Last Thursday we met with the ENT. He said that Kanyon was a good candidate for tubes. The doctor said that sometimes kids do well during the summer months, so we are going to see how he does. If he gets another infection he will be getting tubes. From December 2, 2011 through today he has had 8!
We met with the urologist today. He made a better impression today! He told us what we already knew...that Kimber has Grade II Reflux. He ordered some more tests. We will have to go back to WRMC to have them done. He wants her to start taking a low dose antibiotic daily. This will hopefully prevent future infections and prevent kidney damage. He said that she could be on the antibiotic for years and the reflux may or may not fix itself. He discussed two types of surgery. The more invasive surgery isn't necessary because it is typically done when a patient has Grade IV or V. The other surgery is called Deflux. It is a relatively simple procedure and has a great success rate. If the surgery was successful she would no longer need antibiotics or yearly ultrasounds and VCUG's. He is sending us a referral to Arkansas Children's Hospital. We will go down there with all of her test results and consult with one of the pediatric urologists. If they agree and she has the surgery she will have to have another VCUG to make sure the surgery corrected the problem.
I hate that she is going to have to go through more procedures and possibly surgery. The thought of your child under anesthesia is terrifying, but I am thankful that we know what it is and that it is treatable!
As always, we would appreciate some prayers!










