Access appropriate care for rare haemorrhagic diseases
with with French Association of Hemophiliacs

Access appropriate care for rare haemorrhagic diseases

with 
with French Association of Hemophiliacs

Last update7 avr. 2022

What is it?

The French Association of Hemophiliacs (AFH) supports people affected by a rare constitutional haemorrhagic disease such as hemophilia, Willebrand's disease, platelet pathologies and other coagulation factor deficiencies.

The AFH puts these people in contact with health professionals in specialized treatment centers for medical monitoring and access to treatment.

Who is it for?

Important!

Access to care 24h/24

Target audience
For all
French level
All levels
How much does it cost?
Free
Action zone

France entière

Important!

Access to care 24h/24

Target audience
For all
French level
All levels
How much does it cost?
Free
Action zone

France entière

Why is it interesting?

Access to appropriate treatment

The AFH accompanies helps you have access to a treatment adapted to your pathology.

Meet specialists

We put you in touch with specialised health professionals for your rare disease.

How do I get involved?

Call us on +33 1 76 35 11 57

Telephone line available 7 days a week.

Contact us by email

accompagnement@afh.asso.fr

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Proposé par
AFH

Association française des hémophiles