I am so frustrated right now. Yesterday was soaring to high school event at my youngest jr high. It’s to help prepare and figure put classes to take next year. Well only if your child is not in the sped program. No information was given for sped kids. All these cool classes were talking about? Not for sped kids. Class schedule? Will be figured out by the school. When will we get information about what his schooling will look at? Maybe sometime in April. Why can’t they have a pamphlet something that gives us parents an idea of what high schools will look like? My special needs should going to High School is giving my anxiety and giving me no information at all what it will look like while the rest of the students get information is so beyond frustrating. Especially when it was said that all eight graders needed to go to this. Just you know not my child because he isn’t normal. So inclusive of them.
The Sweet Geek's Blog
Thursday, February 5, 2026
Wednesday, February 4, 2026
Money grubbing apps.
Wow blogger
Vey thing has really become a money grab.Should not be surprised that like everything else blogger now charges to do some basic things on a blog. Well due to medical bills and the expense of one of my child’s meds there is no way I am paying any money to them. So no more pictures on this blog and it seems beyond crazy to me that they limit how many edits you can do on your blog? Like what? Oh well if I have any typos they’ll just stay because so many sites are trying to bleed us dry with fees.
Monday, February 2, 2026
Hi
So it’s been what ten years since my last post? I’m not sure what I’m going to accomplish with posting again just I’m tired and want to release some of my stresses on here.
Where do I start. We found out why my youngest was going through all he was going through. He has a rare genetic disorder called puff-60 syndrome. Less than a hundred in the world have been diagnosed with this. As far as I know he’s the only one in our state. Neither myself nor my husband is a carrier so it was a random mutation.
It’s a bitter sweet answer yay we know what he was! Boo it’s so beyond rare that we have very little to no answers. There is no cure nor medicine to help him with the enzymes his body does not make. Unless many more people are diagnosed with this genetic disorder little to nothing will be done. It’s not profitable to pharmaceutical companies and if they did make something for it we would never be able to afford it.
Monday, August 1, 2016
Insomnia
Tuesday, July 26, 2016
Darkness Fair by Rachel A Marks, book review
Without knowing the sacrifices that will be required of them, Aidan and his motley crew of friends—each with their own role to play—must face the demon threat head-on. They’re the only ones keeping the growing army of Darkness at bay, and if they fail, the future of humanity could be lost.








