I need those times between me and God where I can say what I need to say and cry out and wrestle and not be censored by anyone.

We need time to sit and rest and be with God. We need time to let our fears and frustrations and disillusionment and grief go so that we can let new life spring forth not just in the midst of the weeds randomly despite everything, but in ways that we nurture and water and grow.

So I guess in this rambling post that may not be for anyone except for me writing and figuring this out – I need to find and make time to discern and be open to what God would have me do in this time and place, what God is calling my family to do, our community to do, Wesley to do. I need to trust that it’s okay that sometimes it’s a little too much and it can be heartbreaking and angering and discouraging and annoying. I need to realize that God is bigger than all of this – crazy dreams, long talks on benefits and pensions, things in my life playing up to my fears – and that God is with me and walking with me and comforting me each step of the way even when I want to bless the world and God out sometimes.

Posted in Community, Faith, God's Providence, Grace, Healing, Health, Thankful, Theodicy, Tumor

Update on that Spongy thing inside my Noggin’

  I am completely slacking on blogs right now which breaks all the rules of regular blogging.  Sorry about that!  I’ll catch up soon.  Right now I’m at a great conference and have tried to be as fully invested in it as possible, but there has been a part of me distracted.  Some of you that began following this blog when I started writing after finding out that I had a brain tumor and you walked with me through that journey and the recovery and even though the blog has become a little bit something different, I do still want to give you an update on that good ole brain of mine because I believe that this community of support has been invaluable and really a holy presence in my life and I can’t imagine my life without your prayer and support.

I have been doing 3 month MRI and neurosurgeon check ups over the past year.  For the most part, I try to keep moving with life and I give a sincere and concerted effort not to let these worries and fears rule over my life.  Then comes the time when I get the envelope from Carolina Spine and Neurosurgery in the mail with all of my appointment times and as Mike and I see it, I can feel the background stress and tension in me and those I love.  The unknown is so completely…humbling…scary…difficult.  There’s so much to unpack there but that would be an incredibly long blog and mine are already probably way too long.

Last week I went to my (I don’t really care to remember how many its been now) whatevereth MRI and the techs were asking how I was doing and what I was there for, all that good stuff and I told them my hope that maybe this was the visit where I could be increased to every 6 months or every year instead of every 3 months.

On Monday I met with the neurosurgeon and he said that it was the radiologist’s opinion that the part of the tumor still up there in brain/motor cortex land may have grown slightly but that it was very slight.  His opinion was that he didn’t see a change and disagreed with the radiologist.  We then had a lovely back and forth where I looked at the comparison MRI’s myself and tried to understand and that I got a chance to ask some hard questions.  Since Mike was not with me, I could ask some of the things that I want to know and would like to understand but that I don’t want to alarm, worry or hurt someone else by them hearing the questions or the answers.  Does that make sense?

So even though it was not my most favorite news in the world, I was okay.  My amazing doctor said he was going to take the tumor to the tumor board for them to decide if it had grown or not.  I called Mike and my parents on the way home and was okay.

Primarily I was okay because I was leaving the next morning for a conference and I just didn’t have the emotional energy or the whatever to process it.

Yesterday afternoon while I was in a workshop, the doctor left a message and when I hear him say his name I immediately get a little freaked out on the inside even though he’s a fabulous doctor – like fabulous – but it’s just anxiety producing.  But then he says an AMAZING thing – the tumor board doesn’t see any change.  AND because this place on my lovely brain has stayed consistent this year, I get to stretch the time between MRI’s to 6 months!!!!!!!!!!!!!  (I could probably mash exclamation points for a while on that one.)  That may seem like a little thing, but it’s such an act of hope and grace and peace to me.

And though I didn’t shed a tear on Monday, I couldn’t stop crying off and on yesterday evening.  Is that crazy?  The bad news – I take it and I’m like let’s do this thing.  The good news – I’m a basketcase.  In talking with a dear friend and colleague about this last night I told her as I was trying to process and express my layers of feelings that I really needed to blog about this.  For some odd, crazy reason this is how I started this journey – blogging.  And it has been such a healing and cathartic piece or even peace for me.  There’s something about putting it out there in writing and narrative that makes it something that I feel a little more grounded in.  I guess we each have our mediums – whether it’s walking outside or making pottery or playing baseball or journaling.  And I am thankful for this one.

In the midst of this I know that there are those walking incredibly hard and deep and heartbreaking journeys right now.  I think of the family members that are living this reality right now and the friends and loved ones who have faced challenges that I know not of.  Please do lift up in prayer those who are in the midst of the struggle of the unknown and in this thin place where anger and fear and sadness and grief and life and death and joy and pain are so close to the surface at times.  Each of us walks this journey at times.

And we’re not alone.

I have seen Christ in the colleagues that I’ve shared with here and that continue to uplift and inspire and challenge and hold me accountable.  I have seen Christ in my family who continue to battle for me.  I have seen Christ in the countless people that continue to tell me they’re praying for me or those that just give me space to be…and to feel…and to just cry or laugh or talk about it or not talk about it.  I have seen Christ when I’m by myself and I am vulnerable and just laid bare as a child of God.  Although there is no doubt that I would not have chosen for this piece of the puzzle of life, I have felt Christ’s Spirit and promise more tangibly and have felt the Body of Christ more profoundly and genuine than I have felt in my life.

I am grateful for a community of people that I can keep it real with on the sad days and the angry days and the joyous days and the rock and roll days.  I am grateful for a Savior who continues to be that Great Redeemer and Strong Protector and just that Amazing Grace who support us and girds us up in mighty, mighty ways.

So that’s my brain.

And one of the awesome things – 6 MONTHS!!!!!

Grace and peace to all of you.  I am gratefu for you all.