Have an idea for a way VCF can help? Let us know! This is YOUR Foundation, Community Members will shape and guide its future. But only if you tell us what will help. If you find a resource to help families living with Type 3 VWD, send it our way so we can share it on the website. Have an idea for an educational event? Let’s see if we can make it happen! Are you a fundraising guru? We could use your skills! Together we can make a difference in the lives of those living with Type 3 VWD.
Traveling with a bleeding disorder takes some planning! Check out National Hemophilia Foundation’s tips for travel.
If you ask me, it’s dealing with emergency rooms. The thought of having to go to an ER and explaining about VWD makes my skin crawl! What about you? If you had to pick from the following, which is the hardest to deal with having Type 3 VWD?