Wednesday, December 24, 2008


Merry Christmas

The Cataldo Family

Thursday, December 18, 2008

Finnian

Its been 1 year since we started the Keto diet with Finnian. We didn't get the out come we hoped for seizure free and no meds, but we are almost seizure free with meds on the diet. His quality of life has improved as his number, severity and duration of seizures has decreased.
What is the Keto diet? Well the diet consits high amounts of fats controlled amounts of proteins and carbohydrates. Finnian takes his concoction via g-tube and w just call it his formula. We still try and make him eat by mouth but he doesn't consume enough to take away one of his feeds.
Our formula is made up of RCF fromula soy based, micro-lipids, water and polycose powder. They say if your child can take the Ketogenic formula it is better but our Finnian has a problem with dairy products. So we use the other mixture.
He is due for another calorie increase due to his growth. Right now he is on 1160 calories a day you might not think it is a lot but the majority of it comes from the fats.
Do I agree with the diet? Yes I do one year ago I had an almost 3 year old that was just there now I have an almost 4 year old that can sit up on his own for almost 3 minutes. That was a huge achivement for him.
I hope we can keep him on this for a while so we can improve his quality of life.

Monday, December 15, 2008

Christmas Pictures

Well I had all planned to do the kids pictures last weekend but as always something was up. Finnian had been sick but thankfully no seizures. I am kind of afraid to say that_-- seizures. The increase in the meds seems to really agree with him. The only thing we notice is that he looses his speech when he gets sick. Oh well just something they have to figure out with him.
Maura was as sick as a dog on Friday night so off to the doctor we went on Saturday well she has basically the same thing that Finny had but without the strep throat. By Sunday she was on the mend so downstairs to the lobby to take our Christmas pictures at the Christmas tree.
Click on the picture link to the right and you can see my handy work.

Friday, December 12, 2008

The Playlist

I know when you click on the blog the music plays but if you don't want to listen to Alison Krauss just scroll down and click on someting else.
There are a few songs on it that mean something to me, yeah I know you can all tell I grew up in the 80's but you should see how alive Finnian becomes when he hears some of these songs.
Please listen to "Scorn not his symplicity" I call this Finnian's song. I wish everyone could see him when I play it. It just shows that there is much more going on in his brain than we know. When he hears the first few note of music he taps his chest like he is saying this is my song.

Finnian's friends

As we go through our journey there are many more parents and children going through the same journey.
Finnian's friends are some of the people going through this journey too.

Please click on the link to the right and read about Jude and his journey and also read about Jordan and her journey.

When your children are driving you crazy and maybe your husband/wife, partner, in-laws/out-laws are just take a moment and read about Finnian and his friends and then you will see we don't take anything for granted. Sometimes the smallest things are huge achivements for our kids.

Sometimes we get thrown for a loop but the one thing we all have in common is the strength that we never knew we had, until Finnian, Jude and Jordan came in our lives.

Dear Finnian

My sweet little boy, 4 years ago on Dec. 9th 2004 we were given shocking news. The news we were given was that God had chosen a different path in life for you to follow.He had made you special in a different way.
I was at the doctor's office on my own and I knew something wasn't right, they kept looking at your small sweet head. I found the courage to ask" What's wrong with his head?" The doctor said he saw something but he wanted to make a call and to come to see him in the office after the technician was finished taking all of the measurements. My little boy you were about 6lbs 10oz and about 19" long and yes you were a boy.
So in to the office I went to find out what was wrong. The doctor told me that your right ventricle in your brain was much larger than what it should be. He showed me what it looked like at 6mths and what it looked like now. I don't know where my confidence came from but I was going to do the best I could for you. " I said ok there is a problem so where do I go and who do I see?" "Do you know what happened?" He told me he couldn't say for sure but something had stopped the fluid from flowing out of your ventricle may be a bleed. He also had the name and phone number of a doctor he wanted me to go and see. I told him I would call as so as I had gotten home.
The hardest thing was how do I tell your Daddy that something was wrong. I sat for a while in the car thinking going over how I was going to break it to him never mind Daddy how would I tell Nanny and Granddad?
My dear Finnian I got through it and I made the phone call and our journey began.
To be honest its a journey no parent should make and its a journey no child should have to make. But life is a journey for learning and believe you me I now know more than I ever thought I would and I am still learning.

Thursday, December 4, 2008

Up date on our Finnian

Well our Finnian has been doing pretty good. His bad seizures are down to one every 3-4 weeks. Hopefully with the last increase in Keppra we hope 4-5 weeks but if not we know what to do.
We have an appointment on the 22nd of December with the Genetic doc. Well we have been playing phone tag with her so I decided just to make an appointment and sit accross the table from her and hear what she thinks that our Finnian might have. Blood tests I will do but if he needs anything else we will see.
Will up date on that appointment when it happens.
I hope to be getting the kids Christmas pictures done this weekend well we will see.
Thats it for now

Food Allergy tests finally done

Well our Eoghan had the last of his food allergy tests done today and the results are,
Clams, Oysters, Crab, Soybean,Buckwheat, Almonds, Peanut, Eggs, Dairy and the one that had the highest reaction was Peas. So Eoghan and myself will not be eating Beanie and Barney Peas or peas of any kind. I feel bad for him because now that we know what his triggers are we have to be careful. The best solution is total elimination of all allergic foods. So now I have to be very careful when buying any processes foods to make sure that there are none of the no-no foods in them.
The allergist said that Eoghan would benfit from a gluten free diet but we will wait and see what the GI doc has to say.
Well thats al for now