This blog is about most of what I remembered from childhood to growing up, and some encouragement, reviews of movies and shows, and just other fun things that I like to write about. I'm thankful to continue this blog to share things with those who read it and those who see it because I want to share more. I'm grateful to share what I hope will give people joy and happiness when they read this.
Sunday, October 9, 2011
My Childhood Years Chapter Three
Most of my childhood, has been pretty good and fun. I would say most of my childhood that has been fun, was playing with my sisters or brother and my parents. Of, course i didn't always play, and my other reason it was good is because i had a family that was looking, out for me and taking care of me. Some, of my childhood i was either in the hospital recovering or at home recovering, which wasn't fun at all. I've never liked hospitals, and i still don't like them at all because they're not that fun to go to especially if you are having surgery, or getting bloodwork done. I've had both of those things done lots of times and they were never fun for me. I spent most of my childhood in the hospital, and after i got home from the hospital and was then resting for a litttle while, because i had to rest and be healed from surgery before i could play with toys, or do anything really. I still, had an excellent childhood, even though i spent it in the hospital most of the time. Even, though i'm 17 years old and i still have my Hydrocephauls, i am always going to try my best in school and at home, because even though i have a multiple disability like other kids, and my friends might not have a disability, that doesn't mean i can't do things like other kids without disabilites can do, i mean i might be different from other kids, and my friends but that doesn't mean i can't do what other kids in my school do. I mean, it shouldn't matter what other people might think about my disability, it only matters that you have friends that care about you, think about you, and are there for you, and that goes for family too, only they care, love, trust, think about you, and are there for you. Thats why i love my family and friends so much.
Monday, August 29, 2011
My Child Years Chapter Two
I still can rember some of my trips to the hospital but most without someone telling me. I do remeber the time when i had a seizure because i was shivering all night and my parents had called an ambulance for me and i also remeber being up till three in the morning that day and coming home after, then sleeping till 1:00 in the afternoon. Then there was a time when i got some bad headaches, and had to have a doctor's appointment at the cleaveland clinic, i still remeber on that day when they switched my shunt tap with a spinal fluid test instead, i wasn't very excited about that and i met a new doctor and i was really nervous around him too, because i didn't know him very well and after awhile my headaches were gone and i didn't have to go through a spinal fluid test or shunt tap, which i was very thankful that my headaches went away. There also was a time where they took me off one of medications and put me on a new one called topamax, which wasn't a good medicine for me because it made me feel small and everythingelse big, like a Alice And Wonderland Movie. So then after awhile We switched back to my seizure medication Phenobarbital and got rid of Topamax. I was glad to be back on my medication that i have had for awhile and not be on a new one. When i did have surgery on my tenth birthday, there where some things that had to change for me like, no roller coasters, no jumping too high on trampolines, not doing cartwheels, and especially not putting magnets up to my shunt that could reset it. At first i didn't like the fact that i couldn't do cartwheels or go on roller coasters, but i knew rhat if i did these things it wouldn't be good at all and i am very thank full that i didn't have to go through anymore surgeries and i hope i never have to ever again.
Sunday, August 28, 2011
My Childhood Years Chapter One
When I was little, i wasn't feeling great like most kids, because i was born with this thing called Hydrocephauls. When i was probably 2 and a half years old i had to have surgery at the Cleaveland Clinic to have a shunt put in, and then when i was three years old i had open heart surgery and had to stay in the hospital for a little while until i was feeling better and until i came home. So when it came towards February i was pretty much better and I got to come home on valentines day. Which was a special day because i came home on my cousin's birthday. Even though i got to come home on valentine's day i was still healing and i also had these things called seizures which i usually had either during the day or night. I don't remeber my seizures, which is a good thing but there was one that i did remeber having and that was the night i was with my mom and dad in their bed and even though i was having a seizure i could hear my mom telling my dad to get one of medicines that stop my seizures, sometimes if that didn't work i would have to go to the hospital, which i didn't like very much. On my tenth birthday i had to have my shunt replaced because my shunt tubing broke and made it all the way down to my hip area which isn't very fun to have surgery on your birthday, but it had to be fixed. After i came out of surgery i was very sore for a couple of days, even when i came home too i was still sore. I had someone come over and teach me stuff that i was missing at school, until i was healed and i was well enough to go back to school. I haven't had a seizure at all this year and i am very thankful, and i am very glad that i am doing alot better.
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