THE SHADDOX BOYS

Jacob and Elijah Shaddox are brothers. They live with their mom, Mary, who is the writer of this blog. Jacob is almost 15 and is now three inches taller than his mom! He also has ADHD and gorgeous red hair. Elijah is 11! He also had red hair, but it is lighter and not as thick as his brother's hair. He is hearing impaired(auditory neuropathy) and wears two cochlear implants. He also has tourette syndrome, ADHD, OCD and anxiety! Their mom has been a teacher of the deaf for 20 years now!



Sunday, March 11, 2012

Spring Break

Well Spring Break did not start off well. I got a phone call around 3:15 on Friday afternoon(last day of school) that Elijah had been aggressive again at school. I could hear him in the background yelling. Isn't life grand? I was told what happened and that they were afraid that he might not get on the bus. I was 90 minutes away and there was no way I could get to the school in time. Thankfully, he did get on the bus.

Needless to say, he is grounded for the entire Spring Break. He doesn't get to play with his nintendo DS, the Wii or my iPad. I have also found several web pages with free math and language arts worksheets. He is working on some now and worked on some yesterday.

I did call the doctor on Friday, because Elijah had been having a hard time falling asleep for the few nights prior to this and was awake before I woke up. She upped one of his meds and we had a planned trip to see her for Monday(tomorrow).

He has been pretty good all weekend, but he does show his attitude at times and I send him to his room. I really do get that he has impulsivity issues, but he has also got to learn how to control it or it will always get him in trouble. He has a pulmanologist appointment on Tuesday and Jacob sees the orthodontist on Wednesday.

Needless to say, when Elijah is grounded, I am also grounded. I limit what I watch on TV and he wants my attention since he doesn't have much to do. I would hope at some point, he would "get it" but I guess it is going to take more practice.

Saturday, March 3, 2012

Things Continue to Go Well

Elijah continues to be doing well in school. He had a few instances where he screamed/yelled in class and calling names, but no aggression! We go back to the doctor on March 12th. I am curious to see how this coming week goes. His right ear processor has had not more instances of blinking! That is a good thing!

Jacob spent his second Saturday at the soccer fields refereeing. He has earned some decent money. He is a bit more motivated to work now that he has a PayPal account. I can't believe how tall he looks compared to the kids on the soccer teams he referees for.

We are all ready for Spring Break to start next weekend. We don't have anything planned for Spring Break, except to try to get some rest.

Saturday, February 25, 2012

So Far, So Good!

Elijah had four great days at school. I am hoping I don't jinx it! He had all greens each day except for Tuesday when he had one yellow! It has been two weeks since we increased his medication and I think we are finally seeing that this increase was a good thing. We are continuing with the ticket system at home and I think that being consistent with that has helped. He also earns some gummy bears to put in his ice cream if he has "green" days!

I took him to the movies today as a reward for such a good week. We both enjoyed it and I needed some time with him. Jacob doesn't like to go off to the movies with us!He is a such a teen. He refereed three soccer games today and earned $45. Half of the money went into his savings account and the other half into his PayPal account. He wasn't too excited about earning money, until we set up a PayPal account for him.

Crossing my fingers Elijah continues to have good days and Jacob enjoys his referee job.

Tuesday, February 21, 2012

Would I Change Anything?

If there was anything I could change for either Jacob or Elijah would I? I can surely say for Jacob, that the answer is a NO! He is such a typical kid and now young man. Now for Elijah.... I wonder? Would I change anything for him if I could? How would this change affect him or me?

Elijah has had such a hard journey. He was born premature and struggled to breathe. He was on oxygen for nine months. He is deaf, but does wonderfully with his CI processors. He has asthma, Tourette Syndrome, OCD and ADHD. He is who he is because of his journey. Would I like the Elijah he would be if I took one of these away. I cannot imagine him as a different person.

Elijah has made me a better person, mother and teacher. When I speak to other parents of deaf children we relate in a way that other teachers can't. When I speak to parents of children who are deaf with other special needs, we make that connection. I have walked a similar path as they have. Our journey's may not be exactly the same, but we share a common thread. I hope this connection to other families helps these families with the choices they are faced with. I hope the stories I share with them help them with their choices.

Would I change who Elijah is? No, I don't think I would. He is who he is and I love him for who he is. He has a heavy burden to carry sometimes, but I will be there to help him along the way.

Tuesday, February 14, 2012

Parenting a Child with Special Needs


I have been a teacher of the deaf for 21 years now. The past five years, I have been the Lead Teacher of my department, which means I attend a lot more meetings and am not in the classroom full time any more. Almost 12 years ago my son was born prematurely and diagnosed with a hearing loss at the age of five weeks. he recieved his cochlear implants at the age of 18 months and four and half years of age. At the age of five he started on medication for ADHD and at the age of eight he was diagnosed with Tourette Syndrome and OCD. Needless to say I have had my ups and downs. I was well prepared for the deafness but as far as his other issues, well let's just say, it has been a challenge.

Before the divorce, Elijah's dad was a good support to me. It was a trying time though and having a special needs child is never easy on a marriage. Since our divorce, I have pretty much been the only one at home to deal with Elijah on a full time basis. My immediate family does support me emotionally, but they aren't here 24 hours a day seven days a week. Jacob was only 13 at the time and expecting him to be a second parent is not an option. I was lucky to find a great babysitter for Elijah after school who was a very important person in his life for two years.

Last week, when Elijah had that really bad day, I arrived at the school visibly upset. No one likes to hear that staff at a school are afraid of getting hurt by a student that is your kid. The principal was very supportive and during the conversation mentioned that she has thought of coming by and taking Elijah out for ice cream so that I could get some time to myself! I guess you know it is bad, when people offer that. I told her though that I do get out and have some time for myself. The last year has been one of the best years of my life. I have found someone to share my life with. I am not going to share a lot about her, but I want everyone to know that I am no longer alone in my struggles with Elijah. I have someone who is very supportive and who has become a great step parent. I am happy because I have someone who takes care of me and who I can take care of too.

Elijah's dad is also back more in his life, asking more about his doctor's appointments and about school. He has always been there, but he has had to move five hours away to find a better job. The economy is not great, as we all know and sometimes people have to move. He keeps in contact though and I know once things settle down for him he will be there for his boys.

We parents need to make sure we take care of ourselves. I go out and spend time with friends and make sure that I take the time for myself. Please remember that...take time for yourself and for your significant other.

Saturday, February 11, 2012

Yesterday was NOT a Good Day!

Yesterday was not a good day for Elijah. As you may remember, I posted about him having some bad days in the last few weeks. He bit another student about two weeks ago and then again this past Wednesday. He spent a day in suspension at school on Thursday. Well, yesterday morning he was already in a mood before he got on the bus. He then went to school and basically spiraled out of control. I got a phone call around 8:30 letting me know what was happening and that he was not calming down. I was asked to come and get him.

Unfortunately I work 40 minutes from him and had driven another 20 minutes away to check on some students, so I was an hour away. The principal understood and told me that she would keep him "safe" until I got there. That told me a lot! I called in to work and told them I would be taking off for the day. I had to call someone else and see if we could reschedule an IEP meeting because I had no one else to send(I am a teacher of the deaf and Federal Law says a deaf ed. teacher has to be at a deaf student's IEP meeting, so they can't have it without me.). Everyone knows how dependable I am and thankfully I have never had to cancel on an IEP meeting for an emergency like this.

I finally start driving his way and on the way called the psychiatrist's office and got a 1:45 pm appointment for that afternoon. I got to the school around 10:00 and saw him in the conference room working with a teacher. The principal saw how upset I was and wanted to know what she could do to help me. We sat and talked for almost an hour so she could give me the whole story. I needed to know what had happened so we could talk to the doctor about it. She was very supportive and I explained that we would be going to the doctor.

Elijah and I got ready to leave and he was perfectly calm. He didn't even act like anything had happened. We came home and had lunch. We talked for a bit and I then I called a good friend to talk. I needed a good talk.

We went and saw the doctor who listened to everything. She said it may be puberty coming on which would require him to need more meds. We upped one of his meds by 0.5 mg and may up it more, if needed. We just have to wait and see.

I had noticed that he seemed to be a bit more agitated in the last week or so and there seemed to be more tics. I added the 0.5 mg today and hopefully we will see some improvement in the next week or so. It is hard to know how long it will take to see the effect of upping his meds and we may need to up it more. I think this is the hardest part of Tourette Syndrome. There are just no easy answers.

On another note, Elijah managed to get up on the stage today at the Regional Day School Program's Performance in front over 250 people and say his poem. He even bowed at the end! He can be such a sweetie, sometimes.

Thursday, February 9, 2012

Got the new Controller

We got the new controller and coil yesterday. It was not an easy task. I had to once again call FedEx and have them keep it at the facility so I could pick it up there. I checked on line to see that they had tried to deliver the package, but they didn't leave a note!

I put the new controller and coil on his right ear and now we will see what happens!