Skip to main content

Quarantine is a new normal for many but is not strange to those with disabilities

Life in quarantine as person with a disability is nothing new it's often our reality in some cases. Before this current situation I feel like I once lived in aspect of quarantine in high school for 4 years.

It never really hit me to make such connection to the new reality until today.  In 2009 the beginning of my high school journey

On the first day of school when the school bus came to pick me up the diver inform my mom  that the school i was in route to go to was not wheelchair accessible.. I never really talk out this experiences in my speeches but a few weeks ago I was ask to share my journey with college students majoring in education ask me if I had the opportunity of going to same schools as  my peers and neighbors if wanted too and that was when the light went of in my head to share this experience.

very few of my neighborhood schools are wheelchair accessible so again my parents and I didn't have many choices on placement of school.

Once I got the okay to attend the high school. Mom and I went to register to start school there.  A ramp was there and my perception from myself years back that's all I needed was access to be included.

What really open my eyes was when the administration said they never had a student who has mobility needs and requires other supports as well .
those therapy sessions in a location of a bathroom.
the students who had learning needs and needed extra support like myself only had classes on the 1st floor away from my other peers
from being forgot to attend school trips, award ceremony events they will forget to call my name.. it was even to the point where i ask would you call my name for graduation

The classroom I spent most of my day in was the size of a closet with no windows..most of my days was just about going to school and coming home, being with my family and attending my little recreation programs from time to time that was all i knew for a very long time. I was lost of what the world had to over for people like me until i graduated high school i said they are no more turning back.

in the lunch room my wheelchair couldn't fit under all the tables so i only had access to only one table..

In my 4 years of high school I dealt with isolation at lot


What about those winter months when it snowing and can't go out for a week or so
what about the places you go to and you realize it's not wheelchair accessible.. the friends and family member house that's not accessible so you become limited to the events you can attend

 


from the unreliable transportation like access a ride, working around my personal care attend schedule..

so be kind to those around you we are in this together

Comments

Popular posts from this blog

No shame in my story..its just my life

Growing up I have endured so much in life I  don't know where to start. I was born normal but recieved medical neglect while in inventive care  for 3 months there is still many hiding pieces to this story but it does not stop me from dreaming big. I break barriers..In high school they had no plan for my future because people didn't take the time to get to know me from students to staff..They was so hestited to get to know they always questioned others before the questioned me..They asked my para many times can I talk and she would she yes talk to ketrina. She knows more then what you may think! The frame of my wheelchair fooled many and made them judge mental of me.. They plan on placing me in a day program due to my physical challenges that they thought may impact me in community educational setting..Not everybody in a wheelchair is disabled as you think this word needs to be expanded. My mind does affect my body that's what many don't realize but will need to beco...

A new world start with you

When my heart hit that special place it hit home. It was all from downfalls and people judging me and refuse to realize i was full of potential..at times i wanted to give up but i always got back up and started again..Failing was just never in me I was always a determine person my self confidants back than seems to slow me down often put when I was first brought into an agency called United Cerebral Palsy and having an MSC at SKIP OF NY brought me to a complete new life and world. When UCP heard about my story and what I wanted to do and always continue to thank them for all they're doing for me and my family I earn respect they admire my hard work and how I wanted to reach far in advocacy levels and go to college. They help me make all these great things happen today I always want to thank my dad for his work towards my mission when I first told him about my vision and plans in changing the world for people in the developmental delayed community he smiled and said okay..Later o...

My view on agency programs

When I started  going to a Saturday Recreational Program we did a few things than we do now I would say even if its jewelry making and more than we do now  I would say. Even if its jewelry making or even broad games. Over the years many things open my eyes and allowing me to have a different views I realize that going to this program on Saturdays bored me, I still go a few Saturdays when I want to get time away from home but nothing productive happens there that is where I would like to see changes.I am just like every other teenager out there who enjoys doing different things and being active. All we do is eat and relax and chat with friends many indivduals that attend this program is low functioning to high functioning which I understand but in each person disability, they have abilities and can be productive of some kind.