Lottie Morison retweetledi
Today is #InternationalStutteringAwarenessDay! See 👇 for some facts on #stuttering. We are still recruiting for our sub-group study on #stuttering. To register your interest ➡️ redcap.mcri.edu.au/surveys/?s=4HK….
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Lottie Morison
217 posts
Lottie Morison
@Lottiedmorison
Speech pathologist🗣PhD candidate @MCRI_Speechlang @UniMelbMDHS Interested in kids w/ genetic conditions & complex communication needs🧬 She/Her | Views my own
Melbourne, Victoria Katılım Mayıs 2021
373 Takip Edilen121 Takipçiler
Over the weekend I presented on speech & language phenotyping in CLN2 & CLN3 #BattenDisease @ the 2nd #LysosomalDiseaseSummit in Melbourne
(hopefully we can share the paper soon!)
#BDSRAAus @BDSRA @BattenDiseaseuk @MCRI_for_kids @MCRI_SpeechLang @UniMelbMDHS @UoMSpeechAlumni
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Lottie Morison retweetledi
October is #AAC awareness month. Augmentative and Alternative Communication can include #KeyWordSign, low-tech comm aides like communication books & high-tech comm aides like speech generating devices!
➡️Team member Jen Wong talks about AAC.
instagram.com/p/DApFaulJq4Y/
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Prof Ange Morgan & I have worked with @Unique_charity to create a guide for #CDK13-related disorder.
Unique's guides provide comprehensive, easily digestible info on many genetic conditions.
The CDK13-related disorder guide is now available here: rarechromo.org/media/singlege…
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@MCRI_for_kids hosted a webinar on #PlainLanguageSummaries to communicate research in an accessible way!
Created by @lottiegasp @shaunziegenfusz @TheDLDProject_ these resources can be easily adapted to any research project & available here osf.io/ydkw9/
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Plain Language Summaries of our team’s research on speech, language & cognition in 103 individuals with #KleefstraSyndrome are now available in English, Portuguese, French and Spanish via our website geneticsofspeech.org.au/genes/other-co…
Summary proformas courtesy of @lottiegasp & team
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Lottie Morison retweetledi
The 14th of May is #Apraxia Awareness Day!
Today our team is wearing blue to show support for Childhood Apraxia of #Speech #CAS awareness.
To learn more about our research you can visit geneticsofspeech.org.au
@MCRI_for_kids @Apraxia_KIDS
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90 kids die from childhood dementia in Aus each year.
A new podcast ep from @TheBriefingAU raises awareness + shares what ⬆️ researching funding means for kids living with childhood dementia & their families
open.spotify.com/episode/2ac1eM…
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Lottie Morison retweetledi
Did you know kids with Childhood #Apraxia of Speech (CAS) can have challenges with fine and gross #motorskills? ✍🏽🏃♀️
🗣️ We are recruiting for a study looking at the sensory and motor profiles in #CAS.
Email for more info: geneticsofspeech@mcri.edu.au
instagram.com/reel/C6XDqp_B9…
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Lottie Morison retweetledi
Happy #KIF1A day! KIF1A Associated Neurological Disorder #KAND is a rare #genetic condition.
Our team are working with @KIF1A to better understand #Speech, #Language and Non-verbal #Communication in KAND.
To learn more about the research visit: geneticsofspeech.org.au/media/b4vb0ofh…
KIF1A.ORG@KIF1A
Today is KIF1A Day. A day to raise awareness, drive innovation forward to treatments, celebrate accomplishments our kids work relentlessly to achieve and hold on to. A day to remember those we have lost to this disease. Thank you to everyone climbing this mountain with us.
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Lottie Morison retweetledi
@AngeMorg @MCRI_SpeechLang our wonderful research team casting a speech and language lens on #DEE @geneticepilepsy @Lottiedmorison
GETA@geneticepilepsy
Current research in speech disorders in DEEs with Professor Angela Morgan @UniMelb @MCRI_for_kids #DEE #speech #research
Melbourne, Victoria 🇦🇺 English
An engaging first day of the #GETA2024 conference hearing from families, clinicians, and scientists about genetic epilepsies.
Also such a privilege to hear my supervisor @ingridscheffer speak about #DEEs & precision medicine.
@geneticepilepsy
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Congratulations @MiyaDStJohn !
MCRI - Translational Centre for Speech Disorders@MCRI_SpeechLang
Congratulations @MiyaDStJohn runner up of the Mendelsohn Neuroscience Graduate Researcher Award (Clinical) for outstanding research identifying a set of chromatin #genes as important for #speech, #language, and #neural development in rare #genetic neurodevelopmental conditions.
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Next week 7pm Thurs 18th April AEST we are holding a webinar for Aus and NZ families, caregivers, support workers & clinicians (& anyone else who would like to come!).
You can email me at Lottie.morison80@mcri.edu.au to be sent the webinar details.
MCRI - Translational Centre for Speech Disorders@MCRI_SpeechLang
Join us next week for a webinar on our recent research on '#Speech, #language and #communication in #KleefstraSyndrome' on Thurs 18th April 7pm AEST. For info see the flyer below or email lottie.morison80@mcri.edu.au @kleefstrasyndro @kleefstrasynd @iDefineorg @emmagenetics
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@JacMPennacchia is researching what #mentalhealth
means for young people with complex communication needs (#CCN).
More details about the study are in the flyer below or you can contact Jacinta directly via email to learn more at Jacinta.pennacchia@mcri.edu.au.
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Lottie Morison retweetledi
They’re all terminal. They all progressively rob kids of their cognitive and physical abilities. Bringing these disorders together makes them impossible to ignore. You can see a stationary list here: bit.ly/3uHAJmN #rarediseaseday #childhooddementia
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Lottie Morison retweetledi
Today is #RareDiseaseDay!
We work with kids who have rare conditions affecting #speech & #language.
Our research works to understand rare conditions to transform diagnosis, prognosis & enable precision therapies to improve outcomes!
@MCRI_for_kids @UniMelbMDHS @UniMelb
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Lottie Morison retweetledi
Already #RareDiseaseDay2024 in Aus & so pleased to share with you our first-ever National Recommendations for Rare Disease Care rarevoices.org.au/national-recom… Huge thanks to the RArEST team, @RareVoices ,our clinical working group and people living with rare who codesigned these!
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Tomorrow is the rarest day of the year & rare disease day!
@M4RareDiseases
MCRI - Translational Centre for Speech Disorders@MCRI_SpeechLang
Don’t forget to #ShowYourStripes tomorrow Thurs 29th Feb for #RareDiseaseDay! Just like a Zebra’s stripes, every individual with rare disease’s journey is unique. #Medics4RareDiseases #RareDisease #Genetics #RareAlly
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