Tuesday, March 31, 2009

Beep...beep

The bitter bus has stopped by our house today. I’m totally and completely bitter about having to fight for every ounce of help for Chris. I feel like I spend my days on the phone trying to get help for things that he needs or on the computer trying to research things about what is going on with him. I feel like I’m neglecting the other boys and they really need me. Matthew is starting to act goofy in school by passive-aggressively telling his teachers he doesn’t know things. He’s counting for them like this “1, 2, 10” and I know he knows how to count. We’ve only done it since he was 2. Jonathan is not listening, acting out and hitting. He stopped going on the potty.

Today I called to find out where we were with the Occupational Therapy process with Chris. His initial evaluation with EI showed that he would qualify for it but at the IFSP meeting his case manager felt that he may shut down if we had 4 therapies initially. So, she recommended that he receive Speech Therapy, Physical Therapy, and Developmental Therapy. I’ve called multiple times since his Physical Therapist felt he could use the OT to ask about adding it. Its super frustrating when Chris is having issues feeding, dealing with sensory issues and all that comes with things that are him. He’s not self feeding as well as he had been before. He can’t deal with things that are wet or slimy on him. He freaks with crowds. It seems like he’s over stimulated often. He hand flaps, goes in circles and waves his hands and screeches. He’s biting a lot more and Jon and Matty are running away from him now. His case manager said that she gets to make the decision to add things (Since when is that the rule? It’s supposed to be a group decision! I get a say here!) Then she said “I’m not blaming you since you are as much a part of this team but you could have said you disagreed with what my idea was by not giving him OT right away.” Don’t these two statements contradict each other? Silly me, I thought that if we wanted to add something it wouldn’t have all the freaking red tape involved to do it. I didn’t realize that if his initial eval had in it that he could benefit from OT that if we didn’t add it and went back to relook at it that we’d need to do another eval. No one ever let me know that we had to wait for 3 months to even look at re-visiting his IFSP!

I feel like he’s getting further and further behind….he’s still at a 6 month old level for speech. He’s still at a 6 month old level for social and emotional development. He’s at least gained a bit in gross motor from his initial eval where he was at a 10-11 month old level. Now he’s at a 12-13 month old level for gross motor but still at a 10-11 month old level for fine motor. He’s not able to drink from anything but a soft spout sippy cup. He lacks the motor development in his mouth. He’s not moving things bi-laterally (from side to side) and instead he’s just chewing a bit then swallowing half chewed food hence the big chunks in his poo. I find myself angry and bitter at being around those with “typically” developing babies. I want to isolate myself from them so I don’t see how much of a painful reality it is that he’s not “normal” and will never be “normal”.

Then I called after calling yesterday and Friday and going to the peds office Thursday and talking to them about Chris and his non-sleeping issues. He’s going to sleep at like 2:30 or 3 am on average and waking up around 7 then napping about noon to 2:30 or 3. It isn’t healthy for him. I broke down and tried numerous sleep training techniques with him and nothing is working. They suggested letting him cry himself to sleep no matter how long he was crying. I feel like this is cruel for any child let alone him who can’t let his needs known to us. George decided to do it the other night and I ended up crying most of the night that he did as well. Chris cried for over 2 hours and finally George got him and got him to sleep. I asked the ped about melatonin after doing much research on it. My research showed that sometimes kids who have developmental delays lack the natural melatonin in their brain that tells them there are tired. I believe whole-heartedly that he is one child that this is true for. His ped consulted with his neurologist who felt that we wanted to “drug him up” instead of try to get him to sleep on his own. So, instead we have to do a sleep study to see if they can help pinpoint a behavior issue with him. They want us to go back to our favorite hospital…the one that effed up the original 24 hour EEG in September. And, it takes awhile to get an appointment; he said 4-6 weeks on average. I stopped going to my parents since I can’t handle him on my own anymore. Again, another bitter point here…..

Jonathan and Christopher had their ear surgeries yesterday. We had to be there at 7 am. They did the standard pre-surgery things to get them prepared. They came in to ask questions and Jon did a typical 3 year old thing and hid in a corner in a ball and put his big doggie and baby doggie in front of his face. He cried and screamed that he was scared. I had to hold him down to have them take his temp and put his tags on. He kicked me in the face several times. They weighed him and my skinny minnie weighed 33 pounds! He is just so stinking skinny! Chris was just completely unaware of what was going on. He weighed 28 pounds according to their scale. They came out of surgery and were sleeping. When they woke up they were happy and acted like nothing ever happened. They were super when we came home.

Friday we went to the circus with Jon and Matty. They loved it! Afterwards, we went to Applebee’s (or as Jon calls it “The hungry store”) and they had to have been famished! I’m not sure why since they ate a huge thing of popcorn in the circus but Jon ate a hot dog and french fries and had his lemomade. Matty had chicken fingers, french fries and his lemomade. So, when it came to asking about desert, I let them. They shared a chocolate chip cookie warmed with 3 scoops of ice cream, chocolate fudge and whipped cream on top and crushed Oreo cookies on top of it all. They loved it!

And to top off my lovely day, today marks the one year of my grandfather’s passing. He was an amazing man whom I loved dearly. I’ll forever miss him…….

Monday, March 23, 2009

Cute craft idea

I painted the boys feet yellow, had them press it on a piece of white paper, let it dry and put a beek and feet on it.



We went out to play yesterday and we had to drag Chris in he loved it that much! Matthew was playing with his new bug finder kit. Jonathan was digging to try to find worms....


We had Jonathan's meeting today to see if he qualified for preschool speech services. He doesn't. They said he does have a slight articulation delay but not enough to get services. Then said they want to talk about adding OT for Matthew and will be pulling him out one day a week to work on letters and numbers with him.

Chris' speech person didn't show up today. We're not going to see her next week since that's when Jon and Chris have their surgeries scheduled. 2 weeks in a row for the kid who she admitted needed more than one hour a week of her....OYE! I need to call to see where we are in the OT eval process with him. He really needs some help in the sensory issues department. He doesn't like textures or certain feelings. When I painted his foot today he freaked! He's getting better with shaving cream soap that we use sometimes for bath. He used to shriek and scream when I put it on him and now he's touching it somewhat. He still hates vacuum cleaners, the magic bullet and my hairdryer. Hopefully April 22nd when we have his developmental pediatrician appointment we'll get some answers.

Thursday, March 19, 2009

Our house is like a sick ward

Jon has had an ear infection since February 13th. We've given him 3 different antibiotics and 2 different ear drops to help but he's still oozing out of his ears. Chris has had the croup and a cold. George woke up yesterday sick with a fever and I wasn't feeling well. Today I woke up all congested and feeling the same way I did when I had the kidney stone in November.






Chris has found a new favorite place to play, our stairs.



We're adding more signs with him. He's going to be learing the signs for me, up, down, eat, drink, more, all done and a few more that I can't remember right now. Right now he's done the sign for "more" and "all done".




The thing on here's still not letting me post videos....



We made pizza the other day for lunch.

With the nice weather, we went outside to play the other day. Chris gave me a heart attack! He walked down a stair all on his own. Jon brought out a soccer ball and ran around. Matthew just ran around in circles and laughed. Chris laughed and picked up grass, threw it then would grab sticks and laugh.



Thursday, March 12, 2009

Trip down memory lane or play the who do our kids look like game?

George is in the blue shirt with the yellow party hat
George in the sink


This is me at my parents house when I was a kid.


HE SPOKE!!!!

Monday Chris had speech therapy and we were trying to get him to sign for "more", Wednesday he had developmental therapy and again, we were trying to get him to sign for "more" and he did! We were trying to get him to repeat words. Listen to this clip and tell me what you hear around the 25 second mark????!!!!



http://www.youtube.com/watch?v=wxJpVjnZisI


The video thing isn't working on here so sorry!



Today we went to Chuckie Cheese for Jonathan and Matthew's friend Lucas' birthday. They had a blast! Mr. Chris was even getting in on the action.


















Friday, March 6, 2009

Dr's appoitments galore

3 appoitments in two days....Jonathan and Christopher had ENT appoitments Thursday and Christopher had a GI appoitment yesterday.

Oour appoitment was at 3:15, we got there a few minutes after 3. We weren't seen until around 5. Fun! Jonathan's ear tubes are still in and that is the root of his ear infections. I was told that if they remain in too long they can get infected. He needs them to be removed and he will have patches put on the little holes that will remain. Christopher's left tube is out and non-functioning. He needs it removed and another one put back. I called today to schedule the surgeries but wasn't called back.

The GI yesterday, we were the late ones. We hit traffic and every red light that could have been. We can start trialing the foods that we were told to avoid. So, he cans trial days of dairy, soy and wheat to see how he reacts. Chris has a prescription for priolsec to help coat his esophagus as a help to make sure it’s not inflamed as we do the trial as a precation if his reflux didn’t go away. She would like an endoscopy done at some point but it isn’t something that has to be done right away.


Yesterday during Chris' PT session we tried something new. We used dried beans in a container to have him play in an effort to desinsitise him a bit to different textures. He loves it!








Yesterday we went out for a bit to get presents for George's birthday which is next week. While at Wal-Mart we went to the fish area so we could see the fish there. Christopher got out of the cart (I took him out) and he walked over to the tank, pointed and said "Fesh"! He said it several more times too. This little boy will be getting a fesh soon so he can keep looking at it and saying the word!!!




Monday, March 2, 2009

Happy Birthday Dr. Suess

We celebrated Dr. Suess' birthday today by eating green eggs and ham.







George said he didn't think they'd like them but the boys kept asking for more green eggs. I guess they were a hit!

The never-ending ear infection still hasn't left. Jon started oozing and bleeding out his left ear again....we're going to the doctors tomorrow hoping to start an antibiotic with him, yet again.....we're going to the ENT on Thursday. Both Chris and Jon will be going. Jon needs to be seen for the 3 weeks long ear infection and Chris needs to be seen for the non-functional ear tube and the neurologist said he didn't pass the hearing test even though the audiologist said he did. Then Chris goes to the GI on Friday. I weighed him today....I know he lost some with him being sick but he's back to what he started out at when he was 15 months. He was 25lbs 8 oz tonight. That is even with the calorie booster we put in his milk. *SIGH* Nothing comes easy with this kid.....

George's Aunt Marcia sent me a poem to help comfort and make sense of everything going on with Christopher....

THE WEAVER
My life is but a weaving
between my Lord and me,
I cannot choose the colors
He worketh steadily.


Oftimes he weaveth sorrow,
and I in foolish pride
forget He sees the upper
and I, the underside.


Not till the loom is silent
and the shuttles cease to fly
Shall God unroll the canvas
and explain the reason why.


The dark threads are so needful
In the Weaver's skillful hand
As the thread of gold and silver
In the pattern He has planned.


Author Unknown

Sunday, March 1, 2009

The connection between Einstein and Christopher




Einstein was a premiee, so was Chris. Einstein didn't talk until he was 3; Chris isn't talking right now and he's almost 18 months. Chris has the crazy hair-do, so did Einstein. Einstein lived in Princeton; Chris lives near Princeton. Einstein was a genious.....