Early surgery: Can I get aortic aneurysm repair before it's 5.0?

I had a aortic arch/descending aortic aneurysm. I agree it is stressful knowing it is there. However, it’s also a blessing. Most of us probably had it for years and we’re not aware- once it is discovered it can be closely monitored and watched. Not knowing about them- we are unable to take precautions and alter our daily activities to avoid terrible events from occurring. With my aortic aneurysm I also found a larger subclavian aneurysm- I did have to have mine all repaired- but for the months I knew about them all I could think about was how fortunate I was that it was actually even discovered. Mine were probably there for years my doctors said- in that time I delivered 2 babies, worked a physically demanding job, basically lived my life where there were so many opportunities for something to happen. So when I found mine I just cried that it was found in time to repair. I was lucky to have been immediately referred to Mayo because my cardiologist was not comfortable treating me. I highly recommend if you feel your cardiologist is not taking your case seriously enough or really in any case- seek a second opinion. It’s your body your health and taking control of that can help you feel some kind of control over this. While there are different aneurysms and different recommendations it is is important to find a physician you trust and knows your case. I also wore a medical bracelet all the time until my repair to help me get care faster in case of an emergency- it just gave me a sense of comfort having it on. Little things like that helped me manage my fears. Best wishes to all!

@mermaid1 I hope this will create a link so you see my post below with questions directed to you, It's pretty far down, so if notified
I wrote please scroll. Thank you!

I can only speak for myself but I could not have waited if given a choice . Living not knowing when or if it might rupture would have been to scary knowing that if it ruptured I would only live approximately 15 minutes . Which is why it is referred to as a widow maker. I agree it is very important that you advise your children and siblings to be checked for aneurysms as it is generic.

Do you mean the friends who died (presumably from a burst aneurysm) had aneurysms below the recommended-for-surgery level?

Or even that they hadn't known they had an aneurysm at all? Why did you have the self-pay CT scan? Because you didn't trust your docs' measurements or because their testing intervals were too far apart to make you feel safe in your present measurements?

Not really pertinent, but a personal anecdote - my ex-husband just passed away two months ago from a burst aneurysm. In his case, he knew very well he was past medical recommendations (a reputable local hospital and the Cleveland Clinic. had told him he was in great danger owing to the size of his aneurysm, but he just didn't have the nerve - afraid he's die in surgery.) Finally, his wife ramped up the pressure and he returned to the Cleveland Clinic, which lined up surgery for two weeks after that date (I think they insisted he stop smoking for that period). Whatever, not far from the Clinic while returning home to wait, he collapsed while filling his tank with fuel.

Before this, I was ignorant about this condition - now I've read a good bit including this online conversation. I have tremendous sympathy for you sufferers. The surgery really is a terrifying "Damocles Sword" to have hanging over your heads - also pre-surgery, quality of life-limiting, to never know what activity level is safe.

I'm glad you can support each other here. Perhaps if he'd been a member, he could have been reassured enough to go through with surgery despite the risks. Also to quit smoking at least before the operation. My sons were of course told to be checked. Without such recommendations, how else do people get the diagnosis? It's not that common a condition.

I've been taking 80 mg a day of Valsartin for years. This week I started 12.5 mg of Metoprolol Tartrate twice a day. I don't really notice any difference but I'm going to track my hear rate and BP next week.

Thanks for the link on beta blockers. I’ll follow up with my Cardiologist to see if he recommends them.

I’m not on any of those meds. I planning to read the article while I’m on the plan later tonight. Just on our way to the airport. I’m a sponge for information so I’m sure it’ll be helpful. I’m pretty underwhelmed by my primary physician and the first Cardiologist I’ve met with though. No mention of Beta blockers , I had to suggest the follow up echocardiogram and ultrasound, and I made the suggestion to increase my bp meds. I understand they all want me to remain calm, but the only way that will happen is if I’m provided every slice of information available.

Did you gain any useful information from the Mayo article on beta-blockers, @dwander501? Are you currently taking that kind of BP med?

The next phase of my research is going to be natural things I can purchase to strengthen my blood vessels. I figure I’ll give it my best shot to prolong the inevitable surgery!

I have no family history of heart problems as best I can tell. I didn’t have an elevated bp until last August ‘20. I’m retiring in 45 days to decrease my stress also. Very much interested in learning more about whether I’d be a future candidate for the less invasive surgery Offered at Mayo.
Also, I have a Colonoscopy planned for 3/16. I’ve got to see if it’s safe for that procedure with my condition. Thanks so much.