¿Qué consejos darías a una persona que acaba de ser diagnosticada con Deficiencia Del Factor VII?

Consejos de personas con experiencia en Deficiencia Del Factor VII para personas que acaban de ser diagnosticadas con Deficiencia Del Factor VII

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It is strongly encouraged to join a local bleeding disorder chapter (National Hemophilia Foundation - http://www.hemophilia.org -- or Hemophilia Federation of America - http://www.hemophiliafed.org/), or if dealing with a pediatric case, working with national nonprofits for support (Gabby's Love Foundation - http://www.GabbysLove.org). These nonprofits can be a strong foundation to start with. Research online may yield limited, or mixed results; however, working with these bleeding disorder nonprofits can provide a ton of useful data, advocacy, and often times support in several ways.

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