OMT Parent Voices

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OMT Parent Voices

OMT Parent Voices

@OneMoreThing2Do

One More Thing Parent group advocates for change in systems to minimize the One More Thing that parents of children with disabilities navigate every single day!

Ottawa, Ontario, International 가입일 Mart 2016
123 팔로잉236 팔로워
OMT Parent Voices
OMT Parent Voices@OneMoreThing2Do·
A memorial bench in honour of @GrandmaKim has been installed at Brittania beach. She loved to walk there. Loved the water. And loved people. Please visit and sit a minute.
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OMT Parent Voices@OneMoreThing2Do·
It has been one full year since we lost OMT co-founder @GrandmaKim. We miss her so much. She was a mother, grandmother, sister, friend, fighter and advocate. She was simply amazing. 💗
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OMT Parent Voices@OneMoreThing2Do·
We are so happy to see CHEO recognize and honour our co-founder @GrandmaKim! Kim would be thrilled to know that funds have been dedicated to accessibility in her honour.
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OMT Parent Voices
OMT Parent Voices@OneMoreThing2Do·
It’s been a long time since we used this account! Can’t think of a better time to re-engage than by announcing this fundraiser. gofund.me/29b106ff
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The Globe and Mail
The Globe and Mail@globeandmail·
For parents of kids with complex needs, COVID-19 school disruptions mean losing a lifeline of key supports dlvr.it/Rv7lWC
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Kim McLeod
Kim McLeod@GrandmaKim·
Thank you for this. Peads moms/caregiving are hanging by a thread. Saving Heath systems up front - clearly not long term @fordnation @celliottability cite CHEO Thrive report Pg 50 @AlexMunter ⬇️ #kidscomefirst won’t work if caregivers are ill or dying @OneMoreThing2Do
Eyal Cohen@dreyalcohen

Some new work published today on parental caregiver mortality led by Dr. Anne Fuller @SickKidsNews in collaboration with colleagues at @dceaarhus (including @toftsorensen & @ehrensteinvera) & @UnityHealthTO.

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Julie Drury
Julie Drury@SolidFooting·
NORDpod: The Voice of Rare Disease@NORDpodcast

Listen to the newest episode of #NORDpod: The #VoiceOfRareDisease to join @MatthewZachary as he speaks with @yann_eurordis to reflect on Rare Disease Day & about progress in #raredisease research: nordpod.org What did you do for #RareDiseaseDay this year? 🦓

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Erin Gilmer (Legacy)
Erin Gilmer (Legacy)@GilmerHealthLaw·
This is the reality of disability. It's a system that dehumanizes a person at any age. It's a system where one word, like "mild", may mean you don't get the help you need. It's a system of manufactured scarcity. It's a system that breaks you. Wonderful piece by @Lollardfish.
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OMT Parent Voices
OMT Parent Voices@OneMoreThing2Do·
Quick Poll on Who Can I Talk To? From our parent group. Little surprise for us was having the question added by a member ..15% replied “I really don’t have anyone to talk to” #specialneeds #families
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OMT Parent Voices
OMT Parent Voices@OneMoreThing2Do·
OMT families!! We have a great friend speaking this Saturday. We encourage you to join her!
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