Tuesday, March 25, 2014

Pokemon

The boys have been attending a lot of Pokemon events this year. Besides the MN events they have traveled to Wisconsin for a state tournament, Iowa for a state tournament, Missouri for a regional tournament. In a few weeks they will be heading back to Wisconsin for another regional event. After that it should slow down a bit until July when they hope to go to Indiana for Nationals. If either of the boys get enough Championship points to get invited to World's that will be in DC in August. Shane is very close with only 26 more points to go out of the needed 400+.

They have won hundreds of dollars worth of Pokemon cards, playing mats, baseball hats, deck boxes, trophies....

**UPDATE   MN state tournament was tonight and the boys did GREAT! Tyler took 16th place out of 65 or so in the master division and Shane took 2nd place in the senior giving him more than enough points to get an invite to WORLDS!!

 Also, we just found out that Shane is 15th in the nation for championship points. If he stays in the top 16 he will get a travel award and a $300 Travel Stipend to get him to Nationals in Indianapolis this July. If he were to fall to the 17th-30th he would still get $750 Travel Stipend. There are only 2 more big events before the championship points are tallied up and awards given. Tyler will also have a good chance to get the same as Shane with championship points if he can do well in these next 2 regional tournaments. Technically, Justin has a chance too. ;)


Saturday, March 22, 2014

Reflecting

I have been thinking a lot today about this day last year. I remember it so clearly.  It was the MN state championship Pokemon tournament. Jonah was just a few weeks into this whole seizure thing. I was still scared to be home alone with him, especially at night. My mom was over all day then my sister came to hang with us until they got home around 10pm. I remember being so scared and upset that our little 2 year old had what we thought at the time was toddler epilepsy. Most kids will go on medication and outgrow it in a couple years. Looking back, what I would give for him to have "toddler epilepsy" now. That would be so much less complicated that than the kind of epilepsy he has.

Florida


We are having an AMAZING time in Florida. Everyday has been beautiful. It has been in the high 70s to high 80s everyday. I have been able to spend a lot of time hanging out with Vanessa and James. Sometimes that is hard to do at home as I try keep Jonah safe. I'm so thankful for my husband for making it all possible.




Paper bags

Jonah loves his decorated paper bags!

Barb and Jim are still making Jonah's food. Each meal gets a brown paper bag. 

Family, friends and complete strangers have stepped in and decorated Jonah's brown paper bags. Sometimes it's the little things that make a big difference. 

Thanks to all who have decorated bags for Jonah. We look at and read through all of them! Here are some of them:




Wednesday, March 12, 2014

Venting

My heart sank this morning as I received a text in my bed in Florida that Jonah had a tonic clonic in his sleep early this morning. All the anxiety that has taken 4 days to be lifted came flooding back in a second. I don't know how much of this seizure roller coaster I can handle. It's not fair for Jonah and it's not fair for my other children either. He had just gone 4 days with NO seizures. 

Wednesday, March 5, 2014

Great news, Jonah only had one drop today. That is so much better from the 10+ he was having last week. Let's keep praying the seizures stay away. Thanks. 

-Kristi 

Sunday, March 2, 2014

1 Year Anniversary

Yesterday was the one year anniversary of Jonah having seizures. I was really hoping that a year later they would have been completely controlled with medication or diet.

Most kids with childhood epilepsy can find a medication that works for them and have complete control. Unfortunately, with the kind of epilepsy that Jonah has, his seizures seizures are hard to treat. The BEST treatment for what he has is the ketogentic diet. 

He has been on the diet now for over 4 months. I believe he will become seizure free with it. We just need to keep tweaking it to find his sweet spot.