It Took Me Weeks to Come to Terms With My Diagnosis: Sharon’s Story

…week before the pulmonary emboli. I also found out through testing that I have the prothrombin factor II mutation heterozygous. I have learned a lot from this experience. I have…

UPDATE – Thrombosis Has Deeply Impacted My Family: Gerry’s Story

…relatives had the same SERPINC1 mutation and whether there was a correlation of the gene mutation and the occurrence of thrombosis. All key family members were tested in spring 2023….

To Test or Not to Test: Perspectives on Guidelines Opposing Routine Testing Under Certain Circumstances

The Evaluation of Genomic Applications in Practice and Prevention …

Thrombophilia Resources

…Deficiency & Protein C Deficiency Resources …

Surviving a Silent Killer: Lisa’s Story

…all came back negative. I finally went to a hematologist who did further testing, which revealed that I have MTHFR C677T and the Prothrombin G20210A mutations (heterozygous and homozygous). What…

A Combination of Missed Risk Factors: Gina’s Story

…blood thinner for six months and underwent testing for blood clotting disorders. I found out that I have prothrombin G20210A, or Factor II Mutation, a genetic condition that causes an…

Waiting Could Cost You Your Life: Helen’s Story

…will be on them indefinitely. After following up with a hematologist, I learned that my family has Prothrombin Gene Mutation (Factor II) (a genetic clotting condition). The doctor believes it…

I Had to Figure Everything Out on My Own: Sue’s Story

…that my 23 and Me DNA results showed I have the factor II mutation aka the prothrombin gene mutation. I was tested in the hospital and these results were confirmed….