Information regarding COVID-19 is in constant change, as is the situation regarding vaccination and prioritization for immune-compromised individuals.
If you have any COVID-19-related questions, we’ve created a specific COVID section on our website that can be accessed by clicking here or by selecting the “News & Events” tab from our homepage. In this section, you’ll find the latest news and information about the pandemic in Canada from trustworthy and reliable sources.
Any specific questions that you may have regarding the COVID-19 vaccination, delays between vaccine dosing, and prioritization within your province are best answered by your healthcare team. They’re the ones who know you and your particular situation and are therefore in a position to best address your unique concerns.
Created by, and entirely focused on, Canadians impacted by myeloma, Myeloma Canada is the only national charitable organization committed to providing you with the most up-to-date and reliable information on myeloma. Some of the ways we do this is through our monthly e-newsletter, “Myeloma Matters”, as well as through our social media platforms.
Please don’t hesitate to contact us at firstname.lastname@example.org or toll-free at 1-888-798-5771 with any questions regarding our programs and services.
"You have multiple myeloma." With just four words, the lives of both patients and the people who care about them can be changed in many ways.
Being diagnosed with cancer is overwhelming for most people. And it can be particularly confusing when it's a type of cancer few people know about.
It's important for patients with myeloma, as well as for their families and caregivers, to receive the information and support they need to deal with the diagnosis and its emotional fallout.
If you have been diagnosed with myeloma, or if you know someone who has, you undoubtedly have many questions and concerns. This section addresses some of these concerns and explores ways you can get the support you need, to:
Help you understand more about myeloma and its impact on your life.
Help you manage the issues you may face.
Help you and your family cope with the effects of myeloma.
At times, multiple myeloma patients and their loved ones may feel scared, angry, frustrated and/or depressed. These are normal (and completely understandable) reactions when faced with a serious health problem.
Most people find they can handle their problems better if they can share their thoughts and feelings with others. This emotional sharing can help draw people closer and make everyone feel more comfortable expressing their concern and offering their support.
You are not alone. And you can help others by sharing your story.
Although you may not personally know other myeloma patients, or other people whose loved ones are living with myeloma, your story has the power to touch them in ways you may never know.
We would like to hear from you about how you've learned to live with your diagnosis and how you're overcoming the challenges of multiple myeloma, so we can share your experience with others.
Please send your stories, coping tips and insights on how myeloma has impacted you, your family and/or your friends, along with your permission to publish your comments to: email@example.com
On behalf of all the people with whom your story will resonate, and who will feel less alone as a result of your willingness to share it... thank you!