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Von Willebrand Disease (VWD) - Online Support Group

Welcome aboard, Kaysh from San Fran!

#1

@Kaysh

Hello there and welcome to Living With VWD! As someone who has experienced VWD symptoms for all these years, I’m sure you will have a lot of useful knowledge to offer our wonderful community community. I encourage you to start contributing to discussions around here and even making your own discussions topics! You can check out the “How to Use This Site” tab up top for some useful beginner tips.

I’m glad to hear that you have been able to avoid any serious complications for two whole decades - so hopefully your good fortune continues and also spreads to the rest of community!

Best wishes and let me know if you have any questions or concerns =)

#2

Yes, Thanks for your warm welcome Eisi_BFintern .Yup, i had too many complications in childhood with nosebleeds.BTW.I have type 3 vwd with no detectable von willibrands factor. I hope I run my luck for a long long time.

#3

The rest of us hope so as well - glad to have you aboard!