You can’t fool me, I knew you were sleepy

It just goes to show that we,  as special needs parents,  really know our kids.  Despite all the protesting from Emmett about not being tired,  I knew he was. This picture is from yesterday,  while Gavin was getting his infusion. While he didn't sleep for long,  he passed out across my legs.  He was so sleepy that he was able to fall asleep in the world's most uncomfortable position.  :-) **Thanks for reading**        -Lost and Tired Please join our Autism Help Forum Look for "Autism Help" app at the Google Play Store Posted from WordPress for Android

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Published on Akron Children’s Hospital Blog

I'm really honored and incredibly excited to share with you all that Akron Children's Hospital has asked for permission to post one of my articles on their official blog. Awhile back I had done a review of their mobile app. They somehow discovered that review and wanted to publish it on their site next Tuesday. For those of you that aren't familiar with Akron Children's Hospital, they are among the very best in the entire country. People come from all over the world to have their child treated here. As you know, our kids are frequent patrons of their fine facility. When the post goes live, next week, I share the link with all of you. Thank you Akron Children's Hospital for taking such amazing care of my family and literally countless…

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Nothing quite like the 5am meltdown

My God,  it's way to friggin early to be up already.  However,  Emmett has been up for hours and has already have several meltdowns.  He just screams and screams and screams,  for no decernable reason.  I'm sure there is something behind these meltdowns,  but hell if I know those reasons are. I think that life is just rough for Emmett and he doesn't know how else to handle it. Something will have to give and give soon. I can't keep this up forever.. **Thanks for reading**        -Lost and Tired Please join our Autism Help Forum Look for "Autism Help" app at the Google Play Store Posted from WordPress for Android

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Antibody Infusions: One year down

Gavin had his 12th antibody infusion this afternoon. It's hard to believe that it has already been any earlier since we discovered that he has primary immunodeficiency. I remember hearing that and being completely shocked at the news. How was this even possible? Gavin's never been hospitalized for a serious illness. How could he have made it 11 years without an immune system?  While we haven't found that answer just yet,  we've just chalked it up to God was looking out for Gavin. Gavin has to receive IVIG, once a month,  every month,  for the rest of his life. IVIG is basically,  an immune system in a bag.  It consists of antibodies that have been donated by other people.  They are the specific type that Gavin is missing,  which happens…

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#Autism: Coping with Change

I wanted to talk for a little bit about what happens when routines change. Every child on the #Autism spectrum reacts differently to change.  This post in particular,  is how my youngest son,  Emmett,  has reacted to Gavin being home everyday. You may recall that Gavin has recently been pulled from school due to health related issues. This means, not only is he home everyday,  but his being home has completely disrupted Emmett's schedule.  The unexpected change has plunged Emmett into a state of chaos. It's actually a bit strange, Emmett likes the fact that Gavin's home but simply isn't coping with it very well. Emmett has become much more aggressive since Gavin has been home. He's not eating like he normally would be and he's also not sleeping for…

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Primary Immunodeficiency: One year later

Today will be Gavin's 12th IVIG infusion.  It was roughly one year ago,  we found out about Gavin's immunodeficiency. It was something that completely caught us off guard. While we still don't know the actual cause,  we have made it through the first year without many hang ups. His body has decided to accept the donor antibodies with much problem. So far,  so good. **Thanks for reading**        -Lost and Tired Please join our Autism Help Forum Look for "Autism Help" app at the Google Play Store

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#Autism: Even Daddies Need to Learn to Share

I wrote a few months back about how I resolved our issues with the PS3 by getting rid of it.  I traded everything in and was able to use all the credit to get a Playstation Vita. The Vita is basically a very portable PS3,  about the size of the now outdated PSP. This allowed me to still play games without the kids fighting over the PS3 controller. Anyway,  I'm very careful with my things,  partly because I only really have the PS Vita left.  Everything else have been sold over the years to cover expenses.  I also like to keep my things looking new. My kids,  as much as I love them,  are not gentle with their things.  Because the Vita is the only outlet that I really have…

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#Autism Discussion of The Day: Stress

It's no secret that special needs parenting can be extremely rewarding.  However,  while it can be rewarding,  it's not without stress. This type of stress can become so completely overwhelming that it can and will affect your health,  especially if left unchecked. For today's #Autism Discussion,  I thought we could all share some ways to relieve stress. What kind of thing do you do to reduce your stress level? **Thanks for reading**        -Lost and Tired Please join our Autism Help Forum Look for "Autism Help" app at the Google Play Store

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