Not The Best News……….

Warning: There is a photo towards the end of this post that may be difficult to see or hard to look at if you are squeamish.

What a crazy last few days it has been! I’m not even sure where to begin but here goes!

Last Friday, I took Cannon in for his surgery. Our ride to the hospital always includes a social story. These are stories that gently explains to him exactly what is going to happen to him. To aide in coping. We do it every time he has a surgery or procedure and it helps tremendously as he seems to understand the written word better than the spoken. I was running late but managed to scribble this down as I ran out the door……..



The first part of the surgery was to be the endoscopy. Cannon’s G.I. doctor would do an Upper and a Lower scope to see if he could find any issues or sources of his abdominal pain.  There would also be biopsies taken from all over, as well as blood  drawn for various tests. He has had bouts of extreme lethargy, paleness, etc. and we were so ready to get to the bottom of things. After some time, the doctor came out shaking his head. He asked me when and what Cannon had eaten last. I grabbed my notebook. For as long as Cannon has struggled with G.I. issues….I have been keeping these notebooks. Notebooks that eventually get filed into large binders and stored. I record everything that goes in (food wise), everything that comes out (you get the picture), as well as behavior notes….doctor’s appointments, etc. I have to. I can’t remember anything anymore. So tired! Anyhow, my notebook told me exactly what he had eaten for dinner the night before and what time. He confirmed with me that he had had nothing after midnight. Nothing….yes. A sip of water to take meds and that is it. He shook his head some more and said he found the problem. Cannon’s stomach was completely full 14 hours after he had last eaten. So full he couldn’t even get in there. He said he was in shock. Had taken pictures. He just couldn’t believe how full it was. He had had to pump his stomach. He called this disorder Delayed Gastric Emptying or Gastroparesis. Partial paralysis of the stomach. This, he believed, was the source of all the pain he has been having. I really thought it was going to be scar tissue buildup on his button but no…..this was much worse news. This is a life long, chronic, and painful problem. And it is the cause of the severe bacterial overgrowth that we found in Cannon back in November. A problem so bad….it had taken 4 months (when it should have only taken 2 weeks) of high powered, twice a day antibiotics to get under control. And he still requires a maintenance dose every other day to keep the issue at bay. Stomach contents hanging out for that long and basically stewing….causes the bacteria to build. We could not figure out why it was doing this as we flush his colon daily….but now we know. My poor buddy! The worst part to me is that with Cannon’s limited language…..he has been suffering for so long with this. God only knows how long! And he didn’t have the capability to tell us about it. So….long story short…..his stomach fills up….it isn’t strong enough to break down the food….so it just sits there. Until it is so full and more comes food comes along….pushing it on its way. The bacteria has formed in the meantime. Now it heads into a colon that also doesn’t function. It sits and waits for our daily flush to move it on out. Heartbreaking! Disgusting! My poor buddy!

The only good news on the G.I. front is that all the biopsies and labs came back normal. Thank goodness! No more surprises. The doctor is telling us that right now our only course of treatment is to put him on another antibiotic long term to try to get his stomach to respond and move. The chance of it working is poor. And the concept of him being on yet another antibiotic indefinitely is not so great. But as the nurse pointed out…..the risks are outweighed by his need for the medicine. So, therefore, the doctor feels that this is where we begin. I am going to fill the prescription for now but I am not sold on this idea. Especially as a long term solution. I am going to look into other methods and courses of treatment. This isn’t a super common problem and there are few specialists who are experts on it (more good news) so we will see how far I get. So, that was part 1 of surgery day. Phew! And I thought that was enough.

Part 2 was to be the exchanging of his Chait Button. The button placed in his abdomen that essentially does the job his weak colon cannot. This is the part that always makes me super nervous. As mentioned in previous posts, it can be difficult to remove without issue as well as to re-insert a new device due to the spiral nature of the tube below the skin. That morning, the Interventional Radiologist reassured me that all would be fine and promised to look for scar tissue buildup even though he was convinced… wasn’t there. I waited some more after signing away my consent and was surprised how quickly the doc returned to tell me the procedure was over. Like really surprised. He seemed quite proud to tell that the re-insertion phase only took 30 seconds. Which actually concerned me far more than impressed me. Call it my “mom gut” or whatever…..but it just did. I was then taken to the PACU (Pediatric Acute Care Unit) to wait for my sweetheart to wake up. While doing so, I always work with the Anesthesiologist and nurse to ensure the best wake up possible. The Anesthesiologist gives him a little something to ease his transition from asleep to alert. And stays close by incase we have a problem. We have had some horrific wakes in the past. I also try to have a movie he likes ready to watch, his beloved Curious George monkey ready to snuggle, iPad charged up and ready to go, as well as other distractions at arms reach.  I have also been known to bribe him with the possibility of snacks or milk if he is calm. I also ask the nurse to remove any un-necessary medical tubes, monitors,etc…..because he is so sensitive and can get super upset about those being on his body. We usually remove the sticky heart monitor pads from his chest, IV, and pulse ox monitors if possible. I also wanted to remove the abdominal binder or band that he wears to re-dress the site of his button before he woke. We have a particular way of doing this. We cut a slit in a gauze pad and slide it around the button. This catches any ooze. Place another sterile dressing pad with adhesive tabs over the top of that. And add a layer of medical netting over the top. This keeps the velcro on his band from scratching his back. Finally, he wears the band we had invented by a local prosthetics/orthotics company as a final layer of protection. Here is what that looks like…..


So, I pulled his band off to re-dress and to my complete and total surprise… soon as I took the compression off…..the underlying tube began to move out of his body! I jumped back and told the nurse this was NOT normal. The button should be flush with the skin! He took his finger and pushed it back in and told me it was fine. I protested a bit but eventually re-dressed the area and put his band back on. He was beginning to wake up. This was a VERY good wake-up compared to some in the past. They used a different type of Anesthesia than has been used on Cannon before and this proved to be a good choice. Although it was slightly disturbing as his body made some rather strange contortions and such. The nurse was pleased and allowed him to have some milk fairly soon after wake-up. Followed shortly thereafter by a snack. When we dressed him to go home…..he delayed discharge a bit by throwing up everywhere. I mean everywhere. Yes, even in my hair. But he laid back and rested for a while and soon enough……we were on our way home. To heal and wait to hear back about the biopsies and labs.

At home, he laid on the couch, watched a movie, read books, and just rested. He looked pretty darn good considering and I was encouraged. Until I took the band off that night. THE SAME THING HAPPENED THAT HAD IN RECOVERY! The tube began pushing its way out. I actually got a ruler and measured. It was 3/4 inch out! Cannon was quite freaked out by this.  He cried and kept yelling at me to push it back in.  The next morning, when I went to flush his button, it came out 1 inch! And it did the same when I changed the dressing that night. I called and talked to the G.I. doctor on call Sunday morning because I was obviously very concerned. He said the Interventional Radiologist had to deal with it since they had been the one to put it in. And, of course, they aren’t in on the weekends.


So, Monday morning, with the tube more than 1 1/4 inches now out of his body…..I finally got someone on the phone. They said to keep him from eating and drinking and bring him to the hospital. When we got there and through the check in process…..someone from I.R. came out and told us that they would definitely get to us but it would be about 4 hours. Well, that would have been nice to know before I left home. Sigh. So, I had to keep starving him, distracting him with books and electronics, and carrying him around the hospital (as he had no energy to walk) to try and keep his mind off things. Finally, they brought us back and the resident began discussing things with me. And he was talking about some completely different tube! Obviously he hadn’t read Cannon’s chart. He didn’t even know what the Chait Button was or did. I asked for the Attending. When she came out, I removed the dressing and she saw the problem. She began talking about getting an I.V. in him and starting conscious sedation. I quickly reminded them that this doesn’t settle Cannon enough and he has always required anesthesia. They look dumbfounded and left the room. I wanted to say…..Please someone look at his chart….it’s all there!  When they returned they informed me that not only did they not have the size button needed to fix Cannon’s problem…..they also didn’t have an Anesthesiologist available to help with the procedure. It was at this time, they admitted that the tube that had been put in on Friday was 4 cm too long. He needed the same size he had had in in the first place. Which means they did not have both sizes available at the time of his surgery. I questioned this but as this was not the same Interventional Radiologist….she just shrugged. I wasn’t happy. I expressed concern as it seemed to be coming out more and more each day.  They said the coils of the tube should hold it from here on out.  What about infection….I wondered?  It’s going in and out whenever the compression is off.  They said not to worry.  Now, we had to leave. He’s been waiting all day, un-necessarily, to eat.  And no resolution.   We were told the new button would have to be over-nighted in and Anesthesia would be requested for Wednesday morning. So, we went home….again.

Wednesday morning, we were scheduled for a 9 a.m. procedure but got bumped back to noon.  Another long period of fasting for my buddy.  But all went smoothly this go round.  The right size tube was inserted (the same size he had had prior to the surgery) and there were no problems.  He woke even better than before and we headed home with no nausea issues.

I admit it.  I struggled with being quite angry at the doctor.  Had he been in too big a hurry to notice that the button didn’t fit?  Or did he notice, cram it back in there, and put compression on it.  Can you imagine how that felt to my Cannon……keeping in mind that his sensory issues heighten all of his bodily sensations.  I had to spend a lot of time praying for this man.  For his work ethic, empathy level, future patients, etc.  I am not perfect.  And I don’t know if I would say I am over this……but I am on that road.  It’s over.  Cannon’s ok now.  And THAT is what matters.  (But you can bet I sent the previous pic to our G.I. doc’s email address… he is the President of the hospital as well.)  We do love our hospital.  This was an unfortunate incident.

Back to the Gastroparesis….the new diagnosis.  I am so insanely sad and disappointed to learn about this new challenge.  To say the least.  There have been tears.  Quite a few if I am being honest.  I hate it!  I hate it so much!  But I have to leave it at that and focus on trusting God in this process. I cannot give Satan a foothold…..a way into my thoughts and my relationship with my God.  A dear friend shared Psalm 143 with me.  Here are a few select verses that I am clinging to.

“O Lord, hear my prayer, listen to my cry for mercy; in your faithfulness and righteousness come to my relief.  I spread out my hands to you; my soul thirsts for you like a parched land.  Let the morning bring me word of your unfailing love, for I have put my trust in you.  Show me the way I should go, for to you I lift up my soul.  Teach me to do your will, for you are my God; may your good spirit lead me on level ground.”  

Psalms 143:1, 4, 6, 8, 10  

You may have noticed that the blog has a new song playing when you come visit.  I think it is perfect to share with you know.  Our prayer is that each day…….we will remember and focus on these words and the concept that God is sovereign (the greatest in status or authority or power).  And He is sovereign over us.  He has got this. It’s no surprise to him.  I have to just hang in there and keep doing my best to never stop looking for more treatment options and focusing on doing everything I can to help Cannon avoid pain.  God bless you all!  We will check in again soon!

“Sovereign Over Us”

There is strength within the sorrow
There is beauty in our tears
And You meet us in our mourning
With a love that casts out fear
You are working in our waiting
You’re sanctifying us
When beyond our understanding
You’re teaching us to trust

Your plans are still to prosper
You have not forgotten us
You’re with us in the fire and the flood
You’re faithful forever
Perfect in love
You are sovereign over us

You are wisdom unimagined
Who could understand Your ways
Reigning high above the Heavens
Reaching down in endless grace
You’re the lifter of the lowly
Compassionate and kind
You surround and You uphold me
And Your promises are my delight

Your plans are still to prosper
You have not forgotten us
You’re with us in the fire and the flood
You’re faithful forever
Perfect in love
You are sovereign over us

Even what the enemy means for evil
You turn it for our good
You turn it for our good and for Your glory
Even in the valley, You are faithful
You’re working for our good
You’re working for our good and for Your glory

Your plans are still to prosper
You have not forgotten us
You’re with us in the fire and the flood
You’re faithful forever
Perfect in love
You are sovereign over us

You’re faithful forever
Perfect in love
You are sovereign over us

* Feel free to refresh the page and listen again!  Or watch the video!  Let this beautiful song minister to your heart! *



Team Cannon 2014

In the latter part of April, our family participated in the Piece the Puzzle Autism Walk/Run/ and Resource Fair. We had such a great time with friends and family on that incredibly blustery day! Here are some pics to enjoy…….


(We grew by 3 more friends after this pic.)

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Afterwards, we ate snacks, played, and had a great time together!

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Thank you so much to Karli, Dawn, Ricky, Jennifer, Laura, Cole, Carly, Zane, Luke, Gage, Jace, Yvette, and Grandma for joining us and making this day an extra special day for our Cannon! And for helping to raise awareness for and provide support to those individuals and families who daily live with this epidemic developmental disorder. God bless you! We love each of you so much!

“A friend is one that knows you as you are, understands where you have been, accepts what you have become, and still, gently allows you to grow.” – William Shakespeare

Tomorrow is Surgery Day…..

Tomorrow is almost here and it is a big day. Cannon’s Chait Button is due for replacement and it is definitely time. It opens too easily. (The water in the shower even managed to open it once!) And it leaks a bit. The tough part is that this particular button can be tricky to get out and put back in due to the spiral nature of the tube. I have even had people write into this blog to tell me that this happened to their child. Here is a photo. The tab part that you see is above the skin and what we open and connect a tube and then catheter syringes to to do his daily flushes. The spiral tube is below the skin and goes does into the colon. The cecum to be exact. I believe the technical term is a Chait Percutaneous Cecostomy Tube.



So, tomorrow…..we have to be at the hospital at 7. His tube will be changed at 8 by a surgeon and Interventional Radiologist in the Interventional Radiology Lab. They do it there because dye can be injected and they can see better what they are doing. They will be doing this and checking to see if any scar tissue has developed. This is suspected.

Then, he will be taken to the OR where his G.I. doctor (at 9 a.m.) will be doing an Upper and Lower Endoscopy on him. Cannon has not been doing super great lately. His throat seems to be bothering him and the pediatrician says it is red (but not strep). He has had a lot of unexplained pain and tons of moments where he cries out over and over. Being that he is Autistic and doesn’t always interpret those feelings correctly…..He usually yells “Achoo” over and over at the top of his lungs when this happens. Cannon has also been very lethargic as of late. SO….G.I. will take care of the 2 scopes and getting a bunch of labs drawn. Basic stuff and also checking to see if he is Anemic (again) and doing a thyroid panel.

I am trying not to be nervous. It is hard but I am trying. Failing in some moments. Succeeding in others. I don’t want them to find anything. But I want there to be a solution for his pain. We need that button to go back in. As much as we fought to keep from having to put that thing in him originally….we can’t imagine life without it now. For good reason. It gave us our life BACK! Prior to the Chait……Cannon was being admitted to the hospital every 1 1/2-2 weeks for a week. We do NOT want to go back there.

While thinking about that last statement tonight…..a verse came to mind. John 14:27. “Peace I leave with you. My peace I give to you. I do not give as the world gives. Do not let your hearts be troubled and do not be afraid.” As well as Matthew 6:34. “Therefore do not worry about tomorrow, for tomorrow will worry about itself. Each day has enough trouble for itself.” Some days….a little reminder is all you need to help you recognize the thoughts that are not productive and be able to take them captive. I will be doing a better job of that from here on out. I am committed.

If you happen to have any extra prayer time in the morning…..we would greatly appreciate any prayers for our beautiful boy! Much love!


A Canine For Cannon?

Well, it’s finally time for me to let the “cat (well actually the dog) out of the bag.”

It is with much prayer, thought, research, more research, advice from doctors/therapists, and more prayer that we have decided to pursue trying to get Cannon a service dog. An animal bred and trained just for him. To guide and follow him through life……assisting with so many aspects that are difficult for him and also to become a best friend.

This will be a long, huge, time consuming, uphill undertaking for our family. It entails us partnering with a wonderful org called 4 Paws for Ability, Inc. and committing to raise $14,000 towards their mission. I know. It’s an incredibly lofty goal but we believe with our whole hearts that this will help make our sweet boy’s world a better place. I ask for your forgiveness in advance as I will probably be selling everything under the sun and always advertising some sort of fundraiser over the next year or so.

We struggle mightily with asking for help but that is exactly what I, now, must do. If any of you out there can afford to make a donation of any size….it would be SO VERY greatly cherished and appreciated! Below is the link where you can donate safely and easily online. The money will go straight to the org. If you prefer to mail in a donation….please ask. I have flyers that help to designate Cannon as the recipient. Or be VERY sure to put his name on the memo section of your check. To be sure it is credited to his account.

If anyone would like to do a fundraiser of any sort….please contact me! I am all ears! It can be through a business (brick and mortar or home based) or just done privately. Kids need a service project? We plan to do a lemonade stand and bake sale. As 4 Paws is a 501c3 org….things MUST be done in a very specific way so please ask me questions before doing anything. And always, always, always….if you feel so led…..share this link!

Above all else, we need prayers! We believe in the power of those prayers and in the mighty power of God. Our extensive time praying over this decision has us thinking that this is the right path. And we know that if that is the case, it will happen in His time.

As those of you who are parents know, there is NOTHING you wouldn’t do for your child. It is with that in mind that we begin our uphill climb. May God bless you ALL!