PFS Foundation News

PFS Awareness Hops the Alps into Italy

Aug. 17, 2019 Dear Friends: The Boot has begun kicking Propecia. Last week, Italian health and lifestyle magazine Starbene, which boasts a weekly circulation of 350,000, ran a story on PFS that begins: The entire world, including Italy, is experiencing a tragedy that requires our attention. It’s that of men, often young, who in hopes […]

2019 PFS Foundation Annual Address

Aug. 4, 2019 Dear Friends: Irrefutable. It’s a word we’re aiming to make synonymous with PFS by August 2022, when this foundation turns 10. That leaves us just 41 months. But if recent activity on the research and regulatory fronts are any indication—to say nothing of the surge in efforts by patients and their loved […]

Epigenetic Modifications Do Occur in PFS Patients, New Research Demonstrates

July 20, 2019 Dear Friends: Phase III of the PFS Foundation-sponsored research at the University of Milano (UniMi), which was designed to “study whether epigenetic modifications occur in PFS patients,” has successfully demonstrated epigenetic modifications in PFS patients. Titled Altered methylation pattern of the SRD5A2 gene in cerebrospinal fluid of post-Finasteride patients, the pilot study […]

Germany Joins French Defiance of Finasteride

May 30, 2019 Dear Friends: If PFS awareness is what it takes to unite Germany and France, so be it. Last week brought a slew of media coverage out of Deutschland that closely mirrors what we saw a month earlier in the French Republic. The awareness assault began May 21 with a report on the […]

PFS Awareness Unfurling at a Furious Pace in France

April 29, 2019 Dear Friends: The French are not fond of finasteride. March brought a barrage of media coverage in the nation’s escalating efforts to warn citizens against the medication’s potential dangers. On the broadcast front, three network news programs highlighted the suffering of PFS patients. In a segment on the France 5 program Allo […]

New Spanish-Language Website Ups Our Potential Readership by 500+ Million

April 11, 2019 Dear Friends: Today marks yet another milestone in PFS awareness: Spanish speakers across the globe can now read all about the condition—aka “síndrome post-finasterida” (SPF)—in their native tongue. To access our Spanish-language content, simply click the Spanish flag aside the search box at the top of any pfsfoundation.org page. To toggle back […]

PFS is Front-page News in the Netherlands

February 25, 2019 Dear Friends: PFS awareness is fanning out across Europe faster than a leaky dyke. The latest nation to take up our charge is the Netherlands, via its second-largest newspaper, De Volkskrant, which boasts a daily circulation of more than 250,000. In a 2,600-word story that ran last week, reporter Irene de Zwaan […]