Monday, September 14, 2015

And the Thunder Rolls

My last blog post was kind of huge and really long and had lots of information in it.   It was so overwhelming I had to take some time to let that all just be.  We have had a rough few days around here too.  Alex has some serious sensory issues that we are just figuring out.  He has always had them, but before we knew what was going on he just would have a tantrum and we wouldn't know why.   Now we do and we have been trying to help him around those so he isn't stuck in one place for too long dealing with the same issues for too long.   
He seems to have oral sensory issues and hearing sensory issues and we are not sure which is worse for him, but right now his hearing ones are causing some stress and anxiety.   He has always been afraid of thunderstorms but it seems since the car accident he now relates that crashing sound to the car crashing sound and he can't function.  He gets so freaked out he needs to know what the weather is doing and what radar looks like.  He wants to see all of the alerts and possible  weather conditions for our area.  It is paralyzing for him and we (Nathan and I) are almost powerless to help him stay calm. We have been teaching him self empowerment phases to help calm himself down like "I am safe", "I am calm", "I can do this", and  "everything is going to be ok".  We work on deep breathing and we focus on using his stops and pauses...they are tools he has learned in therapy to center is actions and focus.   Sometimes he is so excited and upset though I am worried he is going to pass out.

I don't believe that he is doing any of this to get attention...in fact quite the opposite.  I think if he could hide from me and the storm he would...he is very upset by the way it makes him feel.   He just doesn't know how to deal with the whole situation all together.   The only one who has had much effect on him is his big sister.  She is a huge comfort to him during the storms. Of course as soon as the storm passes they are right back to cats and dogs as it were...but she is the biggest help when he is all stressed out over the storms.   It certainly doesn't help that I managed to cause both of my kids some distress this weekend with their food allergies...
For the record...Pizza Hut has a lot of Tree Nut allergies on their allergy list...I should have read that list a long time ago...darn it!   And McDonald's Sausage patty has sage in it...both of my poor kids found out the hard way that mom should be more careful sometimes.
Just when I think I have these darn allergies on the ropes they sneak back at us...also after several weeks of elimination diet it seems Cate probably is allergic to Chicken! DAMN IT~

Monday, September 7, 2015

Alex...ASD...Asperger's Syndrome and Us

I have hesitated to post this blog post for a long time...for two reasons.   One I have been concerned that I am putting too much of our life out there on the net.  I have been worried that Alex might be impacted in some way be the choices I am making on this webpage.  The second reason it I am was really waiting for that confirmation that we had this diagnosis. I didn't want to put it out there and then have to back peddle and say oh no...that wasn't it at all.   I do want to be truthful when I am posting..or as much as I can be,
This all being said..,Alex's privacy has been my biggest concern.  He is after all only 8 and has a long way to go.   Over the last few years we have been on a journey with Alex and it has been a windey one.   It really goes all the way back to Parents as Teachers and have some hearing testing done because I was afraid he had some hearing issues.  No one seemed overly concerned that it never changed.   We went to preschool with an overly active kid and into kindergarten with a kid that wouldn't sit still.   The first couple of teacher wouldn't come right out and say there was anything wrong or that we needed to be taking any steps with him.   I would ask is there anything we can do at home to help out.   We would get no information or "just remind him to be good in class"  "tell him to make sure to sit still during quiet time" "make sure he knows that he needs to be quiet sometimes"...it was maddening!  He came home upset everyday because all the other kids were getting happy faces and he was getting frowns.  He just couldn't get it together.
We were leaving Bloomington IL so I scheduled a sit down with his teacher and asked her point blank...do you think Alex has ADHD?  I also see some signs of autism and Asperger's...she said "oh I don't see any of that..he's just an active little boy and you have nothing to worry about."
Of course his dad was relieved and said we needed to put that rest because I had been driving him crazy about this for a while now.   I was not...I just kinda knew that something was not right and we were in for a bumpy ride.  When we got to Salina things did not get a whole lot better.   He found out that his teacher was a lot more involved and wanted him to do homework...my nemesis!  She also met me outside everyday and gave me a report on how Alex was doing.  She wanted me to know he was a great kid and Super Smart...but he was struggling in the classroom.  He was going to do well with some help.   "What?"   He needs to see his doctor...
Of course she can't in her professional opinion tell me that my son to see his doctor, but if it were her child she would take him to see his doctor for an evaluation for ADHD.   "REALLY, you don't say?"
So we went to the doctor and dad and I filled out a survey, teacher filled out a similar survey...if that survey had been read properly at the time it was given when her was in Kindergarten we might have gotten an ASD (Autism Spectrum Disorder) diagnosis then...but the doctor at the time glanced at it...read a few questions and said yep...he has ADHD.  Here is a prescription.  I want to see him every month to check weight and height, have a good day.
Six months went by and we had to increase medication to keep up with a growing boy.  We had to change doctors because our pediatrician was out of town and we found a new one that treat Alex and he really liked her a lot better.  It became apparent quickly that this pediatrician was interested in making sure Alex's needs were met...she began to explore the idea that Alex was in fact on the spectrum and referred us to KU...but that was going to take a year.
In the mean time Alex was struggling at school...with friends, with grades, with tests, and with the teacher.   I decided to go sit in his class one day and observe him the whole day.   It was sad how much of the day he spent distracted.  We had asked for an evaluation at the first parent teacher conference in October...my sit in was in December...nothing had changed in the classroom for him.  He was struggling and I could see why...it was loud and crowded and detracting.     He was going to have a hard time getting anything done in that setting...all the kids faced each other and he had to work with then all around him.

While I was at the school the lead teacher asked me if he was seeing a counselor for the ADHD?
"No, why would he see a counselor?"  Most doctors recommend counseling when you have a child on medication.  "HMMM...I never knew that?"
So we started counseling, it gave Alex someone to talk to other than dad and I.  It also gave him some tools to calm down when he was upset.  He was having these horrible meltdowns...and we couldn't figure out where they were coming from.   In  a couple of counseling sessions we talked about the lack of friends and how mom often had to help him form friendships, and help him maintain them.
I mentioned to his counselor my concerns about ASD and she said she would like to explore that further and had us fill out the survey that we had filled when he was in Kindergarten again.   This time they were scanned by the machine and it showed some autistic tendencies.  It was funny though that the teacher and I answered the questions very similar and dad answered them different.  I could only chalk this up to dad being so similar to Alex.  He is the very image of his daddy sometimes.
At this point the counselor thought it best to refer us to a psychologist in the field for further evaluation.
So that is what happened...it was a rather long interview with lots of questions and Alex was everywhere...of course we had not been able to give him his medication for several days...so he was kind of all over the place.   Thank goodness this doctor was really a children's doctor and he was amazing with Alex and so understanding of all of our concerns.  We walked out of there with a new better understanding of Alex and it is evolving.  He is an amazing little guy and so interesting.  With everyday we learn a little bit more about this fascinating kid and all the little sides of his little world.   Autism Spectrum Disorder is part of his world...it is part of our life...it is not Alex and it not him.  It does not complete his personality or make-up who he is...it is just a little piece of out world that is in his life and it is in our daily life.

If you have any questions please feel free to ask.  We are open to questions.

Friday, September 4, 2015

Because she is AWESOME and silly! We want to keep her safe!

We have had some debate in our live as to where Catie should be sitting now that she is  12 in the car. She is legally old enough to sit in the front seat...she also met the height and weight requirements years ago.   She won't however be riding in the front seat of any vehicle until she is 16 or is in drivers ed and can be driving the car herself.   I am not sure she even ready to think about that yet.
She is still have some PTSD from the car accident.  I didn't even know you could have PTSD from a car accident until we experienced it.  She still fights back tears and panic when I turn too quickly or stop too quickly.  Even Nathan and I have had the same reaction to each other driving, at different times. I seem to not be able to go past the crash site without crying almost hysterically.  We tend not to drive past there since the kids don't like to see mom cry like that.   Nathan almost feels a sense of calm as he drives past there...since he feels like we met angels that day.   I feel like our would almost stopped that day and it flipped it's poles or something.  Back to Catie though....the first time I heard anything about the death seat was the day after the car accident.  Someone said to me "its amazing you walked away from that you know you were sitting in the death seat and all you have is that awesome bruise?"   I cringed and thought my daughter sits in that seat on the way home from school everyday.   What have I been doing.  I started looking into it.   This is what I found first... http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2564455/ Of my gosh...ok Catie...no more front seat for you...Nathan agreed...right away she was pissed off...but within minutes she calmed down and was fine and never said another word about it.  In fact she got really possessive about her seat in the back seat of the car.  She would scream at her brother and throw a fit and temper tantrum ( at age 11) because he wanted to sit there. We finally asked what was going on and she said she felt like she needed to sit in the same place she was sitting in when we had the car accident because we all lived.  Ok...whatever works kid!   Needless to say we have called the doctor...and have put in the call for counseling.   We have to wait for a referral.  It takes months.   She has made comments about not liking having to sit in the back now but she isn't really griping she is just stating that she would rather it have more things to do...more buttons to push...she would rather he brother wasn't right beside her...she just wants to be a grown up.  I think I will take the extra few years and keep her safe in the back.  The last link is the Institute For Highway Safety...It has some startling information...please just take a look at it...the one the thing I was surprised about was the shear number of people killed in auto accidents in 2013.   65% of passengers were killed in auto accidents.  Please buckle up...it only takes a second and it really truly does safe lives.  We are proof!

http://www.iihs.org/iihs/topics/t/general-statistics/fatalityfacts/passenger-vehicles