My team
My Story…
ALS is a progressive nervous system disease that affects nerve cells in the brain and spinal cord, causing loss off muscle control. I've had people I love deeply affected by it and know many others that have watched someone they love be affected by ALS.
I HATE running. But I desperately want to make a difference for someone being affected by ALS. Here's your chance to participate and make a difference!
Description
The ALS Society of BC was founded in 1981 by ALS patients, their family members and healthcare professionals to meet the physical and emotional needs of people living with ALS and their caregivers. The society provides support services to ALS patients and their family to improve their quality of life while living with ALS; equipment loan program, patient transportation support, support groups, psychological support, a camp for children of ALS patients, day of caring for caregivers and outreach and public awareness. The society also supports ALS research to find the cause of and cure for Amyotrophic Lateral Sclerosis.
Recent donors
| Donation date | Donor name | Donation amount |
|---|---|---|
| May 04 | Andrew | $107.72 |
| Mar 08 | Eric | $27.60 |
| Mar 07 | Malcolm | $27.60 |
| Jan 31 | marazao | $27.60 |
| Jan 12 | M Conger | $27.60 |
| Jan 12 | Paige | Undisclosed amount |
| Jan 12 | Anonymous | $11.58 |
