Can You Turn on the Water Please?

Ok, normally the whole "turn the water on" line comes with the general thought of someone going "tee-tee" and needing the water on to go right? Nope. Not for us. I'll admit that all things autism have taken a backseat on my roller coaster the last two weeks. First, my grandmother passed away on Thursday, February 7th. She was 98 and god love her, she had one long and awesome life. Exactly a week later on Thursday, February 14th her sister passed away. (Happy Valentine's Day, huh?) Check please! That's enough of the family passing away for a while if you ask me. Speaking of Valentine's day, I hope everyone had an enjoyable Valentine's day this year. I'll post my cute idea that I made for teachers gifts this year when I get to it. (I need to add that to my to-do list or it will be Christmas before I post it, ha) What did we do for Valentine's Day? Absolutely NOTHING! We literally went to bed and slept and that was perfectly O.K. for this exhausted Momma. And there you have it... the recap of my last two weeks in about 6 sentences.  

Back to the point of this post. I have been a little M.I.A from the blog world the last few weeks, but cut me some slack, it's been hectic! I kind of feel like things are getting back to normal though. John's out of town for work until Friday (weird that's what I consider normal isn't it?) and the kids and I are back to my drill sergeant ways of having things on a list and checking them off so we can survive til' the weekend. Sooooo I got back to researching autism and looking for new reading material and resources, not to mention making my lists for the city schools application for therapies they offer to private school children with disabilities (who knew right?) but that's another post (dang make that two things to add to the to-do list). Tonight I was researching autism and sleep- or lack thereof. Jackson often times has a hard time falling asleep and will sometimes lay in bed awake for hours, yes hours before he finally conks out. 

He then wakes up the next day with bags under his eyes and super lethargic to get moving in the morning. Sure doesn't speed up the process in getting ready for school either. So I wanted to see if there was anything out there to help with the whole "sleeplessness" that he seems to struggle with besides a dose of melatonin every night. Meds are not my first choice in helping him so I am always looking for other ways to achieve the same thing the meds do, well.....minus the meds. 

I came across several home remedies, do this, tried that's of things parents, doctors and anyone remotely internet savvy has posted about on the subject of autism and sleep and the reality is well, kids with autism just have a hard time sleeping sometimes! From weighted blankets to back rubs to black-out curtains, there were lots of suggested aids. I did find that some people recommend noise machines, sounds, etc. So I thought, what the heck. I got on my spotify account and started searching "nature" for any noise-making-theraputic-nature-sounding-ish (that's the technical term there :) uhhh music that I could find. And I found this waterfall earth track that's about 4 minutes so I added to a playlist for Jackson, put that sucker on repeat and told him to lay there in his bed and just listen to the water. 

Once he is asleep, he sleeps like a ROCK (no idea who he gets that from - Dad), but until he falls asleep he hears every creak and crack and gets distracted by even the heat cutting on in the house. It really sounded like a huge faucet on full blast with the volume so loud. But he seemed to lay there and listen and so I left him in his room with faux Niagara Falls, HA! I came back 10 minutes later to find... A SLEEPING BOY! Whoo hoo! Wish I had thought of this about 3 years ago to help him get to sleep faster! Who knew the simplest thing would work for him. 

I am hoping this will be one of those little victories we can check off the list of "things that help with autism" for Jackson, so we'll see if it has the same affect tomorrow or if he gets bored with the whole pretend waterfall. Since I've recently been surrounded by all things "life" that are sad and hard to deal with lately, I thought I'd post on a small victory of a happiness. A sleeping boy and a happy Mommy.  

Fingers crossed for continued running water and a sleeping boy. 

~EM

Commander Mommy - Drill Sargent

Wash. Rinse. Repeat. Wash. Rinse. Repeat. Makes perfect sense right? As a adults that's what most of us do on a daily basis. We get into a routine. A routine that gets us from A to B, from Monday to Friday, from the beginning to the end of a long day. Even all things "routine" can get a bit too repetitive, a lot boring and quickly stale. Imagine the same 5 meals for dinner every week. Mystery meat Monday, taco Tuesday.... you get the picture. Eventually that gets old. Seriously old. Soooo we follow the so called schedule in terms of doing the same things in general everyday, but thank God macaroni and cheese isn't the side item every Thursday. Unless you live at my house...

Boring - maybe. Monotonous - definitely. Effective - Abso-freakin-lutely!

You've heard the line "creatures of habit"...well Jackson is definitely a creature of habit. He could literally do, eat, yes I said eat and play the same things the same way everyday and perfectly content with that. Great, easy enough! That makes it very easy right? Wrong. Not even close. I'll be the first to admit that we are on a schedule, a strict one at that and I try not to veer from it unless necessary, and that's not always easy! He's as stubborn as mule when it comes to changing the "routine". So we stick to whenever possible in every fashion. Especially when I'm a one woman show and John's traveling. The TV stays off, the kids are in bed at 8 on the dot and I'm marking off checklists like a soldier. It's kinda becoming the only way I know how to operate these days (at least if I want to keep my sanity). Jackson is very much a visual learner. I can tell him something 10 times but I might as well ask the door to do what I'm asking. But if I show him or give him something visual and colored to reference, he gets it. It's like "Jackson language". Which is cool. So in an effort to not have the nighttime routine be such a struggle, I made him a visual nighttime chart. Yep, you guessed it. Pictures that are color coded for every task. He can associate the color with each thing on the list and knowing that it's time to move on to the next color and picture really helps him. Come to think of it, doesn't that help us all??? (Even Hallie likes to be instructional on the color block he's on at the moment, ha!) And without further delay... our trusty chart! (sorry for the crappy quality, I am obviously photo challenged today but you get the idea here)

I am in the process of making these charts for everything we do! That's very good in a way, but also means Mom is WAY ACCOUNTABLE for hitting every item on the list! (no pressure there) Here's the other side of that. Yes, these charts are super duper helpful. Yes, they help Jackson. However, I don't want him to only live by those charts and have everything come crashing down heaven forbid we miss something (because let's be real, at some point that will happen). Sneaky Mommy, teacher, drill sargent, care-giver extraordinaire to  the rescue! (ok ok just plain ole Mom doing what she thinks is best for her monkey to the rescue is more like it)

In learning as we go along, I'm finding little things everyday that seem to help Jackson whether it be at home, school, public, self help, whatever. So he operates on a tight schedule, fantastic. Newsflash! Life is not a set schedule! If it was, we'd all have it wayyy to easy anyway. So life happens, you take it as it comes. It's called  change. What was that I said Jackson was no good at? Oh yeah, change! Here's where the "meet me in the middle" strategy comes in.

Have it your way Jackson.... we are going to continue on the visual schedule rigmarole, I can roll with that. What I can't roll with is him depending on those forever. My plan. We'll stick to these "tight, same everyday routine" deals for the next little bit. Then my plan is to start incorporating and teaching him things from these visually. Like... making choices. So our schedules may go from one color block to two color blocks side by side with two different activities and HE will have to decide what he wants to do next, which path to take. It will teach him visually, it will force him to learn to make decisions, it puts him in control and gives him some empowerment. It will force him to communicate his decisions and most of all, it will teach him that he can be a part of his "schedule" and that things don't have to be exactly the same every day. Seem like common sense? Well, it's not.

No blog, book, medical webpage or any other crap resource out there suggested that one. There is no help manual or book titled "Autism Just for Your Kid" out there. So I'm writing my own manual. And apparently, my chart making skills will be stellar by the end of this too. Yes, it's time consuming to make all these schedules and add visual pictures to them that he can actually understand, but if it helps him, it's worth it to me. I hope through doing this to eventually add steps on the schedule that are blank boxes. Meaning there is no schedule. There is no certain thing to do. I hope this will teach him how to cope with change and welcome it. I hope it will teach him to "go with the flow" and be flexible. I hope that it will teach him that he can make his own decisions and feel good about his decisions without a pretty colored box to tell him what to do. See where I'm going with this? I want him to learn how to deal with life, but learn in Jackson terms. I want him to feel like he has been empowered to learn these skills because forcing Jackson with anything has never produced a positive outcome. He is definitely beating to his own drum and that's perfectly okay. My so-called manual may not help any other kid, but it could help lots of kids I don't know. I just know I have said many times that I plan to give him every tool I can to be successful and I that is what I am going to do.

I know this will be a slow process and we will have to go at "Jackson pace" but hey slow and steady wins the race. I'm going to be working with the school too, to incorporate this subtly into his day too. It's not that I mind if the other kids notice, but normalcy at school is key for every kid, so the less noticeable the better for the moment I think. I'll be sure to post updates on how my drill sargent and scheduled ways succeed or fail. I'm not worried if they do fail though. It will just mean we need to take another path. Everything is worth a shot in hopes for a better tomorrow. I wish I had a pretty visual chart to help me sometimes! Ha! I guess in a way, this will be my pretty chart that helps me too.

I have had people ask me, why I am so strict and stubborn about Jackson's schedule. Here's my brutally honest, um polite response to that.... IF at ANY time you think you would like to take Jackson for a couple of days and just go with the flow, you are welcome to do it! I guarantee you will be SPRINTING to bring him back and begging for a schedule at that! Trust me when I say for my sanity (and yours, lol) it's in everyones best interest for Jackson to stay on a productive and clear schedule! And for now,  I'm commander in chief and that's the way it's gonna go!

~EM

The Mummy Test

Ahhhhhh... the MLK holiday. Yes, I was off work and yes I spent the entire day with my two little monkeys.  I don't get too many days at home with them (which may be good for my sanity to some degree, ha) but I often take then time with them when I can and love every minute of it. We stayed in our pajamas til noon, yep noon. Can't say I do that too often either, but trust me, I'm not complaining about having a few lazy hours.

Jackson had a birthday party to go to on Monday for his friend Peter, so at 2pm we headed out to Pump it Up to celebrate and exude some energy for a little bit. Jackson was having a good time for about the first 45 minutes, but a room full of wild boys, bouncing blow-up slides and pegging heads with bouncy balls and you can probably guess how that was bound to end.

Before we reached that point, it was time to leave and head to the doctor. (Phew! Crisis meltdown averted!) Jackson had a EEG (more on EEG here) test scheduled for 4pm. Don't think I got off that easy however. A full on meltdown over missing the cake at the party was the meltdown culprit all the way to the doctor. Ugh... some days I need a raising window in the car. You know like the ones in limos so people can block out the sound from the back to the front. I would have given my left arm for one of those windows during that car ride. We got to Dr. Eastmead's office in Midtown and in we went. Normally I don't like to take Hallie with me, but on Monday she was in tow since John was out of town for work. I was instructed not to give him any caffeine 24 hours before the test, no this, no that blah blah blah, but let's be serious. Jackson is like an operating caffeinated jack-rabbit without the caffeine. Do you really think I give him that stuff doctors??? Really!?!? Ok ok, back to the test. Just had to get that out there. We didn't wait but maybe 3 minutes before they called us back to get started. Lots of gooey gunk, a bazillion wires later and a full mummy headdress and we were ready to go. 

Not to my surprise, Miss Hallie felt the need to be right up in the middle of the action. She held Jackson's hand the whole time and told him, "You're doing reawllly good Jack". I was so proud of her. Only 3, but man she is well beyond her years. She amazes me everyday with how mature she is for her age. She never faltered the entire test. In a way I felt like she relieved me of some of my Mommy duties for this test. She was being the strong warrior for us both and honestly, I let her. It lasted about an hour-ish and Jackson ultimately fell asleep during the test, which he was suppose to do for the latter part of the test. 

As the technician warmed water in the microwave Hallie continued to ask questions and be involved. "What are you going to do with that?", she asked the technician. She told Hallie that was to help remove the sticky stuff from Jackson's hair. Even though that was the answer, she still stared a hole through the technician through the whole process. (ha, my little protective one) Even the technician mentioned how "aware" she seemed to be during the whole process. Normally I don't post pictures from any testing but I feel like this is all part of the journey, so.... head wrapped "mummy style" and another test we can check off the list, here's my little mummy during his EEG. 

Poor thing, he was NOT a happy camper by the end of this experience. I tried to explain that it was just some wrap and that it's ok, but huge shocker here... he didn't care (or even understand). All he knew was that he wanted off that gurney and he wanted that head wrap off! And fast! So fast, that he tried to "assist" in the removal process, which was all but a huge fail of frustration for him.  

On a lighter note, Jackson's latest trick of the trade is to name every female he meets "Woman". So as he was being set free from the mummy gear, he was yelling at the tech saying, "I don't like this you Woman!!!" (lol) Even though it's not funny, we were both laughing at the moment. It was cute, sweet, innocent and typical Jackson in every way. I am more than pooped this week and it's only Wednesday. The results from this EEG will be like most of the other testing, we'll be waiting for a bit to hear results. (big shocker there) Oh well. Glad to have this one out of the way and I think my little dude would second that.  

This will sound silly, but I'm glad Hallie was there on Monday, even if she is 3. I talk to her about Jackson a lot because believe or not, I think she gets it. My very own little pint-sized shrink ha! So thanks to my little peanut for being my rock on Monday. She's the best!

~EM

Just When you Least Expect It

Words. Ohhhh the words. I can't find them. I've had a mean case of writer's block this past week (maybe by inadvertent choice to some degree) But I need to find them. I have been searching for them all week. Multiple times I have thought I was ready to write it all out. A thought or two will come to my mind and I think about writing it down, but end up forgetting the thought 10 minutes later. A good indication I wasn't ready to say what I'm thinking or feeling.  I've wanted to put it all on "paper", but I haven't been ready. Today, I'm trying to be ready. Since our last appointment on January 10th, our lives have changed forever.

The whole idea of "for better or worse" at the alter on the day you marry your best friend never includes the fine print of life. Today I'm living the fine print. All the things that no one tells you will be part of your marriage or life together. All the things that no one can predict or guarantee from day to day. That's where I find myself right now. The best part? I AM NOT ALONE. Because "for better or worse" I have the best man by my side. My partner in crime, my partner in love, my partner for life. 

And with that partnership comes this post. Together. I usually write all of these myself, but today I need my other half to help me. So here we go...

Sitting here in tears, the both of us, John and I write to you. To say thank you for your support. To say thank you for your continued love. To say thank you for reminding us that WE are not alone. A dear friend of John's told him this past week, "God never gives you more than you can handle". Those words are so true. As people we all handle life's trials and tribulations in our own ways, we all react and process differently. That's what makes us who we are. That's what makes Jackson who he is. 

Going in with the expectation of "every appointment is a waiting game" I had no idea we were going to leave there with answers that same cold day on January 10. The neurologist asked me what I thought Jackson had. My reply, "Oh, I don't know" He said, "Yes you do, now tell me." I said, "I think he is somewhere on the autism spectrum and maybe some form of ADD. He replied, "You would be correct". 

His words, "Jackson has Autism. ASD (Autism Spectrum Disorder)-High functioning. (but he didn't stop there) He also has ADHD, OCD tendencies and Asperger's". Holy Sh*t. Didn't see all that coming. (I know Aspergers is commonly known as a form of autism, but our neurologist told us it will soon become a completely separate diagnosis away from the autism spectrum all together and Jackson has all the signs of both, independently and together all in one, but we'll sift through those details in another post). As Jackson and I left the office with reading materials, appointment slips, a prescription paper and more appointments scheduled, I felt frozen. Frozen in that moment. How long have we waited for someone to tell us what we have felt for so long. And how does it feel now that I not only am I hearing it, but it's on paper. I sat in the car for about 10 minutes in complete silence staring at that paper before I called John to tell him. I felt relief, I felt overwhelmed and I felt scared. 

(John's beginning) We have been keeping this very quiet since that day only telling our immediate family and a couple of very close friends.  Not being quite ready to reveal this to all of our other friends, coworkers, extended family, we have been coming to grips that we have a SPECIAL needs son.  The reality of the situation is still sinking in, but we need to be open about our feelings so we can properly handle the situation going forward.  Jackson is SPECIAL.  I mean that in every way possible.  He is truly remarkable.  He makes us laugh hysterically, cry, angry, frustrated & happy.  He is exceptional at memorizing movie lines (gets that from good ole Dad), putting together puzzles (thanks Mom), painting (well, art in general), loves sports, working electronics (future engineer, maybe??), giving the best hugs, and so much more.  It is our purpose in life to make sure that he is given every opportunity to maximize his enormous potential.  Thanks to my best friend and loving wife, Jackson has already starting down this path.  I don't know what I would do without her leading the way with all of the testing and therapy Jackson has undergone up until this point.  There will be more therapy going forward, and we are convinced that this will all pay off in the end.  Speech, Occupational, & Behavioral Therapies are just the starters, but we are so fortunate to have some great people to work with at the Dr. offices and at Jackson's school. 

It is such a relief that we finally have answers (some not surprising, others a little surprising).  For example, I didn't think Jackson would have Aspergers (neither did Ericka), but the more that I have read into it, the more it makes sense.  While I'm sure that we will have more ups and downs along Jackson's path, it just reminds us that we are blessed with such a sweet, caring, lovable son.  As a dad, you never want to have your son/daughter go through anything too trying at a young age as it is hard to comprehend/deal with later in life, but with Jackson, he processes things much different than most the rest of us, and I think he is completely oblivious that his path will appear much different than his friends.  In a way, I think this is a really good thing.  I don't want him feeling "different" than everyone else.  There is a difference between "knowing" you're different and "feeling" different.  

Okay, going to be protective dad here for a minute.  My biggest fear is that other kids will tease/make fun of Jackson through life because he is different or because he reacts to situations completely different than them.  But even more importantly, I don't want Jackson to lose any self-confidence.  There is a time in our lives when we feel like we can "do anything" "be anyone" we want to be, and I don't want Jackson to use his hardships as an out, but rather, I want him to own his uniqueness and channel it to being the best he can be.  I know he has all the potential in the world, and as parents, we plan to give him all the tools necessary to get to the top of the mountain. (John's done typing now, lol)

So, there you have it. Feeling as though our journey has been going on forever (because it HAS), our journey is just beginning. Just when we least expected it, we have answers, just when we least expected it, we are ready to finally put it all out there today. Our story will continue and I hope that through this experience with our little superhero we can inspire you to share our story with other people and to always fight for your children and to stand by them through every part of their lives. Thank you to my amazing husband, who agreed to put some of his thoughts in this post. "For better or worse, in sickness and in health, til death do us part" my friend.

Blessed are you who take the time to listen to difficult speech,
If I persevere, I can be understood.

Blessed are you who never bid me to "hurry up"
Or take my tasks from me and do them for me.
For I often need time, rather than help.

Blessed are you who stand beside me as I enter new and untried ventures, Myself and You.

Blessed are you who ask for my help.
For my greatest need is to be needed.

Blessed are you who, with a smile encourage me to try once more.

Blessed are you who never remind me
That today I ask the same question twice.

Blessed are you who respect me and love me just as I am.

-Author Unknown 

To our sweet Jackson: We will stand by you forever. You amaze us everyday. We love you.

~EM

Filling in "THE" Blank

What's that expression? Close, but no cigar. Yep.... that's about all I got at the moment. (excuse the poor but deliberate English there) Call it what you want, I call it CRAP. Serious CRAP. Sooooo...... of course after I posted my frustrations about this whole "blank" that was left blank, I finally got someone to answer my call later that same day. Go figure. (more on the "blank" here)

I guess it should come as no surprise that every time I take two steps forward, consequently I take two steps back. Or at least it feels that way. Just as I think we are making "progress" with all of Jackson's testing, my phone call for answers didn't quite fill in the "blank" like I thought it would. 

Let's set the scene...me on my cell phone, pen and paper in hand ready to vigorously write every word of the conversation (you should see my shorthand from these medical calls, the dog could write neater LOL)  and then we have the nice lady on the other end of the line at the therapy office. Pretty simple, right? I begin to ask her about the ever so dark blank line from our OT evaluation and why there was no medical diagnosis on the line and her response to me was, "Oh, a doctor has to do the official diagnosis, so our screening for his occupational therapy is limited without a medical diagnosis" (Cue my interior monologue: "Excuse me what!?! I thought that's what you all were doing? She can't be serious? Is this for real?") My real response came out as "That's what I thought you all were doing?" She then went on to tell me that they cannot medically diagnose for Sensory Processing Disorder or anything else OT related, they can only do an evaluation at their office. (Ummmm, NOW'S a FINE TIME TO TELL ME THAT!) So I calmly (yes calmly) asked her what I needed to do about getting to a doctor that can give me those results so we can continue on the path of getting Jackson the testing and things he needs to succeed. We went back and forth for almost 30 minutes and to make a long story short, I needed another referral from our pediatrician for psychology testing and he needs to see a neurologist for the sensory testing. We are also planning to meet with the school about Jackson going into first grade next year, etc. which I explained to her as well. We were coming to the end of our conversation and her advice to me what that I just needed to be calm about everything but that she also maybe should have pushed a little harder for the other testing things for Jackson and that she wanted me to just enjoy my Christmas with my son blah blah blah (yep I was tuning her out by then) Hmmmm, okayyyy. And I'm suppose to still be calm? I could feel the steam starting to come out of my ears at that point. 

I sat there in silence for a minute. How would you respond if someone said "I should have pushed harder for your child"? I simply said I would be in touch with our pediatrician for the other referral and we hung up, although I was ready to BLOW up! For a minute, ok maybe a few hours, I felt like I was failing at all of this for my sweet Jackson. In my mind I was falling just short of success and getting nothing for my efforts. How could I have missed these important things. Why didn't anyone tell me we needed additional doctors and referrals? I guess I shouldn't have been so surprised. Things could only go "according to plan" for so long on this long journey. So, I called my Mom, threw myself a short pity party and put the whole conversation to rest. I just couldn't think about it anymore. Talk about having the scrooge mentality, phew. 

Fast forward, I called our pediatrician's office to send my "cry" for help because I wasn't sure what else to do. Lisa at the office, (an angel in my book) listened to every word of whining and complaining about my phone call. She told me not to worry and that she would call the doctor that we needed to see and demand that we get some answers so we can get back on track.  Keep in mind I have been trying to get in touch with this neurology clinic for a while to see a great psychologist, or so I have been told that he is. Within about three hours she called me back. Whoo! 

Now to fill in that blank. Lisa said, "You're in." THAT was the answer that was missing from the blank. We are in. Finally, we are in. HOLY...... And we are in with a good one, maybe the best? What a sigh of relief. OMG what does that mean? Well, so the neurologist that we are scheduled to see will evaluate Jackson to diagnose or rule out Sensory Processing Disorder and he will also be doing Jackson's Autism and ADHD testing to diagnose or rule those things out as well. He specializes in pediatric ADHD and all forms of Autism. (We do have a psych eval for Autism with EDFTC but not until at least February due to their physician being out on maternity leave) But Lisa's magic has fast forwarded us to another doctor for January 10, 2013. 

That's 28 days from now. Days that will go by fast, but seem like eternity. I called John to tell him and I was so overcome with emotions. I wanted to smile, cry, jump up and down, not to mention I feeling drained all at the same time. (that's a one woman circus of emotion huh? lol)  After years of wondering and searching, we are finally getting "our turn". Suddenly, my world stopped turning for just a moment. Nothing mattered at that moment except knowing my itty bitty monkey is going to get his turn. 

I could HUG and KISS you Lisa! Thank you will never express my gratitude to you. As we approach Christmas, the season of hope and my mind goes a mile a second...

Some days are a rock, some are a stone. For now, I won't look forward, nor behind us.

I am looking for hope and I have fear. What's on the other side of January 10th I do not know.

I cannot predict and don't want to think, I just want to give one final sigh of relief. 

I want to succeed as a Mom for my child, this world is beyond wild. 

And I am not scared of what's to come, though the path is not clear.

So for now, the blank has been filled and my time is served best... right now, right here.

Do not be afraid. I bring you good news of great joy that will be for all people. -Luke 2:10

~EM

Results Minus the Results

It's a chilly Tuesday. It's about time it felt a little more like ole man winter around these parts. (that makes me sound slightly country/ borderline heathen doesn't it? ha) Wanna know a secret? It may come as a shock, but I am developing a serious LOVE-HATE for doctors. I mean don't get me wrong, doctors are wonderful people who save lives everyday, but by golly they can't answer a phone to save their LIFE!!! Secret number two.... I have more test results for Jackson. Yep those ones we've been waiting on since ohhhh about 2 months ago. Good thing I've had Halloween, Thanksgiving and a few blog posts in between to keep my mind focused elsewhere.  

I am finding myself extremely frustrated today. Why, I don't know. Maybe it's just "one of those days". And quite frankly, who cares right? Since when is every day peaches and cream for everyone? If you are one of those people who claims to never have a bad day, stop lying to yourself, we all have a bad day. I feel like a little hamster on the wheel. Running and running, but that darn wheel isn't going anywhere. Hamsters have to be the most frustrated little creatures....

In case you are not fully on the spinning hamster wheel of Jackson's testing, I'll quickly recap. So far, we've had speech, hearing and language evaluations (more on that here) and vision testing. The second set of  OT tests includes the DP-3 (more on that here), Fine Motor Assessment and a Sensory Processing Disorder (SPD) evaluation. Still to go, Psychological evaluations and testing for Asperger's (which is a form of autism), Autism (all ASD forms), and ADHD. My goal in all of this is to hopefully have some firm answers for my little superhero, by April 2013. Just in case you are wondering how long all this takes, April will make 9 months of actual testing and about a 15+ months total of waiting lists and appointments to get some answers (not to mention our previous years of wondering, but hey, who's counting right? haha). Jackson will be just a few weeks shy of 7 by then. If your are a parent out there and you think you are a similar journey, or should begin down the same path for answers, get your rechargeable batteries, you'll be on the "spinning wheel" for a while, but don't ever give up on your little person! I firmly believe that their future depends on your actions today, so whatever you do, don't let that wheel stop turning for them, no matter how long you have to keep it going.

So on to the meat and potatoes of results. 

Jack's results today are the full Occupational Therapy evaluation to include the Fine Motor Skills Assessment and Sensory Processing Disorder. Are you still with me or did I lose you at chilly Tuesday? Ha. All these tests and details and foreign language medical terms can be a bit overwhelming, trust me I KNOW.

Without going into too many details and because I don't think I need to blast Jackson's every area of concern, I'll just recap the areas of testing and results. As you read these, should you find yourself thinking internally: "what does that listed medical term mean?", well... Google it friends. Here we go...

Motor Skills Testing:

• Musculoskeletal Observations
• Fine Motor Skills
• Visual-Motor / Visual Perception Skills
• Oculomotor Skills: 
• Tracking-results: within normal limits (YAY!!!!)    
• Scanning- results: needs therapy                    
• Convergence- results: impaired 
• Accommodation- results: needs therapy 
• Divergence- results: impaired
• Additional Visual Information
• Self-Help Skills 

Sensory Processing Disorder Testing: 

• Sensation Seeking
• Auditory Processing
• Visual Processing
• Tactile Processing
• Vestibular Processing
• Oral Sensory Processing
• Cognitive Skills

And so for all those areas of testing came these results: Occupational Therapy (OT) should begin in January 2013 for Jackson, with a re-assessment scheduled at the end of the school year to observe for improvements. Jackson should also be involved in social interaction group and/or a sensory processing based play group or camp. 

The the most important line on the whole darn report, MD (medical diagnosis) and here's what it says: 

MD:____________________________________

What? Huh? Nothing? What the.....? Okay, what does blank mean? Is this a bad joke because it's definitely not funny. Does that mean there is no diagnosis, yet he needs to have OT sessions? Does that mean we can rule out Sensory Processing Disorder? Does that mean there will only be a diagnosis after more tests? How can you go through all these tests and things for the most important line to be BLANK!!!! I mean if he doesn't have a diagnosis, fine. But write something on that line to say one way or the other. All those results with no real result!?! Ugh! Maybe my frustration today is starting to make more sense. I have called at least (no joke here...) 20 times to ask about this. 

Of course we will be at therapy this week, so I plan to pin SOMEONE in a corner til' they answer me why that little line was blank, so stay tuned and hopefully I'll be able to fill in the blank! 

I guess I can add this to the "speed bump count" on Jackson's journey. But don't worry, I'll get my answers. In the meantime, the plan is to start OT for Jackson at the beginning of the year and hopefully get scheduled for the psych testing next. 

Since that all important line was blank and I'm rather frustrated today; I'll just fill it in for them... 

MD: Milford Done

~EM

You Can't Have That

Ever heard the words "you can't have that"? It's like finding the perfect pair of heels only to flip them over and see just how many 00000's are behind the $ sign on the tag. Shattered dreams.....

So okay, you recover and your on to the next thing. What about repeatedly being told "you can't have that"? That's a whole other story. It's hard enough to process things you can't have (for whatever reason), let alone when you process things a little differently and are told those 4 yucky words. Which leads me to my point. Yes, there is a point here. Ha! I know there are tons of allergies out there with our kids, our own allergies, etc but do you live with one? Do you stare at food labels and read them like a hawk? Well, I do. 

Jackson is allergic to tree nuts. What are those.... well anything like your pine nuts, walnuts, almonds, cashews (especially those little half moon suckers!) and others. But he can have peanuts (for now). Anything that can potentially contain tree nuts, he cannot have. If you have ever been to an allergist you know that little porcupine looking gadget that poke your back with?? Yeah, it has traces of the elements on it when they are testing you for an allergy. Jackson blew up like a balloon before the nurse could even get finished and get out of the room. Cue the epi pen epidemic!!! We have SIX of those suckers! One at school, one at home, one in my purse (always), two back ups, and one that travels in an overnight bathroom bag in case he spends the night anywhere without me and John. 

We figured out this lovely "allergy" a couple of years ago, thankfully at a graduation party for our friend Patrick who just so happened to be graduating as a NURSE! So lots of medical people were on hand at the time we tasted the lovely cashew that caused Jackson to blow up like a balloon. He didn't even look like himself he was so swollen. Long story short here....luckily, with the medical folks there, a police officer and a whole heck of a lot of benadryl, we had him under control pretty quickly actually. (Mr. Cop was trying to pull me over for speeding down Poplar in Germantown, until I rolled down the window and he saw Jackson's face and became our escort instead, hehhehehe I won that one Mr. Po-Po!). But seriously, whew! 

Looking back on that night, it was really scary to see him so swollen! But now we check everything. I had no idea how many foods are made with tree nuts or manufactured in places that touch tree nuts. RIDICULOUS. Especially the good stuff like cookies, muffins, cakes, etc. So last night we were ready to make some cookies from our cookie dough I ordered as part of a school fundraiser. Then I read the label. Yep, you guessed it.... so I delivered the news to Jackson that we can't make those cookies because they have tree nuts in them. Commence breakdown. Hurry Mom, plan B, you need a plan B. Ok, other cookies. No other cookies in the house (of course not, that would be way to easy). So with my crying little man, I offered for us to make muffins. Which I'll insert here, DARN you Hostess! They were pretty much the only ones with the mini muffins pre-packaged without tree nuts! So, I got some other muffin mix sans tree nuts so we could make our own. I offered to let Jackson do all the mixing and make his own. Problem starting to divert! We are working with him on his adaptive behavior skills (you can read about that  here). So I thought if he could try to make these on his own he would feel a great sense of accomplishment, have something sweet to eat, and it's even better for you than cookies! I've lost count on my win win's with this one. LOL

To most kids making cupcakes, etc is cool when you are little but as they get older they are just more interested in eating them, than the whole baking/kitchen labor part. But Jackson was so excited to make his muffins last night and I let him do the majority of the work on his own! He only got upset once or twice with the mix "missing" the mini cup on the pan. (he likes things neat, not outside the lines, so muffin mix on top of the pan will not do for him) But I gave him a napkin and showed him how to clean it up and try to move on and not "obsess" over a little spill. He did pretty good with it! He even set the timer on the oven (he's obsessed with the "countdown" of timers) and then put his hand in the oven mit with mine so we could take out the muffins together. I gave him a toothpick to "stab" the muffins so he could get them out of the pan without burning himself and put them on a cooling rack. 

Super excited and so proud of himself he asked to call Grams (aka my mom) and tell her all about them. (He rarely asks to call people on the phone and usually has to be prompted or helped with his phone conversations on how to respond, so the fact that he wanted to call was so awesome!) He was so happy that he had done it. You wanna know what making muffins really means in Jackson language? That means with a lot of practice and help, he has the will to do better. That means he understands what it feels like to succeed. That means my little monkey can improve in everything he does and there is no limit to what he can do. Of course it takes an entire post about allergies, muffins and yelling at Hostess to get me to the "read between the lines" message here, but my point is just because "you can't have that" doesn't mean you can't have something else that's even better that what you wanted to begin with.

Hanging my hat on a HUGE hanger of success for this one. And my little superhero being super proud of himself... I can't do  much better than that. 

~EM

Frustration, Spilled Milk & a Side of Gangnam?

Sometimes you just have to get it out. Today is one of those days for me. (I'll go ahead and apologize for the small pity party I'm throwing here) Jackson is still sick, day 12. I think a 4th trip to the doctor is in our future tomorrow morning. Poor baby. Whatever this "virus" is or isn't is really throwing him for a loop and a half. And if I am being really honest and candid, I'm SO OVER THE SICKNESS! Not only for him, but selfishly for me too. I'm tired. I want to pull the "I want my Mommy" card, too!  

After a long week of leaving school early for multiple days, missing school all week last week, a lot of sleeping and not a whole lot of eating, I am really starting to worry about my little man. We had therapy tonight and I guess I shouldn't be surprised but we still don't have any more test results even though they were ready before Thanksgiving.  UGH! The "printer" has been messed up at EDFTC or so I am told. I'm sorry but where is the customer service?? I have begged for them to just fax it, email it just any way they can come up with to get me these darn results and still nothing. Oh well, there's always next week, I suppose. Jackson's session didn't go very well today. I could hear the frustration through the door as he was trying to work on his speech. I guess I wouldn't have much patience if I didn't feel well either, much less on a Friday. Feeling helpless, I listened on the other side of the room as my poor little guy struggled and was anything but interested in focusing on his speech. Cutting his session 20 minutes short, his therapist Ms. Courtney opened the door and said he had reached his limit today. 

Game over.... Therapy-1, Jackson-Zilch.

As we continue on our journey for answers, I'll share some of Jackson's "habits". Frustration is putting it lightly for Jackson when things are going "according to plan" for him sometimes. If he spills even one drop of milk, he wants a whole new glass and the world is coming to an end. He has cried and cried over  his spilled milk, multiple times. So much for the saying "no use in crying over spilled milk" huh? He also tends to process things differently. You know how people ask you "If you could be anyone for a day who would it be?" I would want to be Jackson. I wish I could walk a day in his shoes, see his perceptions of how the world turns and really experience things the way he does. 

Often times he becomes very obsessive over things like movies, commercials, the weather, certain iPad games, etc. I mean really... if there was such a thing as the Jim Cantore School of Weather, I would have earned a degree in Meteorology by now! He is also very analytical, which I find interesting. He likes puzzles and he's really good at them. He likes to know how things work, taking them apart and putting them back together, things like that. He's very interested in, surprise... the weather, sports and scores and who's winning or losing. He' also critical when he thinks sports teams/players don't do well. He's very quick to say "they didn't do good, or they need to try again or that was a bad shot" and seldom is he interested in anything but winning. He doesn't understand the concept of losing. He can't lose at anything or there is a guaranteed meltdown. I think he ponders about how technology works. He's very good at using technology too, just ask my Apple iTunes account how easy it is for a six and a half year old to get past a password and buy apps. (cue the OUCH to the ole bank account)

He's also very in-tune with sounds or select words and repeating them, a lot and at totally random times. Like theme songs in commercials, just think "ba da ba ba ba, I'm loving it" from McDonald's. Phone numbers from ambulance chasers, I mean lawyers on tv. For all you Memphians out there....trust me, if anyone ever needed Nahon, Saharovich and Trotz, Jackson could recite Corey B.'s # on command!  Guess that "catchy" advertisement of their phone number is working for at least someone, lol. 

I could go on for a while about obsessions that he has, because there is a laundry list of them, but the last one I'll talk about tonight and perhaps the most hysterical to me is Gangnam Style! O.M.G. I mean, it's really quite funny. Don't even ask me how many times we have watched that You Tube video because I'll never admit to the actual number. I'll just put it this way.... he has watched that video enough to LEARN all the words and dance moves on his own. Now he's no prima ballerina when it comes to his dancing skills, but in his mind he thinks he's on Dancing With the Stars. I even caught it on video....hehehe!!!!

Don't judge my messy den of kids homework, toys and junk. Sometimes you pick your battles so cleaning that day wasn't at the top of my list (sorry). I'm sure this video will go on the list of "I can't believe my Mom did that to me", but I love to capture him in all his happy moments of glory and feelings of accomplishment! It's also "good Mom code" to have embarrassing moments of your kiddos right!?!

After a long week and an unsuccessful therapy session tonight, I'm looking forward to getting up our Christmas decorations this weekend and crossing my fingers for a healthy boy.

TGIF

~EM

Going Out With A Bang!

Yay for Saturday! Ummmm, why is the weekend going so fast? I hope everyone had a wonderful Thanksgiving holiday and time well spent with family, too much food and maybe a libation...or 10 HA! So recapping Thanksgiving, we drove over to John's cousin's house for the day and spent the day playing whiffle ball (yes, we have enough family to make two full teams and fans to cheer us on), knock-out, bocce, corn hole and eating pretty much all day long. But we had so much fun getting to visit everyone. John's Aunt Terry was campaigning for cash to go buy scratch off lottery tickets, which I thought was hilarious and "worth the mention". Ten years from now, this will be funny as hell to look back and remember her walking to the gas station with about $50 of donations, a couple of kids under the age of 5 and a handful of lotto tickets. Have I mentioned I love this family! Never a dull moment and I would NOT change a thing! I'll tell you, I had planned with the best of  intentions on taking all these great photos on Thanksgiving and posting them for the family and ask me how far I got with that???? Absolutely nowhere would be the answer. So FAIL... just put it on my tab. As a matter of fact, these were the only pictures of my own kids I got! What kind of Mother am I? Thankfully... John's Godmother to the rescue! Ginger took lots of photos and is going to send them to me soon! Whoo! 

                                                    

So obviously as you can see above, Thanksgiving was winding down and we were on to the next thing. I feel like we have been running the 100 meter olympic hurdles all weekend! Friday was spent doing very LITTLE black Friday shopping mainly because I am an online junky shopper. Seriously! I need an online shoppers support group ha! But I'll argue my case for a second and say, when you have two kids that have minimal attention spans for comparing "this to that" for Christmas shopping, they don't last very long! I know all you parents can feel my pain here! And on the flip side I can shop online ALL day long and they can play at home. It's a WIN WIN people!!!

The monkeys had finally started to get over the "funk" we have been fighting all week (praise the LORD), so last night we decided to head to the zoo to see Santa and the Zoo Lights (kinda becoming a cousin tradition) Even though we were missing a couple of cousins due to, ehhh sickness is a good way to put it. 

Disclaimer*** Secretly we take the kids to the zoo lights to see Santa because we all get a great LAUGH out of the terrible face that someone always produces from seeing the big guy in the red suit. It's like a cheap thrill for the adults HAHAHA! And boy this year was no different. Miss Ella delivered like a champion! (See terrifying face below as I giggle)

Ha!!!!! I'm so sorry but this picture is hilarious and worth a thousand words. Auntie Ericka loves you Ella!!!! So with the terrifying pic, here's a few more of the fan with "happier" faces. 

Big Christmas tree at the Zoo entrance

Hallie and Ryan, best friends! 

Joe and Kristen

Me and J :)

Jackson and Ella tuckered out!  

Checking out the tree!

Sweet smiles, but double trouble!

Today we are headed to Maryn and Annie's baptism along with a little football later tonight. Go Irish!  Rounding out our weekend, I'll make the extremely fast mention that today is my last day in my 20's! Woah and yikes!!! Good thing I fully loaded the weekend with lots of great family time and love before I celebrate the dirty 30 tomorrow LOL..... Oh well, what is it they say, 30 is the new 18? Ok, yeah I'll go with that. Mentally I feel about 12 most days, so that HAS to count for something right? 

What a blessed and great weekend we are having so far, my cup runneth over!

Going out with a bang... goodbye 20's, hello older and wiser! (HA, yeah right) 

~EM

  

Good Things Come in Small Packages

Happy Thanksgiving eve! My mind has slowly started migrating towards "holiday mode" and man am I ready for the break! Since Jackson didn't get to go to school all week this week, (thank you viral infection) his sweet teacher sent home a small care package of all of his projects for Thanksgiving. We  have an abundance of cutsie art goodies including a pumpkin, a handprint turkey placemat, a headdress and Indian t-shirt,  complete with his Indian name "Cow Jackson" on the back (I have no idea where he came up with that one LOL) and maybe most importantly, his vision screening results from LeBohneur. 

My husband (God love him) is pretty much a blind bat without his "eyes" otherwise known as contacts, so I was expecting the possibility of glasses in our future for Jackson. Much to my surprise however, he is 20/20 in both eyes! Whoooo! I know that sounds so simple and maybe somewhat silly, but since we are racing the Indy 500 of tests these days, these are the first "test" results that we have back that have been different than what I expected and we'll take it! Our OT results are in as well, but I still don't have a copy of those (go figure) so I'll be on the edge of my racing seat until Monday for those results.

As we ski down the slope to being fever free in our house, (YAY!) tomorrow I plan on devoting my entire day to being thankful for relaxation and hugging the necks of family members that we haven't seen in a while. Good food, laughter and love.... that's what I look forward to this Thanksgiving. Wishing you all a wonderful Thanksgiving holiday weekend! I'll be posting.....

I can never have too many kisses from this little man!

Cheers!
~EM

Sunday Not So Funday

Two monkeys with two fevers.....ahhh that's not how I wanted to start out my Sunday. Oh well, I guess we'll take today to really "rest" since Sundays are suppose to be a day of rest, right? Hoping the monkeys are back to normal for school tomorrow, the rest of my day will be spent doing laundry, cleaning and de-germing the house and getting stuff ready for the week. So much for that whole idea on resting, guess I should know better. 

A positive of today is that today is my sister or as she's better known "Auntie Auba's" birthday! (don't worry sis, I won't say your age :) And although Jackson was running a fever this morning he squeaked out his rendition of "Happy Birthday" to Auntie Auba (complete with Cha-Cha-Cha's between every line HA!) Hilarious and yet pitiful too. 

As Jackson's test scores are still setting in, I think I have 3 things I am debating. #1 I am starting to put Friday's scores into my brain folder: plethora-o-info for  Jackson, #2 I am starting to focus on what the next scores (fingers, toes and all things crossed) hopefully coming tomorrow will be. I wonder what they will reveal? Will they be a pleasant surprise? Will I have round two of picking my jaw up off the floor again? Either way, it's just one more step in the right direction. And #3 and maybe the most important, how do I begin to try to make Jackson understand what all of this means? Of course he realizes he goes to therapy, but does he know why? I highly doubt it. Maybe in movie terms since that's relatable for him?

Like the journey of the "yellow brick road"? You are headed to that magic wizard that can grant all your wishes but along the way.... LIONS and TIGERS and BEARS oh my!... but just like in the Wizard of Oz.... those lions, tigers, and bears end up becoming not feared but welcomed. That's what these test scores are starting to turn into. Yes, they scare me (Jackson probably won't care about the scores really or even understand), but I sure am thankful for them because without them, we won't reach that magical wizard that can grant all of our wishes! (call it dumb or silly, I guess that's just my mind making it all relatable for Jackson if I try to explain things to him) I also need to decide if he is even ready to hear my "attempt" to explain these things to him. I can just see it now... A 5 minute discussion (at the MOST, and I'll be lucky to get him still for two minutes), I try to explain things like a "movie" or something relatable to him and then Jackson's reaction "Cool Mom, can I go watch that movie now?" (insert MOM FAIL) Ha... but it will be funny and I'll be ok even if he has no clue what I am trying to tell him.  

He had a hard night last night as we tried attempted to play a game with the kids. Just as playing a family game is simple for me and you, it's like asking Jackson to run the NYC marathon. I won't go into that struggle, but as the journey continues I'll talk about Jackson's habits and "super powers" he has been blessed to have. :)

Hoping you all have a great week and blessed Thanksgiving! Meanwhile my little dude is trying to kick the fever......

~EM

What's Your Age???

Hello loves! Yesterday was not the happiest of Fridays, but as always tomorrow is another day and today has been great! Hallie and I have been to a make-up open house (yay) we went to a crafts fair at our church, we are making Christmas lists, watching football and playing games with the kids. In other words a good family day for a Saturday. This weekend is the first weekend in a VERY long time that we have not had anywhere to be or anything to do. Can I get a hallelujah!?!

In other news, we have more test results. Long post here, so grab your wine and read on.....

Finding the words at this moment is hard. I feel as though I have a case of writer's block in trying to get the words out - even though what I have always known has now been confirmed on paper. Make that NINE pages of confirmation. (I am now starting to see why it takes so long for these tests and the results) 

So, on to (or back to), October 24th....another testing day. We started the process for Jackson's Occupational Therapy (OT) assessment with a parent interview, the OT therapist doing an interview with Jackson and then the actual testing. I also had to fill out a profile for Sensory Processing Disorder (SPD) and Developmental Profile Test (DP-3). And by fill out I mean FILL OUT a profile. You know when you buy a house and it's closing day? Yeah... imagine that stack of pages as you sign your life away only apply to a six year old for testing. I guess I see it as another signing day to "buy" a better future for my sweet Jacks. I thought I would NEVER get through that packet!!! I could have published a documentary of Jackson's life there were sooooo many pages, ha! But again, all so worth it if we can get to the light at the end of ever so dark tunnel. 

So, testing begins... I didn't get to go in for this test like I did for the speech, language and hearing tests. Instead, I got to sit and wait and watch the clock tick by. OMG!!! My nerves were shot and that hour and a half seemed like eternity! (I swear, paint could have dried faster that day) The testing was finally completed, I did my interview part and we left. Ms. Jackie (our OT) said she would have the results back to us in a couple of weeks or so. My interior monologue kicked in...."Weeks? Really? Ugh!" My response out loud was a little more cheerful and along the lines of: "Ok, thank you so much for seeing us and we'll see you soon", along with a grateful sigh of relief. Another set of tests to check off the list and the waiting game begins yet again. Anybody wanna contribute to the "Ericka needs to buy more patience fund?" LOL 

Finally on November 13 (almost 3 weeks later, yes I counted) and we have some results. I thought I was ready....I mean I was ready....I mean I really wasn't ready, was I? My head was a wreck, my heart was pounding. So I get the call, get a few results, continue with my night with nothing really "hitting me yet" and we were scheduled to get the "hard copy" of the results on Friday, November 16 (yes that would be yesterday... and in case you missed how great my day was yesterday, you can read it here). Jackson had speech therapy as usual last night and meanwhile, I had hard, down on paper, pretty (or not so pretty) graphs and charts, recorded results. In Jackson's case, we are doing a series of tests for a multitude of things. I have the results for the Developmental Profile (DP-3 Test) so far. The rest of our results will come on Monday or Tuesday (or in medical time, sometime in 2013.. HA!)

I'll give you the easy to understand run-down as usual. The DP-3 tested Jackson for the following..... Physical Development, Adaptive Behavior, Social-Emotional Development, Coginitive Development, Commincation Development and then  General Development (this is like a composite score of all the other tests combined)

The easiest, most understandable terms I can put these results in is to say that for each of these tests, they give you an "age range" that your child falls into for each test and then an overall General Development Diagnosis. So I review the results: 

            Tests:                                                                                                 Age Equivalent:

Physical Development (carrying objects, jumping, etc.)                                           3-6
Adaptive Behavior (i.e. how make a bowl of cereal, daily life habits, etc.)               4-5
Social-Emotional Development (expressing needs, interacts/plays with others)    3-10
Cognitive Development (what's real/not real, memory, etc)                                     4-2
Communication Development (verbal/non-verbal skills, etc)                                    5-1

Ok, the first one- physical development- ages 3-6? That's not too bad right? Keep in mind he is now 6 years, 6 months (yes they record the months when they test) So I thought the age range of 3-6 was kinda wide, so I asked about the range. WRONG. SO WRONG. 

That was age 3 years dash 6 months. (Cue, my nervous stomach falling from my throat to my FEET!) I know the look on my face had to tell it all. I was shocked. Jackson turns 7 in May and as you can see above, each test score is well below the age of 7. He's 6 and a half and physically 3 years and 6 months? Woah. I almost for a second couldn't wrap my head around that. I wasn't expecting it to be that bad low for any of the tests. I honestly thought his communication would be the worst and it was the best! Phew! Need a deep breathe at this point. You can read the rest above as the same... the first number is the age in years and the second number is the age in months. 

So for his General Development he is: Developmentally Delayed (by years in every category). I knew it, I just hadn't seen it. Seeing it makes it all come full circle. It's hard now to even type it all down. I needed to just take it all in yesterday before I shared it. And although this was the outcome for this test, I don't really want to cry. I want to FIGHT. Fight for him to do better and improve. Fight for him to develop more and more every day. Clearly, we have a ways to go in working on Jackson's development, but we will get there! We have a plan to work on at home, therapy and school for the next 6 months and the DP-3 test will be done again to see what kind of improvements we are making. And he will improve! I firmly believe that. I am still letting all of this sink in and still not sure if it has completely hit me, but we'll continue on the path of nothing but success. There is no room for anything but improvement for Jackson and I won't settle for anything less. 

As it all sinks in...... 

~EM

Hanging. By. A. Thread.

Ahhhh therapy... I could use some therapy of my own right now. Let’sjust say that my morning did not get off to a good start. Chaos was running rampantthrough my house and guess what? It wasn’t the kids causing the chaos today. It’slike nothing was in the normal place, no one can find their shoes (even thoughthey can only be in so many places), dogs are on my nerves for whatever reason…you get the point. You know you just have those days that nothing goes asplanned? You wake up, all is great, then little by little you just hit thedownhill slope to having a “case of the Mondays” on a FRIDAY!  Not to mention I was on the way to dropJackson off for school and then – SPEEDING? I am doing 25mph!!! How is thatspeeding…. Well it is in a school zone. DANGIT! So then that makes Jack latefor school, me late for work and my Friday is really off to a crappy start. Notto mention I now have a mandatory court date right before Christmas. JuuuustGREAT. 

So moving on, we just got home from therapy and I have more of Jackson's test results back! I have to say, honestly...... today I am struggling a little bit, ok a lot. Today is a hard day for me as a Mommy. Getting results is great! Seeing results makes everything very real. So real, that I am not going to post them tonight. I am completely drained. I need some time to let everything sink in. I need some time to unwind. So tomorrow I will post the results from today's session.  Until then, TGIF! 

I am going to curl up with my kids, hold them tight and say GO GRIZZLIES! 

~EM

Lean for Love

I'm starting this post by saying first thank you. Thank you for taking the time to read our story. Thank you for being supportive and thank you for showing the love you have for others. People never cease to amaze me. It's amazing how people can be so giving to those they care about, love and sometimes even complete strangers. And I embrace all of you. I feel like I have always been a very giving and loving person to others in my life and others that I don't know, but it's nice to know that when I need the love, I feel it. The last 24 hours have changed my life. I have received more emails, phone calls, texts, Facebook messages, post comments and tweets than I can even count. People sharing their stories with me, sending love and encouragement, sending prayers, tears and most importantly support for Jackson! Not to mention, it's nice to know you aren't alone.  

Yesterday, coincidentally was John's mother's birthday. She would have been 57. And although I know everyday that goes by he misses his mother (maybe more than anything in the world) I know she is with us. I have no idea where my courage came from yesterday to all of a sudden think I am strong enough for all of this, but I'd like to think our Angel Peggy had something to do with that. I never got to meet the woman that my husband called "Mom" but I hear she was one AMAZING lady. What I do know is the kind of children she raised and the things she instilled in them before her she left the Earth for a better place. I hope that I can give that kind of love to my children like she did for her kids and any other children who's lives crossed her path. It has been over 11 years, but her presence is still felt by so many people today, that I can assure you. I firmly believe she watches over us and I think that sometimes she gives me the extra push of strength when I need it the most. I only hope that I would have made her proud. Weird how things in life line up sometimes isn't it? Sure does confirm for me that we are not steering the wheel of life.  

We have more test results that I will be sharing tomorrow after therapy. I know the results already, but I am getting the full "hard copy" report tomorrow and don't want to leave out anything that could be considered "cool medical terms" ha. I am anxious to get that report, just another piece of the puzzle we'll fill in tomorrow.  

My biggest take-a-way for you all today is - I think all this means we are onto something team! Just as my little superhero tends to lean on things (literally) most of the time, I am leaning on you. And I am asking you to lean back. If you are a parent (or anyone) that has ever had a question, wondered or just felt like you are alone on your search for answers... YOU ARE NOT ALONE. I am an open book. I will be honest, listen and return the love that you have given to my family and Jackson in such a short amount of time. Please feel free to reach out to me if you ever need anyone. I understand privacy and I understand being scared, but sometimes we all just need to lean for a little love. 

After all, this little guy leans for love all the time. 

Jackson and our sweet friend Ava at the
U of M Homecoming Football Game

Sending you all my love,
~EM

Jackson's Journey...4 Tests-1 Answer

To say that our journey will be a long bumpy road is an understatement. Once I catch everybody up to speed my posts will be shorter, I promise! Til then just hang in there with me! I have my feelings, opinions and guesses as to what I think Jackson is experiencing, but I'm not doctor so I'll keep my thoughts to myself on all the "things" I think we are going to ummm be working on to improve. :) All sugarcoating aside, we have some great days and we have some NOT so great days. I will tell you all, as any other Mom with any child, children teach you a whole new level of patience. Or they prove you have no patience. LOL As we have come to realize Jackson seems to have his own ideas about what "normal" means, I decided that Path 2 (from this post) was the way for us to go. 

Yes I have been scared. Yes I have been researching for a long time. Yes I need answers. Are you kidding, I needed answers yesterday. What is it they say? Good things come to those that wait?.... yeah that's for the birds. I have decided to take the early bird gets the worm approach instead. And by that I mean I have been a harassing, nagging, bugging and maybe even annoying parent to every doctor and person that I think we need on our side in order to get answers. After calling almost every single day for referrals and leaving more messages than I should ever admit to, I started getting called back. Ahhh Ha! Being really  extremely persistent can have it's benefits.  

So rewind to October 8. Our first appointment. Having been screened at school for speech and hearing and being told that Jackson had not passed, that came as no surprise. I was kinda relieved he didn't pass the screening to be really honest. It meant two things. One, everything we have been noticing for years is finally starting to surface with hard evidence. Two, I'm not totally crazy. So with those results, I decided we needed a second opinion and I was going to go armed and dangerous! I asked Jackson's teacher to take notes on things she noticed, habits, mannerisms, etc and being that ANGEL that she is, I had 4 handwritten pages of notes. YES! Ms. Beth you are awesome! I also took 12, yes 12 of the exact same drawing produced by my little artistic rockstar from the Lorax (love that movie). Now, I don't know about you but I can hardly remember what I did yesterday let alone days and days worth of things. But Jackson's drawings were of the same scene from the movie, same colors, same patterns and yes I have 12. One for every month I suppose! Ha. (more on his uhhh "obsessions" later) But we had waited so long to get an appointment, I was taking all the ammo I could get together for this. We went to the EDFTC (Exceptional Development Family Treatment Center) after getting a referral to be seen and we were scheduled for a hearing/speech/language evaluation.  Let me just also preface this with, every child that has any sort of special needs is never like the next child with special needs. One test for one child is not the same test for the next child. So for Jackson a Listening Comprehension Test, Oral Expression Test, Oral Composite Test, Hearing Test and Sounds in Words Test were performed. Ms. Courtney is our speech pathologist and Jackson was immediately connected to her. I have never seen a child be SO excited to see someone (that he just met). So I'll give that a checkmark and success for starters. 

After the testing was over, we left. I felt a sense of relief. A sense of success and even though we wouldn't have any answers just yet, I was happy. Skip to October 19. Test results are in and on a Friday night at 6pm, we headed in for some answers. FINALLY! So I won't go into the somewhat hairy fine line (somewhat foreign language) details, but we'll just talk simple "what does that mean in English" terms for now. 

Scores. So every child should be at a certain communication level for their age right? For Jackson (age 6) his scores came back and on the four tests he ranked: 4% for Listening Comprehension, 1% Oral Expression, 2% for Oral Composite and 11% for Sounds in Words.  (Yes, these tests are out of 100%) Diagnosis- Mixed Receptive-Expressive Language Disorder. The good news - He PASSED the hearing test! Whoo! What his disorder means is that for his age, he falls into the categories of needing intervention/has delays/language disorder, thus the diagnosis. So for the next year, we will have speech therapy sessions with Jackson to hopefully improve his communication and speech skills. After a year the goal is to have Jackson be in the 80% range for his age group. How awesome would that be?!?     

Also along with that initial evaluation came the recommendation (and me being slightly persistent) for additional testing. So following that we are on the road to becoming a speech superstar! 

The next steps would be to have Jackson scheduled for a OT (Occupational Therapy) evaluation for Sensory Processing Disorder. One down, lots to go. So our next test was scheduled immediately the same night of our first results. So excited for October 24th I couldn't hardly stand it. 

Eager and ready we'll be reporting on those results soon! Hugs your babies and be thankful that they have so much to offer and teach you everyday. How did I get so lucky to have this kid? 

  

~EM