Caleb has been doing great the last couple of days. The pain is a lot less, but he is still hitting the morphine pump as needed. Today the physical therapist came by and

God has done it! We were told last week in the pre-op consultation that there was a 99.9% the nerve that controls upward movement of the foot would have to be severed and

Last week, we finally got a chance to have the scans on Caleb done to see where everything stood. We had not had any scans or xrays since back in September when he

We have been so busy with everything lately. I am very concerned about the amount of school that the boys have missed because of Caleb being so nauseous constantly from the chemo. If

Sorry it has been a while since the last update, but we have been in a whirlwind for the last couple of weeks. Caleb had 5 days of chemo last week, but we

This has been a hectic, exciting few days for the Murray family. Last Tuesday, both Caleb and I were admitted into the hospital. Caleb had a 5-day regimen of chemo and I was

I know everyone is really busy today with family and getting ready for Christmas, but I felt I needed to write down what I am feeling inside. I have said all along that

Caleb went in yesterday all packed and ready for 5 days in the hospital. His counts were the lowest they have been yet, so they decided to wait until after Christmas to continue

The Bay of the Holy Spirit Revival has posted a YouTube video of Caleb’s testimony on their YouTube and Facebook pages! It has already been shared by 45 people and sent all over

We packed up and headed to the hospital yesterday thinking we would be there this week for chemo. Last week, Caleb started developing mouth sores as a result of the chemo treatments. It