Mikah’s Story

Site created on September 15, 2018

Friends and family...welcome to Mikah's CaringBridge website.  We (the TEAM) have decided to set this site up for Michael and Sarah. Please know they have not asked for any of this, however, it is necessary.   We are gratefully overwhelmed by the amount of people who would like to help and our goal is to have ONE location that you can do just that! We are using this site to keep family and friends updated in one place. We appreciate your support and words of hope and encouragement.  On this site, you will find many ways to help, and a place to get some updates as well as a place for you to send encouraging words! We love and appreciate all of our family and friends for your willingness to help and your love for our family.

On this site, you will also find the link to the MealTrain here (https://www.mealtrain.com/trains/m8orm6), the link to the donation site here (https://sbcbf.org/), as well as a link to a sign up for other items that may be a blessing to Michael and Sarah and the kids here (https://www.signupgenius.com/go/30e0b44aaa723a5f49-love) or please click on the hand and heart icon that says "Ways to Help". Thank you for visiting.

       Dear Family, Church Family, Fire Family and Friends,


On Friday, September 14th, 2018 we received the most devastating news of our lives. We learned that Mikah, our brave and Batman loving four-year old has B-Cell Acute Lymphoblastic Leukemia. It is still hard to think about all that has happened in these last few days. He was first admitted into Pomona Valley Hospital Medical Center on Thursday afternoon the 13th because of Michael’s intuition that something wasn’t right. At Pomona Valley Hospital they confirmed that his Red and White blood cells, along with his Platelets were low but they would need to send him to a children’s specialist to give an exact diagnosis. Michael asked the doctors if Mikah could go to Loma Linda University Medical Center. At first they told us that it is very difficult to get into Loma Linda. Loma Linda University told Pomona they didn’t have a bed open for Mikah on the children’s floor but that they would find a spot. They opened up a spot on another floor until a bed was available in the children’s hospital. After a team of specialist did the bone marrow biopsy, it was confirmed that 91% of Mikah’s bone marrow was full of leukemia and that he would be starting a very aggressive 28 day regiment of chemotherapy the following day. The goal is to reduce the leukemia cells to 0.1% in the first 28 days. We know Mikah is in the very best hands at LLUMC and are so thankful for all the talented Staff and Doctors here. 


Now we begin this journey that we never imagined that we would be on. It is heartbreaking to watching your sweet and lively four year old become sad and somber. We think about our three other children and how life is going to shift so quickly for them also. They are also worried about their brother and just want him home. We know we cannot walk this cancer journey without the love and support from you, our family and friends. We are trusting that the God who blessed us with our children will also be along side us every step of the way in this season of life. We appreciate and are so thankful of the overwhelming amount of Love and Support we have already received. We can’t thank you enough for loving our little Mikah. 




The Carney Family 


 “Therefore we do not lose heart. Though outwardly we are wasting away, yet inwardly we are being renewed day by day. For our light and momentary troubles are achieving for us an eternal glory that far outweighs them all. So we fix our eyes not on what is seen, but on what is unseen, since what is seen is temporary, but what is unseen is eternal.” 2 Corinthians 4:16:19


Newest Update

Journal entry by Sarah Carney

It's been a rough month for Mikah and our family. Mikah's ANC counts came back low a month ago so they put him on a chemo hold and we had to keep him at home from school. We went back to the clinic weekly but his ANC never went above 400 until yesterday we finally got the good news that his ANC is at 1,800. The chemo hold worked. He started back on his daily chemo meds last night but we cut the dose in half. The amount he was taking was just too much for his little body and it was knocking him down. We are all feeling a bit drained and exhausted. The emotional and physical aspect of caring for a child with cancer has put a strain on both Michael and I physically and mentally.

We are looking forward to this weekend's Light the Night event with the Leukemia and Lymphoma Society at the Speedway in Fontana. It is not too late to donate or register to walk with us. Registration and Parking is FREE but if you want to join us in the exclusive Team Love 4 Mikah tent you do need to be registered under our team. We would love to see you there and donations help the LLS find treatments and cures for blood cancers. This has become very near and dear to my heart as I have learned there is little research and funding for childhood cancers. No one wants to talk about kids getting sick. It is very taboo but the truth is there are kids and families hurting as their children battle for their lives.

Light the Night:
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