1/ I have a child with an autism diagnosis and intellectual delay. He is 9. He spends his mornings included in a Grade 4 classroom.
2/ He is not doing what his classmates do. He works at his own pace, with his own (extremely) modified curriculum while he practices sitting at a desk for longer than 20 minutes.
3/ He has the kind of needs that dictate he be supervised at all times. ALL. TIMES. If you have children, consider that feeling when you watch them climb onto the yellow bus and then wave from their window—or when your teenager flies through the kitchen, grabs their lunch and
4/heads out the door. Do you think about what happens a second after that? How they get off the bus, or how they enter the yard? What happens after they walk through the doors of the building? If they know what it means when the first bell rings? If they know how to ask
5/permission to use the washroom or where to go to do so? Do you worry that they may bolt from their classroom? Leave the building? Remove their socks & shoes and leave them somewhere? Do you worry about who will clean them up if they spill something? Who will make sure they can
6/do up the zipper on their coat? Make it to the right classroom? Get on the right bus at the end of the day? Make sure they receive necessary medication on time? That they receive a tube feed properly and on time? That there is someone to tote their belongings if they can’t?
7/Do you think about every second of each day wondering if your child will be where they need to be, when they need to be there and remain safe, clean and fed?

I do. At least, I did.

Logistics of each & every day must be planned. If they’re not—someone is injured. Someone is
8/lost. And someone dies.

I wish I could say this is being dramatic.

If I can’t simply let my child hop out of the car at the curb in front of the school & then head to work—then what DO I do? How do I spend my days not literally vomiting from worry and talking myself out of
9/calling the school every 10-15 minutes to make sure everything is ok?

My son has an EA.
And she is me. At school.
And I once lost sleep & agonized over the logistics of each and every day. But I don’t anymore—because I am privileged to have a 1:1 EA for my child who is with
10/him *constantly*. Every moment accounted for. No divided attention between other children. She is his “School Mom”. And she is invaluable.

I’ll ask you to note that I’ve made it 10 tweets into this thread BARELY MENTIONING *EDUCATION*.

I am not talking about
11/quality of education, good grades, healthy work habits with peers, punctuality or organizational skills.

THAT is a whole other story and a testament to how very broken the education system is particularly for children with differing needs.

I send my child to school so he
12/learn basic day to day tasks, practice routines, be part of a school community and BE SEEN. I send him so I can spend days combing through an endless stream of paperwork for every aspect of his life and maybe get some work done in between. I send him because he is a human
13/being in Ontario and has a fundamental right to an education. He has every right to be there.

My child can ONLY attend school because he has an Educational Assistant. If she is not there, he isn’t.

She is the key aspect to making my family’s life actually happen each day.
14/ She is the human equivalent to that big box building with a yard & unlocked doors that is full of professionals ready to teach.

She is my son’s ACCESS.

If you are upset because your child might not have access on Friday—this is my child’s life every other day of the year.
15/@Sflecce and @fordnation are communicating that she and her colleagues are asking too much to have liveable wages that keep them above the poverty line and safe, supportive work environments.

These two are having a field day vilifying the people parents like me hope for,
16/advocate for, fight for, even pray for. When they are assigned to our children, we are overcome with relief. When they aren’t, we are crippled with worry & sentenced to another year of re-planning the logistics of our lives. EA assignment is like winning the lottery. There is
17/nothing more coveted. When @Sflecce and @fordnation communicate they are being unreasonable—they are communicating that my child is not worth the trouble. They communicate that my child’s safety is not worth the trouble. They communicate that my child’s right to an education
18/ is not worth the trouble.

Calling this out, holding this government accountable & standing with @CUPEOntario is worth EVERY ounce of my trouble.

I am one of the lucky ones. My son has access. Other families do not. A day of “locked doors” of the neighbourhood school is an
19/everyday reality for special needs families across this province.

I will be at the picket line carrying my son’s EA on my back if I have to. She is the backbone of his education, and worth every penny being asked for. It is a damn shame that the value of these dedicated
20/Professionals is even a question. This is not just their fight. It is my fight. This is an attack on the village that supports my child. This is an attack in my child. I am insulted to the core that @Sflecce would even try to turn me against them.

I know whose corner I’m
21/standing in & no number of $250 payments will convince me that those most dedicated to our kids’ education are the ones who show up every day. Not the ones that turn up for a photo op or impassioned speech about the importance of keeping kids in the classroom—that someone
22/else wrote for him. I will stand with those ACTUALLY keeping kids in the classroom. I will stand with Education Workers every. Single. Time.

@CUPEOntario @Sflecce @fordnation #ontedsolidarity @ChandraPasma #onpoli #onted #IStandWithCUPE #39kIsNotEnough

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More from @ottawa_asd_mum

Nov 3
1/The hand off.

My son is severely autistic with an intellectual delay. He is 9 & can use limited words to ask me for juice, to go outside or demand his weekly Timbits ration. Beyond that, we cannot converse. I don’t know how he’s feeling, if he’s nervous, unsettled or scared. Image
2/ I have only the cues and clues we are able to gather from tears & giggles, and the signs of eagerness or apprehension.

I dreaded the day he started school. The thought of handing him off to a stranger in the care of 30 other 4 yos was not something my mind could compute.
3/ Further to that, it just wasn’t an option. I wouldn’t do it. I struggled with the daily challenges of supporting his needs with a 2 year old in tow, in my own home where I could lock the doors and cupboards and use every childproofing device I could find. My son is curious and
Read 22 tweets
Nov 3
1/Children in Ontario have the right to an education. That should be the case whether they have a disability or not. Educational Assistants are ACCESSIBILITY PERSONIFIED for children with disabilities.

They enable access. They allow my child & others to enter a school. Without
2/EAs the doors to education are closed to my child every day of the year.

I am nothing less than disturbed that the government elected by 40% of our population fails not only to value, but to recognize the value of these individuals who care for the province’s most
3/vulnerable children when their mothers and fathers and caregivers cannot.

Let me be perfectly clear. @Sflecce stands before the cameras and makes feeble attempts to turn parents like me against the people we have hoped for. And begged for. And put ALL of our trust in as
Read 8 tweets
Aug 29
🧵🪡
Dear @Sflecce:
I wish you could understand how unsettling, nerve-wracking, *insert uneasy synonym here* it is to approach a new school year as a parent of a special needs child. But you won’t. You may have read a handful of briefings or listened to colleagues tell you
how your government is doing a “stand up” job at special education—but until you’ve fathered children of your own who may need a little more in Ontario, you won’t know.

I wish you could know how maddening it is to hear you talk about how “wonderfully” your govt is
doing at supporting special education when REAL, ONTARIAN FAMILIES have children who cannot attend school, or who are sent home because of inadequate resources, or who are unsafe or who “don’t present with enough challenges to deserve support”.

You don’t support our Boards, who
Read 17 tweets
May 31
I’ll continue to say this as it hurts too much not to. @fordnation is either lying, or is so misguided that he believes the lies he’s being fed.

Both should prevent him from sitting as Premier.

@fordnation has the *GALL* to *CAMPAIGN* on an *UTTER POLICY DISASTER* that is
*CURRENTLY* hurting families and will *CONTINUE* to do so for years because of stupidity and inaction.

The Ontario Autism Program is NOT fixed. It is NOT Needs Based. If does NOT have clinical direction and it is NOT “designed by the community for the community” because
it goes against the most crucial recommendations given by the OAP Advisory Panel.

These policies not only hurt families, but devastate families. They have deprived children of care. They spit in the faces of advocates who have dedicated countless hours trying to
Read 6 tweets
May 19
Daily Reminder that @fordnation HAS NOT fixed the Ontario Autism Program:

What would constitute ‘fixed’?

1️⃣ Adequate funding, with the $600M promise being spent.
❌ Ford did not spend the promised funding and continuously fell short.
#50KIsNotOk #onpoli
2️⃣ A program that recognizes that AGE has no bearing on a child’s needs.
❌ Ford’s program penalizes children by clawing back funding as they celebrate birthdays.
#50KIsNotOk #onpoli
3️⃣ A program that delivers based on recommendations from a clinician who has evaluated the child.
@fordnation has removed clinical input. Funding is determined by an algorithm after a 2 hr phone call between a parent & a non-clinician who has never met the child. #50KIsNotOk
Read 12 tweets
May 10
@MacLeodLisa is my MPP in #Nepean. How unbelievably sad that over the years we’ve become completely desensitized to her antics; this type of story is almost expected. I have autistic children. We have been deeply, deeply hurt by MacLeod’s policies. But we’ve also had enough face
time (or attempted face time) with the Minister to know that #Nepean deserves so much better. Our community has been publicly accused of trying to run her out of office. I think her record might do the job on its own.

We had been invited to an Autism Roundtable in January 2019.
@MacLeodLisa abruptly walked out of the meeting when the questions got tough.

I was invited into the Minister’s office during the first Ottawa protest after she made the Autism announcement that would send the program and families into a downward spiral for 3 years & counting.
Read 13 tweets

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