hope + a new beginning


In the early morning dark, all sleeping in one room at the Ronald McDonald house, we woke Phoebe up to prepare for her procedure.  Brandon had already run out to get starbucks for he and I, and then we gave her the sweater that I had knit per her request (and her pick of yarn).  We also gave her the unicorn as a gift, for her bravery, discipline, and perseverance in this three month intensive part of her journey.  So, wrapped up in that knitted love and comfort, and snuggling “Rosie,” she went back into her procedure.  I was with her until she was just going to sleep, and it makes me cry every time to walk away from her and leave her there, but it was a small measure of comfort to see her snuggled up in that bright yarn and snuggling her new friend.

We have heard back about the pathology report from Phoebe’s recent endoscopy.  Her intestines are showing full healing, healthy whole villi, and little to no active celiac damage.  You guys!!!  We are FLOORED.  We are in shock, disbelief.  It feels like a miracle.  You guys have prayed us through, you have prayed for our girl and God has answered!

Now, we aren’t totally through the woods yet.  Her blood work showed still elevated levels of inflammation, which is a bit perplexing.  I’ve heard different opinions about what this can mean, and I’m still waiting on a call back from the Winston Salem doctor about having another pathologist look over her biopsy results.  So I’ve been sitting on the results for a few days waiting, but I know so many of you are waiting and asking and wanting to know the results and I didn’t want to keep you waiting.  Especially on, what we feel, is still SUCH good news!

Is it all over?  Is the worst behind us?  I don’t know.  We still have a lot of work before us in helping Phoebe grow and in encouraging her to eat more/healthfully.  We plan to do some work with a naturopath going forward.  She will have quarterly blood checks and regular weight/height checks so we can monitor progress.  We believe God has been speaking to us about this season of intense difficulty coming to an end, but my heart is so tender and fearful to hope.  It’s easier to brace for the next wave of the trial sometimes than it is to rest in HOPE and faith.  So you can pray for that for Brandon and I.  Of course, we know that we aren’t fully out of the woods yet, it is too soon, but we do hope that from here we will see our girl flourish.

To those of you who have prayed for this miracle: how can we ever thank you enough?  You have prayed life and healing over our girl and we believe we are seeing these shocking results because of your prayers!  God promises that our prayers are effective and powerful (James 5:16) and that they can make an actual difference in things like this.  God cares about healing and bringing wholeness and restoration, as we saw Jesus constantly healing all the sick ones that He came in contact with, and as we are told that this was part of His earthly mission (Luke 4:18).  It is still part of His mission: taking back the lost ground, healing the broken parts, mending the ruined world, glorifying Himself and making His power and might known in our midst.

To those of you who have donated funds so that we can afford these treatments for Phoebe and so that we can continue her medical testing, how can we ever thank you enough?  You have been a huge part of this process and this result.  You have provided relief and help in a very tangible way to our family.  You have, more importantly, just overwhelmed our hearts with encouragement, with the sense that you are behind us, for us, and with us.  We know one day we will be able to bless others financially as you have blessed us, and we eagerly look forward to returning the blessing.  We will do so in the small ways that we can now.

We will keep everyone posted as we know more about Phoebe and as we continue on this journey.  For now Phoebe’s diet will change slowly and with a different approach than anything we have tried thus far.  She is already so pleased just to have her beloved cereal, and slowly we will phase in other things, but will also phase out things we don’t believe she tolerates well.  I will still need to make most of her food from scratch and from carefully chosen sources, so there is still a bit of work ahead for me in trail + error.

As my mother-in-law gently but firmly encouraged me last night, we will rest in this healing.  That this is the beginning, a new beginning, and we are thankful to our Faithful God and to you!


She’s our girl


Well, it’s time.  I’ve been resisting this for some time, praying over it for a long time, talking it over with our church family, with our small group family, seeking wisdom and checking motives.  I’ve long since moved past resistance to acceptance, and then waiting for the right time, waiting for God’s time and for our move to a new home to be behind us.

This week Phoebe faces another endoscopy.  This will be her third, and I’m hopeful it could be her last.  She has finally finished the three-month dietary course we have been on and now we can take another look inside and see if she has improved.  Since her last endoscopy showed extreme and active celiac damage (as if she was still intaking gluten) after a year and a half on a very strict household-wide gluten-free diet (along with a gluten-free lifestyle in all other products we use), the doctors wanted her on an even more extreme elimination diet of no processed foods, nothing that comes through a facility of any sort.  Everything she eats has to be fresh fruit, vegetables, meats, some simple dairy sources, honey, olive oil, eggs, etc.  Being that she never eats meat or vegetables without gagging/vomiting, it has been quite a challenge to endure for three months.  She has been amazing–but it has brought her to tears many times.  This diet is for the sole purpose of proving whether or not she is super sensitive to even trace amounts of gluten allowed in gluten-free products (most labeled “gluten-free allow 20 parts per million, and certified GF products allow 5 ppm) and/or whether or not she is considered “refractory,” which means her body is not healing even on the strictest GF diet.

So what we are hoping and praying to see on this endoscopy is healthy, healed, whole villi waving around in her small intestine.  Would you pray for that alongside me?

A short time ago a group of strong men, the elders of our church, tenderhearted and gentle, gathered in a circle while Phoebe knelt on the floor in their midst, distracted with some coloring.  They held hands around her, some laid hands on Brandon and I kneeling beside her, some laid hands on her.  And we prayed.  They prayed.  They prayed over Brandon and I.  They prayed for healing for our girl.  They prayed boldly and asked for miraculous healing.  They prayed for protection over our marriage.  They prayed for financial provision.  We knelt and we received it, like being washed in a healing rain.

The thing about having a chronically ill child is that the impact of it happens on so many levels.  The emotions and mental anguish over a child don’t stay in a neat and tidy box, nothing really remains untouched by the life change at some point.  Everything is affected.  The emotional, mental, physical, spiritual, financial, marital impact of it all is continuous, overlapping and crashing into one another like waves on a tumultuous sea.  The weight of worry, the gnaw of fear, the spiritual battle for trust and faith and joy in the face of an uncertain future and so much helplessness–it wears on me, it wears on Brandon, it wears on us all, I’m sure.  This whole journey with Phoebe–it has changed me in a way that only grief, pain, suffering, and agony can.  Those of you who have walked through that dark valley–you know what I mean.

The thing about have a chronically ill child is that you go from just parenting to a heightened level of care-taking.  Everything could be a symptom, everything must be watched and monitored.  There really isn’t ever a time when your guard can be down and you can breathe easy, except in choosing to trust God no matter what the health outcome of your child may be.  The ramifications of having a chronically ill child are far-reaching.  The opportunities she misses out on.  The things I have to say “no” to for her that make her resentful with me, even while I fight for her life.  It is hard and costly and in so many ways, we have borne it out quietly because it feels to soon and too deep and too personal to share all that God has done and is doing in us through this.

We’ve tried for a long time to just shoulder the financial burden, feeling like if God has entrusted this disease to us, surely He will provide all we need to treat it.  I think the major and obvious oversight there was that we would be able to do that alone–without the help of the Body of Christ.  I feel like God has led us to a point where we must depend on others, on the body at large.  We simply have no other choice.  I believe He desires for us to see that YES He will sufficiently provide for all we need through the help of others.  The church is His chosen vehicle for caring for the brokenness in the world.  Christ is in the midst of her, in the midst of us, and the church is His hands and feet to the broken, hurting, sick, needy.  It is so much easier to be on the “giving” end of the spectrum, far more humbling and hard to be on the “receiving” end.  I find myself far more comfortable with being the one to reach out and help others than being the one asking for help.  I have questioned my motives, been in denial, etc. etc., but the reality remains: we have done what we can, we will continue to do what we can to just pay our bills and provide for what Phoebe needs.  But we can’t do it all, and we can’t do it alone anymore.

A sweet woman from our church was on the phone with me asking me about how we are doing with all of this financially and when I poured out the reality of our circumstances and how we feel like we’re drowning silently under the load, she so lovingly reminded me that many people love Phoebe and love us and want to help, but don’t know that we are in need in this way.  She reminded me that it is a gift and a privilege for those who get to give to our need, that they are blessed to do so and not to steal from them that awesome joy.

These words settled immediately in my soul:  She’s our girl.  Yours and mine.  Yes of course she belongs to Brandon and I in the most basic sense, God has entrusted her to us as her parents.  But so many of you who know Phoebe personally and also via what I share of her life on this blog, so many of you love her so.  So many of you know she is hilarious, quirky, vivacious, incredibly outgoing, creative, imaginative, bold, and sanguine.  She is a delight to know!  I think she makes everyone she is around feel like they are her favorite.  She has so much love in her heart it bursts and bubbles out over anyone and everyone she sees each day.  She is wonderful to know and to love, and so many of you adore her alongside Brandon and I.  So many of you have asked how you can help as we battle for life and health for her.  Of course we need prayer!  We are doing all we know to do for her physically.  There is only so much we can do to intervene medically and naturopathically before we realize that there is this great helplessness and dependence on the God who made her body and the God who alone can heal her internally.

So pray with us!  But also–if you are able, if you are willing, if you love our girl and want to invest in her life and in this health journey, then consider giving to us financially as well.  It feels so icky and weird to say it, and I want to make a ton of defensive statements about the medical bills stacked on my counter, the way we’re managing money, etc., but I don’t feel like I should.  I wouldn’t want you to do anything you don’t feel led to do, and I entrust our needs to our great God.

My sister so sweetly began a Go Fund Me for us a few weeks ago.  She has shared it with friends and family and some of you, MANY of you, have already donated there!  But many of you also contacted me to say that you didn’t want to donate through Go Fund Me since they take a percentage of the funds raised.  Some of you have wanted to just send us a personal check, which is wonderful and you can contact me for my address if that is what you would rather do.  I am also creating a fundraising link through You Caring as they have come recommended to me by other families who had health crises and raised funds through You Caring.  You Caring is safe and secure, and also 100% of funds raised go to the recipient.  If you would feel more comfortable giving in that way, the link is here:


Know that every little bit will go to Phoebe’s medical costs and treatments and is a HUGE and tangible way you can help us.  She’s our girl, isn’t she?

Thank you guys so much in advance for blessing us with your prayer, with your love for our family and our Phoebe girl especially.  Thank you for believing God for miracles for her.  Thank you for investing in her life, pursuing her health and wholeness.  Thank you for encouraging us!  I cannot tell you how speechless and humbled and awed we have been by the money that has already been raised.  I want to thank each one of you who have given.  It has brought me to tears many times.  So humbled, so awed.  I just look to the Lord and say, “You bless them, God!  You pour out your rich abundance on those who would so graciously give to us.  You bless them in ways we cannot possibly.  You return the generosity and heap it right back on their heads.”  What an awesome God we serve.  We can rest in Him.  He sees us.  He knows.  He ANSWERS.  I am floored by Him forever.  All praise and glory to Him forever!