Hello and welcome to our family!! We have designed this blog to keep all of you updated on our family and to give hope for families of "O" babies. It continues to be a long road for our little girl
and we would like to share our journey with you.
Thank you for all your love and support.
~Jen, Matt, Kalista and Lawsyn~


Showing posts with label Mehl. Show all posts
Showing posts with label Mehl. Show all posts

Friday, September 24, 2010

Friday already?



"Too bad the week is almost over."

Since Kalista has been home, it is truly amazing how fast time flies each day. On our days off, we never seem to get much done around the house. We are sure that once we get our daily regimen down...it will be much easier.


My taxi service to all my appointments

Here is the latest Kalista news:
  • We saw Dr. Mehl, the pediatric neurologist, this week for her high-risk infant consultation. He is the person who will tell us if Kalista is where she needs to be developmentally. From his exam, she is right where she should be for a cute 4 month old. His only small concern was her neck strength since she has been laid up in bed for so long and not able to get in that quality tummy time. It just means we need to work on sitting her up more and having her hold her own head up. Her reflexes and motor response skills were all age appropriate. Dr. Mehl told us that with everything going on, he is not too concerned if she crawls or walks later than most kids. He also told us she has great communication skills and eye contact. For those of you who have seen or talked to us recently, Kalista is a chatterbox with her "oohs" and "ahhs". Sometimes she even talks herself to sleep. Dr. Mehl told us to look for the "motorboat" sound as the next milestone in speech development. Can't wait for that one! All in all, we don't have to see him until December for her 6 month old follow-up visit and make sure she is where she needs to be at that time.
  • We also saw Dr. Saenz this week for her follow-up on the fundoplication surgery and G-tube. It looks like she is recovering well and we don't anticipate any more visits with him until her final closure surgery at the age of 2 or 3. We asked him about her reflux and the retching that still happens. He told us the retching and gagging, she does multiple times a day, is something she will have to just out grow...poor baby. Nobody likes to see their child dry heave and turn that scary shade of red-purple.
  • So it looks like we have now officially been turned over to Dr. Gossman, the plastic surgeon, for her expertise in tissue expanders. The goal is to make her belly cosmetically appealing for her final closure. The tissue expanders are to create extra skin for the surgeons to work with, so they can discard the scar tissue that is currently on her belly (that purplish skin). She may also get a cosmetic belly button too in the process. We have an appointment with her in the later part of October.
  • We had a few breakthroughs this week in the bottle feeding department. Yesterday, she wanted to suck on everything...fingers...blankets...toys...and even her pacifier and bottle. The last time she truly enjoyed sucking on her pacifier was in mid-July. We'd like to think it means that she is finally feeling more secure about certain items in her mouth and swallowing...but it could also be from the full moon the other day. Odd yet sometimes good things happen when there is a full moon. Since she has been home, we have taken what we learned from OT in the NICU and applied it. So every time she eats now, we make sure we give her different textures in her mouth and have recently started just placing a small amount of milk in a bottle for her to taste and she seems to be more accepting of it. We hope she will catch on and eventually bottle feed most of the time. We know it might be a while from now, but every step counts.

Thursday, September 16, 2010

No Tears


Kalista laying on the pediatrician's table

Kalista saw Dr. Berent (pediatrician) today for the second time this month. We had to see him two days after our discharge from the hospital and then today for Kalista's big "four month old immunization" shots. We had a list of questions to ask Dr. Berent too...poor guy....but we're glad he took the time to listen and answer all of them. It's so true what experienced parents say when they tell you to write down all your questions before you see the doctor...because it works. Twelve questions answered in a matter of ten minutes...pretty efficient! So back to Kalista....it was the big shot day and she did so well. Matt held her and nurse Suzy worked her speedy shot giving skills. Boom boom boom....DONE! No tears!!!. We know that our little girl has been through so much more, that a few little shots would be easy peasy. We hope in two months that Kalista will be just as tolerant and forgiving for her six month old set of shots. Cross our fingers!

So in the grand scheme of things, Kalista is going to be seen by many specialists in the next few weeks and months for all the areas we need to address due to her omphalocele. She truly has a fuller schedule than her parents. In the next month we are scheduled with four different specialists: Dr. Saenz (surgeon), Dr. Mehl (neurologist), Dr. Nigam (cardiologist) and Dr. Gosman (plastic surgeon). Somewhere in the mix we are supposed to see the dietitian/nutritionist and occupational therapist for the feeding issues. Thank goodness for our smart phones or we would be all over the place!