Bug in Air

Bug in Air

Tuesday, June 14, 2016

Fun, Sun... & Back Inside

Rayleigh has had good weeks and bad weeks since our Make a Wish trip to Disney World. The good weeks are really good and the bad weeks still aren't as bad as this time two years ago - or even as bad as this time last year which was during her Charlotte's Web Hemp Oil Days. 

We switched Rayleigh from Charlotte's Web Hemp Oil to Palmetto Harmony CBD Oil a few weeks before the Disney World Trip in February. It has been better for Rayleigh at seizure control. In April and May she had several days where she only had 1-2 seizures a day (from 5-8 last year). And the "bad weeks" that I mentioned have nothing to do with seizures really, in April Rayleigh's chorea movements flared back up during a short stomach bug that she had. Then they appeared every week but only for a few days. We were keeping Rayleigh's neurologist updated but weren't concerned because this has happened before with her involuntary movements. 

But then she had a flare that lasted 10 days and that just wasn't her norm so we contacted the neurologist and she recommended started Artane/Trihexyphenidyl. This is a medicine commonly used to treat Parkinson's but it helpful for similar movement disorders as well. Within 1 week her chorea movements, which were quite aggressive at the time, subsided almost completely. Rayleigh was back to falling asleep on her own at night without the disruption of constant movements and she was able to enjoy her days again! And her favorite part - she was able to get back in her routine of school of therapies! When her movements are violent we pretty much have to put everything on hold because she needs constant one-on-one care to prevent her from hurting herself and to keep her calm. Part of Rayleigh's chorea includes anxiety and possible depression - heartbreaking.

After we got the chorea pretty well controlled Rayleigh developed Dystonia. Wikipedia defines: Dystonia is a neurological movement disorder in which sustained muscle contractions cause twisting and repetitive movements or abnormal postures
Our Bug's dystonia involves her head turned and locked to the right, her legs want to be bent, and she keeps her shoulders far back so that her arms hang back too. 
We went up on the Artane medicine (two times actually at this point, to 3 ml twice a day). This seems to be helping although she still has random days of strong Dystonia which is puzzling. Our girl is a puzzle. A beautiful, confusing puzzle that you just want to solve.

This blog is titled the way it is because one of the major side effects of Artane presenting for Rayleigh is heat intolerance and sun sensitivity. This is a first for us really, she's definitely been on medications that can cause these effects before but she's never experienced that side effect luckily - until now. It's been a huge bummer for us this summer. I'm having to find fun things to do indoors and that's just not where she loves to be in the summer, usually. Rayleigh loves to go in the backyard with bubbles, and books, and coloring books, and children's music, and Mommy. We used to spend at least an hour on a blanket in the backyard any given summer day. Now, her maximum time in the sun is 15 minutes and in the shade maybe 30 minutes depending on the humidity. She starts to get red in the face and little sweat beads, even heat exhaustion. I'm so nervous about heat stroke that at the first sign of her getting too warm I immediately bring her indoors to the air conditioned house. 

Hopefully this side effect wears off over time as her body gets used to the new medication. Until then, we will be at Target, the library, and the science museum in hopes that we can return to the zoo and walking parks soon! 

On the lower dose of Artane she was still able to be in the sun for a little bit before getting too hot. My sunshine angel.

Daddy added these lantern lights on each end of her bed - I think she likes them!

This was taken right after getting outside, a few minutes later was the first time that we had to go back inside because she was getting too hot. 

We have lots of fun indoor activities like Kinetic Sand, manicures while she's in her stander, switch activated Minnie Mouse toy, reading stories, coloring together, making crafts together, and having friends over for play dates!
One last thing I should note is that her seizures are drastically lower these past few weeks. She's even had some seizure free days!! Most days she only has one seizure, if there are other factors in play (constipation, too hot, full moon, sick) then she might have up to 4 but that has only happened twice since the change. The change being fewer seizures but having chorea/dystonia. We love her neurologist and are working together to lessen this dystonia without disrupting the seizure control she has! Her neurologist believes that the exchange of seizures and movement disorders are because her brain, all children's brains, is changing as she gets older. The pathways develop and new things can evolve for children with neurological disorders. Let's hope that we can get the dystonia calmed down and keep the chorea movements and seizures at bay - in a perfect world! 


Sunday, March 20, 2016

Rayleigh's Wish Come True

Three weeks ago from today we were boarding
an airplane with Rayleigh for the first time.
Our destination? Disney World! 




Make a Wish Oklahoma granted Rayleigh the most magical trip to Disney World. Better than we could have even dreamt up! Rayleigh, Michael and myself were sent to Orlando, FL to stay in the most exclusive resort you have ever heard of! It is called Give Kids the World Village and only families going on the Disney World trip can stay there. It is almost fully run by volunteers and everyone staying there has a big commonality - we have a child facing a life-threatening illness AND love Disney! 


Rayleigh did wonderful on the flights - not a single seizure on the airplanes! 

Rayleigh got to meet the pilot and see the cockpit!

Enjoying a little Frozen on the flight :)

We were greeted at the airport by a GKTW volunteer who helped us get the
rental wheelchair van that Make a Wish arranged for us!


So from here I will just share a bunch of pictures! 
Day 1: Magic Kingdom
She was mesmerized by Mickey!



We have arrived at Magic Kingdom!






Rayleigh was loved on by so many princesses that week!










On the monorail back to the car at the end of Day 1
Can you tell that she enjoyed Magic Kingdom?!??

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Day 2: Animal Kingdom in the morning and afternoon & Hollywood Studios in the evening
Rayleigh with Mayor Clayton - the Mayor of GKTW Village



She LOVED the Festival of the Lion King show!



Excited to go on a safari ride!










When we first arrived at Hollywood Studios we went to a Disney Jr. play and Rayleigh loved that!  Then we got to meet all of her favorite Disney Jr. stars!
Doc McStuffins
Jake from Neverland Pirates
Sofia the First

Daddy even got to Nerd Up in the Stars Wars Launch Bay

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Day 3: Epcot in the morning, then back to Magic Kingdom!
Rayleigh got to pet a horse at our village before breakfast on Day 3!
We didn't last long at Epcot. Rayleigh ended up having her first bad day, a cluster of seizures threatened to ruin the day starting at 10am. We quickly sought reprieve at the First Aid station in Epcot and because the seizures just kept coming hourly, we ended up staying in the station over 2 hours and had to give her a rescue medication while there. Luckily it is one that wears off fairly quickly, but it sedated her for almost 3 hours. After she started waking up we headed to Magic Kingdom. But we were able to see some neat things on the way out of Epcot ;) 
Epcot's Flower & Garden Festival was going on while we were there




Magic Kingdom Princesses:





On Day 3 at Magic Kingdom she went on the Dumbo ride, Peter Pan's Flight, It's a Small World, and the Magic Carpets. She really really enjoyed every single ride! After riding rides and meeting princesses we found spots near Cinderella's Castle for the nighttime show and fireworks. She really got a kick out of that, too! Our girl is definitely a Disney girl!!! 

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Day 4 also turned out to be a pretty seizure-y day. We mostly explored all of the fun things to do at Give Kids the World village where we stayed! We also went out to visit Disney Springs for some shopping and lunch. We got back to the village in the afternoon and just in time for some very special visitors! Rayleigh's Grandma, Uncle and Aunt drove in to stay with us that night and go to SeaWorld with us the next day!! 

She rode the carousal at GKTW a couple times that week :)
Once in her wheelchair in this spot and once with Michael and I holding her on a pony

Daddy showing Rayleigh a Chewy backpack - no, he didn't buy it ;) 

Rayleigh getting her nails painted at the La Ti Da Spa at the village

She also got some light makeup and a dolphin tattoo! Mommy, Daddy and her Aunt also got aquatic tattoos so we could all wear them to Sea World the next morning!




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Day 5: SeaWorld


Ready to see some penguins!

Good thing we bought a towel at the Shamu Show earlier that day! She needed it as her blanket
because it is literally 32 degrees in the penguin exhibit!

Brr! After this we headed downstairs in the exhibit to watch the penguins swim under water, she liked that a lot!

A penguin caretaker saw our Make a Wish shirts and asked if we'd like to go backstage and pet some penguins!!!!




Rayleigh liked these loud guys! She even threw them a fish (with Mom's help of course)!


It was such a super fun week! This trip was so magical and wonderful and stress-free! Everything was taken care of for us by Make a Wish and Give Kids the World! I know it's cliche but we really did make memories to last a lifetime. We can't think the team that made it possible enough!