Pages

Life with a boy and his Hypoplastic Left heart Syndrome, now Heart transplant and partial Liver from Aspergillius. Also, a girl and her Tethered Spinal Cord Syndrome, Neuro Endocrine Cell Hypoplasia, Lumbar Hemangioma, asymmetrical gluteal cleft, Pectus Carinatum and two Super Sisters and one yummy baby brother.

Tuesday, June 23, 2009

Perfect

I knew posting about Gator's ears would make me feel better. I am so glad I have you guys. I think that we are going to PCMC because the dr.s that our ped recommended aren't covered by our insurance. So I am going to see if Grimmer can see us. Par recommended from Arna's momma, he is at PCMC. It sounds like most of you have had it done there, another reason I feel better... Thanks again everyone.

3 comments:

Lacey said...

I agree with Julie. Grimmer is the way to go. We love him.

Mom of twins ♥ said...

Good luck with everything!

Molly said...

If Dr. Grimmer can't see Gator for some reason, go with Dr. Smith. He did Alice's choanal atresia surgery and he put her tubes in. I just realized that out of all her doctors, he's known Alice the longest, since she was 1 day old. He's great!