LOVE – Songs of my Soul for Now

In an hour I go to the hospital for my second brain surgery and it feels super surreal to write that.  I wanted to post a quick blog before I go to say thank you to everyone who is praying and who has been supporting us.  We can feel your love and the community surrounding us!

I spent this past week with 30+ students from Gator Wesley touring around the state of Florida doing our Spring Tour – singing, dancing, rocking out, reading scripture and so much more.  There’s a song that they sing in one of the sets (and I love the mash up that they do) called “Set a Fire” by United Pursuit Band and one of the lines says, “There’s no place I’d rather be…but here in Your love…”  I’ve felt that from each of you.

Campus ministry is this crazy special place where things intersect – struggles, fears, hopes, dreams, silly Vine videos, lots of laughter, and experiences that both challenge and inspire. The students this week have inspired the heck out of me.  I’ve been ministered to in their music and their passion and their faith, and even more than that in their zest for life!  There weren’t many stops during this tour where I didn’t feel moved in some way and though I couldn’t figure out how to share that with them without becoming a blubbering hot mess, I want to let them know how special this week was for me.  Even the trampolines.  And the cold water of the spring when knocked off a raft.

Two of the songs that they’ve been singing are two favorites of mine that I’ve been holding dear over the past few weeks.  They didn’t know that when they picked the songs how much they have been resonating with me and yet again, I know that God is weaving all of this together in mighty ways.  The first is Meredith Andrews’ “Not for a Moment.”

http://www.youtube.com/watch?v=qoh26pC2RT8

And the second is by an amazing band that we hosted here at Gator Wesley called Bellarive.  It’s their song, “Taste of Eternity.”

http://www.youtube.com/watch?v=-uAqdtzo4F8

These have been the songs of my heart.  Worship taps into a place that breaks down the barriers that we place.  It digs in between the walls that we’ve built to protect ourselves and the layers of stress and muck that this world provides.  May the scales on our hearts and our eyes be removed that we may see God more clearly and know God more fully, as God draws us to God’s self.  I know that no matter what happens today, I know that I am God’s and God is ever in the midst working things together for good.

Y’all have humbled me speechless with all of your texts, facebook messages, tweets, and cards and I hope that each of you feels the love, hugs, fist pumps, and high fives that we have for you!  Thanks for being on this journey with me.

Much love!

Cheers to a new haircut!

Grace and Peace,

Narcie

The Anger Stage

So it’s there.  A little bit after the parental units, but nonetheless, the anger stage is in the house.  I, like most of you, know about the stages of grief and it’s almost worse that I know this and realize this and can clinically say, why of course, Narcie Jeter, what you are experiencing is a quite substantial dose of the anger and sadness stages of grief.

Lord knows why it took me so long and why I went into survival, defuse the situation, and keep bouncing along mode except for the fact that I just really don’t want to deal with this.  I really don’t want to think about surgery again.  I really don’t want to show the kids the scar from the last time and let them know this is all going to be okay.  I really don’t want to feel so freaking ticked off and frustrated and distracted and weepy.  Weepy.  And not in a nice, cute crying way, but watching old episodes of Dawson’s Creek and crying like a nutcase.

I don’t really know how to make this feeling go away so besides the Dawson’s Creek marathon which is strangely always comforting (nutcase, I told you), I’m trying to blog it out.  Maybe if I articulate whatever this is…since I don’t really have a punching bag and I probably shouldn’t throw things against the wall so late at night.

I don’t actually know what I want.

I don’t know if there’s an answer.

I don’t even know if there’s a question.

Things I know:  I love my family.  I trust God.  I know there are many, many people praying.  I appreciate that greatly.  I love what I do – all of it – silly, serious, and in between.  I am tired.  I am worried.  I am scared.  I am loved and cherished by an amazing man who is more than I ever deserve or imagined.  I have done this before and I know all will be fine and it’s a great doctor and facility.  I can’t decide if this is a big deal or not a big deal or if it’s just normal, which is weird and not quite right.  I’m already wondering about the next surgery or what will happen…  I have the two silliest, sweetest, most unique and precious and precocious children imaginable and I swing between the hope that they may never know anything about this because I wish I could control things and realizing that this isn’t just my story but our story.  I realize that there are a heck of a lot of people dealing with things more awful and challenging and I sometimes feel whiny and weak for even articulating this.

And yet.  When I start typing and I stop feeling the waves of anger for a bit and I stop crying along to “I Don’t Wanna Wait” like a sad sack, I know that God is carrying me and holding me each step of the way, which ironically in some ways makes me cry more.  And for the record, I’m not writing that as a pastor and I don’t care a hill of beans if anyone reads this, but it’s just good to feel and know that.  Even as silly as that may seem to some.

Thanks for being on this journey.  Thanks for praying.  Even if I don’t always answer the emails, comments, facebooks, fast enough or at all, know that I appreciate them and I read them.  They help that “held” feeling when it’s denial, anger, sadness, and yuck city.  Love you all.  Especially my crazy WNWers that would let me share my Dawson’s obsession.  And if any of you reading this make fun of me for my silly, trashy, and immature tv watching….you’re going to get it.  (I kid.  Mostly.)

***I also realize that I write plenty of run-on, stream of consciousness sentences, and I, nor the English major inside of me, actually cares.  So ha!

Surgery Date

It’s official.

Surgery will be on May 10th and pre-op on May 3rd.

Thanks for y’all’s prayers, your comments on the blog, your comments on facebook and all of the messages!  Much love to each of you.

All of us greatly appreciate it.  As I know more, I’ll let you know.  As I process more, I’ll try to post.  The in between time makes this a bit surreal but I know that God is with us.  I know there are quotes out there like “Never trust quotes posted on the internet” – Abraham Lincoln, and I don’t know if this one is completely true or not, but as my uncle Carlee would quote John Wesley saying, “The best of all is, God is with us.”

Here We Go Again.

In December I had an appointment with my neurosurgeon in Charlotte and since it was the last day of classes here and was a 7 hour drive, I decided to cancel it and find a neurosurgeon here in Gainesville.  I didn’t make this decision lightly and I looked up all sorts of things about the awesome program here and I asked around to a number of people.  I saw my new neurosurgeon for the first time on Valentine’s Day (ha!).  He ordered an MRI to be done the Monday after our spring break trip to Costa Rica (March 11th).  On Tuesday, March 19th while Mike and I ate lunch with Evy, the nurse called and said that the doctor recommended surgery.  She then set an appointment for me to talk to him about this for today, March 28th.

Mike and I of course called our parents.  I didn’t want to say anything about this before we knew anything, but needless to say, we’ve been pretty distracted this past week and because I try to be a reasonably transparent person, it was hard to preach on Palm Sunday or for either of us to function without a twinge of something always in the background.  My parents came to visit last night so that Mom could go with us to the appointment and Dad being the great MacMac that he is, could hang out with the kids this morning since they’re on spring break.

Three years have passed since the first surgery.  To review, my doctor in Charlotte removed what he could of the tumor but left a strip near the motor cortex of the brain.  The type of tumor I have is an oligodendroglioma and very thankfully it’s a grade II (low grade).  At the time, research and common practice said that you take a watch and wait perspective and treat symptoms.  Now, research says that you resect as much as you can of the tumor so that it does not increase in grade.  They will use computer guidance to make sure that they are as precise as possible in removing as much as they can of the tumor that remains.  All of the risks associated with brain surgery are still at play here (duh.), but even more than that, because this is on my motor cortex, there could be temporary weakness in my right arm, hand and face.  As he said, scenario A is much like the first surgery – I come in on Friday and have surgery, I go home on Sunday, and I go back to work on Wednesday (this is also because I’m a crazy person that likes to work – yes, I know).  Scenario B is I go into surgery on Friday, hopefully still leave on Sunday depending on some things, go back to work in two weeks, and then possibly do physical therapy and rehab for a month.  If removing as much of the tumor as possible gives me a higher means of this not turning into something worse, I’m willing to risk either scenario.  The doctor’s suggestion is to take the “earliest elective opportunity” to do the surgery.

I’ve decided to do the surgery in May – most likely either May 10th or May 17th.  What does this mean for our family?  The kids were 1 and just turning 3 when the first surgery happened so they thought Mommy was on a trip of some sort.  They’re 4 and 5 now so we’ll be handling things a little differently.  They’ll still be in school so that should help.  I am blessed with an incredible extended family….and in essence I consider y’all a part of that as well.  Mike has been an absolute rock in all of this and I can’t begin to thank him for living out the weight of our vows every day.  The irony of asking him today – do you want to have the surgery around our 11th anniversary (May 11th) or around your 34th birthday (May 16th)?  I know that God is with us and will provide – whether that’s within the surgery, recovery, sanity, financially or us trying to squeeze in two more days at Disney before June 6th when our passes expire =0).  I’m also looking at the beginning of May so that I can be present for all of the end of semester fun, but before things ramp back up for summer.  I didn’t plan on a surgery during my first year here in Gainesville, but I know that there’s an amazing staff, student leaders and board here and we’ll be good to go.  As always, I’m pretty open with questions – so if you have one, ask me.  I also tend to use the blog to process and answer things as I can. (Don’t be afraid.  I’m not “broken” or an invalid, and I’m still the same person.  Human as can be, but trying to figure it out….so ask, don’t just wonder.)

As soon as I get the actual date of the surgery, I’ll definitely post it and I will hugely appreciate all of your prayers!

So all that to say, I don’t have any big actual blog “reflection” tonight.  We just completed the Maundy Thursday service and I’m pretty spent at this point, which I guess is just about right with Good Friday coming tomorrow.  I am increasingly struck this Easter season that there’s no fast forward button between Palm Sunday with the Hosannas and Easter.  I also appreciated a song that my parent’s sent me when I told them this last week.  It’s Tenth Avenue North’s “Worn.”  Hope that during this Holy Week we are reminded of our redemption, peace and hope in Christ in the midst of the sometimes dark despair.

For those visual people out there that want to pray over an image….rock on.

Miraculous

I got a phone call on Friday after a long week of good, fun, tiring and yet rewarding work.  It was not a number that I or my phone recognized and I’m usually tempted to let those go to voice mail since you never know if it’s a survey or a wrong number or who knows.  But for once, I didn’t.  It was a student who had something to give me.  A pastor of hers knew that she was a student at Winthrop so she wanted to pass something along to me.  That’s all she really said.  So I had no idea what this could be.

When she stopped by Wesley, she handed me a beautifully colored picture.  I love rainbows and bright colorful things so I liked the picture instantly.  She then said that it was a Mandala and as the picture says on the back – it’s a contemplative practice.  Rev. Annie Edwards who I don’t know, created this for me during my brain surgery in 2010.  She started it at 11:45 am and finished it at 1:30 pm – truly roughly the time of my surgery.  As she writes on the back, “This was done for you during your surgery, with love and compassion.  Your Dad is my friend.”

It’s beautiful and something I’ll treasure.  As are the prayer shawls, books, pictures, everything that has been passed along to me that I can share with others.

I am admittedly sometimes flippant about the surgery and I in some ways am pretty successful at brushing it off.  In my day to day life – I don’t walk around with a sign around my neck that mentions it.  When I get an invitation to the survivor’s dinner for Relay for Life, I am more often than not – surprised.  But I think, as is often the case with the things that we are flippant about, most of my bravado comes from a place that is truly grateful and humbled by the outpouring of love and support – so much so that I don’t know if I can express how much it means or how much even when it’s not at the forefront of my mind – that I depend and rely on the prayers and the Spirit of mercy and grace that I feel ever present.

It’s not something that I’m afraid to talk about, but it is something that’s deeply personal.  So yes, I keep it on the About Me part of the blog – though I’ve debated that – and it becomes a part of the fabric of my life.  Not definitive of all of who I am, but yes a defining moment….among many.

One of the things that struck me on Friday was yes, the picture, but also what the girl from Winthrop who I’ve never met, said to me as she delivered.  She talked about what a miracle it is.  I asked her what she meant and she said, “You.  It’s miraculous.”  No, this is not a big head moment.  I’m not slapping myself on the back. But part of me did want to slap my forehead at the “Doh!” moment.  I don’t know about you but I think it’s easier for me to see the miracles around me – my students, Spring, healing of friends and family, the birth of a child – but it’s harder to see ourselves in that way.  I don’t know if we can even wrap our minds around that.  But we can sure as heck be grateful.  And hugely grateful at that.  For the prayers of so many, for the love that encircles us, and for the hope of the resurrection.

During this Holy Week, my hope is that I not rush straight to the resurrection but that I take time to attend to the twists and turns between Palm Sunday to Maundy Thursday and that I’m attentive to all that is the darkness and despair of Good Friday because we all have felt and walked and witnessed times like that.  And that when I hear the Good News of the resurrection on Easter morning that I feel both the impossibility and the miraculous and the ever present and real hope and promise that it offers.  May we know and see the miracles in each of our lives, our communities and the world around us and may we claim and treasure them!

 

**  Dad’s reflection on this time period – Holy Saturday Redux - http://wtmcclendon.wordpress.com/2010/06/16/holy-saturday-redux/  I think about it around this time of year…and I appreciate his honesty.

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.

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.

Would life change for you?

I know I haven’t posted much about the tumor lately and to be honest I haven’t wanted to.  This is not because I haven’t been thinking about it but the opposite.  I think this summer when everything happened, I didn’t really process or take the time to think about everything because it was so fast and then it was the school year and semester and you know how crazy that is.  With a little bit of a break over the past couple of weeks, it’s been tough.  I have a friend who says she only blogs on the bad days, but for some reason, I don’t.  I’m not saying that I haven’t had challenging days and hard days and have not blogged, but when I’m really wrestling with something, I just don’t always want to articulate or “sermonize” it.

After Christmas I did my latest MRI and the next day went and saw the neurosurgeon.  He said there was no change, so the little line of tumor on the motor cortex hasn’t grown and for that I’m thankful.  He didn’t really say anything new, but for some reason I took it more to heart.  I asked him whether I should get off of the seizure medicine or not and he said that was up to the neurologist but he also warned that it is more likely that I will have another symptom whether seizure or otherwise before an MRI would actually pick up a change.  Then he said that it’s not a question of if the tumor will come back, but when.

Now, I know that he’s said this before and I know that this type usually recurs but for some reason it hit me worse this time.  I think it’s because there’s a huge part of me and a sense from a lot of the people around me that everything’s fine now and back to normal and that I have to lead my life as I’ve always lived it.  And I do really want to do that.  It’s hard to tell if I should just go about business as usual or if my life really has changed completely.

I am a huge fan of wikipedia.  That may be completely against my English teacher self and I know it’s not always right or accurate but if you want something quick and consise – especially when I’m trying to figure out history during the Tudors or looking up actors or actresses – it’s a great site.  Did you know that I didn’t even look up “oligodendrogioma” which is the tumor that I had/still have a piece of?  Didn’t even think about it in the rush of the summer and semester.  The diagnosis and the treatment and much of the article follows exactly what we’ve been doing and I didn’t even think to look there.

Now part of me is glad that I didn’t.  I didn’t know that the median survival times for a grade 2 is 11.7 years or for a grade 3 is 3.5 years.  That’s a median I know and as the doctor said I could still live to be 80.  But how does knowing that information affect my life?

Not that we ever know specifics or a particular time table but if you knew you had say 5, 10, 15, 20, 30 years to live, how would that affect how you live your life?  Would it?  Would you change what you eat or how much you exercise or if you take your vitamins?  Would you spend more time with friends and family and try to make more meaningful relationships?  Would you change careers or look at fulfilling your hearts desire in a different vocation?  Would you live your life differently?

I’m not talking about Tim McGraw’s, “Live Like You Were Dying” song and sky diving and rocky mountain climbing – love the song but that’s too cheesy of segue for even me to post.  I’m asking a real question.  How would you live your life differently?  Or would you?  Maybe it’s better just to keep on keeping on and keep fighting and do the best you can and not change anything.  Or maybe we should be living our abundant lives to the fullest every day regardless of any prognosis, time table, or outcome?

I don’t know.  I don’t quite know how I feel about this yet or if this changes anything.  I know that I believe that prayer is powerful.  I know that when I read that article or I read other materials about this tumor that it is miraculous that I have come away from this with very little deficits – not being able to remember names and numbness and tingling every now and then is significantly different than what could have happened.  I thank each of you and my community folks for this.  I know that God walks with those on the 3.7 year side as well as those that live to be 80 and that God’s mercy, love and grace is shown to each.  I know that we all have “stuff” to deal with and for each of us it can be a long and winding road.

When I think about New Year’s resolutions or I think about the future, I think very much of how we live our life.  How do we let our lives speak?  Would you live your life differently knowing…?”

Here are some quotes from the beloved Parker Palmer:

“Verbalizing is not the only way our lives speak, of course. They speak through

our actions and reactions, our intuitions and instincts, our feelings and bodily

states of being, perhaps more profoundly than through our words.”

“Our deepest calling is to grow into our own authentic self-hood, whether or not it conforms to some image of who we ought to be. As we do so, we will not only find the joy that every human being seeks–we will also find our path of authentic service in the world.”

“We need a coat with two pockets. In one pocket there is dust, and in the other pocket there is gold. We need a coat with two pockets to remind us who we are.”

“Humility is the only lens though which great things can be seen–and once we have seen them, humility is the only posture possible.”

“As a young man, I yearned for the day when, rooted in the experience that comes only with age, I could do my work fearlessly. But today, in my mid-sixties, I realize that I will feel fear from time to time for the rest of my life. I may never get rid of my fear. But . . . I can learn to walk into it and through it whenever it rises up . . . naming the inner force that triggers . . . fear . . . Naming our fears aloud . . . is the first step toward transcending them.”

No Negative is Positive

So that’s what the doctor said today.  No negative change is positive news.  Mike and I went to see Dr. Smith today and he showed us the scans.  I like to have visuals so I’m glad he showed them to us.  There’s still a bright part that could be scar tissue, swelling or still some of the tumor – but as Mike said – there’s no new players in the band.  Ie. there are no new negative things.  So that is good!

Mike started asking a lot of questions in typical deep voice, serious form and Dr. Smith responded, “Right…you’re the questions guy.”  That was funny.  He asked why the image still looked like that with like a hole there and he said that I would never have another normal looking brain MRI again.  The brain doesn’t grow back and the tumor was in part of the brain matter so therefore some of it is gone.  Very little though.  Ridiculously I was taking it very personally that Mike was talking about my brain and part of it not being there even though I know I’m still me and I’m okay.  Anyway, the funniest thing of the afternoon – Mike says well we only use a small percentage of our brains anyway, and Dr. Smith says something along the lines of well she didn’t really need that part anyway.  Yay!

Mike is excited by all of this news!  No negative change is a positive report.  We’ll keep doing MRI’s every 3 months for awhile and we’ll see what happens.  Dad on the phone earlier asked what could have made the news perfect?  Well that my brain is normal of course.  That it’s not always going to look like that on an MRI.  That there’s no bright smudgy line that’s still there.

But hey – I’ll take “No negative is positive” any day of the week.  This paired with some folks dropping off some paper towels as donations to Wesley – have made the day sunny again – and even in my un-air conditioned building – that is good.

It’s been hopping

If I’m ever not blogging it’s because I’m swamped or maybe even more than I’d like to admit – I’m afraid to “voice” something.  A friend of mine who I love commented on my facebook a few weeks ago when she heard about the campus ministry funding cut – something along the lines of “feeling like Job lately?”

Don’t want to go there because I’m not asking for any other challenges headed this way, but after going to Presbyterian’s Ballantyne office for the MRI yesterday I returned to Wesley to find that our air conditioner has officially passed on to the other side.  When there’s an explosion and smoke and then the awesomely amazing Adams Services guy shows you wires burned in two and half the thing on the inside is black and no fans are moving – that’s not a good sign.

It’s an even worse feeling when he has to bring in the “big guns,” ie. the owner of the company to give me the bad news that it’s good and gone and they can’t rig it up any other way.  The thing worked hard for us so I am thankful for that.  I’m also thankful that it’s not too hot so far today and no one tell the Wesley students that there won’t be a/c tonight - we’ll make do and I want them to still come!

I couldn’t sleep for a long time last night trying to figure out where in the world we’re going to get $8,000-$11,000 for an air conditioner and even more importantly for the winter – the heat pump so that it’s not just straight up gas heat.  I looked up grants and wow that us.gov sight is a monstrosity of crazy info.  I know that somehow, someway we’ll come up with the money to make this happen.  Somehow we always do and I know that God and the people that support this ministry are faithful.

For the past two days Mike has been recording with Tom Conlon in the worship/fellowship room at Wesley.  Many have said this room’s acoustics are like magic and even without AC, the magic room came through.  In walking up to the building this morning and rolling up the trash cans and recycle bins I began to ask myself why do I care about this building so much?  Why do I care about this space?  In the sceme of things what does it really matter?  When there’s bills to pay and things to repair – what stops us from just chucking it all?

My answer is both simple and sincere.  There is magic that happens here.  Tears are rolling down my face just thinking about it which makes me either really sappy or beyond emotional.  This is not a Harry Potter kind of magic but one that happens when community is formed and shaped and grows and changes and is found.  This building is so much more than just a building to me because both as a student and as a campus minister I have witnessed the powerful things that have happened here.  We have shared much laughter and some tears, we have shared in worship and I have seen someone’s call to ministry unfold at an Ash Wednesday service, we have cooked dinner as family and have hung out as friends.  This is part of what the students mean when they talk about Wesley being a home away from home. 

Yesterday after getting back from the MRI I talked to a student who has been coming here for 2 and a half years to use the prayer room several times a week.  He’s only been to one Wesley night but he comes and uses the prayer room as often as he can.  Yesterday he stopped me in the hall and said thank you for us providing this space for him and for people just to come and be.

I think about the student groups and the gospel choirs and the other campus ministries that use this place and how this building and the things that it stands for and witnesses to is greater than we know.  Yes it is just a building – with windows that aren’t the greatest, an exterior paint job that needs some help, and a vacant lot that is probably one of the worst parking lots imaginable – but it is ours and it is home to both the sacred and the sacrilege – the holy and the profane – the mysterious divine and the completely human.

So we’re going to somehow make this work.  Somehow.  By the grace of God and a lot of prayer and hopefully some creative solutions.

Today at 1:15 pm we’ll go to the neurologist and see what’s up.  Do I think a tumor has grown back?  Nope.  Was I very tempted to ask the MRI folks yesterday?  Heck yes.  Am I apprehensive?  Sure.

Ann Curry tweeted this this morning – “The most beautiful people we have known are those who have known defeat, known suffering, known struggle, known loss, and have found their way out of the depths.  These persons have an appreciation, a sensitivity, and an understanding of life that fills them with compassion, gentleness, and a deep loving concern.  Beautiful people do not just happen.” – Elizabeth Kubler Ross

The only way I see this beauty is through the eyes of the community that surrounds us.  We get to the other side by the grace of God, the One who sustains us, and those that God has joined with us on this journey.  As I wait and hear what’s up today and as I begin trying to figure out that ever lovely money question for air conditioners and programming and all that Wesley jazz – I am thankful for the arms that cradle each of us in both the good and the bad, the light and the dark, the joy and the loss.

I’ll leave you with a song that Tom Conlon played at Wesley a few weeks ago.  Love this song.  It’s called “Leaning”…

Here’s his “Sacred Things”