GI (gastroenterology) update- It is no secret that I don't have a need for fad diets and weight loss videos, but in fact, struggle to keep on the pounds. I know, I know, you wish you had that problem ;-). I have never even been in the 1st percentile of the growth chart, but have been slowly following my own curve since birth. Some of you may not know that I had a g-tube (surgically inserted into the stomach so you can tube feed through a port) placed at about 2 weeks old so I could eat. I had no suck or gag reflexes so I could not eat orally. Luckily, after about 1 month of being home I was able to start eating and then got the g-tube out when I was 6 months old (sometimes my mom regrets that decision). So now, I eat pureed foods made by Chef Mom. She's not a bad cook- but more variety would be nice. We put lots of things in my food to help me gain weight, like: cashew butter, coconut butter, regular butter, avocado and Duocal (a calorie supplement that is essentially modified corn starch - which makes my mom cringe every time she adds it). But alas, I struggle to meet my weight goals because my muscles are constantly contracting and working all the time.
Sleeping in my big hotel bed! |
At this last visit to see Dr. McSweeney (GI doc) I gained over a pound in 3 months! I now weigh 35.49 lbs. and am 42.5 inches tall. Mom and I were so thrilled! The doc was not as excited (she's new- we won't hold it against her). She would like to see me get on "the chart" so I have a little "reserve". So, here we go- upping the Duocal and feeding me like a spring chicken!
I also suffer from reflux and chronic constipation. Not fun. But, we are managing it and I am comfortable most of the time.
On Tuesday night Mom and I drove up to Boston to stay in a hotel. We had appointments all day on Wednesday, starting at 8am. We got to snuggle and watch TV together. I think hotel rooms are pretty cool.
Waiting for eye exam |
For the next appointments at the CP (cerebral palsy) clinic, my Dad was able to come along. After getting Liam and Addy off to the babysitter he drove up to meet mom and me.
Waiting for Dad |
Neurology- Next we met my new neurologist. He is there to help manage my seizures. Yep- they're back! As a baby I had infantile spasms, which are a type of seizure that occur many times a day (the highest day my mom counted was 89). Once those were treated I stayed on medication until I was about 2.5 years old. Then I no longer needed it. Unfortunately, 70% of people with infantile spasms will develop seizures later in life. Mine started again last October, right before I turned 6. After a few episodes (two of which were pretty scary with trips in the ambulance), mom, dad and doctors decided I needed to start taking medicine again. I've been doing great, but then I had another few episodes two weeks ago- 2 were even at school! Most of my seizures are described as generalized tonic-clonic, and they occur mostly related to sleep. Mom and Dad record me overnight and watch the video the next day to see if I had any seizures. I do not make much noise so Mom doesn't wake up. It is a little scary. We are looking for some kind of monitor that would have an alarm if I started having a seizure. In the meantime, I have to increase my medication. The neurologist mostly manages my meds. I take 3 main things for seizures and muscle tone (mine is really high). We talked today about something called a Baclofen pump. Baclofen is a medication I already take, but it has side effects. With the pump, a little machine is put into your back and a tube delivers the medication directly to the nerves to help calm them. Then you go in every few months for a refill! You don't have the side effects since the rest of your body does not have to process the medication. Of course, putting a pump inside your body has it's own problems. The doc said I am probably too small yet for the pump. I think mom was glad about that for now.
Dad distracting me from the orthopedist |
Sitting in traffic watching Beauty and the Beast |
- functional vision assessment
- augmentative communication clinic
- PT equipment clinic
- Orthodontist
- Audiology test
- Movement disorder specialist
- fittings for 3 new braces
- Physiatrist
And of course, follow-ups with all of the people we saw today!
Tomorrow a nurse is coming to our house for more evaluation of me! I feel so special! Can't wait to go on vacation to Florida next week, I can barely handle the spotlight!
I happened across your blog and so glad I did. Kai, you are AMAZINING, and oh so handsome! I love the pics. Sorry to read about the seizures, they are scarey. My own daughter with CP also suffered from seizures, was severely cognitively impaired, and had many of the same problems. I want to tell you and your Mom about a network I belong to that consists of hundreds of other CP families, and invite you and your Mom to check us out. We are the Cerebral Palsy Family Network. We're always thrilled to have guest bloggers and, would love for you and your Mom to join us! You can also find us on Facebook and on Pinterest. Hope you revisit your blog soon. I look forward to reading more about you. Also would love to hear about the type of Augmentive Communication devices you use and like :o) Please come visit us. You would be a wonderful inspiration to so many of our families!
ReplyDeleteLee-
DeleteThank you for reading Kai's blog! I briefly checked out your website. It looks like a wealth of info! We would enjoy being a guest blogger.
At this point Kai does not have an adaptive communication device. Everything he "writes" on the blog is my interpretation of what he may be thinking. Unfortunately, we have not tapped into his world yet- but hope to in the future!
I look forward to reading more on CErebral Palsy Family Network.
THANK YOU for your quick reply :o) I love your creativity and "interpretations" for Kai! I hope you're successful in finding Kai the right AAC devices that will open both your worlds :o) I'm anxiously looking forward to the day when you will be writing about Kai's first experience with a communication device. If you ever have questions or want to "talk about" the Baclofen pump please don't hesitate to email me. My daughter was one of the first pediatric patients in the country to get the pump for CP and was on ITB therapy for 15 years. For us it was the answer to our prayers but I've read of some families that didn't realize the same level of success. If you ever want to treat CP Family Network to a guest blog, and can find the time, you can email it to cpfamilyblog@gmail.com. The only thing they ask is that it be 400-500 words and be CP related. Thank you for accepting my offer to blog!.. Now that I found you and Kai, I look forward to your future blogs. If you want some insight into whats out there for augmentative communication devices, I put up tons of pins on our Pinterest sight that will give you some insight. Also, I'm not sure if you've had time to check out Medtronic's Baclofen page. My daughter had the Medtronic pump so I'm very familiar with their site. It gives a very thorough description of ITB therapy. Big HUGS and Happy Holidays!
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