Glossary of Genetic Terms

Available equipment

Please consult the list below or the ALS Canada Equipment Catalogue for more information about which pieces of equipment are available through our program.

Mobility assistance and lifts

Bedroom and other equipment

Bathroom assistance

 

Please note that the ALS Canada Equipment Program is not a trial program. This means that we do not loan equipment for the purpose of testing what devices are best for you. Instead, we facilitate loans or funding assistance once someone’s equipment needs have been assessed and recommended by a professional.

The ALS Society of Canada’s (ALS Canada) vision is a future without ALS. To achieve this vision, new treatments that can help with symptom management and slow down and someday stop the progression of amyotrophic lateral sclerosis (ALS) need to undergo clinical trials on humans to ensure that they are both safe and effective before being approved for widespread availability.

Today, more is known about this relentlessly progressive motor neuron disease which causes paralysis and leads to the death of approximately 1,000 people in Canada each year. And while the prognosis of ALS is variable and its progression difficult to predict, (i) we know that it can move with startling swiftness – leaving a very narrow window of time to slow it down, often further compressed by delayed diagnosis.

In this Toolkit you will find the following resources:

A resource that supports and empowers advocacy efforts aimed at improving the lives of people living with ALS (Amyotrophic Lateral Sclerosis).

Donation type (select one):
• General donation
• In memory of…
• In honour of…

Amyotrophic lateral sclerosis, multiple sclerosis, and muscular dystrophy can sometimes be confused as the characteristics and symptoms of these diseases can overlap. People living with ALS, MS, and MD often require the same kinds of wheelchairs and assistive devices. However, ALS, MS, and MD are separate and distinct diseases.

Bulbar ALS is a subtype of ALS that destroys motor neurons in the corticobulbar area of the brain and brainstem. This area controls muscles in the face, head, and neck including the jaw, lips, throat, and tongue.

You are probably reading this booklet because your Mom or Dad or someone else special in your family has Amyotrophic Lateral Sclerosis. It is a long name and for short it is often called ALS.

This glossary contains a list of scientific and medical terms and definitions that are relevant to amyotrophic lateral sclerosis (ALS). It can be used by anyone from within the ALS community including recently diagnosed individuals, caregivers, medical professionals, researchers, as well as by the general public. The research glossary was developed to help support knowledge-sharing by helping to provide clarity around terminology that may be unfamiliar to our readers.