Ride For Lupus
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Welcome to Ride For Lupus, an annual charity motorcycle ride in support of the SickKids Foundation at the Hospital for Sick Children where 100% of the proceeds of this event go directly to the Pediatric Lupus Research unit at HSC (Hospital for Sick Children).


*information provided directly from Dr. Earl Silverman, MD, FRCPC

• HSC diagnoses between 60-70 new cases of Lupus in children and adolescents each year.

• SickKids follows between 200-250 patients with Lupus throughout the course of any given year.

• Dr. Silverman (lead in the department of pediatrics at HSC) has treated over 650 children with Lupus since he began working at SickKids over 25 years ago.

• SickKids sees more Lupus patients than any other hospital or facility in the world – including institutions for adults with Lupus

• 20% of those Lupus diagnoses occur before the age of 18

• Lupus is present in 1/1000 Caucasian women

• Lupus is present in 1/500 non-Caucasian women

• Prevalence rates of Lupus are 5x less common with men

Lupus is a chronic illness. The cause is unknown, and there is no cure. This nickname for the illness is “the disease of 1000 faces” because the symptoms vary so drastically from patient to patient, and is often a challenge for doctors to diagnose. Patients can live for years with this disease and not have the proper treatment due to a misdiagnosis or Lupus simply not being recognized.

Lupus is an autoimmune disease where the body’s immune system becomes hyperactive and attacks normal, healthy tissues; this results in symptoms such as inflammation, swelling and damage to joints, skin, kidneys, blood, heart, lungs, brain (causing cognitive dysfunction), and other organs. Along with chronic fatigue, muscle weakness is also an issue. With this, general stiffness occurs all over the body, is quite painful and doing simple movements with limbs can be a major task.

Under normal function, the immune system makes proteins called antibodies in order to protect and fight against antigens (a substance capable of inducing a specific immune response) such as viruses and bacteria. Lupus makes the immune system unable to differentiate between antigens and healthy tissue. This leads the immune system to direct antibodies against the healthy tissue, not just the antigens, causing swelling, pain, and tissue damage (just to name a few). For more information about lupus, please visit www.lupuscanada.org

Having being diagnosed myself at a young age, it is my hope that with your help we will be able to conquer this disease in our lifetime. Please check out the upcoming Events, Register and Donate links above. Note that a donation does not register you for the event, as these must be done separately.

Why the Purple Butterfly?

Ride For Lupus - Butterfly Rash The purple butterfly represents the rash most Lupus patients have, more often than not on their face. It is called the Butterfly rash, is purple and expands over the face from one cheek bone, over the bridge of the nose and over the other cheek bone, looking very much like a butterfly has landed on the face, hence the name, Butterfly rash. This is symbolic for all Lupus patients.
Donate to Ride For Lupus

SickKids Presentation

Ride for Lupis -presentation 2014
We presented Dr. Silverman, head of the Pediatric Lupus Research Unit at the Hospital for Sick Children, with a cheque in the amount of $2,405.00! Every cent of this goes directly to the lab where they are currently working on if/how Lupus is genetic.

  © Ride For Lupus 2014
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