Mia's Lymphatic Malformation

We are Mia's parents, Rich & Brandy. Our little girl was born with a rare mass called a Lymphatic Malformation. She has been to several hospitals, seen many doctors & specialists, had many CT & MRI scans in addition to several surgeries. As you can imagine, all these visits and treatments are not free nor inexpensive. Any money we recieve will be used for her existing & future medical expenses.

For more up to date status on Mia, please visit her blog;
http://ourprincessmia.blogspot.com/