TORONTO (October 29, 2018) – To mark World Psoriasis Day, the Canadian Association of Psoriasis Patients (CAPP) today released new data on the barriers to treatment that Canadian psoriasis patients face and is calling on patients and their loved ones to get serious about advocating for change at their new website, www.PSOSerious.ca
The report, Pso Serious 2018: A Report on Access to Care and Treatment for Psoriasis Patients in Canada, highlights the changes to the care and treatment environment for psoriasis patients in Canada over the last four years. While there have been advances in the number of treatments available, there is still work to be done to ensure equitable access to these treatments as well as to dermatological care in Canada—particularly in rural and remote parts of the country.
Psoriasis impact beyond skin deep
Psoriasis is a chronic, debilitating disease that impacts more than one million Canadians of all ages and about 125 million people worldwide. There is currently no permanent cure for psoriasis and patients may experience recurrence of symptoms throughout their life.[i] Psoriasis is also associated with an increased risk of developing other chronic systemic diseases, including heart attack and stroke, diabetes, cancer and liver disease.[ii]
“What many people don’t know is that in addition to its physical manifestations, psoriasis can have a significant impact on the psychological health of patients with psoriasis, and their families,” said Kathryn Andrews-Clay, Executive Director of CAPP. “People with psoriasis have an increased risk of depression, anxiety and suicide – which is why access to care and effective treatment is so important to their overall well-being.”
Significant barriers decrease quality of life
The report revealed significant barriers to the three things that psoriasis patients need to thrive – access to phototherapy, dermatologists, and to a choice of treatment:
With the results of this report, CAPP will advocate for better access to care and treatment, including phototherapy, for psoriasis patients. All patients interested in sharing their story and advocating on these issues are invited to visit www.PSOSerious.ca.
About the Canadian Association of Psoriasis Patients
The Canadian Association of Psoriasis Patients (CAPP) is a national non-profit organization dedicated to be a resource and advocate for psoriatic patients and their families to improve patient care and quality of life. CAPP’s vision is to ensure equal access to best care and treatment for all psoriasis and psoriatic arthritis patients, while its mission is to be a resource for psoriatic patients and their families to advocate for improved patient care and quality of life.
[i] Pso Serious 2018: A Report on Access to Care and Treatment for Psoriasis Patients in Canada.
[ii] Canadian Associaton of Psoriasis Patients: Living With Psoriasis (http://www.canadianpsoriasis.ca/index.php/en/psoriasis/living-with-psoriasis) Accessed October 25, 2018.