“I write my name…..on my leg…..”

On Sunday I gave Gabriel a couple of mothers day cards to sign. He wanted to keep the pen, so I gave him a blank piece of paper. Before leaving him alone I  reminded him “write on paper”. About a minute later I hear him say “I write my name (Pause)….on my leg”. I turn the corner and sure enough both legs are covered in black pen marks!  I can’t help but smile!  There he goes being all 3 again….pushing the boundaries just to see how much he can get away with. Needless to say the pen had to go to time out.

This was the 2nd incident this week that I found myself with wonderfully conflicting emotions! Soo frustrated because we have been over the “write on paper” bit about 70,000 times….at the same elated that the my sweet boy is wanting to write and telling me about it!

The first incident was on Wednesday morning as he was getting dressed to leave the house. I was holding the shorts he was stepping into, and he bent down and bit me! Twice on the arm!

I immediately sat him down and said “No! We do not hurt each other in this house. That hurt Mommy! Tell Mommy “I’m sorry, I won’t bite”

to which he replied…”No I not! I go to time out.”

He then took about 5 backwards while saying “I walkin backwards”.

Sits down for 3 1/2 seconds, stands up, walks to me, gives me a hug while saying “I sorry”

Seriously melt Mommy’s heart! He not only figured out his wrong but knew what to do to fix it.  The best thing is these were 2 things that had been BIG headaches for me several months ago before doose hit our lives. Makes me feel normal 🙂

Things with the diet seem to be going well.  He has not had any  “big seizures” in several days now. He does continue to have 1-3 little head drop or quick partial falls a day. My husband reminds me these are still seizures and our job as his parents are to advocate for NO seizures.

We go for his follow up appointment with the nutritionist and doctors tomorrow afternoon. I am slightly anxious…just because I don’t know what we will find out or if things are going as well as we hope.

 

Mother’s Day Powell Gardens

We went to Powell Gardens, a local botanical garden, today for Mothers Day. Gabriel and I met parents and my sister as well her husband and his mom and brother. I was sure to schedule things around his medicine and meals (he ate lunch right before left and he ate a waffle in the car before we drove home). Obviously, Mother’s Day has taken on a whole new meaning for me this year. Not all about me…but about my heart full of love and hope for my boy!

"Cheese" Look at this sweet face peaking through one of the forts at Powell Gardens. Amazing shot of his face! These are hard to come by!

 

Gabriel's adorable cousin, LYDIA!

They say cousins are your first friends. Hope these two stay close friends for a lifetime.

Overlooking the lake. Trying to get pose of all of us facing away from camera. As usual G is looking the opposite way. Oh well 🙂

All the mommies! Left to right:Sharon Treese, Lisa Treese, Amy Russell, Barb Fluchel (notice both kids have their hands in the mouths!)

It was a fun afternoon. It was nice to be in an open public space and not have to wear his helmet! He has been pretty steady on his feet lately. He still have 1-3 small head drops or trips each day but they are not enough to necessitate extra head protection.

 

 

NO! Stop! What are you doing?

Today, I got to say things “No”, “Stop” ,”Not safe”, and “What are you doing?”. My little man is acting like a regular 3 year old, pushing the limits 🙂 So exciting.  He was a total chattberbox today, asking lots of questions, bossing my around. “You STAY THERE! “Put your glasses ON!”

He went to the church nursery for 2 hours today while I was in my mom’s meeting, then we went the local children’s farm, and then he played outside for hours after his nap.  He is so great about his helmets! He just goes to grab one anytime he is going to play outside! We maybe going a little overkill with them on good days like today, but he isn’t bothered by them and gives us extra peace of mind.

Gabriel and Grandma transplanted the flower he started at school yesterday.

He loves his new t-ball tee!

He even kind of let Grandma help him.

Last week, at this time I felt like I was hanging off  tallest building in town, gripping on for dear life, hoping not to plumet to into certain disaster. This week, things are much better. I’ve been saved from the immediate danger and have my feet firmly planted on the rooftop. The only problem is I am still on the rooftop and I belong on the ground!

Doose has certainly turned our lives inside out, upside down and caused all kinds of crazy….but for today…the view from up here on the rooftop is good. My kid did have not seizures today, he is talking, laughing and playing.  He has had 2 good days in a row. I made sure to stop and write down a few of victories today because we will need them for darker days when the rooftop seems too high and unsteady.

 

 

Back to school!

Gabriel got to go back to school today! He even ate lunch there! Chuck’s mom spent the day in the classroom with him, just to be sure he didn’t have any seizures or other issues.

Playing Dominos with one of his school friends.

Playing outside. Apparently he ran to the top of the play structure first thing.

He loves the diggers on the playground. He does a great job wearing his helmet. I heard all the other kids were really nice about it too.

Our boy loves trains! So fun to see pictures of his day and hear a great report. Since, he only goes one day a week, next week will be his last day of school for the year. Sniff, sniff…his first year of “big boy school” has gone by so fast.

Better days and Waffles

We have had several good days with little man. He had 0 seizures today! Woo hoo! Yippee. His little personality is starting the shine through again. He has been playing with his toys a lot and asking us to read him books and play puzzles. He is not interested in watching tv because he wants to play! (OOPS…I was wrong…he had 1 very small seizure early in the morning but bounced back after medicine!)

I channeled my inner Rachael Ray again tonight, and taught my mom how to be a Keto Chef.  We worked together and made Gabriel’s Pecan Applesauce Waffles.

Here we are hard at work.

Getting set up: Recipes, ingredients, cups and scales

2 waffle meals ready to eat! (We made 8 total)

While, we cooked Gabriel and my dad played trains.  After watching Chuck take pictures of Nonna (my mom) and Mommy, Gabriel insisted that we take a picture of him and Papa too!

We were cooking for about an hour and a half.  When we started Gabriel had just eaten a pizza and was having a great time playing. By the end he was begging for a waffle. I felt so bad having to say no 🙁 but at least I have some food ready for the week!

 

What A Day.

The facts of today are good.

  1.  Gabriel only had 1 seizure, which was not until 8 o’clock at night.
  2. He had an EEG that did not show seizure activity.
  3.  He had an awesome time playing with his friend Jack at Crown Center.

Even with many good things it was a roller coaster day.  G and I got home about 12:30 from our playdate. Chuck immediately informed us that the hospital had called to inform us that Gabriel’s doctor had scheduled an EEG for him at 1:30. We quickly gathered everything together and hit the road, while calling the doctors office to find out why we were getting the EEG.  We found out the EEG was to determine if some new facial movements were seizures.

Since Gabriel was having his first good day since Monday, none of the distinct issues occured. There were several “events” during the EEG but we don’t know what they were. Our doctor called and left a message before we even got home that the EEG was not showing seizures and to call back. By the time we got home and called back we had missed the doctor. Which means we are waiting until Monday. So hard.  I am trying so hard not to be consumed by fear and worry.

I was looking up a verse about Moses online and Bible Gateway had the following verse as the verse of the day:

“Do not be anxious about anything, but in every situation, by prayer and petition, with thanksgiving, present your requests to God. And the peace of God, which transcends all understanding, will guard your hearts and your minds in Christ Jesus.” Philippians 4:6-7 NIV

The perfect verse for me. It is one I have tried to weave into my life for the last several year. Perfect timing because it was the verse for the day starting at midnight.  I read it 12:30…way after I should have been in bed but I was awake nervous and worrying…about my son, my husband, myself….our whole little family.  My request to God is that Gabriel gets to be a fully functioning member of society during his life on this earth and that his life is long and full.

Bad Days and Brownies

Sigh…we have had 2 bad days in a row. Which we hate! Monday was awesome…so we knew Tuesday would be bad. There is a clear pattern of a bad day after a good day. We were saddened that today was bad as well. I can’t count the number of times I have thought “this is as bad as it gets” over the last 2 months, just to be confronted with something worse. The day began at 2:30 a.m. with a 4 minute seizure that led to mouth clicks. He rested but did not sleep until 6 a.m. when he got hysterical because he was so hungry. Today was difficult because he had several quick and aggressive seizures that cause him to fall down. Afterwards he cries (I don’t know if it is frustration, or pain) and will not let me console him. He also had tons of little mouth clicks (well over 100) that disturb him. On top of the seizures he can’t seem to go to sleep even though he is tired. He was very upset for a solid 3 hours today. I spent 2 hours driving him around in the car. He would quiet down and almost fall asleep. Whenever I would pull in our driveway he would shake his and scream. We stopped by a friends house and sat outside on the lawn and he sat in a swing for a few minutes. He seemed calm and relaxed the whole we were there. We did have some up moments in the day. He watered flowers with Grandma, chair danced to Yo Gabba Gabba and around 5 (after his first dinner) he perked up a bit and started talking. I went to small group tonight and got a report that he was talking and playing while I was gone.

 

BROWNIES!On a brighter note….I got to cook Gabriel brownies! Now that he gets some extra calories the nutritionist sent me some yummy snack options.

 

I had to do some grocery shopping because I did not have flax seed meal, coconut oil. Since everything has to be brand specific as well, the only ingredient I already had were the ground macadamia nuts.

 

Mixing in the sour cream….seriously….yummy!

 

The foil pan I created per the recipe directions (first time I have followed instructions on creating a baking device!)

 

Finished product. (Hard to see but they look like brownies!) This pan made 10 snack servings for him. He liked them A LOT! Maybe next time he will eat them slowly enough for me to get a picture!

More Calories!

We got approval today to give Gabriel more calories per day. He will have 10 extra calories per meal and an extra 100 in a snack. We are very excited as we hope it will give him more energy. He was asking for food all the time and clearly got exhausted about an hour before it was time to feed him. We are also adjusting his ratio from 3:1 to 3.25:1 (giving him a little more fat and hopefully more energy)

It was so fun to give him a snack of Keto Fudge and strawberries today. The extra calories clearly helped because he did not eat all of the brand new mac-n-cheese we made for his dinner.

We were so excited to finally have a mac-n-cheese offering and he did not seem to like it. I think he doesn’t like the aftertaste of cream. Everytime we to get him to eat cream he will take a couple bites, then a few seconds later make face and kind of shake his head and shiver.  We are going to try again with a super sharp cheddar cheese, hoping to hide the heavy cream flavor. Hoping we find a mac-n-cheese he likes.

He had a lot of energy today. Went to a playdate, then open time at his gym. We are planning to take him to his day at Child’s Day Out tomorrow. We are going late so he will skip snack time but we are packing a pancake and jell-o for him to eat lunch at school. Hopefully, it will go well. He loves being around other kids and is clearly missing it.

Now I need to go print off all of his recipes and rebuild our cookbook. Very excited that we have snack recipes now and need to update all the old recipes with the new ratios. I am truly thankful we have nutritionist to work with and figure out all the calculations for us.

 

Thrill of VICTORY, Agony of Defeat

Today began with the victory of a new meal Gabriel will eat!  Chuck worked with me last night, as I channeled my inner Rachel Ray, to create a pecan, applesauce waffle for our little guy. The applesauce waffle makes 4 meals that he will eat! So far, we have eggs and cheese, Keto Pizza, Keto Blueberry Pancakes and Pecan, Applesause Waffles.

We used applesauce, cream, eggs, pecans and a few other ingredients to make something a little bit sweet and CRUNCHY for him! I can tell he is really missing crunch and specifically toast. He asks me everyday for bread or toast and mac-n-cheese. (We think we may have a solution to the mac-n-cheese arriving from Amazon on Tuesday).

Showing off the beautiful creation. It actually looks like a waffle! (Notice him sitting in his chair behind me. He runs and jumps up there every time he thinks he might get food).

Chowing down the waffle! No time to stop and smile! The cup on the side, is filled win an AMAZING chocolate whipped cream sauce, that he would not touch! We are putting extra cream, in some form, on his tray at every meal.  My hope is at some point he will try and like something!

The agony of defeat portion of the day came when Gabriel had a 3 minute seizure that began while he was sitting in his chair after dinner. Chuck ran out to the garage for a second to grab something and came back to him seizing.  Seconds before he had been chatting with his Grandma Gaye, who was in the next room. That is how fast and without warning they happen.  He has had other seizures this week but this was the first time he had one in the afternoon in the quite a while. Sometimes the sets back feel small sometimes really big. Tonight felt like a big one.

We are trying to focus on the VICTORIES! I was chatting with a friend on the phone today and she challenged me to write down the victories. No matter how small, write them down and post them somewhere right in our faces. I am totally doing it! Our victories for today are a new meal, and a fun night checking out train displays at the mall.

Anyone else struggling with focusing on the defeats? Want to join me in focusing on and celebrating the victories?

 

 

 

 

Grocery Shopping Alone

I never imagined there would be a time when I would miss taking Gabriel to the grocery store with me. Let’s face it grocery shopping with a young child can be time consuming, chaotic and exhausting.

I ran into Hy-vee to get tomatoes for Chuck and suddenly found myself very sad. This local store offers free cookies to kids. It has been a favorite routine of G and I go to grocery shopping here. He was always in a good and silly mood while munching on his cookie. We would sing silly songs while walking down the aisles, he would ask me to spin him around in the circles in the cart, or give the cart a huge push and let go.

We have been able to avoid foods he is not allowed to have so far. I know the time is coming when we will have to say no to cookies, chips, cake, ice cream and all other foods that he might see while we are out and about. I know it  just food, but it makes me sad that his brain doesn’t work right, and because of this he is going to feel excluded and sad.