Bed Campaign: Update

Abel is 21 years old and is a person with autism.

Abel is 21 years old and is a person with autism.

We have gifted 14 beds, blankets, and pillows to our kids thanks to your generosity!

85 of 240 kids in our program needed beds. Now, 14 of those kids get to sleep in a real bed. For many, it’s the first time they’ve had their own bed, much a less mattress, blanket, or pillow. For kids with disabilities, having their own space to sleep both makes their lives easier and also helps their families greatly.

Mercy moms, staff members, and community members made all of the beds by hand,

Our team delivered each bed to each home.

Over the next few months, our team will be providing beds to another 41 kids.

Marta is 31, has epilepsy, and survived a brain aneurysm. She is pictured here with our president Walter!

Marta is 31, has epilepsy, and survived a brain aneurysm. She is pictured here with our president Walter!

Meyling is 11 and has cerebral palsy.

Meyling is 11 and has cerebral palsy.

Joshua's coming to the US!

Joshua (2 of 10).JPG

Joshua is coming to the US!

Thanks to the generosity of The Child Foundation, Joshua and Majoyre, his mom, will be in South Florida for the next few months receiving treatment.

Joshua and his mom in Managua after receiving their visas

Joshua and his mom in Managua after receiving their visas

Joshua was born with a hemangioma on his upper lip that quickly grew in size over the first few months of his life. Hemangiomas are benign tumors made of blood vessels that normally disappear naturally but, in some cases like Joshua’s, sometimes continue growing.

The mass causes Joshua pain and has prevented his teeth from developing properly. The growth could continue expanding and causing him pain without medical intervention. Further, local dentists have refused to provide the dental care he needs because they’re unfamiliar with treating kids with hemangiomas located in and around the mouth.

Walter, the director of the Mercy Center in Nicaragua, took Joshua to the US embassy in Managua to get their visas in order. After a long process of letter writing and rescheduled meetings, Joshua’s approval came through and so we’re buying their plane tickets today!

Joshua (3 of 10).JPG

How to help

  • Pray for a smooth transition as Joshua and Majoyre make their way to the US, for his treatment and medical professionals, and for smooth recovery.

  • Reach out to friends in the South Miami/Coral Gables area. Joshua and his mom don’t need housing. They will, however, need friends and especially friends that speak Spanish. If you know someone (especially a Spanish speaker!) that could spend time with Joshua and, please reach out to:

  • Send a card! If you’d like to send a card (in Spanish!) to Joshua, mail one to:

    • Joshua Hernandez

      c/o Child Foundation Charity
      9485 SW 72 Street
      Suite A230
      Miami, FL 33173

Nimsy's Progress!

Nimsy amazing progress.jpg

“The proof is in the pudding applies.”  We are all so pleased with how Nimsy’s leg has grown. Dr. Gordon told Elizabeth (Nimsy’s mom) that he’d hire her if they ever moved to the USA.  He has been so impressed with how well Elizabeth has handled the turning of Nimy’s leg frame.  The current plan is for them to return to Nicaragua in September. That seems like a long way off to them right now as they are both extremely homesick. 

We sincerely thank each of you for caring, praying and investing!  One child at a time, one step at a time.

Nimsy: An Answered Prayer

Nimsy Mirana Gonzalez Castillo (1 of 2) 2.jpg

Nimsy’s family always believed that, one day, she would be able to walk like a normal girl.

She was born with a birth defect called a “tibial hemimelia.” In layman’s terms, that means she was born with a short, improperly-placed tibia.

Last week, Nimsy and her mom Elizabeth traveled here from Nicaragua under the assumption that they would be in the United States for four months, returning in June with a prosthetic leg.

Elizabeth has told us that, from the day of Nimsy’s birth, she has been praying for a miracle that somehow God would heal her leg and extended it. But based on x-rays taken in Jalapa, Nimsy’s team of doctors thought lengthening was not an option. Amputation was a painful, disappointing prospect.

Needs:   - Prayer for comfort as Nimsy will face challenging surgeries and therapy for the next 6 years  - Lodging from May - December of 2019 in St. Louis  - Prayers for strength as the Gonzalez family


- Prayer for comfort as Nimsy will face challenging surgeries and therapy for the next 6 years

- Lodging from May - December of 2019 in St. Louis

- Prayers for strength as the Gonzalez family

After a week of firsts for Nimsy and Elizabeth—from sub-zero temperatures and sledding to airplanes and customs—we traveled to St. Louis to the orthopedic specialist at Shriner’s Hospital taking her case. After reviewing new x-rays and manipulating her leg, Nimsy’s doctor proceeded to announce that amputation was not the only option.

“Yes, I can extend her leg,” he told Elizabeth and Nimsy.

Both immediately cried tears of joy.

Rather than amputating her leg, Nimsy’s surgeon will begin a process of slowly pulling apart the segments of bone in her leg so new bone will form in the gaps made. This slow process leads to regeneration and increased bone length.

This amazing news presents some challenges. 


First and foremost, Nimsy’s surgeon has told us that leg lengthening is the most excruciating orthopedic process he’s ever encountered. From multiple painful surgeries to months of intensive physical therapy, Nimsy will experience pain unlike anything she’s encountered. As her bone grows, the muscles in her leg will become tighter and her joints will ache.

Second, the family will be separate from each other for the rest of 2019. Nimsy’s father and brother will remain in Nicaragua while she and her mom will stay in St. Louis. After this year, they will return to Nicaragua for a year, come back to the US the following year, go back to Nicaragua, then come back to the US one final time, repeating the cycle three times.

Name *

Primarily, Nimsy and Elizabeth will live in St. Louis as they need to be near her orthopedic specialist. Two months of lodging have been graciously at the Ronald McDonald house but after that we need help  to find a more permanent place for them to live. (Thank you Pediatric World Project! ❤️)

We ask for prayers for Nimsy as she's going to experience difficulty during this time, prayers for their family separation, and prayers for funds to help provide housing for them. Ultimately, we are so grateful that Elizabeth’s vision of Nimsy’s future will come true. At the end of this 6 year journey, Nimsy will have two full-functional legs!

If you have any St. Louis housing thoughts, please reach out to us:

"Every Child Should Have a Bed" campaign.

Can you imagine tucking your little one into the bed pictured here?  It actually cannot happen because there is no mattress, no comfy blankie, and no pillow. It hurts my heart. It feels wrong. This has been bothersome for years and this Christmas we are hoping to make real change. Would you give the gift of a bed to a child in The Mercy Kids Foundation?  The cost for one bed is $100. and included in that price is a mattress, pillow and one blanket.  There are currently 85 of our 240 kids needing a bed. It is our goal to change that 37% to 0%, and your gift can help make that happen.

This is a “bed” for a mom with her three kids. The oldest has CP and spends many hours on this wooden platform.

This is a “bed” for a mom with her three kids. The oldest has CP and spends many hours on this wooden platform.

This last year we were able to purchase fifteen beds but our primary focus has been to get the Mercy Center open and running.  The center opened in April and has been extremely successful. Despite the political upheaval in Nicaragua we are flourishing. The staff is both efficient and effective with all our donated funds, and our attached newsletter gives just a few success stories.

If you donate toward our “Every Child Should Have a Bed” campaign we will send you a picture of the bed you purchase with your recipient’s picture.  If you buy ten beds, we’ll send you ten pictures.  This is our commitment to you. 

The kids with disabilities are the heart and soul of our program.  Most of our kids live in extreme poverty in a single parent home.

Pictured here are parents in the program sanding a bed. This helped reduce the cost of the bed. Each parent that has a child attending the center is required to give back. #teameffort

Pictured here are parents in the program sanding a bed. This helped reduce the cost of the bed. Each parent that has a child attending the center is required to give back. #teameffort

The moms are not able to work because caring for their child is so intense.  Your gift will not be used to buy sugar for their tea; we are wanting to buy a bed for their child. It is hard for me to think of a bed as a luxury.

We covet your prayers for the changes that are happening in Nicaragua with the kids and families experiencing disability. Without you; there would be no us.  We cannot say that enough.

Yours for the children,

Ron and Mary




Another loss for The Mercy Kids

Danny de Jesus Marin Quiroz (1 of 2).jpg

A couple years ago Pastor Carlos found a young woman and her son in an abandoned building.  Pastor Carlos saw the little guy had disabilities and the mom looked young and vulnerable.  He immediately brought them both into his home.  After helping them regain strength and a sense of stability, he found them find a place to live. UNICEF offered Sarah and Danny a room in a project where they had with space available.

Sarah was in the abandoned building because her husband had been killed on a motorcycle after they’d been married for only a few months.  Motorcycles often rob people of their lives in third world countries where there is no order on the road. Only in her mid-twenties, Sarah was now widowed, unemployed and had a child. The negative stigma associated with widowhood and with disability isolated Sarah. Her situation became more and more desperate. Disabilities carry complications in rural, uneducated areas. She was in a community without support, encouragement or help.

Pastor Carlos provided necessary support to Danny and his mom. They were able to get food, emotional support and Carlos helped her get more connected to resources for Danny’s medical needs. Danny became a sweet, central kid in The Mercy Kids.

It is with deep sadness we announce that Danny has passed away from pneumonia. It’s a terrible loss for Sarah and she needs to be covered in prayer. While we rejoice that his disability has been fully healed in heaven, our hearts are so broken for her.

Please lift up the team in Nicaragua in prayer. This loss carries so much pain for our staff.  There was something irresistible about little Danny.  His spirit was beautiful and he will be greatly missed. 

Of course, thinking of Danny running, jumping and worshiping Jesus is a beautiful thought but death is painful as well.  It’s final and it hurts.

- Mary Nelson

The Mercy Center: Four Months-lives changed!

      The Mercy Center Staff: Rolando, Nintzy, Abelito, Walter, Amilkar, William, Ellen, and Fany!

      The Mercy Center Staff: Rolando, Nintzy, Abelito, Walter, Amilkar, William, Ellen, and Fany!

On April 18, 2018 the political climate of Nicaragua changed dramatically. The conflict continues and our people struggle even more to come by the bare essentials needed for life.  Food and gas prices continue to climb and basic health care has moved from being scarce to nonexistent.  It’s truly heart-wrenching to watch the country collapse.  At present, the estimated loss is over 2.5 billion dollars.

Sally (my married daughter) and I went down in July to celebrate the three-month mark of the center.  Witnessing, first hand, the services our center provides encouraged our hearts. Our team is tight, focused and professional.  We’ve been able to add a physical therapist and her skill set filled our gap.  The team now covers education needs, basic speech needs, health care needs, and each child receives physical therapy.

It was humbling having the moms come up and pour out their gratitude.  They have such a sense of belonging, they feel understood and look forward to their day of therapy.  The moms are diligently doing their “homework” and the proof is in the pudding (note bragging points below.)

The Mercy Center operates three days a week and does home visits on Monday and Friday.  We continue to look for physical/occupational and or speech therapists willing to go down for a short-term trip.  We also desperately need connections to orthopedic surgeons willing to donate their services (stateside or in Nicaragua).

Thank you so much for your continued support. Without you, there would be no “us.”



Alex is at the top of the “success” lists. His club foot underwent six months of procedures and is now in the final recovery stage. This salty little guy would be a great presidential candidate. He is truly an amazing child.



Our journey to help families affected by disability is not without pain as we helped the family of this sweet child bury their daughter. She passed away due to pneumonia.

DSC_3200 (2).jpg

Bragging Points....

· Elias is feeding himself for the first time  —   age 15

· Rommy is almost walking alone —age 11

· Ismara was speechless in April, now a bubbling        extrovert

· Ciara (photo above) was pulled from school because of bullying, at the center, she’s flourishing– age 7


Ellen Moore......

I cannot express in words my gratitude to this amazing woman.  She loves these kids so much and her love for them has encouraged every single mom involved.  It is just beautiful to see Ellen in action.  The team meets and greets each mom/child as they arrive.  A member of the team immediately takes their child and warmly smothers that kid with kisses and then more kisses.  This is clearly the fingerprint of Ellen.  Her beautiful smile makes everyone excited to be part of the program.

In February, Sally and I went to visit Milagro in the hospital. She had pneumonia on top of her Zika diagnosis.  The experience was nothing short of horrible.  We were skeptical she would make it through the night.  Her body was writhing in pain and her mother was needing to hold her all night in an upright position for her to be able to breathe.  The hospital lacks any actual real medical equipment beyond the rust covered IV pole.  It was a daunting and scary scene.  My momma’s heart broke for Milagro and her devoted mom. 

Milagro might not live long but her mom and our team are committed to helping her live life to the fullest.  Her spirit is sweet and the team loves this child.  The Zika virus is a terrible thing!

Ways to Get Involved:


  • Pray for the Mercy Kids
  •  Pray for the team
  •  Come visit

 Please consider partnering with us financially.

  •       We are hoping to buy a van. 
  •        Our center is also not fully funded yet {our monthly expenses}


Spanish logo with words and box.jpg

The Mercy Center: Month One Success Stories

On April 17, 2018 our front doors opened.  We had a wildly successful pilot month.

Team Members serving in Nicaragua

  • Ellen
  • Walter
  • William
  • Abeltio
  • Amilkar
  •  Fany



Jana, a visiting occupational therapist from South Africa was a godsend!! She brought to the table some skillsets that will be treasured going forward. After one month this boy, Elias, age 15, shines as the face of the mercy center. His mom has had to feed him his entire life.  He now has the range of motion and the coordination to be able to bring food from his plate, to his mouth all by himself.   What an encouragement his progress is!!

WhatsApp Image 2018-05-17 at 10.04.52 PM.jpeg

Abelito, a Nicaraguan, is excited to have a job where he can use his skills but also express the love he has in his heart for the most vulnerable kids in his country. He knows the deep need and is grateful for the opportunity to serve in the center.

WhatsApp Image 2018-05-17 at 10.04.14 PM.jpeg

Ellen helps Katerine’s mom learn ways to keep her daughter safe. She is one of the most challenging Mercy Kids as she is CONSTANTLY moving but doesn’t have the mental capacity to stay safe.  Ellen is always willing to serve wholeheartedly.


Naomi’s mom was hesitant to commit to the work of being a willing participant of the Mercy Center . . . at first.  She did not understand the whole concept of a physical therapy center.  Now, after one month, she is one of the strongest advocates as she already sees progress with Naomi’s range of motion, cognitive abilities and is so excited to be part of the center.


This is Nyeli.  When she arrived to the Mercy Center she did not make eye contact with anyone.  She was insecure, shy and withdrawn.  Now Nyeli smiles and laughs and enjoys all the therapies offered. What a blessing to see her develop.  We want as many of the kids to move toward independence as possible.  Our team is making a difference!!

 On a more difficult level . . . I am sure many of you are aware of the political turmoil in Nicaragua.  This has been building for many years. The problems are deep seated and we covet your prayers.  The people, the ordinary people, like you and me are really suffering.  Food and gas prices have skyrocketed and the availability of both are always in question. As one would guess the list of issues is long.  We hope and pray for change, most definitely, but . . .   at what cost? Please join us in prayer for peace, for safety and ultimately that God’s perfect ways would reign and control the little country of Nicaragua. 


Ways to Get Involved:

  • Pray for the Mercy Kids
  •  Pray for the team
  •  Come visit

 Please consider partnering with us financially.

  •       We are hoping to buy a van. 
  •        Our center is also not fully funded yet {our monthly expenses}


Spanish logo with words and box crop.jpg

Alex's Story

The Mercy Kids Foundation (1 of 21).jpg

This is Alex González.

He is five years old, has more personality than the average 15-year-old, and was born with a club foot. 

When he as an infant, he received corrective casting and surgery for his foot. Due to poor medical care, his foot rapidly regressed and walking became increasingly difficult. We're praising God because this wonderful little person is receiving treatment! 

On our most recent trip to Nicaragua, we randomly decided (or so we thought) to get Alex x-rays of his foot. We took Alex, along with another sweet little girl in our program, to the local radiologist where we paid $20 for an x-ray of his foot and celebrated with ice cream. We'd known for years that he needed treatment but hadn't known where to begin.

Less than three hours later, we received word from a friend that an appointment had opened up with the leading club-foot doctor in all of Nicaragua. It was Monday night and the appointment slot was Wednesday morning at 8 AM, more than 6 hours away by car. Alex and his mother would have to leave their home for at least 6 weeks to receive treatment, live with someone they'd never met, and handle the pain of club foot casting. It was only the second time they'd have traveled more than 4 hours from their village. 

We were afraid that this would just be too much for the family to process in less than 12 hours. But when we told them the news, Alex informed us he wanted to make and pack spaghetti to bring with him for the trip and his mom cried as she had been praying for years for that day to come. They truly couldn't have been more excited! 

The following morning, we left for Léon, a six hour truck ride south, for Alex's treatment. The little man bravely handled the casting of his foot and we're so happy his treatment is going well!

Our long term goal through The Mercy Kids isn't just basic care. Rather, we hope to provide treatment that will change lives and open futures to our 265 kids that otherwise wouldn't be possible. We can't wait to share how Alex's life changes after his casting and surgery!

Scroll down to see images from our trip to Léon.

To sponsor Alex for $25 a month, please email:

Partnership with His Hands

We're delighted to announce that His Hands Support Ministries has established a sponsorship program for our Mercy Kids! Through this program, sponsors provide monthly donations of $25 a month per child and 100% of that money goes directly to caring for the Mercy Kids.

For several years, our dream has been to connect individual kids in Nicaragua with families that can not only provide financial support but also provide prayer for each child by name. His Hands has made that possible!

This January, God brought a team of His Hands volunteers to Nicaragua. While they were there, they began photographing and interviewing each of our 265 children. 

Because of their faithful work, more than 20 of our children have been sponsored! To sponsor a child, follow this link below.

UPDATE! We're so grateful that Deyvin is now sponsored! Please consider sponsoring one of the other sweet kids in the Mercy program. 

Right now, one of our most urgent sponsorship needs is Deyvin Rosales Hernandez. 

Deyvin is 18 years old and has cerebral palsy. The difficulties of his disability, however, are compounded by his extreme poverty. Deyvin receives almost no care, lives in a plastic shack, and does not receive the medical treatment he needs. 

To sponsor Deyvin, follow this link. $25 a month provides Deyvin food and other household supplies.