Better Late Than Never {Thoughts From Me}
Here’s a little fact about me: I am 35 years old and I don’t drive. *Gasp* You heard me right. I’ve never even had a driver’s license.
About 6 months ago, I received my first permit but even then I haven’t driven much. I have this weirdly irrational fear of driving that is really hard for me to overcome. That is until recently.
Last week, I just felt it was time to get started on really learning to drive. So I have been. This week, I decided I needed to come “home” to my hometown where I grew up and spend some time with my best friends who have all been proactive in helping me learn to drive.
And you know what? I am doing it! I really am.
I don’t know why I have felt afraid to do this for so long. Yes, there are dangers and it’s always a risk but it’s something I’ve been needing to do. I need the independence and I need to be able to take my kids places, just me and them. I’m well on my way to making that happen and I know they are so proud of their Momma. Seriously, I thought they’d be driving before I would!
So this is what I am up to right now. Learning to drive about 20 years later than a normal person. Better late than never though!
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September Update {Epilepsy Awareness}
Life is been full of doctor’s appointments for us lately. It’s not leaving a lot of time for other things to be done. Being on the road is definitely time consuming but of course, my children’s healthcare is more than worth it.
Jackson started Parent Child Interactive Therapy a few weeks ago. We are doing great with this therapy and have already passed through the first part of the series after 2 weeks of sessions with our therapist. We are now moving on to the next step which is to give Jackson demands and work on his temper issues, as well as building discipline. We hope this will help both us and him learn to better deal with our day to day and also help with his breath holding spells. Time will show us if it does or not.
Emma sees the neurologist this week as well. It will be our first visit. We hope he will be able to tell us why she is toe-walking since no one can tell us that. Once this is done, we will move on to repairing her toe-walking.
Last week we ordered Jack a helmet. Hopefully, it will be done soon and we will be able to use this for both of his therapies. It will be great for his headbanging as well.
Laycie and Winston are doing great right now. No issues for them which is wonderful.
That’s it for a current update and where we are at with our day to day issues.