THE SHADDOX BOYS

Jacob and Elijah Shaddox are brothers. They live with their mom, Mary, who is the writer of this blog. Jacob is 19 and is now four inches taller than his mom! He also has ADHD and gorgeous red hair. He is a freshman at a technical college studying computer maintenance. Elijah is 15! He is in 9th grade and he is not in ROTC at his high school. 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! Mary just started her 25th year as a teacher of the deaf. She is also in her last semester of graduate school to be a diagnostician! She will graduate in December of 2015!





Saturday, September 18, 2010

Four Weeks into School

We are four weeks into school and things seem to be going well so far. I have been running crazy busy at work, but things finally seemed to calm a bit this week. I actually got some quality time in my office to get some things done! I am hoping this continues. I have to travel in a few weeks, but that is another story!


Jacob is LOVING school. He has had a few bumps in the road with an Algebra test and a test in Biology. I am keeping a close eye on it and emailed the Colonel over his ROTC class to help intervene. Jacob went to a lock in that the ROTC held last night and LOVED it. He did say a few kids got rowdy and everyone had to do push ups, but he wasn't really complaining. He loves wearing his ROTC uniform and takes great pride in it. This week he got his name badge with SHADDOX on it. I am so glad he has started off the year well. These four years will fly by and I want him to really enjoy them. I have so many regrets about my high school years. Nothing awful, I just wish I had done more!

Elijah has had a good four weeks at school. He has had a few days with "poor behavior" but nothing like we have seen in the past. He has had no physical aggression towards anyone and I am hoping that continues. He seems to like school more this year. He is taking NO medications while at school. He takes his medication in the morning prior to school. Last year he took one medication at school. He was on this medication for tics, but it wasn't seeming to help anymore, so the doctor wanted me to slowly take him off of it and we did that this summer. The new medication for tics he takes in the morning and did take in the afternoon, but I stopped the afternoon one. Tics had decreased and it was hard to know if it was really helping or not.

We went to the neurologist this week and he agreed. The less meds Elijah has to take the better. Sometimes there will just be tics and IF they are not INTERFERING too much into his life than no meds. He has gained a lot of weight and that is a concern. Last night he had what seemed like more tics, but nothing to serious. For now all I can do is observe and decide from day to day what to do. Elijah is also not the best reporter of how his tics affect him or if it is a "good" or "bad" tic day. I think his hearing loss plays a part in that. He has come a long way with language but he is still a deaf child who hears with cochlear implants, who is a bit behind in his language skills. I can guarantee this, there is no other child like him! He and Jacob both are one of a kind!

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