Shortly after his second birthday our Little Landen was diagnosed with a Proxisomal Biogenesis Disorder (or PBD) a rare yet fatal genetic disorder. It hasn't been easy for us to share and this site has been created to help us keep everyone updated with doctors news, information and what is going on in our journey. We know we have tons of family and friends support and love. We hope and pray that we are blessed with many more years to watch our sweet baby grow!
My Little Landen
Monday, July 25, 2011
Another Loss in Our PBD Family
Wednesday, July 6, 2011
Landen's Ears, Therapy and Doctors
Tuesday we went to Flagstaff to see if there was any improvement in Landen's ears. The mineral oil treatments did the job in the left ear but not the right. The audiologist tried again to get the wax out herself but his ear canals are just too small for her instruments.
The PT was a wonderful guy as well he is one I haven't seen there before but he agreed that Landen would do well with a walker and was even able to make some heel inserts that keep Landen from leaning too far back when he tries to walk. Its going to take some time to get the walker because in the state of Arizona a child like Landen
The best news of all Landen has gained weight! He is now 24lbs 9oz meaning he has gained almost 2lbs in the last 6 months considering he has only gained 4lbs 10oz since his first birthday the last two so quickly is so amazing! Its no wonder with the way he has been eating lately. Landen for the first time is out eating Brayden! I forgot to write down his height so I can't tell you exactly how many inches he has gained but I know he has gotten a little taller.
Now we are looking forward to our Omaha trip at the end of the month and August 8th will be Landen's birthday!!! Which also happens to be the first day of school here meaning the day Landen turns three he will start receiving in home services as well as out patient in Kingman!
Wednesday, June 29, 2011
Grand Canyon
It was a fun trip! Eva didn't tell the kids we were coming she convinced them I was too busy to make the drive up so it was a surprise. I also made Victoria a cake since she celebrated her birthday the day before it was a surprise
It seems like forever since I've spent time with Eva's family and I miss them already. One of the highlights of my trip was when me and Ethan were walking together and he grabbed my hand and said "I love you Aunt M,
We spent the day walking and checking out the rim. Even Jacob seemed to handle everything very well and walked most of the day with us. We had dinner at the canyon and then Scott and I took the boys to Eva's hotel room to rest while they went to do some star gazing. That's when I was able to get Tory's cake out. I just set it on the table for her to find when they got back. Rebecca spotted it first but Tory's reaction was the best!
Saturday was a long day we didn't get much sleep cuz the only hotel room we could get was in Williams so we had to drive the 50 miles there after the cake before we could fall asleep ourselves. Then it was up early the next morning with the kids. Scott really wanted to go to see the IMAX so we left Brayden with Eva thinking we would be able to catch up with them but because it was so crowded in the park and we had bad cell reception we really didn't meet up till late. Then we had lunch and
Tuesday, June 21, 2011
California
Wednesday morning. I left somewhere around 6:30am it is supposed to be a 8 1/2 hour drive but I knew since it was just me alone with the kids to plan on more like 10. It took 12 hours!!! I was so tired that I had to pull over and rest twice and on top of that my GPS got me lost and made me travel through farmville to get to their house. I was so glad to finally be there and so were the kids.John Graduated Thursday morning. I can't believe how grown up little scrawny Johny looks in his uniform! It was exciting I was so proud of him. Even if I could barely hear anything above the screaming of my tired kids. Unfortunately the Army didn't ask me when my kids nap time was so they could take that into account when planning this event! We all walked down John's class room where the students and teachers we all gathered for a little celebration. Its amazing how well they speak french. I took several years of french in High School and in College and can barely remember enough to introduce my self and ask what time is it! That is when my camera broke... don't know what happened to it? It was working just fine and I set it in the stroller and picked it up again and it just wouldn't work so we had to head out and get a new camera (no I cannot live one day without mine). John and Heather too
Being with family is so fun the kids were all giggles and smiles with all the attention they got from their aunt and uncle. Friday they took us to the Santa Cruz Boardwalk. We had so much fun playing on the beach, (it was too cold to get in the water) riding park rides and eating
Saturday and Sunday we went to the beach and played some more. It was grey and cloudy the whole week we were there but even with the gray clouds the ocean is still beautiful! Saturday was Seventeen mile drive and Pebble beach which was beautiful. Brayden loved the wet sand he would hold onto my hands and run town the beach toward the water. He would smile and laugh as long as the water only got his toes if it touched his diaper he would cry. It was really cute. Landen was having a bad
Sunday was Carmel beach which was beautiful! The houses around are so cute I want to live there! We actually weren't their very long although we did manage to wear ourselves out. Landen was in a much better mood and enjoyed the texture of the sand. He would pat it and pick up handfuls. We had to keep stopping him from wanting to rub his face in it. Brayden was a silly boy he loved getting his legs covered and stealing everyone's attention. J
Just hanging out at the house with John and Heater was so much
Now we are planing on going to the Grand Canyon on Friday to meet up with my sister who gets there with her 5 kids tomorrow and then having them spend a day here. I'm so excited!
Monday, June 13, 2011
WELCOME TO HOLLAND
by Emily Perl Kingsley
I am often asked to describe the experience of raising a child with a disability - to try to help people who have not shared that unique experience to understand it, to imagine how it would feel. It's like this...
When you're going to have a baby, it's like planning a fabulous vacation trip - to Italy. You buy a bunch of guide books and make your wonderful plans. The coliseum. The Michelangelo David. The gondolas in Venice. You may learn some handy phrases in Italian. It's all very exciting.
After months of eager anticipation, the day finally arrives. You pack your bags and off you go. Several hours later, the plane lands. The stewardess comes in and says, "Welcome To Holland".
"Holland?!?" you say, "What do you mean "Holland"??? I signed up for Italy! I'm supposed to be in Italy. All my life I've dreamed of going to Italy"
But there's been a change in the flight plan. They've landed in Holland and there you must stay.
The important thing is that they haven't taken you to a horrible, disgusting, filthy place, full of pestilence, famine and disease. It's just a different place.
So you must go and buy new guide books. And you must learn a whole new language. And you will meet a whole new group of people you would never have met.
It's just a different place. It's slower-paced than Italy, less flashy than Italy. But after you've been there for a while and you catch your breath, you look around…and you begin to notice that Holland has windmills...Holland has tulips. Holland even has Rembrandts.
But everyone you know is busy coming and going from Italy...and they're all bragging about what a wonderful time they had there. And for the rest of your life, you will say "Yes that's where I was supposed to go. That's what I had planned".
And the pain of that will never, ever, ever, ever go away...because the loss of that dream is a very significant loss.
But...if you spend your life mourning the fact that you didn't get to Italy, you may never be free to enjoy the very special, the very lovely things...about Holland.
Saturday, June 11, 2011
Some video's of Landen in a walker that the PT is letting us use. Unlike the one from the school district this one is the correct size and he is able to use it alone. Watch how good his walking is getting. Even though he doesn't have his braces on in the video he is keeping his legs closer together and picking his knees up!
Thursday, June 9, 2011
Just the Start of aBusy Summer
The rest of the week has been busy with therapy and meetings. Yesterday we went to Flagstaff for a hearing evaluation. I've been noticing for about a month now that even with his hearing aids in Landen does not respond to noise anymore. He doesn't turn when you call his name or respond to clapping which has always been his favorite. I've been so worried that his hearing has gotten even worse so I made an appointment a few weeks back for him to be seen. They wanted to do a booth test which has never worked very good for Landen but at his age they wanted to try it. A booth test for those of you who don't know is when they put him in a sound proof room on my lap and face him straight forward then they play sounds on speakers there is on each wall. The hope is that if he hears t
While we were in Flagstaff we got to visit with the Burdick family... they are Ezra's family... the girl who has the same disease as Landen and is the same age... It is always nice to visit with them it is such a relief to be able to talk face to face with someone who knows what you are going through. It was fun to see Ezra she is outgrowing Landen and is looking so healthy and big. She did a little assisted walking back and forth between Joleen and I. She is also learning some words and signs to help her communicate which gives me hope for Landen. Her family is wonderful and so helpful to us.
Today we had Landen's IEP (individualized education plan) meeting with the school district he will be allowed services at home and will be having a lot of in home instruction coming this fall. Its almost that time of year for us to start making our annual trips to all of Landen's doctors in Phoenix I will be having a meeting on the 6th with some of the people from CRS (childrens rehabilitate services) to see which ones I can see through them and get referrals for Capstone (CRS and Capstone are insurance Landen is provided through the state) since when he saw them last year he was on a different insurance. It gets very confusing dealing with multiple insurances both private and state. Plus different hospitals and doctors in different towns and to top if off several of his doctors from St Joseph's in Phoenix are now at Phoenix Children's Medical Hospital changing things up again. But in the end its what we have to do there is no way we could afford all of Landen's care on our own. I
We have some fun things planned for this summer including (now that the cat is out of the bag) a visit to California next week to see my brother John, a visit from my sister Eva and her kids when they go to the Grand Canyon, our trip to Omaha for Landen's medical conference, and a trip to Oregon to see Scott's family... to top it all off I'm hoping to make another trip to Utah after my brother Isaac's little girl is born. So we may not be seen much of this Arizona summer after all!!!