Preparing for round 2 of the headache infusion

When Lizze left the neurologists office this afternoon, she left with a little present called a hep lock. Basically, the hep lock is a 6 inch pieces of IV tubing coming of the catheter, that's still in her arm. This makes it easier and less painful with they start the IV on day 2. I had to flush the hep lock out tonight and was really surprised to see that they were not using needless equipment.  I thought everyone had pretty much switched over to needless. Flushing her hep lock really took me back to doing my time in the ER for medic school. I really miss those days.......but at least Lizze doesn't need to be stuck again for the 2nd infusion. Hopefully, the port will remain in so Wednesday…

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Anyone else hate the tags on clothing?

I don't know about you folks but I have grown to hate these things on clothing called tags. I hate them and so do my kids. I've lost track of how many of these little bastards I've cut off of various items of clothing over the years. For the love of God, please stamp the tag information on the shirt itself.  It's got to be cheaper than stitching in multiple tags. If I was in charge for a day.    

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Headache Infusion Day 1: Update

https://www.youtube.com/watch?v=VadtUii6OUs 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.  ;-) For more ways to help the Lost and Tired family, please visit Help the Lost and Tired Family.

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What kind of help could your #autism family use?

I was asked in a recent post,  what kinds of things would could a non-profit do to benefit my special needs family?  She was asking a really good question and so I thought I would pose the question to my readers as well.  What could a non-profit autism organization do to help your family? Please leave your feedback in the comments below.  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.  ;-) For more ways to help the Lost and Tired family, please visit Help the Lost and Tired Family.

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Does “Lighting it up blue” really help anyone touched by #Autism?

Disclaimer: I'm adding this disclaimer because there is always going to be someone that takes a post like this the wrong way. I'm not saying the Autism Speaks or by extension, Light it up blue, is a bad thing. I just feel like it's more about the organization and less about the people they are supposed to be helping. Again, I'm not saying that's the case. I'm simply sharing my thoughts and opinions. These are my opinions based on my current knowledge and understanding. I remain open minded, regardless of my opinions. I would ask you to do the same. Why would I of all people, question the purpose of the light it up blue campaign? I can already see the hate mail flowing in after this but here's the…

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Off to a good start

Emmett and I got Elliott off to school with no problem. All the stars aligned this morning and I had a level of cooperation that I rarely ever see. I'm super proud of them. :-) 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.  ;-) For more ways to help the Lost and Tired family, please visit Help the Lost and Tired Family.

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Operation Crush the Migraine Begins

Lizze has begun her headache infusion and now we will simply have to wait and see if it works.  Please keep her in your thoughts and prayers. She can use any and all positive thoughts. 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.  ;-) For more ways to help the Lost and Tired family, please visit Help the Lost and Tired Family.

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Living on the edge

This is a pretty big week for the Lost and Tired family. Lizze has her migraine infusion for the first half of the week and I'll have the boys.  We're really feeling the pressure in many areas of our lives right now. Most of that pressure are things outside of our control. In a lot of ways, that sorta makes it worse, at least for me.  By nature, I'm a fixer and when I can't fix things, I really stress out.  Right now, the focus is on the immediate things, like Lizze's headache infusion. At this exact moment in time, this is really all we can do.  If the procedure works, that will be a huge win for both Lizze and the rest of us. This migraine has really incapacitated…

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