
This Christmas we will continue the tradition we started at Christmas last year. It was such a blessed and meaningful outreach that changed lives and continued thru the whole year.
Soon, we will be sharing details about the families we will serve this Christmas. These are families who have children who have been diagnosed with and who are undergoing treatments for cancer.
Once again, we will not be focused on giving gifts alone. Our support will take the form of providing tangible help which will alleviate some of the stress and burdens which come with enduring the crisis of cancer, especially during Christmas.
God bless you all and have a blessed Christmas
Mark
So, how can we provide the tangible support which will help ease the family's current burdens? I have provided a link to the Amazon wish list the family has put together. When you look at the Amazon list your 1st reaction will likely be to think this is a strange Christmas wish list. Of course there are some toys for the kids on the list, but many of the other items are necessities for changes they need to make in their home to provide the best environment for Micah.
Amazon list link: https://www.amazon.com/reg.../gl/guest-view/2BT52QU1SHVN4...
One of the best ways to help families enduring childhood cancer is to bless them with gift cards which meet immediate recurring needs which come with making frequent day long trips to Children's Hospital.
These are the gift cards Micah's family indicated would be most helpful:
PLMK via message if you do buy anything from the amazon list. Items purchased will disappear from the list and I will not otherwise receive record of those purchases.
Checks can be made out and sent to:
Compassion Network
PO Box 3055
New Kensington, PA 15068
Here is the link for online donations

Micah as a newborn

Micah at home

Micah at home

Valentines Day 2023

Micah at 6 months

Micah's first birthday

Medical Problem Discovered

Micah after cancer diagnosis at Children's Hospital

Prayer Request - December 2023

Micah after his first surgery - December 2023

Continued Prayers for Micah

Valentine's Day 2024

Valentine's Day 2024

April 2024 - Micah has his first MRI after the surgery

May 2024

July 2024 - next scan reveals two lesions

August 14, 2024 - second surgery and port placed for immunotherapy

September 23, 2024

2nd Birthday!

2nd Birthday!

Valentines Day 2025 - tumors not growing

February 2025

June 2025

June 2025

June 24, 2025

June 24, 2025

September 2025 - Best news yet! First time seeing regression without surgery. PRAISE GOD!

3rd Birthday! November 2025

3rd Birthday! November 2025
On November 5th, 2022, a baby boy was born to a local young couple. Micah, their 2nd child, was expected to arrive around Thanksgiving Day but decided he wasn't waiting any longer.
Like any parent, Micah's parents were grateful to be blessed with a healthy, happy son who thrived and was growing just as a newborn should. They watched his unique personality emerge. They eagerly anticipated milestones that mark the development of every child; recognizing mom's face; the babbling which leads to his 1st words; rolling over, crawling, standing and those monumental 1st steps.
Sure, there were the sleepless nights which temporarily interrupt life as a parent of young child. Right around Micah's 1st birthday on November 5th, 2023, Micah and his sister dealt with a round of colds, ear infections and a bout of pink eye.
Not long after his birthday, Micah's mom noticed that Micah's left eye was looking swollen and appeared to be a little "lazy". Over the following couple of weeks, Micah had two appointments with their pediatrician. The symptoms with his eye were not getting better so the pediatrician recommended they have a CT scan done to see if they could diagnose what was possibly at the root of his eye problems.
On Thursday, December 7th, Micah had a CT scan done at Children's Hospital in Pittsburgh. The results turned the family's world and Micah's bright future upside down. The scan revealed a tumor right below/behind his eye. Hoping for the best outcome, they immediately conducted a biopsy procedure and were then left to endure an agonizing week waiting for the results. Micah's parents hung onto their faith praying for a miracle. Family, friends, members of their church and many others on social media joined them in seeking the Lord's grace and healing for Micah.
The results were not easy to hear. Their one-year-old son, Micah, was officially diagnosed with Alveolar Soft-Part Sarcoma (ASPS). This is an extremely rare type of cancer that unfortunately does not respond to chemo or radiation. And, if left unchecked, this type of cancer is known to spread quickly and is often fatal, especially for children.
Micah's doctors consulted with numerous experts to find the best treatment options with the greatest chances of success. Sadly, Micah's parents were only given one treatment option, and they were told that option needed to be done as soon as possible. Their son would have to undergo major surgery.
The tumor had to be removed in its entirety, including any surrounding tissue which was proximal to it. In little Micah's case, the surgery would require removing his eye and everything within his eye socket. The surgery (exenteration) was quickly scheduled for Friday, December the 22nd, 2023. A whole team of doctors from several specialties would be brought together to perform a lengthy surgery.
Once the surgery was scheduled, Micah's parents shared how scary it was because everything was unknown and they had never gone through anything even remotely related to Micah's condition.
On Christmas eve, Micah's parents shared this update: “Happy to announce that Micah is home from the hospital! We have multiple follow-up appointments in the coming weeks but grateful to be home for Christmas. Best Christmas present that I could ask for... he acts like we haven't been in the hospital for 2 weeks and that he didn't get surgery two days ago. Crawling and walking like it's nothing.”
In April of 2024, Micah had his 1st post surgery MRI. The MRI proved the surgery was a success. The tumor was gone! Praise God! Micah would need to be scanned quarterly for the foreseeable future since ASPS is so rare, and it is known to present itself in other places at random intervals.
The next scan was done in July 2024. This time, the results were not so positive. The scan revealed two lesions near where the original tumor was removed. A biopsy was performed to determine if those lesions were cancerous. Everyone was praying and agreeing the lesions would be benign.
On Tuesday, August 6th 2024, Micah had his biopsy/resection surgery. Surgeons removed one lesion and pathology confirmed it WAS cancer (ASPS). We were heartbroken.
The location of the new tumor meant Micah would have to undergo a much greater invasive surgery to completely remove the cancer. Since ASPS does not respond to chemotherapy, radiation or other cancer killing drugs, Micah would have to start a different treatment regimen.
The only known treatment that has been proven to have some positive results on eradicating this type of cancer is immunotherapy. In other words, Micah would be given immunotherapy treatments in the hopes his small, young body would kill the cancer and fight off any spreading.
We thanked everyone for their prayers and support and asked them to continue to intercede for Micah. We hung onto this verse and believed for a miracle. "With God all things are possible" Matthew 19:26
On August 23, 2024, Micah went to Children's Hospital to have a mediport placed in his chest and to receive his 1st immunotherapy treatment. His treatments are given every three weeks which requires us to be at Children's Hospital each time. At this time Micah was also put on a highly specialized, organic diet to help his body fight the cancer and to rid his body of contaminates which can come from processed foods.
November 5, 2024 “Not gonna get sappy, but this handsome little man turned TWO today. He sure is one tough kid. With many tough situations this past year, he continues to have a smile on his face. We thank God everyday for our Micah man.”
February 2, 2025 **Update** Micah is getting scanned after being on immunotherapy for the past 6 months. As of this scan, the tumors appear to be the same as before. Although we are hoping that they go away fully, it is a blessing that they have not grown or spread. Thank you for your continued prayers for our little Micah man! We continue to pray for healing.
June 1, 2025 **Update** Micah’s scans this past month were not as clear as we were hoping. Micah will unfortunately be having surgery on Tuesday to remove a suspicious “nodule” from the base of his lung. Once they remove it, they’ll be able to tell if it is cancer and discuss further treatment options.
We pray for Micah’s continued strength. We pray that his surgeon will successfully be able to locate and remove the small area of concern. We pray that the current immunotherapy will continue to keep the cancer from growing/spreading. We pray for healing, and we pray for strength for the whole family. Amen.
Micah's surgery on June 3rd went well. The surgeon was able to locate and cleanly remove the “nodule” - Praise God! Now the hard part once again. We wait on the unknown to find out if it was cancer.
June 24, 2025 **Update** Sadly, the area of the lung that was removed WAS cancer. The good thing is that it is out and it appears all the affected surrounding area was successfully removed. The doctors told us to start adding herbal supplementation to Micah's highly specialized diet.
September 10 2025 **Update** This is THE update that we have all been praying for and waiting for - This past week, Micah had his usual 3 month scans. Not only were his lungs clear, but also one of his tumors in his head is completely gone! Praise GOD!
This is the first time that we have seen regression without surgery. We are hopeful that the medicine continues to help his body fight the rest of the cancer and keep it away.
November 5 2025 Such a bittersweet day...My BABY is THREE! Blessed to be this handsome little man’s mama. So proud of how kind, loving, and STRONG he is. Grateful for him everyday day HAPPY BIRTHDAY MICAH!
I would like you to meet Jace, our 2nd pediatric child. He turned 2 years-old on November10th. On February 25, Jace was taken to the hospital because he was experiencing what would best be described as stroke-like symptoms.
Life took a drastic turn for Jace and his family that day. Doctors found a large, rare brain tumor called Atypical Teratoid/Rabdoid Tumor (ATRT). They were told ATRT is a rare and aggressive form of cancer which would require immediate, vigorous types of treatment.
Treatment began by subjecting young,15-month-old Jace to two intense rounds of chemotherapy. Then, over the following 5 months, Jace had to undergo three painful stem cell/bone marrow transplants, the last of which was done in August 2025. Once the results of those transplants were positive and Jace's stem cells were producing new cells, they were allowed to go home. Each of the transplants required extended stays at Children's Hospital.
The next step in Jace's treatment required Jace, mom and dad, and his brother to spend 6 weeks at the Ronald McDonald House in Philadelphia. Jace now had to undergo 28 straight days of proton radiation treatment at the Children's Hospital there. Mind you, mom had to take a leave from her full-time job when they 1st learned of Jace's diagnosis. Now, Dad would be taking at least 6 weeks off from work to take the family to Philadelphia.
Remarkably, little Jace handled the radiation treatments rather well by the grace of God. On December 2nd, just 12 days ago, Jace was able to “ring the bell” signifying the end of his radiation treatments. Now the family faces four weeks of waiting. Jace is scheduled for scans on January 13th which will show what the last 9 months of treatment have done to the tumor.
There have been a couple of negative effects Jace has experienced due to the size of the tumor and its location. He has lost hearing in his right ear and is experiencing weakness on the side of his face. I need not say Jace and his family need and desire your prayers. Jace has been through so much over the last 9 months. That is the 1st and most important thing everyone reading this can do. Please take a little time as often as you can to lift little Jace up in prayer.
Between now and January 13th, Jace's family, like Micah's, will be completely changing their lifestyle and their home environment. Every effort has to be made to minimize the allergens, contaminates and any other possible enemies of keeping Jace healthy. Purifying the air and water in the home, changing what Jace eats, changing how they cook and even the cookware they use, to name but a few, had to change.
For Jace's family, purifying the water is a significant challenge. They have well water at their home and the Iron content is very high. They have been given quotes of $6,000+ to make the needed changes to their water system which they simply cannot afford. So, basic purification system for the water they consume is a priority need.
There are also ways our ministry will be tangibly helping this family during this difficult time. I have asked the family to create an Amazon wish list. In addition to some toys for the kids, you will see a number of things they need to create the healthiest environment possible for Jace. New cookware, socks that do not have plastics in them, clothes that do not have contaminates, and things for the house.
amazon list link: https://www.amazon.com/reg.../gl/owner-view/333V73979DTKP...
This is the same list of items + a couple that cannot be purchased thru amazon, in particular the water purification system:
https://registry.wegotthis.org/registries/jace-spears
One of the best ways to help families enduring childhood cancer is to bless them with gift cards which meet immediate recurring needs which come with making frequent day long trips to Children's Hospital.
These are the gift cards Jace's family indicated would be most helpful:
Checks can be made out and sent to:
Compassion Network
PO Box 3055
New Kensington, PA 15068
Here is the link for online donations to the Compassion Network:
https://www.paypal.com/donate/...


June 2025

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