If you are a PNH patient who is having difficulty finding a PNH specialist or accessing treatment, please contact us at firstname.lastname@example.org.Si vous êtes un patient atteint de l’HPN et que vous éprouvez des difficultés à trouver un spécialiste de l’HPN ou à obtenir des traitements, contactez-nous.
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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