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 live a very normal life. I can do whatever I want. I add a note to review with my doctor every year for my physical. The doctor that treated me said to check every five years. Do whatever your doctor suggests.
I have been diagnosed with a fusiform aneurysmal dilation of the celiac artery 1.8 cm x 1.4 cm just below its origin on Oct 28 2021 . The VA is my primary and they can not take the case so they are looking outside the VA . I have no pain or symptoms. They found it doing a CT scan for my heart and chest arteries. The only other case beside yours is a 30 year old male with 3 gunshot wounds to his abdomen. They are supposed to be formed by trauma . I had a bad accident 34 years ago and had trauma to my kidneys and broke my left femur. How was your 2019 test . Did the doctor tell you what activities you can do or not do ?
I was diagnosed with a Fusiform Celiac Artery Aneurysm Oct 28 2021 from a CT scan that was to check out my heart and arteries . It is 1.8 x1.5 cm . With no symptoms. The only trauma I have had was a car wreck 34 years ago that was very bad.
I’m 62 years old in good shape and the VA here in Hampton VA is my Primary Care sines I have retired, the VA here can not help me because it is so rare. I have read all these post from being to end and have only seen 1 post about a Fusiform Celiac Aneurysm on this group. I’m sure when the VA clinic finds me a Vascular Doctor it will be a wait and see as well. But I agree, to be so rare there are a lot of post on this site . So if there is anyone on here that has been diagnosed with a Fusiform Celiac Artery Aneurysm I would like to talk with you. The only post I saw I think was in 2019 on this group.
Before the diagnosis I was walking on the beach a lot , riding my bike, playing golf , and other wise doing what I wanted to.
Today marks three years since I had my celiac aneurysm surgery. Unfortunately they were unable to stop the blood flow even with the stents and coils they did so we continue to monitor it. unfortunately the aneurysm grew a little on the last visit but it seems the blood flow and pressure is not as big a concern as it was prior to the surgery. Best of luck to all. If we are here writing we are the fortunate.
Hi! My husband Greg was diagnosed last August with a celiac trunk aneurysm of 1.2 in size that has shown growth from previous scans. He has a lot of esophageal pain and difficulty swallowing so it is hard to determine where his pain is coming from. He is in the “watch and see” phase now but recently also having a weird “shocking or twinge type pain in his lower right rib cage area” - any connection?
Hello @auntbrenda44
I've been thinking about you. I hope you are recovering well from your surgery last Friday. When you feel up to it, will you please post an update?
I will definitely pray for you, @auntbrenda44.
Dear Teresa, thank you very much for your kindness. I welcome and am grateful for prayers. Blessings to you.
@auntbrenda44,
I'm so glad that you felt comfortable enough to make a decision.
Thank you for letting me know. I'll be thinking of you on Friday and I'd be happy to pray for you if that is OK with you.
Hi Teresa. My surgery is scheduled for this Friday. It will be an open repair. Thank you for your encouragement and comforting thoughts. I sincerely appreciate it.