The CTMA was created to support and create a networking infrastructure and public awareness public awareness of the rare neuroimmunologic disorders of the central nervous system. The Canadian Transverse Myelitis Association (CTMA) was incorporated on July 12, 2010 as an organization dedicated to advocate and support those who have these rare neuroimmunologic diseases.
This scholarship is offered in the memory
of Graeme McDonald who passed in March 2020 . Graeme leaves behind a legacy of
generosity in helping The Canadian Transverse Myelitis Association as he was
the designer of our logo, pamphlets and many of our virtual run medals. The
Canadian Transverse Myelitis Association and its Board of Directors want to
recognize that Graeme used his incredible talents to help others and this will
be memorialized through the recipients of this scholarship.
How to Make a Donation
Donations can be made by cheque and sent to:
The Canadian Transverse Myelitis Association
263 Malcolm Circle
Dorval, QC H9S 1T6
Or you can click here to donate through Canada Helps
.
IT'S TRUE! THE CTMA HAS JOINED THE TRUEARTH FUNDRAISING PROGRAM
The news is out! We are continuing our fundraising efforts with TruEarth!
We’re so excited to explore this new avenue with sustainability in mind and we hope you are too!
Learn more and see what is available to fill your cupboards here:
http://tru-earth.sjv.io/CTMA
The Blusson Spinal Cord Centre is a unique facility dedicated to
advancing world-leading integrated research and care for people with
spinal cord injury.
Learn more
The goal of this trust is to help families who cannot afford the
necessary items that their child may need as a result of Transverse
Myelitis
Read more
Bring awareness and support to those who live with Transverse Myelitis by purchasing and wearing these bands and help us in
Shining the light.
$2 or 3 for $5 plus shipping.
Buy now
Find support for yourself or your loved ones. The
CTMA has compiled a list of resources to help those living with
Transverse Myelitis.
Read more
Your donations will make a difference in the lives of
patients of TM, their families, physicians and whole communities across
our country.
Donate
Although we always do our best to create events on our own, The CTMA are always looking for volunteers to organize.
Read more