Celiac Artery Aneurysm: Anyone else with same illness?
Hello! I was recently diagnosis with a celiac artery aneurysm in June 2016. I underwent a embolization w/ coils procedure since the aneurysm had grown while in the hospital. I was trying to reach out to someone who suffered the same illness but have not been lucky. I would like to locate someone with my same illness. I would appreciate any help. Thank you
Interested in more discussions like this? Go to the Aortic Aneurysms Support Group.
I recently had a abdominal CT to check on a hernia, but they found a celiac artery aneurysm measuring 11 mm. I have an appointment with a vascular surgeon this week, but my husband & I want me to have surgery for this, although the aneurysm is not very large.I don't even know if he has ever performed this kind of resection before. We live 3 hours from Dallas & may decide to have a surgeon there do the operation. Any advise would be helpful.
Hi .... Ive had 2 ultrasounds 3 ekgs and 4 cat scans in the past 2 weeks . theyve mentioned disc degenerative to me for my lower back and this aneurysm but nothing else . I do have viens that stick out in my arms and another parts .. Idk this is very depressing
Thank you for sharing your experience @marylisa !
Very curious if they ever spoke the words Fibromuscular Dysplasia or Ehlers Danlos to you? I also have frail arteries and have those diagnoses.
@bobrush welcome to Mayo Clinic Connect... the journey is a long one with MALS and can be overwhelming. This is a wonderful group and you will get a variety of experiences that I believe will be helpful in your journey. Have you had a GI work up yet? What symptoms have you been experiencing? I have been navigating MALS for quite sometime and will try my best to support you. Understand the frustration and depression that comes along with this. You are not alone. Thinking of you.
Hello I'm 42 and was just told I have this as well. I cant work at my normal job because its all heavy lifting. I cant even pick my little girl up anymore. It's extremely depressing . ive never been the type to let a little pain keep me down but I'm speachless after hearing I have this... Like others I go back in 2 weeks for another cat scan... I just dont know what to say anymore
I too am being followed at this point every six months. 1.3 celiac artery aneurysm, but also a dissecting mesenteric artery. all of this is scary and there seems to be so little reassurance from the docs. When I asked if I am safe to travel my vascular surgeon stated I should stay close to home re insurance. This makes me a little more nervous that something can go wrong but there has been no advice as to what they can do to repair or stabilize these conditions.Like many of you express there seems to be no cause for this.
I have been diagnosed with a celiac artery aneurysm. I had a stent put it my celiac artery 3 weeks ago. I have a lot of genetic testing and everything came back negative. My artery is thinning and I am worried about long term effects. How are you feeling? I feel so much better since I received the stent. I did have complications from the surgery my bronchial artery ruptured and I had to have emergency surgery to repair it. I would like to follow up with a specialist to find out why this happened to my celiac artery.
I have had my liver thoroughly checked out and all my other organs because its a bad place to have chronic pain. The tests showed nothing. My blood tests are good also but I will bring it up again when I see the vascular surgeon. Thanks for your response. Also, my pain use to be worse so I take that as a good sign. And I think I'll try to get an appointment at an internist.
It's been 2 years since diagnosed with 1.2 aneurysm. Just received my annual CT scan recheck and all is good. No growth. Luckily no other symptoms for this very rare condition. It's difficult at times not to think about it but I can't do anything about it anyway so just need to wait and watch.