Showing posts with label OCD. Show all posts
Showing posts with label OCD. Show all posts

Monday, November 19, 2012

Let Me See Redemption Win . . . .

I am the mother of two special needs children. 

One boy with Asperger's, mild Tourettes, OCD, Anxiety, Sensory, and Insomnia that is 8 years old. My daughter is 7 and suffers with Sensory and a severe anxiety disorder. 

I praise God for good days, and I am learning to praise God for the oh so bad days. 

This past Saturday my son had a melt down at his cousin's birthday party. His meds were wearing off (which is always an emotional time daily) and then his feelings were hurt that we had to leave the party early . . . . ended in him punching me over and over to get away and then running down the street. 

These sort of days don't happen every day any more, but when they do, it is taxing. 

When Christopher was just days old, God gave us a pediatrician that is so much more than a pediatrician. 

She is a friend. 

An advocate. 

A shoulder to cry to.

She sent me this song song this morning when she should have been sleeping! I wanted to share it for any of you that are worn. Weary. Tired.

There is hope my friend.

His name is Jesus. When we are at our weakest, His strength then shines through. Why? Because we are out of the way! That's why I think so much changes in the night time hours! When we are sleeping our "selves" are out of the way and He works miracles!

My daughter this morning asked me to take a battery out of the clock. I asked, "why?" She responded, "Because I want to control it."

Oi. What a teachable moment God gave me.

"Kaitlyn, you know there are going to be many times in life that we can not control what is happening." I said.

The conversation continued and while it was more than she could comprehend, it was a start.

I pray you are strengthened this day and that you take the time to seek His face.

Shalom.



Tuesday, September 4, 2012

Thankful For Good Days

Several, several months ago, Christopher's psychiatrist wanted him hospitalized.  He refused to make any adjustments on his ADHD medication, even after several months of concern that his impulsion was once again, out of control.  He was endangering himself, and his sister, or anyone else he was around when his medication didn't work.

The side effect of two of the medications Christopher was taking (Abilify and Focalin) was aggression.  He said the only way we could know if the child, my child, was being aggressive because of his behavior, was to take him completely off one, and then the other.  Gradually.

Since I did not want my son hospitalized where I would not be able to be with him, I chose the long road of decreasing meds, using my oils when I could; but trying to make them last because we just could not afford to replenish them.


While Christopher is home schooled, because he was in the gifted program in Kindergarten, he was allowed to continue to be a part of the PATS program in 1st grade through Escambia County School District.  I just took him each week instead of him riding the bus.  No big deal.


By the last three months of school, his writing had become so poor it was no longer legible.  I could not get him to sit still and keeping his attention on the subjects was impossible.  Our daily schooling consisted of repetition . . . . mainly focusing on how we respond to people, emotions, how to process, "What do we do when we get angry, Christopher?"  etc.


Out of desperation I spoke to his therapist.  They were not working on his writing and abilities at the time, so she was shocked when I showed her this.






I then spoke with his PATS teacher, and yes, she was concerned as well as Christopher had been unable to complete ANY work in the last several weeks.

We suffered through the rest of the year and most of the summer.


A few months ago we had to put Christopher back on medications because we simply could not continue buying the oils and the impulsion was absolutely exhausting me and taking its toll on the rest of the family.


While one medication was working well, his ADHD medication was not working and the horrible side effect was not sleeping, up and down all night and hallucinations.  It was a rough few months of trial and error.  The hallucinations seem to be under control and I believe were medication related; however, he is now regularly having full body tics.  While we haven't "gotten there yet," and probably never will the way the body changes and metabolizes, it seems we are making progress in the attention and impulsion area.


We started back our 2012/2013 school year a few weeks ago, just a couple days a week to start getting in a routine.


We have had good and bad days since we started back; but today, my son thrived!


We worked from 9 a.m. to noon; broke for lunch and finished up lose ends from 1 p.m. to 2 p.m.  Last year we used a computer program and he loved it, but would HATE to write and fought me all day on it; and while he still does not like to write, he is doing so much better using things printed straight off the computer!  


Christopher has only written on the THICK lined Pre-K and Kindergarten writing paper.  His writing is HUGE and he often runs out of space.


Today, for writing, we talked about how to write dates correctly, margins, and proper spacing between words.  Yes, this is something he was taught in Kindergarten, but, as his home-school evaluator explained to me, Christopher will always be ahead in areas because of how smart he is, but he will also be behind in areas because of his disabilities.  It is my job to push him along and encourage him in the slow areas (reading, writing, and spelling) and challenge his brain in mechanical, mathematical, cultural, scientific areas.  (Yes, pray for me.  I hated school and passed by unknowns reasons.  Seriously.  Pray hard!)


My son will be 8 this month. With the months of regression he had earlier in the year, he couldn't take what was in his brain and put it on paper, couldn't complete a thought verbally without getting confused where he was or what he was even talking about, and writing his own name was impossible.


Today, for the first time EVER, he wrote on wide rule paper and writing WELL!  It takes him a LONG TIME to get the information from his brain to the paper, BUT HE IS DOING IT!
 





He had one spelling error.  I wrote, "When I grow up . . . . . "  He traced that, but everything else he wrote himself. 

Very proud!

Thursday, February 5, 2009

Following Through...

Hey ya'll, Christopher's teacher called Chris first thing this morning regarding the email he had sent her stressing our concerns. Please pray for Ms. Casey and the other students. Pray also for Anthony, the little boy that is causing so much problems. Ms. Casey has had a headache since Monday regarding her dealings with this young boy. He is abusive to everyone in the classroom. So, this morning, Christopher and I prayed for Anthony. I would appreciate it if you would pray for Anthony also. He is 5 years old; a year older than Christopher. Please also pray for Christopher. I've mentioned before Christopher was diagnosed with ADHD/OCD. Last week we had to increase his medications as it seemed like nothing was working. We aren't seeing a difference with the change either. He has become more emotional that ever, throwing himself down and screaming, tackling his sister (the younger one). We don't know if this is the wrong medication or if it's behavioral.

We were sent an application for the SuperNanny show; in fact, we got it the same day we were told to leave our home because of the black mold. I think it's time to follow through and get the help we need.

Thanks for listening, well, reading.

Later.