Autism, Aspergers, Rob Gorski,Special Needs Parenting, Reactive Attachment Disorder, Fibromyalgia,

Tag Archive: autonomic disorder

Dec 29 2012

My advice to parents new to #autism

I wanted to take a few minutes and say something to all the parents that are new to the #autism journey.  I’m not an expert by any stretch of the word, however, I have accumulated a great deal of experience over the past decade. 

One of the first things I can tell you is not to listen to everyone who tells you what to do.  I know that ironic, considering I offering advice but let me explain. 

Autism is profoundly different for every person that’s diagnosed.  This means that no two people with autism are exactly the same. 

I find that all too often, people forget this truly important autism fact. They will try to tell you what to do because it worked for them.  Maybe it will also work for you as well. However, what you are more likely to find is that what works for someone else’s child may not work for yours.

You have to learn to trust yourself.  You have to learn to do what you feel is best. 

You can take in all the advice you want, but at the end of the day, the decision remains yours to make. 

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Something I have noticed as well is that people tend to romanticize autism and make it out to be this amazing gift. While this can certainly be the case for some, it isn’t for others. 

The truth is that sometimes autism can be an absolute nightmare and people just don’t want to talk about that.  In my opinion, the only thing that not talking about it accomplishes, is creating confusion in the public arena and decention within the community itself.

Look, autism is different for every single person and family out there.  That’s not just my opinion that’s a fact. It would stand to reason that everyone’s experience with autism could be different as well. Right?? Right!!

Some families are more profoundly affected and like my family, will face a great deal of challenge on their journey. 

On the other side of the coin, some families will have far less challenge on their journey.  While their journey isn’t necessarily easy, it will be easier than others.

Something good to remember is that everyone’s experience is relative.  This means that two people can experience the exact same thing, differently.  This is so true when it comes to autism.

There will also be times when you feel like you’re going crazy. Trust me, I’ve been there.  In fact, I’m living downtown there  and have been for sometime. There’s nothing wrong with you. You’re tasked with a parenting situation that most other parents couldn’t even imagine.  Personally, I would think it weird if didn’t feel like you were going crazy from time to time.

You’re likely to feel a cornucopia of emotions. 

Guilt will likely be among the most difficult to bare.  Guilt is something that I have personally struggled with for years.

There may come a time when you may even live in the city of denial, especially in the beginning of your journey. It’s entirely possible that we’ll run into each other in the small town of resentment. I have been known to make an appearance in resentment from time to time.

That may sound scary and unpleasant. That’s because it can be scary and unpleasant.  This is life we’re talking about here, not some fairy tale with a guaranteed happy ending. Real life is messy and very often times unfair.

The only advice I can offer is that it’s perfectly okay if you feel one or more of these emotions. I mean, you’re only human right? I know I feel these emotions and more, quite often in fact.  I hear from other parents all the time about how they feel the very same way. 

I think what really matters is how you handle these feelings.  If you try to bury them and pretend they’re not there, you may find yourself in trouble.  Instead, I’ve chosen to embrace these feelings and let them teach me more about myself and my limitations.  It helps me to keep myself centered and not take on more than I can handle. 

Honestly, I could go on and on but let me just say this. 

You will be undergoing a journey that while difficult at times is rewarding in ways you can’t yet imagine.  Experiencing life with an autistic child can be truly amazing.  You will learn to see the world in ways most people never will.  You will find joy and happiness in the tiniest of things and never take anything for granted. 

You will celebrate victories and and be prouder than you ever thought possible.

One of the most amazing moments of my life was when I realized that my kids were the ones teaching me.  I mean, sure, I’m teaching them as well but they are teaching me to appreciate life in ways I might not have otherwise. 

If you read this blog, you know that our lives are extremely difficult.  Having said that, I’m happy. I’ve managed to find happiness in an otherwise overwhelming situation. We aren’t rich and so money is always a struggle but we somehow get by.  My kids are made happy by the little things in life.  They appreciate nature and see things in unique ways.  I absolutely love watching the way they work. 

The bottom line is that you’re a special needs parent to now.  You’re part of a group or community that is constantly growing, and growing in many different directions.

You will hear many things from many people.  There things will often conflict with each other.
It’s frustrating because so much of what people rely on as fact is really nothing more than opinion.

My advice to you is find a doctor you trust and therapist that knows what they’re doing and works well with both you and your child.  It also helps to connect with other parents and people with autism themselves, within the community who can offer advice based on their own personal experience and who understands what you are going through.

Never ever think that you are alone.  While you may be alone in your house, you’re not along in the world.  We are all here for you and want to help in any way that we can. 

If you visit Lost and Tired, you won’t find me trying to shove my opinions down anyone’s throat.  I simply share my personal experience that I have gained raising 3 boys on the autism spectrum.  Maybe something that I have done or shared here can be useful in your life, maybe not. You can at least learn from my mistakes, of which there are many.

If nothing else, you will find people who care and can empathize with you because they have been there themselves. 

Sometimes, just knowing you aren’t alone can help you make it through the day. Sometimes just making it through the day is a victory in and of itself.

Good luck and please remember you aren’t alone.

Permanent link to this article: http://lostandtired.com/2012/12/29/my-advice-to-parents-new-to-autism/

Dec 18 2012

Autonomic Crisis: Selling the Drama

Gavin had bloodwork done about an hour or so ago. At this point, he seems to have stabilized enough to be sent home. We’ll know more when the blood work comes back

Thus far, things have been interesting.  Gavin was in full on drama queen mode.

He was screaming and crying for no reason, other than trying to get the attention of the pretty nurses.  Very frustrating on our end because his behavior made things more difficult on everyone. 

I missed Elliott’s promotion and Gavin‘s acting like a drama queen. 

This has nothing to do with aspergers, autism or overstimulation.. It’s all about getting attention and cresting a scene.  That would be the reactive attachment disorder. 

I realize that none of this is his fault per say. However he is responsible for his choices, and quite frankly I’m sick and tired of the drama.  I love Gavin, I always have and always will.  Having said that, I don‘t have to love his behaviors and trust me, I don‘t. 

I know that some of you out there can understand how frustrating this type of behavior can be.  My heart goes out to all of you, especially you Carl. If there’s a person on this planet that completely understands its him. 

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Permanent link to this article: http://lostandtired.com/2012/12/18/autonomic-crisis-selling-the-drama/

Dec 18 2012

Autonomic Crisis: Waiting to be seen at @AkronChildrens Hospital

We have actually been for awhile now and are still waiting to go back.  It appears that they are pretty busy at the moment

We have to wait for a room with a monitor.

Gavin‘s slowly become more stable as time goes on.  Hopefully we’ll get back there and we can figure out what’s going on. 

We had to miss Elliott’s promotion. I saw him as he was going do to the dojo and I let him know that we were going to have to be with Gavin at the hospital and he was really disappointed.  He didn’t want to be doing the promotion in the first place, so this really sucks. 

Thankfully my parents are there with Emmett to cheer him on and take pictures.

I friggin hate this. 

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Permanent link to this article: http://lostandtired.com/2012/12/18/autonomic-crisis-waiting-to-be-seen-at-akronchildrens-hospital/

Dec 18 2012

Autonomic Crisis: Heading to @AkronChildrens Hospital

I spoke with Dr.  Moodley’s office at the Cleveland Clinic.  We were originally going to be taking him to the ER at Cleveland. However, as we are getting ready to go, I received a call back instructing me to take him to Akron Children’s Hospital instead.

I don‘t know for sure why they wanted this. However, it’s likely they either don‘t want him to travel that far or there isn‘t really anything we can do at Cleveland that they can’t do at Akron.

Either way, this day has very quickly gone right down the shitter. 

I’m very close to losing what’s left of my mind and just beating my head into the wall until it all goes away. 

Hopefully, Gavin will be stabilized and we can take him home and make a plan for going forward.

Please keep Gavin in you thoughts and prayers. 

Permanent link to this article: http://lostandtired.com/2012/12/18/autonomic-crisis-heading-to-akronchildrens-hospital/

Dec 18 2012

Autonomic Crisis: Gavin seems to be crashing

We just got home from Gavin‘s martial arts promotion.  Gavin did really well and I will have pictures up when I can. 

Right now, we have a problem.  It looks like Gavin is in another autonomic crisis.  After promotion we got spend some time with him in his classroom.  He didn’t look good to me and I asked him to check his heart rate.  He did and it was 50 bpm, standing up. 

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That would explain why he was so shaky and pale.

I had him sit down and take it again.  This time his heart rate shot all the way back up to 138 bpm. That’s almost a 100 bpm difference.

That’s not good at all. 

Your body is supposed to compensate when you transition between sitting and standing.  There should be almost no difference or change in your heart rate or blood pressure.

Gavin‘s body is not compensating at all.  Truth be told, I’m really worried. 

Despite having moved him out of our house for behavioral reasons, we love him the same.  Nothing will change that.

I’ve placed a call to Dr.  Moodley’s office at the Cleveland Clinic.  He is Gavin‘s autonomic specialist and the goto person for this type of thing.  We are waiting to hear back and find out what he wants us to do. 

We aren’t sure if we should take him all the way to Cleveland or bypass Cleveland and go to Akron Children’s Hospital, as it’s much closer.

At the moment, Gavin is still at school.  His teachers are keeping a close eye on him and Gavin insists that he’s okay.  We figured there’s nothing we can do at home that they can’t do at school so we would wait to hear back from the doctor before deciding, what if anything we should do.

I’m at a point to where I want him admitted until they figure out what the hell is going on with him.
His body can’t sustain a heart rate of 135+ bpm indefinitely.  At some point he will crash and we want to figure this out before that happens. 

Please keep him in your thoughts and prayers. I will keep you all posted, as always.

Permanent link to this article: http://lostandtired.com/2012/12/18/autonomic-crisis-gavin-seems-to-be-crashing/

Nov 28 2012

Operation Hope: New problems and tough decisions

I mentioned the other night that we had some more concerning news about Gavin‘s autonomic issues.  His specialist at the Cleveland Clinic decided that the pros outweighed the constant when it came to adding Ativan to Gavin‘s daily medication routine. 

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You may remember that this was discussed briefly before Thanksgiving the doctor that was filling in for Gavin‘s doctor was not comfortable do this and pulled the plug. 

However, Gavin doctor is back and pushing forward anyway with Ativan.

I actually picked it up from the pharmacy yesterday.  The pharmacist was uncomfortable with this as well and went on the record as stating just that. 

Here’s the problem.

Gavin‘s heart rate is still out of control. The Ativan is supposed to help suppress his heart rate and bring it down to a more normal range, thus making him a bit more stabilized. No one is disputing that.

The concern is how the Ativan is known to interact with Clozapine. Clozapine is the most tightly control medication in the country and a very hard core anti-psychotic. Clozapine can have very serious and even fatal side effects of not closely monitored. That’s why it’s so tightly controlled. 

Apparently, the combination of the Ativan and the Clozapine is known to increase the risks of side effect for each respective medication.

This is one of those situations where, as a parent, we have to weigh the pros and cons of a situation and do what we feel is best. 

In this situation, there is a increased risk of side effects.  Gavin has been on the Clozapine for well over a year and is generally considered to be at little risk for side effects now.  We don’t know that anything bad will happen.

Having said that, we do know for sure, that Gavin‘s heart rate cannot be allowed to continue the way it is.  It’s too high and basically means that Gavin is in a state of constant autonomic crisis. At least to some degree anyway. 

It basically comes down to this.  Something bad may happen by adding the Ativan.  However, something bad is going to happen if we don’t get Gavin‘s heart rate under control.

It’s a horrible position to be in.

The reason we have decided to go forward with this is because Gavin‘s doctor is among the best in the world at what he does. We also know that there is a difference between a potential problem and an accident waiting to happen.

This wasn’t something to decide lightly but based in the information at hand, this was the best decision.

It doesn’t feel good to be in this position and have to make these types of decisions. At no point in life, does anyone ever teach you to be prepared for this type of situation, let alone what to do. There’s no guide book for this.  Trust me I’ve looked. 

Of course, the symptoms we are supposed to be looking for could be difficult to notice in even the most typical of children.

The reality is, Gavin is many things but typical is not one of them.

I will say that this weighing pretty heavy on me at the moment because with Gavin not being home, I have to rely on others to makes sure nothing happens.

I hate this situation. 

Permanent link to this article: http://lostandtired.com/2012/11/28/operation-hope-new-problems-and-tough-decisions/

Nov 14 2012

I need little victories

Elliott’s off to school and Emmett’s literally bouncing off of every surface he can.  Lizze has an appointment this morning and Emmett and I are going to do some running around before picking her back up. 

I want to try and get some work done around the house today and try and make our mortgage payment. 

That will feel good.  One step closer to being caught up. 

Right now, I need every little victory I can because I’m feeling pretty defeated at the moment. 

I’m also suppose to hear from the doctor again today about Gavin.  Hopefully, we’ll have a game plan that will allow things to stay the way they are and at the same time, help medically stabilize Gavin so we can get him into residential care.

That’s the ultimate goal right now because it’s the only chance Gavin has to get the help he needs to function safely within society.

Permanent link to this article: http://lostandtired.com/2012/11/14/i-need-little-victories/

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