Monday, September 21, 2009
A Plea to MOOs
We're doing an all out blitz for information lately on tissue expanders versus compression. We're still not sure we have all the information on each of those, but we definitely don't want to put Karsie through a surgery if she doesn't have to.
Therefore, if you're a MOO (Mother of Omphalocele) or know one, or know information about:
1. Compression Method/tissue expanders; and
2. Who does them around us in Southern Cal (or the west coast)
...please let us know.