Brisan and Parker Stults | Living with Niemann-Pick Type C

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Brisan at CMH 2-18-11

On Saturday February 19th Brisan returned home from Children's Mercy Hospital. Jenn had taken him in on Wednesday evening with concerns form our carousel & his school nurse along with ours that something was going down. He had puffy cheeks, feet were swelling, and his abdominal area was pretty hard. Back in September, these were similar things that took place. We wanted to be cautious and even more proactive to prevent him from going into distress.

Jenn had asked for them to culture the inside of his g-tube hole but at the given time the consciences was that might not be the problem. Over the next day it did grow and sure enough it was another Staph infection. Along with that he has an upper respiratory infection of some kind going on to.

He is at home resting and appears he will be making a recovery with the antiobotics and game plan they've set fourth for us at home.

*Should be posting Parker & Duncan's birthday pictures soon! Also a news video of our family from a few years back.

Parker At KCI Airport

Can you believe it is mid February already? About 3 weeks ago Parker received his new chair and he seems to really like it. I say me and Jennifer like it to ! 🙂 He has been having issues with his balance because of the cataplexy. When we let me out of his chair he starts to giggle then it is “man down”. That has been our little joke in the house if him or Brisan falls down. Not that them falling down is funny because it is some serious business. They get hurt, break noses, and just look like they got in a bad bar fight.

It is hard to see these kind of things because it means Niemann-Pick Type C (NPC) is really doing it's dirty business. When you first see the boys you kinda of think they look “OK”. Then you interactive with them and it is all apparent. We contemplate what it would be like if they were just more typical kids their age. What would they say, do, and their activities. What would their voice really sound like? They are very sweet and we do know their voice but it is so few times we get to hear it more everyday.

We are very thankful for every single person that comes to our website, donates, and especially lifts our family up to the Lord. It is hard to stay focused when your pulled in so many directions to keep the Lord the main priority. I mean giving him every single piece of your life. In retrospect if this was all meant to be easy with or without this disease in our life, would we really develop the appreciation for his grace? Would we develop the since of gratitude that his blessings provide? It is about continuing forward and being thankful in every little way. Thank you!

Parker lately has been having gelastic cataplexy attacks very frequently. We've had both Brisan & Parker on medicine to help this but the last 3-4 weeks Parker seems to be reacting differently to the changes Niemann-Pick Type C is placing on his body. This is all to be expected.

Parker laughing is a joy to watch because he is so innocent with his sweet soul. The bad part is when he does start this laughing “fit”, it creates a loss of muscle control & tone. He essentially becomes a noodle and falls. Saturday (1/29) he was out of his chair getting a diaper change and he stood up for a few moments and then accidentally fell into the corner of the wall gashing his head open. We've been trying to get video of him trying to walk and when he has these cataplexy episodes. Hard to plan for those things…

Sadly we have to keep him and Brisan more in their chair although we hate doing this. The other challenge is we can't be a 100% of the time hovering over both of them to keep them safe. It just isn't possible and especially with a little squirrelly three year old running around.

Starting on the next school day (depending on when that will be with all the snow expected tonight), we will be sending Parker to school with his wheelchair just like Brisan. Now that doesn't mean he can't get out and roam around but it will provide a safe haven for when he is unstable. This has worked well for Brisan at school. It just takes one good fall to do some serious damage. You and I don't think much about this because we typically have enough control to protect ourselves on a fall. It would be like free falling out of the sky and hitting the ground. There is nothing you can do to soften or protect yourself from the impact.

Last week Parker fractured his nose (1/22) because he fell. That all happened within a matter of minutes.

Here is a video we shot on Sunday (1/30) showing Parker laughing. He was going really good earlier before I grabbed the video camera to record. You'll notice he has a couple good head drops along with the vertical gaze palsy (issues with moving the eyes up/down/side to side. the “awkward” eye movements.) Plus the poor kid needs a hair cut????!!!!

Last July 2010, my parents (Mike) helped organize a fundraiser for Brisan & Parker. During that time through mutual friends they were introduced to Hazel Kinder who lives in Columbia, MO. That is about 1-1.15 hrs from Kansas City. During the late 80's through the late 90's she lost 3 of her son's to Niemann-Pick Type C disease.

I can't imagine going through this whole situation during that time when the internet was just getting started and networking to find support with other families. We are thankful that she wanted to be apart of our story and journey.

KOMU.com out of Columbia, MO did a small story on the event.

Happy birthday to Parker & Duncan! Parker turned five this month and Duncan turned the big three!

Here is a video from their party. I was going to say short video but it is much longer :).

Thank you so much to all that came out even with all the snow! They both had a great time. Also thank you to Lee & Julie Bailes for taking pictures (will update this post as soon as we have them uploaded to get on here).

[ View on Youtube: http://www.youtube.com/watch?v=_hGZCnfvFsU&hd=1 ]

We haven't wrote for a few weeks. I went out of town for work last week and Mr. Parker on the 8th turned the BIG # 5!

The new year has started off well. Things for work (Mike) have been going well and progressing nicely. Jenn has started her master classes for school. I know she is so excited (minus the homework). Still trying to find suitable insurance but the price tag is very scary. It is well more than our mortgage yet we know we have to make a decision as soon as possible.

Brisan has been doing much better but he did develop a rash around his port-a-cath this week which caused us not to be able to access his port for their DDVAP infusions this week. On that note…looks like they have made arrangements to keep the supply of the drug to us :). Thank you for your prayers! The rash is essentially a yeast infection. You don't want to risk injecting that into the bloodstream because of the risk of all kinds of non fun stuff for him. We are applying topical and an oral medication to get through it. Brisan is a funny boy…. cute as well. He doesn't like to take a nap and we are glad he is being  himself since we've got a hold on that previous eye infection.

Mr. Parker… oh Parker! We should be getting his new wheelchair anytime (like six months later). It is identical to Brisan's but his will be blue. Still issues with bleeding but they are much more controlled. Now that doesn't mean we can tame him during the times we need to get the bleeding to stop :(. He has been enjoying school but you can clearly see his struggles walking and transitioning to different services. End of last week I went up stairs to check on them and he was stuck on the floor in between his bathroom door and the hallway.   He doesn't know how to compensate to get up since he couldn't lean forward to gain leverage to be able to do so. Hard to imagine that 5 years ago we were blessed to have him!

Duncan's 3rd birthday is upcoming on the 28th this month! This boy is something else…oh wait, maybe normal for the most part? He never ceases to amaze us. One day I came down from upstairs and he said “Hi Dad, whats up?”. LOL We've been working on potty training with him. I think he owns more underwear than all females combined on our block. It's like he needs to make a fashion statement!

Duncan was evaluated for potentially going into a pre-k class like Parker but the school district is saying he isn't smart enough to be a peer model yet not “dumb” enough to be apart of the program. (No that wasn't there exact words). We felt he should qualify based upon other areas. He especially has two older brothers that are poor models for him to interact with. We would like to get him around other kids his age as much as possible. It would be nice if we didn't have to work to be around him all day and just have a blast with them all!

Thank you again for everything!

[cincopa AwAAEbaOqDwD]