Project FAVA (@projectfava) 's Twitter Profile
Project FAVA

@projectfava

Project FAVA: nonprofit working to drive medical research to treat the painful fibro adipose vascular anomaly, a rare disease connected to the PIK3CA mutation.

ID: 1148059502442418177

linkhttp://www.projectfava.org calendar_today08-07-2019 02:41:30

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National Organization for Rare Disorders (NORD) (@rarediseases) 's Twitter Profile Photo

NORD is proud to announce the launch of the COVID-19 Critical Relief Program for #raredisease community impacted by #COVID19. The program supports patients & families facing financial challenges & helps with essential non-medical expenses. Read more: rarediseases.org/nord-launches-…

Project FAVA (@projectfava) 's Twitter Profile Photo

proserarediseaseday.kudoboard.com/boards/virtual… #RareDiseaseDay love for those living with FAVA and other PROS conditions

Guillaume Canaud (MD, PhD) (@canaudlab) 's Twitter Profile Photo

Fantastic news today for patients with PIK3CA related disorders (PROS)! Alpelisib obtained FDA approval. This is for us a fantastic achievement. We started in 2016, identified alpelisib (BYL719) has a promising compound and developed a mouse model. 1/n fda.gov/drugs/resource…