We place a check in the good news column and it begins to sink in that we have not one but both of our children now facing a life time of concern over potential complications that come from an NF1 diagnosis. As always, this is where we ask God to give us peace and strength to weather the storms.
48 hours later...
We met with Dr. Korf and our Ravin Williams, genetic counselor, at our UAB Genetics Clinic. This is the follow up exam to Helen's positive test for NF1. We could share so much about what we learned but again, the good news column gets another check mark since we know of no medical concerns at this time. She will return in a year for an annual exam. Here is the interesting information...
If not for Little Philip's tumor, no one would have suspected he has NF1. The genetic markers for NF1 are 6-8 cafe au lait spots on the skin (CALS), and/or freckling in the armpits or groin. Most often these CALs are present from birth or shortly thereafter. Little Philip has 2-3 CALs which is pretty standard for caucasians with no freckling.
Helen has 2 faint CALs. That's it.
Both of our children's genetic test show that they have the exact same genetic mutation resulting in NF1. But neither exhibit the usual marks. Why? As Dr. Korf stated, we are an atypical situation.
Question we asked today:
If Philip's NF1 is so atypical but he has a largely inoperable tumor, is that indicative of a potential tumor concern in Helen as well? Why not provide a baseline head/neck MRI?
Not necessarily, but there is no scientific link between the type of genetic mutation that results in NF1 and the way in which the condition manifests itself in a patient. There is no effective treatment to shrink or remove neurofibroma tumors. You can only attempt to treat symptoms. So there is no point in doing an MRI unless symptoms are present (headaches, back paint, etc.)
Because of this, and pretty much for the betterment of scientific research, we elected to have the genetic blood test today ourselves. Dr. Korf reminded us that each of us is 38 years of age and have no known NF1 medical concerns. We could speculate that Helen's NF1 would progress in a similar path through life. We pray this is the case. Maybe one day our family genetic testing will add information to track what NF1 mutations can better predict associated complications. Right now that is not possible. Maybe the additional of our two tubes of blood will lead to effective courses of treatment to kick this genetic condition to the history books for good.
We know that it is statistically impossible that one of us did not pass NF1 on to our children. It does not matter who did it, and we have talked about this extensively. If this test provides another genetic link to finding out more about NF1 and how to find a cure or a course of treatment, then count us in.
There will be no guilty feelings or thoughts when we find out. God provided us with the beautiful ability to pass on to our children Daddy's gorgeous brown eyes and Mommy's stubborn will power. What brings this mother's heart the greatest joy is seeing that God has also passed on to us two tender hearts that show early signs of chasing after the will of our heavenly Father.
There is a reason this is happening in our family. God intends it for His glory and we pray that we are salt and light to those in fear and darkness facing a new diagnosis of NF in their family. We cannot make it go away but we will come and walk alongside other local families to support and encouragement them.
Next week Little Philip will see Dr. Woolley, his ENT, to make sure that his tumor is not causing any concerns in his facial nerves, vocal chords, and other surrounding tissues in his neck.