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

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

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