PAF – Patient Worthy

Patient Advocate Foundation Provides Co-Pay Relief for Rare Disease Patients

Post author:Trudy Horsting
Post published:February 21, 2019
Post category:Familial periodic paralysis Multiple Myeloma Myelodysplastic syndromes Rare Disease

What is the Patient Advocate Foundation? The Patient Advocate Foundation (PAF) is a non-profit, formed in 1994 that has one primary aim- eliminate the barriers to treatment too many patients…

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Cómo y por qué usted debe recibir dinero para la medicación HFHo

Post author:Patient Worthy Contributor
Post published:January 16, 2017
Post category:Homozygous Familial Hypercholesterolemia Rare Disease

Si usted o su ser querido está viviendo con hipercolesterolemia familiar homocigota (HFH), que va a estar encantados con esta noticia - y se lo merece, también! La Fundación Defensor…

The PAF is increasing its efforts to fund co-pays for those suffering from HoFH.

How and Why You Should Get Big Money for HoFH Medication

Post author:Alisha Stone
Post published:November 10, 2015
Post category:Homozygous Familial Hypercholesterolemia Rare Disease

If you or your loved one is living with homozygous familial hypercholesterolemia (HoFH), you’re going to be thrilled with this news--and you deserve it, too! The Patient Advocate Foundation (PAF) just announced on November 2nd,…

Patient Advocate Foundation Provides Co-Pay Relief for Rare Disease Patients

Cómo y por qué usted debe recibir dinero para la medicación HFHo

How and Why You Should Get Big Money for HoFH Medication

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