Thursday, July 12, 2012

Tuesday, June 19, 2012

Jetty turns 3!

I slept through my entire party but I hear it was a great time. A bunch of family came to see me with presents, Daddy grilled burgers and hot dogs, Poppop brought crabs, and Mommy made me a cake. Maybe next year they will wake me up!

Sunday, June 10, 2012

Daddy took me swimming today to cool off. I've been very tired lately so it was nice to take a refreshing dip. I'm gearing up for next weekend as that is when I turn three!

Friday, June 1, 2012

We went out for dinner to celebrate Grandma's birthday!

Thursday, May 17, 2012

I was hesitant at first... thought Clay was driving this thing!



Monday, May 14, 2012

I'm feeling great! Been very sleepy but feeling so much better. Mommy had a great Mothers Day thanks to the herb garden I made her.
I am a month away from my 3rd birthday and I am really looking forward to it!
Daddy took me, Clay and Olive to the dump this weekend. I was excited to get out of the house but... the DUMP?... Really Daddy?

Monday, May 7, 2012

Swinging

Olive let me sit in her swing. I even got a break from my oxygen and did ok.
I am doing GREAT! My seizures are at an all-time low. I am tired a lot and still need oxygen all the time but am happy to be home with my family and doing well.
Mommy wants to send pictures of me to the hospital to show them how well I am doing. Thank you to everyone who has been thinking and praying for me. I know that has a lot to do with why I am doing so well.

Wednesday, May 2, 2012

I've been doing well the last few days. I really enjoyed the boat ride but got some sunburn on my face... Thanks Daddy.

Went to my cousin Brenna's birthday party Monday night. I slept in my stroller the whole time but heard it was a good time.
I received a package today all the way from Montana! The Seacats (dear friends of mine) sent me this heart stone that they find on the river banks.

I'm still hanging in there. My seizures aren't too bad and my nose is healing nicely. My breathing is the same but this oxygen machine really helps. I really like having food in my belly again rather then getting it through IVs.

Sunday, April 29, 2012

Went on a boat ride this afternoon! The weather was great and I was feeling good too! I require oxygen all the time but my seizures haven't been bad at all.

Saturday, April 28, 2012

Jetty's Baptism- 4/28/12- Fleetwood Residence



So today I was baptized by a very nice gentleman named Reverend Vance. I am not sure what a Baptism is but it consisted of my family, great food, and a wet forehead.










That brother of mine is always a jokester.






Friday, April 27, 2012

Clay and Olive sure are happy to have their big brother home. I just wish they'd ease up on my face a bit!
I've been doing a lot of sleeping since I got home. I guess I am just catching up from the past several weeks.

Thursday, April 26, 2012

It's 9:30 pm and i am more calm than i have been in weeks. It's amazing how much better I do at home!
This is what was waiting for us!

Heading home

Mommy and Daddy are here this morning to take me home. We are waiting for the medical supply company to deliver the equipment to us here in the hospital and train Mommy and Daddy how to use them. They want to use ambulatory services to get me home but Mommy nixed that! There have been many visitors (doctors, nurses, specialists, case workers, etc) from all over the hospital that have met me at one point over the last few years, come by to say goodbye as they have heard that I was leaving. My nurse today is in awe and thinks I am famous. Hopefully we are out of here in a few hours!

Tuesday, April 24, 2012

Mommy and Daddy sat down with all of my doctors this afternoon to talk about my future. I wasn't there but Daddy said he now knows where I get all my strength from and he was very proud of Mommy, as am I.

The Attending Pediatric Doctor said that my abilities to breathe on my own have come to an end. Sometimes I can make it a few hours without the bipap machine but that's about it. Much of this is due to my long stretch of seizures that are very severe. My Neurologist said that Ohtahara Syndrome is fatal and most don't live past 1 year. He also said that my seizures have progressed as expected to the point that they can not be controlled with medicine. Mommy and Daddy requested that I get to come home. Everyone agreed with their request as long as we could get the proper equipment available at the house. The discharge nurse (who Mommy had been talking to over the last few days) spoke up and said that it is already arranged and should be set by Thursday. The doctors all grinned knowing that Mommy gets things done!

On Tuesday, July 7th 2009, the worst news imaginable was delivered to Mommy and Daddy when they were given my prognosis at a similar meeting to today's. As hard as that was for them, it did not prepare them for today. I write this most difficult post to date with a heavy heart as my days are numbered. I am so excited to get to go home and enjoy them with Clay and Olive who I haven't seen in over 3 weeks. Daddy promised to put the boat in the water and take me for a cruise. This is going to be a special weekend for my family and I am really looking forward to it.

I must end this post with a quote from one of my favorite writers... "Don't cry because it's over, smile because it happened". - Dr. Seuss