Mami, Papi, and the girls.....

Mami, Papi, and the girls.....
stories from our little corner of the world.....

Saturday, August 13, 2011

BPI Clinic Day

On Wednesday we made the trek downtown to Children's Memorial's BPI Clinic.  Going into the appointment, I hoped the Dr. would be happy with what they saw and I hoped that based on her progress we wouldn't have to go back for another year (it had been 8 months since our last visit).  We got the girls all excited about going to Molly's Cupcakes, the novelty cupcake bakery across the street, and the adults excitement was in a restaurant called Sultans Market which is next door to CMH. 

We absolutely love Sara's specialist.  She has such a nice way with the children and families.  We have always appreciated and trusted her expertise and kindness.  The clinic nurse is wonderful as well, but unfortunately we didn't see her this time.  My hopes proved to be in the right place because the Dr. was happy and said she wouldn't be a candidate for any surgeries and that we should come annually from now on.  She also told us that Sara no longer had any restrictions except for something like football where there is an opportunity for strong impact in the shoulder. 

At the moment I took everything for what it was and was very pleased, and I still am.  But when I started thinking about no restrictions, my mind went flying.  NO RESTRICTIONS!  I didn't know if I should laugh, cry, be shocked, seem surprised....no restrictions.  Although she hasn't had complete recovery, this is my girl, and it is her moment to fly.  She will always be in therapy to keep her muscles loose and to continue to stretch her range, but this is who she is and will always be.

Sara has always been very in tune to her BPI and we have always felt that there is no reason to keep her injury a secret from her.  We wanted her to understand why we were going to so many therapies and why we were doing home exercises.  She is also aware of her vascular birthmark on her BPI arm, and she takes people aback when her little two year old voice exclaims that it is her hemangioma when she is asked.  So I began to think about the importance of reminding her in our daily conversations that she can do and be anything she wants to be.  And when I asked her what that would be....she said a tap dancer.   Of course she understood my statement at a very 2 year old level.  But I hope that when she gets to be an adult, that she never has felt the feeling of road blocks or my nervousness with her arm as something that held her back.  So today, and I am sure for her whole life.....we will be telling her that she has the whole world at her fingertips.....and today is her day to fly............

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