Why it matters to us

If you have visited the workshop, it is very likely that we have told you our story and that you have also seen the adapted equipment that we have at home. For those we haven't had the chance to meet yet, you should know that one of the most important people for us has this disease. When that happens, we have no power over it! So we wondered what we could do...

This is why this page exists, so that one day, with your help, we can talk about ALS, this incurable disease, in the past.

 

What is ALS?

Amyotrophic Lateral Sclerosis (ALS) is a fatal neuromuscular disease that results in eventual paralysis of the body, for an average of 2 to 5 years.

WITH YOUR SUPPORT, the ALS Society of Quebec can:

• Support and accompany people affected by ALS and their families at all stages of the disease throughout the province of Quebec;
• Contribute to research, the source of hope;
  
• Raise awareness and make the disease known to the general public, government authorities and medical and paramedical stakeholders.

 For more information about SLA Quebec, visit https://sla-quebec.ca.

 

How to help?

By making a purchase with Atelier Arbor, you will have the option to add a donation during your checkout on our online store.

You can also make your donation directly on this link.

Once a month, we'll post the names of generous donors on our social media!

The ALS Society of Quebec will send you your receipt for tax purposes by email in the months following your transaction. For any questions regarding your tax receipt, do not hesitate to contact the ALS Society of Quebec by email lcourteau@sla-quebec.ca or by phone 514 725-2653 ext. 108. 

 

 

Here is the contact information for The ALS Society of Quebec if you have any questions regarding your donation:

The ALS Society of Quebec

5415 rue Paré, office 200, Mont-Royal, Qc, H4P 1P7

Phone: 514-725-3653

E-mail: info@sla-quebec.ca

Charitable organization number: 119153187RR0001