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TSC In the News
Canadian TSC Educational Series – 2nd Session
Join us on Thursday June 13, 2024, at 6:00 pm EST for the 2nd session of the Canadian TSC Educational Series for caregivers and patients with TSC. This second session will focus on ‘What is routine follow-up in TSC: Across the ages’.
The symposium will be held on Google Meet.
Don’t forget to register using the link below:
Click here for link to: Registration for the Canadian TSC Educational Series
We hope to see you there!
TSC Awareness Month – fundraiser
Hi Everyone! May is TSC Awareness month.
Cathy Evanochko is a member of our VIP group and Chair Person for the TSC Canada non-profit, charitable organization dedicated to raising public awareness and support for individuals with TSC and their families. Her daughter has TSC.
Cathy created a fundraising website with Sipology to help raise funds to help with research and develop awareness about this disorder. Use this shopping link to help support TSC Canada!
https://fundraise-ca.sipology.com/collections/may-tsc-awareness
40% of all proceeds are returned to TSC Canada. All items are priced $15 each and there is a flat shipping rate of $3 per order.
Let’s all pitch in and make a difference in the lives of individuals and their families impacted by TSC.
#tsccanada #TuberousSclerosisComplex #fundraising
Canadian TSC Educational Series – Session 1 Video
For those who were unable to join us for the first session of the Canadian TSC Educational Series for caregivers and patients with TSC, we have posted the video here:
The next session is scheduled for June 13, 2024, 6:00pm-7:00pm. For more information and to register, please use the link below:
Canadian TSC Educational Series
Join us at 7:00 pm EST on Thursday March 21, 2024 for the first session of the Canadian TSC Educational Series for caregivers and patients with TSC. The first session will focus on Diagnosing TSC and Understanding its cause.
Please use the link below to register.
Registration for the Canadian TSC Educational Series
TSC Canada & TSC Alliance Research Collaboration Webinar
Did you miss the TSC Canada ST & TSC Alliance Research Collaboration Webinar? Watch it here:
Webinar – Thursday December 14th @ 8:00pm ET
Please join the TSC Alliance and Tuberous Sclerosis Canada Sclérose Tubéreuse (TSC Canada ST) on Thursday, December 14 at 8 pm ET to learn about the TSC Alliance’s ongoing research collaboration with Drs. Mark Keezer and Phillipe Major. They will be talking about ongoing efforts for the TSC Natural History Database and Biorepository and answer any questions regarding research for TSC in Canada.
Please register for the webinar using the link below.
BRI Symposium – Thursday November 16, 2023
BRI Symposium – Thursday November 16, 2023.
The symposium is from 8:30 AM – 5:00 PM. Registration is free and attendees are welcome to attend virtually.
The Keynote speaker is Dr. Petrus DeVries who will talk about both autism and TSC.
Presenting the TÉCUM Program
Are you an adolescent or young adult with epilepsy or a family member or caregiver of such a person? The TÉCUM program (Transition en épilepsie complexe de l’Université de Montréal) is hosting a symposium that is meant for you!
On Thursday, December 7, 2023, from 5:30 to 6:30 p.m., Dr. Mark Keezer (CHUM) and Dr. Philippe Major (CHUSJ) will present the transition program. There are two options to attend the evening conference:
1. Come to the CHUM at 1000 rue Saint-Denis, room A.02.9209A/B. Snacks will be served on site.
2. Attend the online presentation. The link will be provided upon registration.
It is mandatory to register via the form. You can scan the QR code (in the attached poster) or click here to access the registration form.
Speakers will present in French, but English subtitles will be available live.
Educational Series on TSC
An educational series to empower patients and their families with knowledge and resources related to TSC, are being planned by Canadian health care professionals. They want your input on frequency, timing, and topics of the educational series.
Please take 1 minute to complete the survey:
Attention: Résidents du Québec
l’Institut National d’Excellence en Santé et Services Sociaux (INESSS) et en cours d’évaluation pour le remboursement par l’assurance-médicaments d’un médicament pour le traitement en appoint de la sclérose tubéreuse de Bourneville.
l’INESSS à un questionnaire (ci-joint) pour que les patients et des proches aidants puissent participer à l’évaluation. Le questionnaire est ouvert à tous les patients et proches aidants de personnes atteintes de la sclérose tubéreuse de Bourneville, qu’ils aient essayé ou non ce médicament.
Les personnes doivent envoyer le questionnaire ci-joint rempli à plan.commentaires.inscription@inesss.qc.ca.
Si vous avez des questions ou besoin d’aide, vous pouvez contacter par courriel : marie-eve.fleury@rqmo.org ou info@rqmo.org.
Vous trouverez plus d’information sur comment faire un commentaire à l’INESSS ici: https://www.inesss.qc.ca/thematiques/medicaments/medicaments-evaluation-aux-fins-dinscription/faire-un-commentaire-sur-un-medicament.html.
