Funded through CIHR-IMHA and Muscular Dystrophy Canada
Visit us at: https://neuromuscularnetwork.ca/
Learn more and apply: neuromuscularnetwork.ca/news/2026-nm...
#fellows #graduatestudent #researcher
Deadline to apply: April 4, 2026
🔗 | Learn More: neuromuscularnetwork.ca/opportunity/...
#NeuromuscularResearch #ClinicalResearch #Canada #AcademicJobs #ResearchJobs
Deadline to apply: April 4, 2026
🔗 | Learn More: neuromuscularnetwork.ca/opportunity/...
#NeuromuscularResearch #ClinicalResearch #Canada #AcademicJobs #ResearchJobs
Hosted by SCN and @medicinebydesign.bsky.social, our Careers Beyond Academia seminar series continues on Feb 18, 2026, featuring Sonam Dubey and Ben Wang, with a focus on #ClinicalResearch 🩺
Register here. ➡️ https://stemcellnetwork.ca/training/careers-beyond-academia/
Hosted by SCN and @medicinebydesign.bsky.social, our Careers Beyond Academia seminar series continues on Feb 18, 2026, featuring Sonam Dubey and Ben Wang, with a focus on #ClinicalResearch 🩺
Register here. ➡️ https://stemcellnetwork.ca/training/careers-beyond-academia/
Register Here: bit.ly/CMTUpdates
Speakers:
Rami Massie: Update on CMT1A: Clinical trials & genetic therapies
Rita Horvath: #CMT: Clinical & Research Updates
#letstalkNMD
Register Here: bit.ly/CMTUpdates
Speakers:
Rami Massie: Update on CMT1A: Clinical trials & genetic therapies
Rita Horvath: #CMT: Clinical & Research Updates
#letstalkNMD
🔗 | Register here: neuromuscularnetwork.ca/event/17-02-...
#NMD4C #letstalkNMD #duchenne #steriod #neuromuscular
🔗 | Register here: neuromuscularnetwork.ca/event/17-02-...
#NMD4C #letstalkNMD #duchenne #steriod #neuromuscular
🔗 | Learn more about their work: neuromuscularnetwork.ca/news/2025-de...
🔗 | Learn more about their work: neuromuscularnetwork.ca/news/2025-de...
This months edition features new employment, funding and training opportunities, major community milestones, upcoming webinars, events, news and the latest research from across the Canadian neuromuscular network
🔗 | Read it here → zc.vg/EmdGo?m=0
This months edition features new employment, funding and training opportunities, major community milestones, upcoming webinars, events, news and the latest research from across the Canadian neuromuscular network
🔗 | Read it here → zc.vg/EmdGo?m=0
Deadline to apply: April 4, 2026
🔗 | Learn More: neuromuscularnetwork.ca/opportunity/...
#NeuromuscularResearch #ClinicalResearch #Canada #AcademicJobs #ResearchJobs
Deadline to apply: April 4, 2026
🔗 | Learn More: neuromuscularnetwork.ca/opportunity/...
#NeuromuscularResearch #ClinicalResearch #Canada #AcademicJobs #ResearchJobs
Speakers:
Rami Massie: Update on CMT1A: Clinical trials & genetic therapies
Rita Horvath: #CMT: Clinical & Research Updates
Register Here: bit.ly/CMTUpdates
#NMD4C #Neuromuscular #letstalkNMD
Speakers:
Rami Massie: Update on CMT1A: Clinical trials & genetic therapies
Rita Horvath: #CMT: Clinical & Research Updates
Register Here: bit.ly/CMTUpdates
#NMD4C #Neuromuscular #letstalkNMD
🔗 Apply by May 31, 2026: neuromuscularnetwork.ca/opportunity/...
🔗 Apply by May 31, 2026: neuromuscularnetwork.ca/opportunity/...
can-acn.org/meeting-2026/
Date limite demain le 6 fev pour soumission de résumés et demandes de bourses de voyage
can-acn.org/fr/congres-2...
can-acn.org/meeting-2026/
Date limite demain le 6 fev pour soumission de résumés et demandes de bourses de voyage
can-acn.org/fr/congres-2...
Theme: Resolving unsolved cases in rare genetic and non-genetic diseases. 👉 Access the full details and criteria: https://loom.ly/YzdmNGY #ERDERA #RareDiseases #ResearchFunding
Theme: Resolving unsolved cases in rare genetic and non-genetic diseases. 👉 Access the full details and criteria: https://loom.ly/YzdmNGY #ERDERA #RareDiseases #ResearchFunding
Learn more and apply: neuromuscularnetwork.ca/news/2026-nm...
#fellows #graduatestudent #researcher
Learn more and apply: neuromuscularnetwork.ca/news/2026-nm...
#fellows #graduatestudent #researcher
If you or a loved one has #SpinalMuscularAtrophy, we’d love to know what you think about gene therapy, prenatal testing, and family planning.
Get more info & complete the survey @ redcap.link/SMAperspecti...
**Please consider sharing with others in your #SMA community.
If you or a loved one has #SpinalMuscularAtrophy, we’d love to know what you think about gene therapy, prenatal testing, and family planning.
Get more info & complete the survey @ redcap.link/SMAperspecti...
**Please consider sharing with others in your #SMA community.
Learn more and apply: neuromuscularnetwork.ca/news/2026-nm...
#fellows #graduatestudent #researcher
Learn more and apply: neuromuscularnetwork.ca/news/2026-nm...
#fellows #graduatestudent #researcher
If you or a loved one has #SpinalMuscularAtrophy, we’d love to know what you think about gene therapy, prenatal testing, and family planning.
Get more info & complete the survey @ redcap.link/SMAperspecti...
**Please consider sharing with others in your #SMA community.
If you or a loved one has #SpinalMuscularAtrophy, we’d love to know what you think about gene therapy, prenatal testing, and family planning.
Get more info & complete the survey @ redcap.link/SMAperspecti...
**Please consider sharing with others in your #SMA community.
We’re kicking off the year with new research, opportunities, events, and updates from across the Canadian #neuromuscular community.
🔴 | Read our newsletter → neuromuscularnetwork.ca/january-2026...
#NMD #RareDisease #Research #Canada
We’re kicking off the year with new research, opportunities, events, and updates from across the Canadian #neuromuscular community.
🔴 | Read our newsletter → neuromuscularnetwork.ca/january-2026...
#NMD #RareDisease #Research #Canada
With MDC, we’re proud to support two early‑career scientists advancing #NMD research: neuromuscularnetwork.ca/2026fellows
🔴| Dr. Haley Geertsma, CHEO Research Institute
🔴| Dr. Isabelle Demers, Université de Sherbrooke
With MDC, we’re proud to support two early‑career scientists advancing #NMD research: neuromuscularnetwork.ca/2026fellows
🔴| Dr. Haley Geertsma, CHEO Research Institute
🔴| Dr. Isabelle Demers, Université de Sherbrooke
🔗 Apply by May 31, 2026: neuromuscularnetwork.ca/opportunity/...
🔗 Apply by May 31, 2026: neuromuscularnetwork.ca/opportunity/...
As we get the new year started, we’ve got three NMD4C deadlines you won’t want to miss that are all closing next week. Learn more & apply: neuromuscularnetwork.ca/news/2026-nm...
As we get the new year started, we’ve got three NMD4C deadlines you won’t want to miss that are all closing next week. Learn more & apply: neuromuscularnetwork.ca/news/2026-nm...
Read more → zc.vg/LUFW5?m=0
Read more → zc.vg/LUFW5?m=0
🔗 Register here: bit.ly/Dec2025Rounds
Speaker: Dr. Tefani Perera | Resident, University of Calgary
Date: Tue Dec 2, 2025
Time: 5:00pm ET
Register Here: bit.ly/Dec2025Rounds
#Neuromuscular Mystery Case Rounds #letstalkNMD
🔗 Register here: bit.ly/Dec2025Rounds
Join the global rare disease community this December, in Germany or online. 🌐
Co-organised by ERDERA, RDI and IRDiRC.
✍🏼 Programme & registration: https://loom.ly/1fhf8zI
#RareDiseases #ClinicalResearch
Join the global rare disease community this December, in Germany or online. 🌐
Co-organised by ERDERA, RDI and IRDiRC.
✍🏼 Programme & registration: https://loom.ly/1fhf8zI
#RareDiseases #ClinicalResearch
Register here. ➡️ stemcellnetwork.ca/training/wor...
Register here. ➡️ stemcellnetwork.ca/training/wor...
Meet Mak, Linges, Micah, Ayça & Burak, our heroes showing what life is like for the 300M people living with a rare disease.
Full video 🎥 youtu.be/7J1oTfoIOGw
Let’s bring about equity in more ways than even we can imagine!
#ShareYourColours
Meet Mak, Linges, Micah, Ayça & Burak, our heroes showing what life is like for the 300M people living with a rare disease.
Full video 🎥 youtu.be/7J1oTfoIOGw
Let’s bring about equity in more ways than even we can imagine!
#ShareYourColours
ERDERA’s new call will focus on solving unsolved rare disease cases through variant validation and advanced technologies.
🔸Info: https://lnkd.in/erMJCeGn
🔸Register to the webinar: https://loom.ly/d45a8o8
#ERDERA
ERDERA’s new call will focus on solving unsolved rare disease cases through variant validation and advanced technologies.
🔸Info: https://lnkd.in/erMJCeGn
🔸Register to the webinar: https://loom.ly/d45a8o8
#ERDERA