I was walking with my Dad last night and he was talking about how well Gavin did the other night when they went out to eat. Gavin didn't a really good job and my Dad had a great time with him.  He did point out that Gavin has no restraint when it comes to eating.  That's nice to have him notice that because it gives him a better understanding of why we have to watch him so closely. First hand experience is priceless..... My Dad has some projects planned for this summer.  He wants to involve Gavin and get him some hands on,  real life experience.  I'm so proud of how well Gavin did.  He really is a great kid and I love him very much. **Thanks for reading**  …

How do you know when your day is not going to go well? How about when your 6 year old asks you what a period is. It gets even worse when he's not satisfied with it's the dot at the end of a sentence. **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 so please forgive the auto-correct induced typos

Elliott and Emmett both have been handfuls today.  However,  since Gavin arrived home it's like they're on speed or something.  They just don't stop and I'm going to lose my mind. I have decided that I'm going to find a new happy place. I need a new happy place and I need it now. I'm putting the call out to all of my readers.  If you have an extra happy place could I borrow it please.  It can be slightly used,  I don't mind. Maybe you know someone that's trying to unload their happy place.  I'd be interested in taking it out for a spin and if I like it,  we can work something out. I really appreciate it... **Thanks for reading**        -Lost and Tired Please join…

Gavin arrived home a little while ago from his antibody infusion. Lizze said he did very well and was polite to everyone.  Awesome job Gavin. However,  Gavin is experiencing some side effects today.  He's really tired,  which isn't surprising but he also has a headache as well. Gavin procedure was changed a little today by means of increasing the infusion rate.  Hopefully these symptoms will not last and he'll be back on his feet ASAP. At least he's not puking all over the place. Knock on wood... :-) **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 so please forgive the auto-correct induced typos

One of the things we really struggle with when it comes to raising 3 boys in the #Autism spectrum is meeting the various sensory needs. With the whole insurance/therapy fiasco,  we have been having to do as much at home as possible because they haven't been able to return to therapy yet.. Today I did some things with the boys outside,  while Lizze and Gavin were at his infusion. It may look like they're just coloring on the sidewalk but they are also getting a little sensory workout as well.  Both the boys are barefoot and walking on the rough cement.  They are stepping on little pebbles and tolerating it quite well. They are barefoot because their shoes are still wet from last night's water fight.  The front walk is…

As a father and husband to both 3 boys and a wife with special needs,  sacrifice has been part of my life for a long time. Sacrifice is something that is not exclusive to me but instead common to most parents.  Having said that,  as special needs parents,  the sacrificing is much more frequent and will happen for a much longer period of time. I think this is all pretty common knowledge. However,  despite all the sacrifices I still have the need to feel like I can still do things for myself. It promotes a sense of normalcy. For many years,  my special things was renewing my XBOX Live account.  It renewed on my birthday so that was my birthday present every year. I sacrificed my XBOX awhile ago in…

Gavin has yet another antibody infusion this morning. The reason I say yet another is simply because I lost count of where we are. Anyway,  he goes this morning,  with Lizze to Akron Children’s Hospital. The infusion takes a few hours and than he will be home once again. It think this may be his 14th or 15th monthly infusion. For those new to my blog,  Gavin suffers from primary immunodeficiency.  The antibodies he receives every month via infusion, replace his missing immune system. Gavin's natural antibody levels are less than half of what they should be.  Not only that,  but what he does produce is defective,  meaning they don't work. Every month he receives donor antibodies via IV infusion. He does really well and his body tolerates the foreign…