Dig out your craziest socks and help us in make a difference on Saturday, July 6 at the 2024 BC Rugby Provincial Championships for the Crazy Socks for ALS Day.
The ALS Society of BC and BC Rugby are thrilled to announce the exciting and fun-filled charity fundraising event called “Crazy Socks for ALS Day” on Saturday, July 6, as part of the 2024 BC Rugby Provincial Regional Championships. Prepare for a day brimming with joy, togetherness, and, of course, crazy socks!
Dive into the spirited Crazy Socks for ALS Day and be part of an impactful journey toward ALS awareness and fundraising while combining the excitement of regional junior Rugby.
Let’s make a difference together: join us for a memorable “Crazy Socks for ALS Day” to show our support for the ALS community. Together, our goal is to raise $3,999 to purchase a Travel Buggy Power Chair for ALS BC’s Equipment Loan Program. This advanced equipment is not just a luxury but a necessity for newly diagnosed ALS patients, helping them maintain independence and social connections.
All participants, Coaches, Officials, staff members and fans attending the popular BC Rugby event are encouraged to wear the wildest, craziest socks on Saturday, July 6 and donate via this secure online page.
Two people wearing the ‘Craziest’ pair of socks at the event on Saturday, July 6, will WIN prizes, all thanks to the generosity of BC Rugby supporters! O’Neills offers one lucky attendee a fantastic prize pack full of amazing merchandise. And the Vancouver Highlanders are giving away a one-of-a-kind signed rugby jersey to another lucky person. The prize winners will be chosen that day – don’t miss out on these fantastic chances to make your day even more memorable at the event!
If you can, share photos of your Crazy Socks for ALS Day on social media with the hashtag #CrazySocksforALS. It will help amplify our message and inspire others to join the cause.
Here’s how you can participate:
- Wear Crazy Socks: Show off your wildest socks at the event
- Share on Social Media: Post photos with the hashtag #CrazySocksforALS
- Donate: If you can, contribute to our $3,999 goal to purchase a Travel Buggy Power Chair
- Join the Fun: Attend the championships and participate in the activities
WHAT IS ALS?
Amyotrophic Lateral Sclerosis (also known as ALS, Lou Gehrig’s disease, or motor neuron disease) is a disease that gradually paralyses people because the brain is no longer able to communicate with the muscles of the body that we are typically able to move at will. Over time, as the muscles of the body break down, someone living with ALS will lose the ability to walk, talk, eat, swallow, and eventually breathe.
ALS is not contagious. There are no effective treatments for ALS and no cure. Approximately 80 per cent of people with ALS die within two to five years of being diagnosed.
ALS can hit anyone, at any time, regardless of age, gender or ethnic origin.
There is no one thing that causes ALS. Rather, ALS is recognized as having multiple interacting causes that are likely based on changes in people’s genes, and possibly contribution of environmental factors. A number of genes have been identified as playing a role in the development of ALS.
Research suggests a potential connection between high-impact sports and ALS, though this research is ongoing. Athletes, particularly in contact sports like football, hockey, boxing, and rugby, may have a higher risk of developing ALS compared to the general population.
PLAYER SAFETY IS PRIORITY
BC Rugby’s number one priority is player safety and adheres to World Rugby’s policy of ‘Recognise and Remove’ when dealing with concussions or suspected concussions.
Anyone on or around the Rugby pitch has a responsibility to be aware of the symptoms of concussion and are encouraged to annually complete World Rugby’s online Concussion Management module to learn more.
We also strongly encourage parents, guardians, partners or housemates of Rugby players to complete the online module to be informed.
World Rugby has a Concussion App with all the basics of Concussion Management. Download it now from the Apple Store.
ABOUT ALS SOCIETY OF BC
The Amyotrophic Lateral Sclerosis Society of British Columbia (ALS BC) was founded in 1981 by Dr. Andrew Eisen, ALS patients, and their families to address the physical and emotional needs of people living with ALS, their families, and caregivers. The Society’s mission is to cure ALS by funding research while advocating for and supporting those affected.
Learn more about the ALS Society of BC here.