Cedars did a really great job of getting us in quickly. I'd mentioned when I faxed the registration packet over last week that Dr. Krakow (with both Cedars and UCLA) and Dr. Danielpour (the Neuro with Cedars) had both mentioned concerns over the size of Caitlin's fontanelle at the D12 regional and had recommended getting an MRI done as soon as possible. Of course, if you've been reading this blog (or my Facebook updates) very often, you know that getting an MRI through Kaiser and Dr. Tiller has been almost impossible. Of course, as soon as word got to Dr. Tiller that two of his important colleagues thought Caitlin needed an MRI (and should have had one earlier, no less!) he called Cherylle directly and offered to do whatever was necessary to get one going for Caitlin. Uh huh. Too little, too late, buddy. The letter to Kaiser and to the LPA's medical advisory board is already started - I'll post it here when it's done. As parent coordinators, Cherylle and I feel that we have a responsibility to make sure other parents know who is out for your child's interest and who is not!
Anyway, on Thursday I started getting calls from Cedars - first from Tami, the clinic coordinator with the Skeletal Dysplasia Clinic, to get us in to see Dr. Rimoin, and then from Cathy, the genetic counselor, to get a brief medical history for Caitlin and to let me know that SHE'D ALREADY REQUESTED AUTHORIZATION FROM OUR INSURANCE FOR THE MRI. Apparently the word of Drs. Krakow and Danielpour was enough - imagine that?
So today we left home early, dropping Evan off in the cafeteria at Newhall Elementary to eat breakfast there, and headed down to West LA. At the last minute the appointment got moved to the Pediatrics division in a different building, but we found it alright. The fun part was that the intake nurse obviously had little experience with dwarfism, which was an odd way for an appointment with the top dwarfism genetics expert to start - but she did just fine. We had to educate her on a few things, but you all know that that's pretty typical for us :-) After she did the initial vital stats, a Dr. Mencias came in to see us. She was an intern with the genetics department, and was also still learning, but obviously knew a lot more already. She was really nice, and did a great job of trying to make Caitlin okay with the fact that she was being examined - which thanks to all the doctor appointments she's been through lately she's having a hard time with.
Dr. Mencias asked a lot of the typical questions, complete with a quick family genetic history. It always amuses me to have geneticists ask if there is any history of dwarfism in the family, since achondroplasia is autosomal dominant and there is no recessive gene, but I guess it makes sense - they're always looking for the exception to the rule. That's how you learn, right? She did a fantastic job with Caitlin, though, and Caitlin was actually relatively calm with her until she needed specific measurements. Cherylle and I had to both hold her still for the head circumference, and Cherylle ended up laying down with her on the exam table to help keep her calm. It didn't really keep her calm, but it kept her still enough to get the measurements.
Dr. Krakow works full time at UCLA now, although she consults with Cedars, but because she'd seen Caitlin at the regional she decided to drive over to see us and join in with Dr. Rimoin on the consult. She asked us if turning Caitlin back around (rear facing) in the car had helped with her nausea problems on drives, which it had, thanks to her advice. She told Dr. Rimoin about what she and Dr. Danielpour had seen at the regional with Caitlin's fontanelle, and he concurred. He was a bit mystified as to why Dr. Tiller had been so reluctant to approve an MRI - we explained that Dr. Tiller had thought the anesthesia was risky, but Dr. Rimoin seemed to think that death from something that could have been detected by an MRI was riskier. Strange - that's what we thought, too - and what we had told Dr. Tiller. Hmmm - that's another blog post.
Anyway, Drs. Mencias, Krakow, and Rimoin all thought Caitlin was in great shape overall, except for the problem with her fontanelle. She's not showing any problematic symptoms - no clonus, no muscle tone problems, no bulging soft spot or forehead veins - but they all still felt it was something that needed to be followed up on asap. They also felt that her increased snoring combined with her minor apnea problems on her last sleep study warranted ordering another one. They also wanted us to have her seen by their ENT, and after the results of all of the above were in, Caitlin will get a followup appointment with Dr. Danielpour to see what, if anything, needs to be done.
Man, just like when we saw Dr. Krakow at the regional - it was so nice to see doctors who say what we think before we say it! It's almost like we've all been reading the same thing - like the Health Supervision for Children with Achondroplasia! You'd think the American Academy of Pediatrics knew what they were talking about, or something!
Well, we'll see how it continues to go - there are quite a few authorizations to get through. I'll keep you updated!
Here are some pics from our recent adventures -
Here's Caitin waiting for the doctors - already worn out from fighting the nurse.
Here she is coloring at lunch across the street after the appointment was over.
Here's Evan getting ready to ride the motorcycle with daddy for the first time this weekend! Woot!
Here's Caitlin looking ridiculously cute in pigtails on her way into daycare on Thursday :-)
Here are the kids with my parents on Sunday - we met up with them halfway between both homes, which fortunately happens to be in Santa Barbara. Beautiful!
Finally, here's a shot of Caitlin on her first night in a big girl bed - it's Tink, of course! The most beautiful fairy of all...
See y'all next time!