Can anyone tell me about the drug Wilate used to treat VWD
I take It. It’s factor 8 and has less things in it to react to is what I was told. I don’t feel as sick after taking it. Not sure what else you wanna know about it.
my daughter has VWD and also has EDS hypermobility and was told that NAC would help her EDS yet I'm tyring to find out if it is safe to take
We share the same journey – what makes daily life hardest for you?
Does anyone with Type 1 VWD wear a medical alert bracelet?