This page posts your websites, blogsites, books, and radio interviews.

Niki shares her grief from losing her infant daughter who was born with factor X at her blospot: http://mommyduffy.blogspot.com


Marilyn has a website for her film called BAD BLOOD.  She also welcomes you to become a fan of BAD BLOOD on Facebook.

click this link===>BAD BLOOD


Linda, from Florida shares her blogsite called Fibrinogen Free, that tells about what it is like to have been diagnosed with congenital afibrinogenemia. 

click this link===> Fibrinogen Free


Andrea, from The Philippines has a blogsite about her daughter, Star
click this link===> www.fortheloveofstar.blogspot.com



Rosamund, from Kidderminster, Worcestershire UK
A blogsite called FunnyBlood about life with vWD
click this link ===> FunnyBlood


Ryanne from Calgary, Canada has created a blogsite. 
click this link ==> Hemophilia is for Girls


A friend of Kathy from Kent, Washington has created a website for Kathy's daughter.
click this link ===> Helping Hannah


Laura has a website for those with vWD and other ....
click this link ===> Von Willebrands Disease ......YES it is real

Josephine and Patrick have a website:
www.havingvonwillebrands.org


Cheryl, from the Pacific Northwest writes about her stepdaughters who are born with severe factor V deficiency in a book titled Pooling Blood.
for book info, click this link===> www.poolingblood.com

Also, listen to Cheryl's iUniverse radio interview about her book (click, download and turn on your speakers):
for radio interview, click this link===> radio interview