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Author: Jon

Generous

A Jon Post

Last week the generosity of the Kingdom of God and its King was on full display.

Sunday, the 1st, I flew to the town Benjamin and his family live in. It’s only a 1 hour flight but it’s about a 14 hour drive and it would cost more in fuel to drive than the ticket on the airplane so I flew.

It started with the kindness of our friends Wayne and Tracey Greenwood organizing a place to stay and a vehicle I could use while I was there, all at no cost. I had planned to stay in as cheap a place as possible and use public transport but was able to stay in a house with a wonderful family and use a vehicle for the entire 5 days I was there.

Mozambique is notoriously difficult to get things like buildings/houses built so I had a tough task before me. I had 5 days to scout the building site, coordinate with SOMEONE/ANYONE about building a house and work out all the details (materials, payment, land permissions, etc.) that needed to be settled before a brick can be laid. Not a small assignment.

On a whim, the day before I left, Layne reached out on a local Facebook page, asking for contacts or references for a good construction company in the area. A local businessman’s wife saw the plea and forwarded us her husband’s phone number the next day. I called him up. He agreed to a meeting the morning I called and, over a cup of coffee, I explained what we wanted to do. His company does not do cheap work. As I showed him what I had hoped to build for Benjamin’s family, and told him our budget he grimaced and explained that it wasn’t even a third of what he would usually charge to build something like that.
Once again, the generosity of our King is immense.
He probed more into what we do and why, we agreed that we could reduce the size a bit but even with these changes, we didn’t have the money to do it. A couple minutes later… he looked at me, confirmed our budget one more time and said, “Jon, we’ll build it for you.” And that was that. For less than half of what he would usually ask, he promised to build a home for Benjamin and his family.

I spent the rest of the week going to Benjamin’s little rented house (a single room about two meters by two meters) and visiting with his family, going over details of the build, walking to the building site, (it’s about 2 kilometers from the end of a drivable road), and visiting with other former Casa Ahavá patients or their families.

Our King’s generosity is a stunning thing.

Thank you, to everyone who contributed to this. We will hope to be posting pictures as things develop; we hope that’s very soon.

Family

Family

Friend

Friend

Zacarias' Widow Teresa and Two of Her Children

Zacarias’ Widow Teresa and Two of Her Children

UPDATED: ***All Funds Raised*** There Are Things We Don’t Know How to Say

A Jon Post

There are some things that I love to share, some things I love to show, some things I love to enjoy with others;
My wife’s spirit
My daughters’ laughter
My Christ and His power
A cold crisp morning and the sun rising above the mountains
Casa Ahavá’s patients voices and stories and laughter
The deep truths that come from sharing in those voices, stories and laughter

And there are some things I don’t know how to say. There are some things I dread sharing, things I put off or delay the telling of, things I know no creative way to chronicle;
Zakarias died two weeks ago
Benjamin went home today to die

Zakarias

Zakarias

Benjamin

Benjamin

I don’t have an inspired way to narrate my feelings or how those events affect me. I’ve spent the last 2 weeks trying to put words on this page and kept failing and failing.
We knew that we would outlive our patients when we started Casa Ahavá. We knew that the well of mourning would only grow deeper.
Every patient Casa Ahava had in 2013 has died and many from 2014 have followed them to eternity.
So we wait.
Come quickly, oh Great King.
We want to see them again.

These have been expensive months for Casa Ahavá. A large part of the finances for our ministry go to helping patients who are too poor to afford it, to travel across the country to see the families they have left far away and return to finish chemotherapy treatments. Since November we’ve sent 4 patients on this round trip journey and 3 more on one way journeys. We also make great efforts to support the families of those patients who have passed away, especially with funeral costs.

Last week, as I was talking to Benjamin about going home to spend the time he had left with his wife and four children, he asked me for help. “Brother Jon,” he began, “I need help. I do not own a house and the house my family stays in we have been renting. I own a small plot of land in my town and would like to build a grass house for my wife so that when I die they will not be thrown out with nowhere to go.”
I nodded my understanding.
“This little house would cost about $150 to build but if you can’t cover all of that I could ask my old boss (the owner of the fishing boat he worked on for 15 years) to help too.” Benjamin finished.
I told him I could not give him a final answer right away but committed to help in some way.
A grass house for his wife and children?
Last night Layne and I sat with Benjamin and told him we’d like to help him build a house out of concrete blocks and cement. His eyes widened and he insisted that it did not have to be some huge house and that his wife and kids would be fine in a small home.
I made this commitment knowing;
1. God has always provided for the things Casa Ahavá needs.
2. Those who read this blog have been so faithful to help with things like this.
We want to raise about $3000 dollars and build Benjamin’s family a home. He will not have long to oversee the building of it and we want to ensure his wife and kids can remember their husband and father in a home built in his memory.

Can you help?

If so, please click on the “Help Build Benjamin’s House” button below and you will be taken to our secure Paypal portal where you can donate specifically to this need. We will update this post when this need is met.

***Update! In 3 days the Kingdom of God has responded and more than covered all needed funds for Benjamin’s house. As of now, I (Jon) plan on going to visit him at the end of February or the beginning of March to help him and his family make this happen. Thank you!***

Through all of this, please pray that his pain stays manageable, his wound stays clean and his hands grasp firmly the rope that pulls him to his Savior.




 

Not the First or the Last

A Jon Post

It wasn’t the first or the last time I will plead that a test return without signs of cancer.

Regina

Regina – Returning

Regina will be coming back to Casa Ahavá. She wasn’t cured. God heard our prayers, He listened to us, He wept with us, He knelt beside us, and He withheld the miracle. Regina has cancer on her lungs. Her CT scan stared unblinking at her doctor and I from its fluorescent backlight. It screamed its unapologetic truth at us through her lung tissue and chest. Two spots showed their wispy contrast against health and oxygen. Two nodes where they did not belong gaped back at us from that fluorescent box. Cancer. Metastasis. Pain.

It wasn’t the first or last time I will start a conversation with someone, “This is going to be hard. You are sick.”

Regina will spend the holidays with her family north of the city called Beira in a little village named Marumeu. From there, at the beginning of next month, she will get on a 4 hour train ride, then a 16 hour bus and return to the only place in this country where there is medicine for her. Here in Maputo.

It wasn’t the first or last phone call I will receive informing me that someone has died.

Separation

Pedro – Separation

Pedro’s brother called me.
It had been a month since any of Pedro’s family had answered their phone. Pedro’s number stopped working soon after we got him home and his two brother’s number hadn’t been working since the first week of November. Finally, last week, I got a phone call from a number out of South Africa. Pedro’s brother wanted me to know… Pedro closed his eyes for the last time two weeks ago. He held Marcos, his newborn son close, and finally ended the pain of separating his soul from his body. Pedro finally met face to face with the one who passed the test on his behalf.

It wasn’t the first or last time I will remove gauze and tape from a wound and feel the drop in my chest at the sight of a tumor that has only grown, not shrunk.

Unwavering

Benjamin – Unwavering

Benjamin’s pain level has increased though his courage and smile are unwavering. His tumor has grown as he has waited for his body to recover and be ready for another round of chemo. He rests a lot, hoping the pain behind his tumor will diminish and that he may experience a pain-free day. He has been waiting for days now.

These are not firsts nor lasts

Here at Casa Ahavá we have times when it seems like battles are won and we walk in the sun and there is only laughter and relief.
The last weeks have not made up one of those times. These last weeks, there has been shadow. Death’s dark sting has pricked Casa Ahavá twice… Tomás also died last month.

Remembered

Tomás – Remembered

Tears have leaked from eyes more than laughter has burst from smiles.
Now in our mourning we wait for our Comforter.
I’m so glad that Jesus Himself, asks the Father to send us a Comforter, a Counselor, a Helper, an Intercessor, a Strengthener… who will remain with us forever.

Come oh great Comforter. How we need your help, intercession, strength and comfort now.

Devastated

“This X-ray doesn’t show me what I need to see” said Regina’s doctor yesterday.
Last month Regina finished her 6th month of chemotherapy and over the past few days she’s had an ultrasound, blood tests, and an X-ray taken of her chest to find out if there are still signs of her breast cancer.
“The ultrasound and blood tests look good though” her doctor continued. Still, he looked at me and I could tell he was uneasy with declaring her cancer in remission and her treatment course finished. It takes a few days for the Central Hospital to schedule and perform an X-ray for a patient, a result of a valiant effort to keep up with the constant demand in a city of 2 million people combined with the limited resources of a developing country.
“I tell you what,” I said, “I will take her to a private clinic this afternoon and pay for an X-ray there, then tomorrow I’ll bring that back to you so you can feel better about making an informed decision and we can all rest easier about her health.”
“No problem.” Her doctor replied, “Just swing by in the morning and I’ll look at it then write up her discharge papers and she can be on her way home the next day!”
“Perfect!” I said, “See you in the morning.”
Regina and I left the doctor’s office smiling and I could see in Regina’s eyes the anticipation and joy of being so close to going back to seeing her family. That afternoon we sped through a little private clinic up the road from our house (where we’ve taken Pedro and Filomena for emergencies in the past) and got a quick X-ray done.
This morning I found Regina’s doctor in the oncology conference room busily doing his best to care for the hundreds of patients he is responsible for. He looked up at me and smiled and, when I asked if he had a sec to look at Regina’s X-ray, he quickly moved aside his current task and held out his hand for the X-ray.
When he pulled out the plastic film and held it up to the light, his face clouded over.
“This isn’t what I wanted to see.”
My heart sunk. Still… I hoped.
“This isn’t what I hoped for.” He reaffirmed.
He indicated a cloudy section, contrasting with the dark around it, and said, “This should be cleaner.”
“What do we do?” I asked.
My heart was racing. Regina, dear sweet Regina, oh, how I wanted to send her home tomorrow. Oh, how I wanted to get her to the “nice” bus at 2:00 AM tomorrow, the one with air conditioning, with a TV, with a bathroom. Oh, how I wanted her to see her grandchildren, all waiting and hoping that their grandma would be home soon.
“She needs a CT scan.” said Regina’s doctor. And he pulled a little piece of paper out and started writing instructions to the CT scan technician.
Carcinoma of the breast, suspected it has metastasized to the lung or bone.
My heart sunk further.

Beach Day

Beach Day

Regina

Regina

Metastasized.
The word no cancer patient ever wants to hear.

After a few more minutes of conversation with the doctor, I called Layne. She was at home with our three girls and Regina was preparing to leave early tomorrow morning. I told Layne what the doctor told me. We agreed that Layne needed to tell Regina right away.
So, three kids running, playing, crying in the background, Layne approached Regina and started, “Regina, Jon talked to the doctor. We have some bad news…”
Regina listened stoically to the report. Her face betrayed little emotion as it began to sink in. She tried to keep doing the cleaning Layne had found her in the middle of. Soon she was leaning against the wall… crying… asking God for reasons that didn’t come… looking for answers to questions too terrible to voice.
Sitting on a bench back at the hospital, praying and venting my frustration I shook my head over and over.
Not this one. Not this one. Cancer! You shall not have this one! My heart and soul screamed out, desperate for a confirmation to my challenge. I sat, lungs and throat sucked dry and raged against a disease that ravages so many people I love here.
NOT THIS ONE, CANCER! My silent scream echoed out to an empty courtyard.

I don’t know if I’m right. I don’t know if Regina will have a clean CT scan. I don’t know.
But I pray.
I pray.
Layne told Regina the plan. For the next 8 days we will pray. Regina will pray. Regina’s friends and family will pray. Our friends and family will pray.
We pray for a miracle.

We pray for a clean CT scan.

Don’t make us liars.
Pray with us.

My Hat in My Hand

A Jon Post

There are a few things running around my mind. I’ve decided to make a blog out of it.

Layne is traveling this week, I’m at home with my three girls, Casa Ahavá is empty, two of the most recent four have transitioned out.
Inês finished her treatment and is with her family, hopefully, with cancer in remission.
Pedro… well… if you’ve read the last few posts you know a bit about his story. He’s home, still alive, still paralyzed on his right side, still smiling. His newborn son has a name; Marcos Pedro Mavango. Pedro is in a good place.
Campande and Sara are both visiting their families between treatments and will be back tomorrow.

There was some work that needed to be done on the Casa Ahavá rooms that was easier done with no one in there (re-laying broken concrete and tile, re-painting the kitchen floor, etc). We spent some money on some nicer counters and cabinets for Casa Ahavá’s kitchen and are very pleased with how it came out.

And so here I sit, home with my kids, mind spinning, thinking about washing diapers, washing kids, washing dishes, washing my sins, washing my wife in the water through the word (whatever that means), washing Casa Ahavá’s floors, washing my kitchen floors (I knocked the toaster over a couple days ago, you know how all those toast crumbs get in the bottom of those things? Yeah… ALL over my kitchen).

I’ve also found myself thinking a lot about money this week. Money I spent on Casa Ahavá (paint, tile, grout, cabinets, toilet cleaner), money I spent on my family’s groceries, money I spent on a plane ticket to send Layne to America. We’ve written on here about how we’re in need of support, how our expenses are higher than our income. How does it then follow that I flew to America last month for a wedding, and that Layne flew to America this week for a birthday trip?  How do I look supporters or potential supporters in the eye and say we need more help? I know that you all have entrusted me with these resources and I feel that it’s important to be honest and open about how I use them.

I went to the USA last month to be Javan and Holly Mesnard’s best man at their wedding. The plane tickets from here to Phoenix were paid for by a generous person who wanted to make sure Javan was blessed. No donated money was spent on that travel.

Layne is in the USA right now. Last year in January I decided I wanted her to go on a “girls trip” with her sisters, mom and niece for her 30th birthday which is this year the same year has her mom’s 60th. We’ve been saving a little bit of money every month since then to pay for this trip.

We do take vacations from time to time. We do try to rest from time to time. We feel like it’s important to find time and memories outside of our full time ministry at the hospital and Casa Ahavá.

This week, while the other two girls were sleeping, Anaya was playing with her stuffed animals. She held her stuffed bird in her arms and said in a pleading and mournful voice, “Don’t die birdie. Don’t die in my arms. Just don’t die yet. I love you birdie.”
Anaya is 3.
This not an uncommon way for her to play. She often plays at dressing bandages, helping her sisters and toys while (pretend) sick and vomiting.
Jovie often pretends that Chauncey, her stuffed elephant, is sick and needs to be rushed to the hospital.
Jovie is 2.
These are the things that keep my mind spinning and my heart questioning about how we’re doing as a family. I don’t think it’s bad that my 3 and 2-year-old are so familiar with death and sickness. But I don’t know if it’s healthy for my 3-year-old to be pretending to have a seizure (like Uncle Pedro) while she’s lying in her bed.
And so I pray.
I was in church recently and there was a guest speaker talking about the dreams God gives us and what He purposes for us to do. He started walking around the room, asking people what they wanted to be. He didn’t come to me but when I started thinking about how I would respond to that question the answer was immediately obvious. I want to be a loving husband and a righteous father. That’s all I really want. Those two things are much more important to me than Casa Ahavá.
So, we take Sabbaths. We take times to rest away from sickness, pain, and death. We try to give our daughters a world full of life and joy mixed with the pain and sorrow they see every day.
That may be hard for some people to support. Some people may prefer that I spend more time and effort on Casa Ahavá than I do on my wife and kids. That’s really, really, really fine. There are lots of missionaries and ministries around the world who are doing INCREDIBLE things for Jesus. They need your help too and I’m sure there are plenty that share your values.
For those of you who are on board with me, please don’t be offended if I splurge now and then for my family. I can’t work a few overtime hours to make some extra spending money so I can take my family somewhere nice for the weekend. I can’t work towards a promotion and the extra money that comes with middle management.

I live with my hat in my hand, hoping that my priorities are straight, that my wife feels loved, that my kids are fathered well, and my patients are served with all that’s left over.

My Kids

My Kids