PNH Patients,
Aplastic Anemia & MDS International Foundation has released a webinar for PNH patients regarding COVID-19.
You can watch the free webinar by following this link: https://youtu.be/apMyOo7YSeA
For regularly updated information on COVID-19 from the Public Health Agency of Canada, please visit: https://www.canada.ca/…/d…/coronavirus-disease-covid-19.html
The Canadian Association of PNH Patients is a not-for-profit Canadian organization formed in 2009. The mission of the organization is to connect Canadians affected by Paroxysmal Nocturnal Haemoglobinuria and advocate for the best possible care for patients and ensure they are equipped with the most current tools and information to help them live well with the condition.
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