#Autism: Through the eyes of Denise

This is a guest post by Denise. She responded to my request for people to come forward and let me help them share their story. My goal with this little project is to help everyone have a voice and to show the world how different #Autism is for everyone. I'll be cleaning up the format in short order and make a few tweaks to the process. I have already received a huge response to this and I'm so excited to be able to be a part of this.  Thank you Denise, for opening up your lives for all of us to see. :-)  Please note that I have not edited or censored this story in any way whatsoever. These are Denise's words...   Meeting Autism: A Work in Progress  …

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Please keep Emmett in your thougts

I just got back from the pediatrician with Emmett.   Basically,  there isn't anything that we can do. He likely needs longer cycles of Prednisone.  Currently he takes it 2x a day for 3 days. He may need to do that for 5 days instead. The problem with that is Prednisone suppresses the immune system. He would need to do that once or twice a month and that wouldn't be safe. For right now,  we're are doing 1 teaspoon of Benadryl 4 times a day.  That can help reduce the allergic reaction his body is having to the virus that is apparently causing the sores. We will see immunology hopefully next week.  It was also recommended that we see infectious disease as well. For now,  at least the Benadryl will help…

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I should have stayed in bed

I woke up this morning to the realization that today is Friday the 13th.  Honestly,  I'm not a superstitious guy but having said that,  it's Friday the 13th. I have already been back and forth to the Ford dealership and in a little bit,  Emmett is being seen by his pediatrician for the second fever flare.  We spoke with immunology last night and the said there is nothing we can do aside from 1ml of Benadryl,  4 times per day.  It's something about reducing the inflammation. Outside of that,  all we can do is manage the pain and do our best to keep him hydrated. The doctor told us if we even suspect that he may be dehydrating or stops drinking that we are to get him to the ER…

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I’m so friggin tired

Elliott woke me up because he had an accident.  This never and I mean never happens to Elliott. Because his bed is unusable at the moment,  him and I are camped out on the couches... I'm sooooooooooo tired..... **Thanks for reading**        -Lost and Tired Please join our Community Autism Support Forum Posted from WordPress for Android so please forgive any typos as auto-correct and I don't see eye to eye. :-)

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#Autism: Sharing our treasures

I always love to share my kids creations with you all. What I really love about sharing their creations is why I'm sharing them.  My kids are actively making things just so they can share it with you. I think that's pretty cool.  :-) So once again Elliott has created something to share with you all. He didn't name this one but he's proud of it nonetheless. Gavin wanted to share his Halo action figure collection with all of you as well. **Thanks for reading**        -Lost and Tired Please join our Community Autism Support Forum Posted from WordPress for Android so please forgive any typos as auto-correct and I don't see eye to eye. :-)

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#Autism: When you’re told there is no hope

Lizze and I are so pissed off right now I can barely write this.  Because of that,  I'm going to keep this short and sweet. Basically,  we received a phone call about Emmett's speech therapy.  Emmett has been having speech therapy for 180 days now and has not progressed fast enough is not caught up yet.  Insurance has stated that Emmett will never catch up and so they will no longer cover speech therapy for him. In other words,  they are essentially saying that there is no hope for him and that we should give up. I don't have words to express just how pissed off I am right now. I realize insurance is about the bottom line but who the fuck says something like that?  How do they sleep…

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I’m really starting to lose faith

Poor Mr.  Emmett John is once again facing another medical issue.  He has finished up his last day of Prednisone the other day for his then current flare and has already started another flare.  I don't think that we have ever seen this happen before. If you look below,  you will see just one of the large mouth sores.  Since she these are not herpes related, there is very little we can do.  In fact, the only treatment is Prednisone and Unfortunately,  there is a major draw back to using that.  Basically,  it suppresses his immune system and leaves him susceptible to things like pneumonia.  He just recovered from pneumonia a couple of weeks ago. We have a few calls in right now because we don't know what to do. …

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#Autism and Eggshells

Elliott is easily the most sensitive of our 3 boys.  He recently spent some time at Grandma's house coloring Easter Eggs.  Actually,  it was more like one Easter Egg, but it was a very special one. Elliott and Grandma had carefully drained the egg out of the shell,  so the egg was hollow. They hand painted it and it looked beautiful.  Elliott was so very proud of his egg.  When he brought it home,  he asked me to take a few pictures and share them with all of you. However,  during the picture taking process,  there was an accident and Elliott drop his precious egg. The egg was only slightly damaged and Grandma took it home with her and fixed it right up.  When Elliott and Gavin went over to…

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