Thursday, September 29, 2016
Depression
Having a Job
Tuesday, September 27, 2016
Feeling like an Outcast
My days in elementary school were miserable. I didn't get my first real friend until 4th grade. After that, I never kept many friends. I always had a small circle of close friends. What changed? To be honest, I have no clue. Even though I started to make friends, I still felt like no one understood me. No one would really know the struggles I go through each day, being in a wheelchair. I remember thinking things would be different if I had a friend with SB.
Now, as an adult, I am becoming more involved in the SB community. I see now I barely fit in, still. I think and act differently than most in this community. It's nice to meet others who have been through the same struggles I have, but sometimes that is all they want to talk about. The conversation can get very depressing that way. So, have things changed? No. I still don't fit in. Truth is, I never will and that's okay. As long as I am friendly with others, willing to take an interest in people, and not focus so much on myself things will be fine.
Editor: Esmé Nicolson-Singh (redsbreadslady)
Monday, September 26, 2016
Wisdom
Saturday, September 24, 2016
High School
Friday, September 23, 2016
Disabled or not.
Sunday, September 18, 2016
My Biggest Fears
Saturday, September 17, 2016
Exercise
Friday, September 16, 2016
Making Friends
Thursday, September 15, 2016
Relationships
Wednesday, September 14, 2016
Don't you wish you could walk?
Monday, September 12, 2016
Drivers license
Sunday, September 11, 2016
Childhood to Adulthood
Growing up with Spina Bifida was tough. As a kid I was picked on in school. I didn't have many friends. I didn't have my first real friend until 4th grade. I didn't start going out and doing things unil I was about 15 or 16. Things weren't all bad though. I had my siblings to do stuff with when I was bored. I always got my medical supplies I needed right on time. I had parents who cared for me, things you don't appreciate at a young age. I remember thinking "I can't wait until I am adult, things will be better then." Boy was I wrong. At 18 I tried to look for a job and couldn't find anything. There was a program I was in to help me find work but they were basically a middle man. I was doing everything on my own and they weren't helping much. I had to find a new provider for my medical supplies since the other one was for those under the age of 18. You get so much help as a kid but once you become an adult you get dropped so fast with no idea of what to do. I guess that isn't any different from anyone else's experience going into adulthood. Then I found out if I work I will be cut off my medical insurance. That wouldn't be any good since I have many doctor appointments and could not afford my bills on my own. Now I live off SSI. Is it annoying? Yes because it feels like a handout. I don't feel like a responsible adult. But it is what it is. I am writing this as a warning for others with SB. Don't make the same mistakes I did. Don't think life will get easier, it won't. Adult life will smack you right in the face. Be involved with others who have SB. I grew up without having anyone around to understand my frustration and now I am barely getting to meet others with SB. To any parents who have a young child with SB remember this, do not make his/her disability your disability treat him/her like you would any other child. Let them set their own limits. To any young kids and teens who have SB I say this, You are disabled, not unable.