SpA Awareness - A FREE webinar

More than 500,000 Canadians live with spondyloarthritis—more than rheumatoid arthritis, ALS, and MS combined. The Canadian Spondyloarthritis Association (CSA) is the only national charity solely dedicated to supporting people living with spondyloarthritis. In its various forms this includes ankylosing spondyloarthritis, psoriatic arthritis, enteropathic arthritis, uveitis, etc. The CSA provides education, advocacy, and community resources to empower patients and promote early diagnosis and effective treatment. Through collaboration with healthcare professionals and ongoing research initiatives, the CSA is committed to improving the quality of life for all those affected by spondyloarthritis. For more information, visit sparthritis.ca.

Canadian Spondyloarthritis Association

Join the CSA for a FREE webinar on Spondyloarthritis Awareness

<p>Here’s a chance to learn why SpA conditions (particularly AS) are often difficult to diagnose. Understand why the time to diagnosis can be quite lengthy for some and how to make the most of your diagnosis and time with healthcare team. Join the Canadian Spondylitis Association &amp; Dr. Sherry Rohekar for this free event offered to CSA members</p>
<ul>
<li>The process in diagnosing SpA</li>
<li>Why is it often a longer process for females to get diagnosed</li>
<li>Knowledge base of physicians and what you can do to help.</li>
<li>How to work with your rheumatologist during the diagnosis process</li>
<li>How to work with your rheumatologist once a diagnosis is made</li>
<li>How can patients help</li>
<li>How to ask for a referral</li>
<li>How to work with your doctor to set goals</li>
<li>Q&amp;A</li>
</ul>




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SpA Awareness - A FREE webinar

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SpA Awareness - A FREE webinar

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