Dear Friends and Family,
Am I the only one that wonders where time goes? For those of you that have checked this blog and have not found an update... I'm sorry. Let me bring you up to date on what has been going on.
First up to the plate is Becky:
Beck has completed all of her testing and it was sent to Mayo. It has been concluded that she has PSC (primary sclerosing cholangitis) I could explain it to you but it would be easier to 'google' and read up on it. As far as what this means to Becky is that she will have to have cancer testing every 6 months and a colonoscopy every year (Yes at 23!) I have spoken at length with her doctors and specifically her Oncologist (Cancer doctor) although PSC is specific to the liver and ducts it has a very high relationship with the colon and in almost all cases will end up with cancer in either the liver or colon. Best is to stay on top of the disease and catch it early. You ask: Is there a cure: No.
Is there something to be done? Not really. What then? Beck rests... in the Lord. She has an amazing outlook on things. Her faith is and continues to grow strong. Lots of prayer.
We trust the Lord with our daily activity in guiding us and lean not to our own understandings... when you are faced with a young person; your child with an illness, you have many things that you learn and the one that comes to mind as I type this is that: Who is the One that loves her more than me (her mother) that One is the Creator, the Savior, the Healer... Beck is in the Lords hands and has been all along. When you say that and believe it... you can't help but find the rest and comfort of a love that is unshakable... indescribable... and for some just not understandable. Remember we love and serve an AWSOME God!
Back to Becky; She had the pain spinal stimulator removed. If you recall she had a device placed along her spine that went to a little box (much like a pacemaker) in the hip that was suppose to be an alternate way to control pain. Well... it didn't do much after all. Plus, she couldn't have an MRI which Mayo wanted to have done. When it was removed she had an MRI it again confirmed PSC and the cirrhosis which we knew about. It also revealed that Becky has "spots" on her liver. Here is the thing... we don't know what the spots are; yet. I'm not certain that we will know soon either.
Some of you may wonder why they don’t just do a liver transplant. Both the liver transplant team and Mayo have told us that at this point it would be more dangerous for her to have a transplant now (meaning a negative outcome; death) verses waiting. After digging a little deeper it appears that when a liver transplant is done or considered that the patient has about 3 or so months mortality time. After that was explained we were able to understand why they just continue to do... very little... because there is no cure there is not much that can be done but treat symptoms.
Well, praise God she is not at the 3 month mortality point!
I tell friends that if you were to see Beck you would never guess she was so ill. I also have to explain that what you don't see is when she gets home after being at church for an hour or two her need to sleep for 5 to 6 hours because it wears her out that much. She is making it to church and I enrolled her in a one hour class for cake decorating which she loves to do. These outings are pretty much the only time she gets out. In April she is in one of her friends wedding as a bridesmaid. She at first wondered if she would be able to stand up that long and have that long of a day (to be honest I wondered too) but she agreed to be in it and I feel that overall it will be good for her, although exhausting!