Catherine Stratton, MPH
cathsmstratton.bsky.social
Catherine Stratton, MPH
@cathsmstratton.bsky.social
Epidemiology PhD(c) @UofT; @CIHR_IRSC CGS-D & @fdnPETF Scholar; MPH @Yale; VP & Research Chair @moyamoyafoundation #KnowledgeTranslation #KnowledgeSynthesis #RareDisease #PainScience #Disability
Reposted by Catherine Stratton, MPH
Have you checked out our online knowledge synthesis course? Bring a project to work on and walk away with a protocol that's been reviewed by experts!

Starts in January 2026, learn more here! bit.ly/42AoohE

@andreatricco.bsky.social @cathsmstratton.bsky.social @sporalliance.bsky.social
December 2, 2025 at 6:02 PM
Reposted by Catherine Stratton, MPH
DEADLINE EXTENDED TO NOVEMBER 27, 2025 - There’s still time to register for the Digital Health Literacy for Older Adults (DHLOA) in-person knowledge mobilization event!

Sign up as a Person with Lived Experience: tinyurl.com/bp5bn6wr

Sign up as a General Attendee: tinyurl.com/48x8x5e2

/1
You’re Invited - Join us for the Digital Health Literacy for Older Adults (DHLOA) In-Person Knowledge Mobilization Event!

Sign up as a Person with Lived Experience: tinyurl.com/bp5bn6wr

Sign up as a General Attendee: tinyurl.com/48x8x5e2

/1
November 25, 2025 at 6:21 PM
Excited to share this work which extends the Template for Intervention Description and Replication (TIDieR) to include pediatric-specific considerations: lnkd.in/gzFq_P52

Wonderful leadership by @martinoffringa.bsky.social!

#ClinicalTrials #ReportingGuideline #Pediatrics #ChildHealth
LinkedIn
This link will take you to a page that’s not on LinkedIn
lnkd.in
October 17, 2025 at 10:17 PM
Reposted by Catherine Stratton, MPH
Do you want to learn more about #KnowledgeSynthesis from the experts? By the end of our online course, "Intro to KS for Knowledge Users", you'll have a protocol ready for registration.

Apply & find out more here: bit.ly/42AoohE

@cathsmstratton.bsky.social @andreatricco.bsky.social
September 17, 2025 at 5:53 PM
Reposted by Catherine Stratton, MPH
Check out our July 2025 e-newsletter for the latest SPOR Evidence Alliance updates, including patient-led research spotlights, publications, and engagement opportunities!

📩 Read it here: mailchi.mp/smh/spor-evi...

#PatientOrientedResearch #PatientEngagement #KnowledgeMobilization
July 31, 2025 at 11:59 PM
Reposted by Catherine Stratton, MPH
We're thrilled to share that KTP grad student @cathsmstratton.bsky.social & scientists Drs @andreatricco.bsky.social and Jennifer Watt were awarded funding for their projects thru the Canadian Institutes of Health Research Spring Project grant competition!

Congratulations to all of the grantees! 🎉
July 24, 2025 at 7:55 PM
Reposted by Catherine Stratton, MPH
Check out our May 2025 e-newsletter for the latest SPOR Evidence Alliance updates, including patient-led research spotlights, publications, and engagement opportunities!

📩 Read it here: mailchi.mp/smh/spor-evi...

#PatientOrientedResearch #PatientEngagement #KnowledgeMobilization
May 30, 2025 at 5:01 PM
Reposted by Catherine Stratton, MPH
(2/2)

PhDs for Public Impact fellows focus on engaging the public through their scholarly work. See the full group of 2025-2026 fellows at the link below.

Congratulations again to Catherine, and all of the new cohort!

www.cgpd.utoronto.ca/public-schol...

@sporalliance.bsky.social
Connaught PhDs for Public Impact Fellows – Centre for Graduate Professional Development
www.cgpd.utoronto.ca
May 27, 2025 at 7:13 PM
Reposted by Catherine Stratton, MPH
(1/2)

Congratulations to KT Program grad student @cathsmstratton.bsky.social on being awarded a Connaught PhDs for Public Impact Fellowship from the Centre for Graduate Professional Development at the School of Graduate Studies, @uoft.bsky.social!

@andreatricco.bsky.social
May 27, 2025 at 7:13 PM
Reposted by Catherine Stratton, MPH
Join RareKids-CAN in acknowledging World Moyamoya Day - a day dedicated to raising awareness and knowledge about moyamoya, a rare and progressive condition affecting the arteries in the brain.
May 6, 2025 at 8:06 PM
Reposted by Catherine Stratton, MPH
I am presenting at an Open Science event on March 21st & would like to get the patient community involved & influencing how I present the patient perspective. If you have 5 minutes, please consider completing this survey to share your feedback: docs.google.com/forms/d/e/1F... Many thanks!
Open Science: What do patients or people with lived experience think?
My name is Laurie Proulx and I have lived with a chronic condition for most of my life. For the last 15 years, I have been active as a patient partner in research. On March 21, 2025, I am presenting t...
docs.google.com
March 13, 2025 at 3:08 PM
It’s #RareDiseaseDay! With ~1 in 12 affected, RDs represent a significant burden for patients, families, & systems. The RD diagnostic odyssey is a call for improved awareness. The fact that still, only 5% of RDs have a therapy is a sobering reminder of the work we have to do. #RareDiseaseIsNotRare
March 1, 2025 at 2:10 AM
The @moyamoyafoundation.bsky.social is gathering input from #moyamoya patients on what they’d like to hear about at upcoming educational events. Please follow this link: docs.google.com/forms/d/1wxF....
Responses are de-identified and are not part of a research project.
https://docs.google.com/forms/d/1wxFeR…
February 26, 2025 at 12:42 AM
Most #RareDisease #registries require a confirmed Dx for inclusion. This is important for accurate calc of risks & outcomes, but accuracy is also threatened when people who remain undiagnosed are missed. This can perpetuate inequities: “If someone’s not counted, they don’t count.”
February 6, 2025 at 1:12 AM
The #RareDisease #DiagnosticOdyssey is a glaring example of health inequity. A Canadian Organization of Rare Disorders survey found pts saw 5.9 clinicians & received 3.2 misdiagnoses over 3.7 years before receiving an accurate Dx. RD awareness is crucial. #RareDiseaseIsNotRare #RareDiseaseTruth
February 4, 2025 at 1:05 AM
It’s #RareDiseaseMonth! While there is no official definition, #RareDisease (RD) generally refers to conditions affecting <1 in 2k people. There are an estimated 10k RDs. Despite each RD being uncommon, 1 in 12 Canadians is affected by RD. #RareDiseaseIsNotRare #RareDiseaseTruth
February 3, 2025 at 12:31 AM
A big step forward! While the roll out of the National Strategy for Drugs for #RareDiseases has been slow with a series of agreements with provinces, this investment mitigates existing disparities. We must continue advocating for the inclusion of other drugs & sustainable support
Government of Canada signs bilateral agreement with Ontario for Drugs for Rare Diseases www.canada.ca/en/health-ca... @markhollandlib.bsky.social

Get weekly updates: CanadaHealthwatch.ca/newsletter 🍁
January 27, 2025 at 1:34 AM
Reposted by Catherine Stratton, MPH
Member spotlight! Amanda Doherty-Kirby is a valued patient partner of the SPOR Evidence Alliance, and has contributed to many knowledge synthesis projects.

Check out her spotlight in our December 2024 newsletter: shorturl.at/LG45U

We are grateful for her partnership!
January 24, 2025 at 10:00 PM
Sharing a new protocol publication regarding #MetaAnalysis in the context of #LivingSystematicReviews, led by my fellow lab member:
journals.lww.com/jbisrir/fullte…. Well done, Menelaos!
@andreatricco.bsky.soci
al
https://journals.lww.com/jbisrir/fullte…
January 24, 2025 at 12:06 AM
#HappyNewYear, everyone!
May each day bring comfort, fresh opportunities, and moments of happiness. Here’s to embracing new challenges and celebrating every win as we step into 2025. #NYE #NYE2025 #HappyNewYear2025
a black background with the words happy new year written in white
Alt: a black background with the words happy new year written in white
media.tenor.com
January 1, 2025 at 4:18 AM
Wishing everyone a wonderful holiday season that is restorative and fulfilling #MerryChristmas #HappyHolidays
December 26, 2024 at 4:01 AM
If you are interested in #moyamoya and #LargeLanguageModels, please consider completing this study survey from Boston Children’s Hospital. Eligible for patients, caregivers, advocates, clinicians, and researchers! #RareDisease #Neurosurgery #Neurology

Link: redcap.tch.harvard.edu/redcap_edc/s...
December 17, 2024 at 2:35 AM