Anyone out there with Behçet's and vasculitis?
Firstly, if you're on the receiving end of a lot of medical gaslighting, keep searching. It took me 6 years to finally get to a rheumatologist who would run an HLA-B51 antigen test.
Secondly, anyone out there with Behçet's? What are your main symptoms and what is working for you for treatment?
I have a 5 cm ascending aortic aneurysm. It looks like I have pulmonary artery hypertension as well. That artery is nearly aneurysmal. Wicked dry eyes! They are the worst. I've been in a bad flare up for weeks now. I have a massive number of contact allergies now. Basically, soap is out to get me. My ANA titer is 1:1280, speckled. Arthralgia, mouth sores, nasal lesions...
And it still took me getting my genome sequenced and finding a way to scan the file for pathogenic variants to get to that HLA-B51 antigen test.
I have no guarantee that this new rheumatologist will even act on what he now knows. So if anyone with Behçet's has a decent doctor, I'd love that info, too.
Interested in more discussions like this? Go to the Autoimmune Diseases Support Group.
I need to mention that antiphospholipid syndrome to my cardiovascular surgeon. I thought I'd been checked for that back when I first saw the cardiovascular surgeon. Turns out, I haven't. Thank you!