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.
We share the same journey – what makes daily life hardest for you?
Do any of you with VWD experience petechiae and fatigue?
Does anyone with Type 1 VWD wear a medical alert bracelet?