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Update on Zakarias

A Layne Post

I’ve wondered what to say. I keep thinking, “I’ll write after his doctor’s appointment.” Now that doctor’s appointment has moved two times, thanks to Dr. travels, and I have decided to delay no longer. It is time for an update!

Papa Zakarias, his wife Theresa, and his 2 year old daughter Maria have been living with us for a month now. He has 4 other children at home, 14 years old and younger, whom his mother-in-law and sister-in-law are caring for as the children continue their school studies.

Before he came, we communicated multiple times with Papa Zakarias about expectations for why he would come back to Casa Ahavá. We understood and he indicated that he understood that he was coming for hospice care and that the hospital could only provide pain management, something that is not offered in Beira, the city where he lives.

The first week he was here we had lots of conversations about the future to make sure we were all on the same page. Turns out we weren’t. Papa Zakarias hopes that chemo treatment would be beneficial and wants to ask an oncologist again if that is possible. Jon has had personal conversations with 3 oncologists at the hospital who have all indicated that chemotherapy could no longer help him but Zakarias wants to hear it for himself.

This change in his outlook did take Jon and I by surprise and we have had to make a bit of a mental shift to know how to best support and love him. A decision about treatment is not something Jon and I have control over. Jon helped Papa Zakarias make an appointment with one of oncologists at the hospital and hopefully on Monday he will have a meeting with him. If he does not begin treatment, as of now, we believe he will return home to be with the rest of his children. If the oncologist believes it beneficial, he would stay here during treatment. Theresa and Maria would stay during the first few cycles to see how he managed.

If the oncologist reconfirms that chemotherapy is not an option, before going home, they have a few decisions to make – if his wife will have the time, strength and resources to care for him in their home as his health deteriorates and if he will be able to manage his pain with only Tylenol. Hard decisions! Pray for them!

We are sure that his time here with us has not been in vain. We have been trying to help him get his affairs in order before his time comes. Papa Zakarias is a veteran of Mozambique’s War for Independence and he has access to some monthly income and benefits (ex: transport and medical discounts and free school fees for his children). He also qualifies for a monthly income for his age and years of work. He and Jon have been down at government offices filling out the proper paperwork making sure everything will continue to go to his wife and children.

We also continue to address their spiritual health. I want so badly for them to know and understand the Lord’s deep love for them and the sacrifice that was made on their behalf. Pray with us. I keep praying that the Lord would use dreams and visions and meet Papa Zakarias right where he is – in such a bold manner it would be undeniable. It is our desire for Papa Zakarias that he would come to the end of his life full of peace and full of hope for the next life.

How is his current health?

He is weak. He is unable to eat much. If he walks around and does too much in a day, his whole body feels the consequences with aches and exhaustion. He has had a secondary infection that he is treating now. He struggles a lot at night, unable to sleep and sometimes experiences body tremors. The tumor on his liver is growing and protruding, causes great pain and discomfort.

Pray with us that we would love him and his family well.

This is All We’ve Got Right Now

 

A Jon Post

I’ve been trying to write this for a while now. I hate it. I’ve started a few times and keep ending up feeling like I’m forcing something out and trying to do a nice mix of emotion, encouragement, spirituality, faith, and all the other nouns or adjective-nouns that are used to describe what we do/write.

I can’t do that right now.

So here you go:

Eliza died last month. Her tumor grew so big it shut her throat and she couldn’t eat or speak. She died in pan. We couldn’t be there.

Filomena is suffering immense pain, her weight has dropped dangerously low, and her phone number, our only way to communicate with her stopped working. A neighbor in her town far to the northern part of this country tells us she’s been admitted to the hospital there and is dying.

Zakarias came to live with us along with his wife and two year old child. I’ve had many conversations with him since he arrived last Tuesday about his health. He’s dying. He only came back because the pain was too intense and there was no way to get any medicine to control it so he came here. We are trying to help him.

We’re finding moderate success.

He’s dying.

Dosma at the Beach

Dosma at the Beach

Two weeks ago a young man named Dosma, an 18 year old boy who had come back to the hospital from his village of Calimane, died. I had known him almost two years. About a year and a half ago I took him to the beach and the little shopping mall that’s near the beach. We spent the afternoon talking and thinking about home, the farm, school, his first girlfriend, his mother, my money, his desire to be rich, his need for Christ.

He died two weeks ago.

This has been a tough start to 2014.

Pray for us.

Come Meet Eliza

A Layne Post

I knew Eliza a long time. She had a big personality, one you could not miss. She was full of faith and had a love for God’s word, despite the fact she was unable to read. All day long you could catch her singing songs to her Lord. She was a prayer. When she felt pain, her response was to cry out to God. One weekend Jon was quite sick and I remember her knocking on the door, walking into the living and passionately praying to the Lord for his healing.

She loved her family. She spoke with her mother and sister daily. Her daughter, son, and grandchildren were her pride and joy. It was difficult for her to spend so much time away from them. We were honored to have her come and stay with us, to become a Grandma around here.

She loved to cook and thought her cooking was some of the best in the country – no one else could get it quite right. She had all the tricks to the perfect this or that. She served people through her cooking – Jon and I as well.

When Jon traveled, she would come in to play with the girls, feed Jovie, and just sit with me. She helped teach Jovie to walk and patiently chatted with Anaya, even when Anaya would only speak of Katy Duck (her stuffed animal).

Eliza knew she didn’t have long. She was confident in her Savior, and last week she was redeemed, saved from this life with all its sorrows and pain, and she is living in freedom with Him.

We interviewed Eliza and asked a few questions about her family and her sickness. This was to send to her family on a DVD so that they could see her talking about them and about her life while she still had strength and life. She gave us permission to share it here as well. We hope you have the time to honor her and remember her by watching this video.

A Thrill of Hope

a thrill of hope

Thanks Tara Craver for sharing

We are home. The trip was long and our girls are still not recovered – struggling with night and morning coughs and jet lag. I keep asking Jon to reassure me that it will get better… and it will, though it seems like it is dragging. I caught the bug before leaving the States and was determined to get home and get our house ready for Christmas. So before all of our bags were unpacked and laundry was done the tree, garland, and lights went up. This year I am enjoying a little Advent calendar with the girls, and while they may not understand it all, perhaps little bits and pieces will stick.

On Thanksgiving day we received a heavy email with a health update from our dear Eliza. She left for South Africa to start radiation the day we went on furlough to the States. The treatment has not gone well. Her throat has swollen and she is unable to eat food. She has stopped talking and can only use gestures to communicate. Her brother came by our home a couple of days ago to ask for help to get her home. We are so very blessed by our supporters in that the financial side of that is not a problem – Thank you! What we need from you is prayer. Pray that Eliza, who is currently on breathing tubes, will improve and stabilize enough to get on an airplane and make it back to Mozambique, her home country, where  she can be around family and those that love her.

Yesterday we were able to make our first visit back to Oncology! We wanted to arrive as a family and introduce ourselves to all the new patients. Our girls are such a blessing there. It was fun to watch our Karasi being toted around, chill as could be. Anaya is becoming more and more comfortable, and we are able to talk with her more about our “job” there. It is sweet when she suggests that we pray for people. We saw two patients that we knew and the rest were all new! Pray with us as we develop new relationships and ask the Lord to guide us in the selection of 4 new patients for Casa Ahavá.

This holiday season, surrounded and so very aware of this weary world, we feel the thrill of hope, and we rejoice! Christ our Savior has come.

Snapshots

A Jon Post

Following are a few snapshots of our lives over the last 2 months from a family that did a pretty poor job of communicating with all of you about where we are/what we’re doing. If you don’t have time to read it all please just skip to the end where I list a couple prayer requests.

#1 Week of September 22-28
A mad scramble to figure out if we would be able to get 2 our patients home, to the hospital, or to life-extending treatment in South Africa before we left. A mad scramble to find out if one of our patient’s tumor was operable or he needed to go home, and a bus ticket to send another one home who had finished her treatment and needed to spend her remaining days/months with her family.

Family minus Filomena

Family minus Filomena

Zakarias, the surgeon didn’t respond before we left, we did not know if his tumor was operable, he stayed in our house.
Tomás and Eliza, the day we left for the USA (September 24th) we were up first thing in the morning to buy last minute bus tickets to send them to South Africa for more treatment.

Filomena The Day She Left

Filomena The Day She Left

Filomena, we purchased a bus ticket and sent her home a few days before we left for the USA to make sure she was with her family after she was discharged with no more options to fight her cancer.
September 24th, we left our house at 11 AM and arrived at Layne’s parents house 40 hours later with all three girls in tow. Thankfully we had the gracious help of Jon’s parents who came to visit us and joined us in our long journey to the USA and helped tremendously on the plane.

(whew, that was a long first snapshot but we did a really bad job of telling everyone who reads this blog that any of that stuff happened before we left)

Jovie Meeting the Dolphins

Jovie Meeting the Dolphins

Anaya Running with Dolphins

Anaya Running with Dolphins

#2 Time in Corpus Christi, TX
The Texas State Aquarium with our girls. Grandparents helping them swim and play, as well as cousin time. Sitting with sweet, sweet supporters. Trying to recover from the jetlag and help our girls sleep in new places with new surroundings.

#3 October 30th More Travel
Flight from Corpus Christ to Phoenix. Left Layne’s parents place at 8 and arrived at Jon’s brother’s house 7 hours later. This was our first plane travel with our three girls alone. They are super stars.

Layne and Her Dad

Layne and Her Dad

#4 More Family Adjustments
Man… it’s hard doing this furlough thing with 3 little children. We could not ask them to be better sports through all of this but a new bedroom for a month, a new bed for a month, different living space for a month, meeting lots of people (supporters) for the first time on an almost daily basis. Well… it’s tough. Our girls are super stars.

#5 Time in Chandler, AZ

At Uncle Joe's Duck Pond

At Uncle Joe’s Duck Pond

Seeing more sweet, sweet supporters. Time with other Grandparents. Time with LOTS of cousins, girls napping in the car a lot.
So there are a few, far from comprehensive or descriptive, snapshots of our lives since September. We are currently in Chandler, Arizona in the USA trying to connect with those who pray for us and give to this ministry. We have been trying to sit down with each of you and we still have a little under two weeks to do that. We are very sorry that we haven’t pursued you and communicated with you all well enough to do that “sit down” better. We are finding out that we need to be more diligent with some things and one is our personal and purposeful communication with team mates.

They See Us Strollin...

They See Us Strollin…

Anaya Loves Karasi

Anaya Loves Karasi

In closing this little “snapshot” post. Can we ask you to pray for two things?
Would you pray that our children’s health improves? I don’t know if it’s because they don’t have American immunities built up or if it’s just a bug they would have picked up either way but all three, Anaya, Jovie, and Karasi have bad coughs and are very congested. It’s hard for them to rest and, thus, hard for their parents, especially Layne who still feeds and comforts Karasi in the night. Would you pray for them?
Would you also pray that each airplane on our return flight has LOTS of open seats? Neither Jovie nor Karasi are ticketed for those flights and are traveling as lap children. Anaya still needs plenty of help and attention on the flights and Jovie needs space to move so if we all try to jam into three seats it’s just really hard. Would you pray for our flights? Would you pray that a check-in agent magically upgrades us to first class? Would you pray that we have 15 seats to spread out on and rest on for the 40 hours of travel?

Karasi Loves Jovie

Karasi Loves Jovie

We love you guys. Thanks for loving us, even though we lost touch there for a bit.