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

Tag Archive: infusion

Feb 01 2013

The 1st IVIG Infusion of 2013

Today is Gavin’s first IVIG infusion of 2013. This makes 2 years of successful treatment for his primary immunodeficiency.  When I say successful, I mean hasn’t gotten much worse.

He hasn’t gotten seriously I’ll and his dosage has only needed to be increased once.

He will need these infusions for the rest of his life but he does really well and never complains about the 4+ hour procedure. 

It’s amazing how fast time has gone by.

It feels like we just got blindsided by the diagnosis yesterday.  I remember getting the phone call letting us know that he had a severely compromised immune system. We were totally shocked because in all his 11 years, no one had ever picked up on this.

It was the gastro doing a followup blood panel to rule out celiac disease that was responsible for the discovery.

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Looking back on things, it’s amazing that Gavin was never really a sick child. Actually, it was a blessing and still is.

While it’s a blessing, it’s also something of a medical mystery. Was Gavin born with this or is it something that occurred later in life? No one has the answer, at least yet.

We take each day, one at a time and each infusion, one month at a time. It’s not easy and honestly really scary but Gavin is a real trooper about this and Akron Children’s Hospital takes excellent care of him. Hopefully, I’ll be able to say this once again, this time next year.

This site is managed via WordPress for Android, courtesy of the @SamsungMobileUS Galaxy Note 2 by @Tmobile. Please forgive any typos. I know how to spell but auto-correct hates me.  ;-)

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Permanent link to this article: http://lostandtired.com/2013/02/01/the-1st-ivig-infusion-of-2013/

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/

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/

Nov 13 2012

Autonomic Crisis: 11/13/2012 Further Complications

Lizze and Gavin are on their way home. For whatever reason, his infusion finished much faster than anticipated.

His HR has not dropped below the mid 130′s since at least 8am this morning when we first became aware. 

He did top out today at almost 160 bpm.

I have been in contact with nurses with neurology at both Akron Children’s Hospital and the Cleveland Clinic.  They are speaking with the respective doctors and will call us back when they know what to do. 

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Another huge issue is that because Gavin isn’t living at home right now, we have no first hand knowledge of what’s going on with him. 

We don’t know what for sure, how controlled everything has been for him. 

This isn’t a knock on his grandparents in any way.  It’s just that when dealing with something this serious, we need first hand knowledge, so we can accurately report symptoms to his doctors. 

This is possibly going to put a huge wrench in Operation Hope, at least our side of it anyway.

Lizze and I are going to meet with Dr. Patti tonight and figure out WTF we are supposed to do in a situation like this. 

The question at this point is whether or not we need to more him home and if so, how do we insure the wellbeing of everyone else involved?

Goddammit.  I really hate this entire situation.  It’s like we’re screwed either way and there’s no better or safer solution.

Permanent link to this article: http://lostandtired.com/2012/11/13/autonomic-crisis-11132012-further-complications/

Nov 13 2012

Autonomic Crisis: 11/13/2012 Please pray

Lizze just called me from Akron Children’s Hospital and told me that Gavin’s heart rate is so high that it keeps setting off the alarms. 

Right now, his resting heart rate is in the 140-150 bpm range. 

While they were sitting in the lobby waiting, his HR was in the high 130′s.  He’s not nervous about his infusion at all.  In fact he looks forward to them.

The problem is that it’s not good for his heart rate to be that high, let alone a sustained HR that high.

We are making phone calls in order to figure out what we are supposed to do.  His autonomic specialist is at the Cleveland Clinic but Gavin does have a kickass neurologist at Akron Children’s Hospital as well.  In fact, this doctor is the one who has handled every one of Gavin’s crises thus far. 
Emmett just left for my parents and I’m going to be making more phone calls and helping Lizze out anyway that I can while being trapped at home. 

Permanent link to this article: http://lostandtired.com/2012/11/13/autonomic-crisis-11132012-please-pray/

Nov 13 2012

23 IVIG infusions down and a lifetime to go

Today marks Gavin’s 23rd antibody infusion. December will mark the 2 year anniversary of Gavin being diagnosed with Primary Immunodeficiency.

Depending on how Lizze is feeling in the morning, she may be taking him for his infusion.

It’s easier for her to take Gavin than it would be for her to stay home the ever energetic, Mr. Emmett John.

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It’s really hard to believe that it’s been almost 2 years on this immunological journey. It’s been a long road.  A road that was at times, quite scary. It’s a lot for a kid to have to cope with and for the most part, Gavin does really, really well.

We have the typical issues of him being demanding to the staff or at times, downright disrespectful.

Overall, I’m really proud of him because I can’t imagine having to do this each and every month.

For those that are aware, Gavin receives IVIG infusions every month because his body doesn’t produce enough.  What he does produce on his own, is defunct.  This basically, means that Gavin has a significantly compromised immune system.

Ironically, he has never really been a sick kid.  I mean he had ear infections and that sorta thing but never anything serious.

That’s a miracle, considering.  Nevertheless, we are very grateful for that miracle.  :-)

We actually found this whole thing out on accident.

Gavin’s gastrointerologist ran a blood panel testing for certain foods allergies and that how we found out.  We were completely caught off guard. He had gone 11 years without anyone picking up on this and never getting seriously ill.

We have Akron Children’s Hospital to thank for not only discovering this but taking such good care of him over the past 2 years.

I can’t say enough about Akron Children’s Hospital. They are simply amazing and I don’t think there is another way to describe them.

I feel like we should have a little celebration for Gavin’s 2 year anniversary next month.  Maybe a cake or something.  To me, this is a pretty big deal and should be celebrated.  Especially considering that this all takes place in oncology.  Every single month, we realize just how much worse it could really be.

If you ever need perspective in you life, volunteer in a children’s oncology ward.  I promise, it really does put things into perspective.

Permanent link to this article: http://lostandtired.com/2012/11/13/23-ivig-infusions-down-and-a-lifetime-to-go/

Sep 13 2012

Positive

Lizze came home from Gavin’s infusion at Akron Children’s Hospital bringing news of how well Gavin did.  :-)

This is really positive as Gavin doesn’t always make the best choices while at the hospital.  She even said that things didn’t go his way,  and yet he took it in stride. 

Way to go Gavin.  :-)

It’s really nice to be able to post positive news in regards to Gavin. 

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This was posted via WordPress for Android, courtesy of Samsung’s Galaxy S III. Please forgive any typos. I do know how to spell but auto-correct hate me.

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Permanent link to this article: http://lostandtired.com/2012/09/13/positive/

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