Acquired Von Willebrand syndrome

Posted by mtevcm @mtevcm, Feb 16, 2023

I was recently diagnosed with Acquired Von Willebrand syndrome. I went to the hematologist initially because I was seriously concerned about massive bruising I was getting. Now, she has done tons of bloodwork. I've been tested for blood cancers and autoimmune disorders, as well as CAT scanned to see if there were tumors in my chest or abdomen. Nothing. I have other symptoms too, including late onset seizures and unexplained all over body itching, as well as joint swelling. Please help. I am also looking to get a second opinion.

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Hello @mtevcm Acquired Von Willebrand Syndrome is relatively rare. It helps to know you’re not alone so I’m happy to welcome you to Mayo Connect where I was able to find two other members associated with this condition in our forum. @koryw208, who has AVWS and @susanellis, whose daughter has this syndrome. They may be able to share some insights with you.

This conversation ~High Platelets~ is where @koryw208 discusses her experience.
https://connect.mayoclinic.org/discussion/high-platelets/?pg=6#comment-792936
There are quite a few replies with @susanellis in this discussion regarding,
High platelet count: What does this mean?
https://connect.mayoclinic.org/comment/251998/

Since this is such a rare condition, I’d encourage you to get that second opinion at a larger teaching institution such as Mayo Clinic. Mayo has 3 campuses in the US, Rochester, Mn, Jacksonville, FL and Phoenix/Scottsdale AZ.

Click on this link to lead you to the Mayo Clinic main page. You’ll find numbers for the campus most convenient for you. An appointment request starts with a simple phone call.
http://mayocl.in/1mtmR63

Are you currently on any treatments?

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@loribmt

Hello @mtevcm Acquired Von Willebrand Syndrome is relatively rare. It helps to know you’re not alone so I’m happy to welcome you to Mayo Connect where I was able to find two other members associated with this condition in our forum. @koryw208, who has AVWS and @susanellis, whose daughter has this syndrome. They may be able to share some insights with you.

This conversation ~High Platelets~ is where @koryw208 discusses her experience.
https://connect.mayoclinic.org/discussion/high-platelets/?pg=6#comment-792936
There are quite a few replies with @susanellis in this discussion regarding,
High platelet count: What does this mean?
https://connect.mayoclinic.org/comment/251998/

Since this is such a rare condition, I’d encourage you to get that second opinion at a larger teaching institution such as Mayo Clinic. Mayo has 3 campuses in the US, Rochester, Mn, Jacksonville, FL and Phoenix/Scottsdale AZ.

Click on this link to lead you to the Mayo Clinic main page. You’ll find numbers for the campus most convenient for you. An appointment request starts with a simple phone call.
http://mayocl.in/1mtmR63

Are you currently on any treatments?

Jump to this post

No treatments. I am interested in learning the underlying cause and to find out if I should be seriously concerned.

REPLY
@mtevcm

No treatments. I am interested in learning the underlying cause and to find out if I should be seriously concerned.

Jump to this post

Anytime you have a blood condition it should be taken seriously. From everything I’m reading about AVWS it can be complicated to diagnose, as you’re already finding out.
Acquired Von Willebrand Syndrome is usually associated with an underlying disorder and it looks like your doctor has been trying to determine the cause.
I found a good article that was quite informational on AVWS. Hopefully it gives you some insight.

https://ashpublications.org/blood/article/117/25/6777/24352/How-I-treat-the-acquired-von-Willebrand-syndrome

I really think your idea of the second opinion is a very sound.
Again, as in my earlier post, I’d suggest getting a consult with Mayo Clinic (all the info is in the previous post) a teaching college or larger medical facility near you. It would be worth the further investigation.

REPLY
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