We are all keeping busy; school, church, work, sports...all the things we love and enjoy!

We are all keeping busy; school, church, work, sports...all the things we love and enjoy!

We haven't updated on Blake's health in a while. In a nutshell, Blake's progress is slow and isn't really where the doctor wants it to be. We all know that it is a long process to get him to a stable point; Dr. Mc Omber (pictured here with Blake) thinks it will be at least a year before we can look at maintenance medication. So until that point, Blake is now taking 6 pills a day. At our last appointment, Dr. Mc Omber told us that he feels that Blake's liver is swollen as it is trying to clear all the copper out, and he is concerned that some of the other filter organs may be working harder to compensate. We have another appointment in 6 weeks, and lab work to complete before that. When you see Blake, you would never know that he had a sick liver, as the boy eats non stop and is pretty active. He is a very good patient, and the team at Phoenix Children's Hospital loves it when he comes in. We ask that you continue to pray with us that we can get him leveled out on his medication schedule and that the medicine will continue to do its job.








August 12th began the new school year. Craig II is in 9th grade, and Blake is in 5th grade. The phrase of "time flies so quickly as they get older" is now more evident than ever. Both boys are doing really well in school so far this year. Blake was bumped up to advanced math (he didn't get that gift from me), and Craig II is taking an engineering class that he really likes (again, not a gift from me)- they are already looking forward to their week off in October. :)
Blake had another appointment today - we see the doctor every 6-8 weeks. I will start by saying that we love Phoenix Children's Hospital and Dr. McOmber! He is awesome and so concerned with Blake's health and treatment. Blake had to have his medication adjusted, as his liver is not getting rid of the copper as fast as the doctor would like to see. So now Blake has to take 5 pills a day instead of 3; 2 in the morning, 1 in the afternoon, and 2 at night. The good side of this is that it will bring Blake one step closer to a maintenance program. The downside of this is that as the liver is trying to get rid of more copper, there will be abdominal pain. And the hard part, for me as the Mom, is that I can't do anything to take the pain away. Please pray that the side effects from the additional medication are minimal, if there are any at all. Dr. McOmber also doesn't see a need for another biopsy anytime soon - we are so glad to hear that. Blake's food restrictions still remain the same; not as fun, but we are adjusting.As soon as things settle down a bit - I will post more frequently. :)
After trying to be patient for 6 weeks (not one of my strengths), we received word today from the Mayo Clinic that Craig II is only a carrier of the gene that causes Wilsons’ Disease (meaning he doesn't have the disease). You have no idea how happy we are. God has answered our pray. Craig II is on his way to camp up in Big Bear, California today with the Jr. Higher’s from church and I couldn't wait to tell him the fantastic news. So I found out which bus he was in and made the call. He is so happy!!! He too has been waiting, wondering if and how his life was going to change with a diagnosis. Now we can all relax and move forward and focus on taking care of Blake.

