Times Colonist

PATIENTS SHOULDN’T BE FORCED TO GIVE UP TREATMENTS THAT ARE WORKING

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Mina Mawani, President and CEO, Crohn’s and Colitis Canada

Last November, I penned an opinion piece for the Vancouver Sun titled Crohn’s and Colitis Canada calls on B.C. to mandate

‘No Forced Switch’. In the months since, policymake­rs across the country have taken notice of our advocacy campaign. To date, more than 4,500 letters have reached the offices of elected officials who now have a better understand­ing of the needs of people living with Crohn’s disease or ulcerative colitis, the two main forms of inflammato­ry bowel disease (IBD). But the stakes are still high. We cannot allow private or public payers to force any of the 25,000 British Columbians living with Crohn’s or colitis to give up a treatment that’s working well in exchange for a lower cost alternativ­e. This is a possibilit­y in the province and a worrying prospect for people who have finally found stability. As we prepare to mark World IBD Day on May 19, there’s no better time to raise your voice to keep this issue top of mind. Canada has one of the highest rates of Crohn’s and colitis in the world. Nearly 250,000 Canadians live with one of these chronic diseases which cause frequent and urgent washroom trips, fatigue, joint pain, abdominal pain, internal bleeding, and unintended weight loss. While we still don’t know an exact cause, researcher­s believe the diseases are triggered by a combinatio­n of elements, including genetics, environmen­tal factors, and abnormal immune system responses. Living with Crohn’s or colitis can be debilitati­ng and there are no cures, but medication­s can stabilize a patient’s condition and allow him or her to lead an active, healthy, and fulfilling life. This is the goal for all patients, but there are no one-size-fits-all treatments. It can take many years for a person with Crohn’s or colitis to find a drug that works for them, and more often than not this means a process of trial and error. Switching medication­s can jeopardize long-term remission, cause stress, and lead to unnecessar­y flare-ups. Once a patient has found remission, the last thing they want is to put their stability at risk. For this reason, we believe that doctors and their patients have the right to remain on a treatment option best suited to a patient’s individual circumstan­ces, without undue interferen­ce from government or private payers. We are calling on British Columbia to take Nova Scotia’s lead in protecting doctor-patient decision-making and mandating ‘No Forced Switch’. Crohn’s and Colitis Canada will always celebrate the introducti­on of safe, effective, and more affordable treatment options. New treatments hold great promise for patients in Canada, especially for people who have failed to respond to existing therapies and are running out of options. However, treatment decisions must never be made on the basis of cost alone. The decision to change treatments should only be made by patients in consultati­on with their doctors. We are asking for a ‘No Forced Switch’ policy to help ensure the best interest of the patient remains at the heart of every treatment decision. We need your help to make that happen. Please visit action.crohnsandc­olitis.ca and let your local representa­tive know how critical this issue is.

NUMBER OF BRITISH COLUMBIANS LIVING WITH CROHN’S OR COLITIS: 25,000 NUMBER OF LETTERS TO ELECTED OFFICIALS CALLING FOR NO FORCED SWITCH: 4,500

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