Aortic Aneurysms – Introduce yourself & meet others

Welcome to the Aortic Aneurysms group on Mayo Clinic Connect.

An aortic aneurysm is a bulge in the wall of the aorta. The aorta begins deep in the heart as it emerges from the powerful left ventricle, gently arching over the heart, descending into the chest, and finally into the abdomen. Some aortic aneurysms can be harmless; others can lead to catastrophic problems. I invite you to follow this group and connect with others, share experiences, exchange useful information, and learn about aortic aneurysms.

Get started rby clicking the +FOLLOW icon on the group page here: https://connect.mayoclinic.org/group/aneurysms/

There are some great conversations going on right now that I think you’ll like. Grab a cup of tea, or beverage of your choice, and lets chat. Why not start by introducing yourself?

Interested in more discussions like this? Go to the Aortic Aneurysms Support Group.

Profile picture for houston13 @houston13

@teresalee Hi Teresa, it is normal to feel stressed by this whole situation, every one in this forum has gone through the same feelings. The good news is that you found you have an aneurysm before it became an emergency, there are plenty of stories of people that have dissected and had to have emergency surgery in this forum and those are the few that survived.

You can monitor and plan, you seem to have the right care, a surgeon who is following you periodically and a cardiologist. At 4.7 cm your aneurysm is on the large side and seems to be growing so surgery is probably more a when than an if.

Take care of your body, keep yourself active, stay in shape without straining too much, avoid lifting that would cause you to hold your breath as BP spikes significantly during those moments. BP is the most critical element to control, your cardiologist should be helping you ensure you maintain it within your normal limits, high BP is the worst enemy of aneurysms even for short periods. Lastly try to keep calm (stress doesn’t help BP) you are doing everything right,, find activities that bring you joy and help you relax.

I had a 5.2 cm aneurysm repaired and also a bicuspid valve. The valve was left in place as it was highly functional, I get it monitored every year and at some point it will need replacement. In your case with symptoms of the stenosis already is likely they will replace it at the time of the repair.

The risks are highly related to your general physical health and whether you have other health issues. I was in very good shape and the surgery went as smooth as it could have gone, it is tough but I was out of the hospital in 5 days back to work in 3 weeks. Everyone different though.

Take care and stay calm (easier said I know) you are doing the right things.

All the best

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@houston13 thank you for the advice. these are things I did not know. I was only told to lose a little more weight ( I am 5 foot 2 and 73kg so do need to lose around 20kg) and to keep my blood pressure down. Now reading about others experiences makes me feel less alone. I am so grateful I found this group.

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Hi Teresa! First, take a breath. What you are feeling is completely understandable, and nothing about your reaction means you missed something or should have known more. You were told pieces of information over time without the full picture being put together for you, and that is disorienting for anyone. You did exactly what a thoughtful patient does. You listened to your doctors, followed up, went to your appointments, and when something didn’t make sense, you went looking for reliable information. Finding Mayo Clinic and learning the word aneurysm on your own is not a failure on your part—it is a gap in communication that happens far too often with aortic patients.

A 47 mm thoracic aortic aneurysm in the setting of a bicuspid valve is something that absolutely deserves close monitoring, and your concern about the growth rate is reasonable. The stress you’re feeling often comes less from the number itself and more from not knowing what it means for your future, your safety, and your day-to-day life. Uncertainty is the hardest part. Your job right now is to REDUCE your stress. Posting here will help with anxiety and most posts get responded to pretty fast. @houston13

Here are the most important things to anchor to right now. Knowledge is power. Stay very close to a major medical center that has a dedicated thoracic aortic specialist department, not just general cardiology. Meet your thoracic surgeon now, not the morning of surgery someday. Even if surgery is not imminent, that relationship matters. You deserve time to ask questions, understand thresholds, and know what the plan is long before decisions become urgent.

You are not behind. You are not late. You are not being dramatic. You are learning about a condition that most people only hear about when something goes wrong, and you are doing it in a controlled, proactive way. For a bit of perspective: I survived an acute Type A aortic dissection in 2015 and emergency open-heart surgery. I learned the hard way how critical it is to understand your aorta, your numbers, and your care team before a crisis. The fact that you know now means you have power, options, and time.

You are doing the right things. Keep learning, keep asking, and make sure you are surrounded by specialists who do this every day. You're going to be fine. Peace.

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Profile picture for teresalee @teresalee

Hi, my name is Teresa and I am actually from Australia. Whenever I need to know anything medical I always look up Mayo clinic.
Around 8 years ago I went to the doctor with chest pain, shortness of breath, after a few tests I was diagnosed with bicuspid valve with mild stenosis. I started seeing my cardiologist every 2 years and just before Christmas this year I went for my usual stress test etc and had an abnormal test so had a ct scan, I followed up with my cardiologist a week later and he told me that my aorta was much bigger and he was referring me to a surgeon. I was confused and felt that any question would sound dumb (I thought I should have known what a large aorta meant) that’s when I asked the question on google and the Mayo clinic gave me the answer, I had an aortic aneurysm. so the surgeon called and got me in within a week. This stressed me, he explained to me that I had a 47mm thoracic aortic aneurysm and that he would have to keep a close eye on me. So I am scheduled to have a follow up ct in November 2026. The growth of my aneurysm I was told is faster than normal as it went from 44mm to 47mm in 2 years.
I feel like I have not been well informed because the first time I heard someone tell me I had an aneurysm was just a couple of months ago and I didn’t and still don’t know what questions to ask or what to do with this shock information. I have been very stressed about it.

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@teresalee Hi Teresa, it is normal to feel stressed by this whole situation, every one in this forum has gone through the same feelings. The good news is that you found you have an aneurysm before it became an emergency, there are plenty of stories of people that have dissected and had to have emergency surgery in this forum and those are the few that survived.

You can monitor and plan, you seem to have the right care, a surgeon who is following you periodically and a cardiologist. At 4.7 cm your aneurysm is on the large side and seems to be growing so surgery is probably more a when than an if.

Take care of your body, keep yourself active, stay in shape without straining too much, avoid lifting that would cause you to hold your breath as BP spikes significantly during those moments. BP is the most critical element to control, your cardiologist should be helping you ensure you maintain it within your normal limits, high BP is the worst enemy of aneurysms even for short periods. Lastly try to keep calm (stress doesn’t help BP) you are doing everything right,, find activities that bring you joy and help you relax.

I had a 5.2 cm aneurysm repaired and also a bicuspid valve. The valve was left in place as it was highly functional, I get it monitored every year and at some point it will need replacement. In your case with symptoms of the stenosis already is likely they will replace it at the time of the repair.

The risks are highly related to your general physical health and whether you have other health issues. I was in very good shape and the surgery went as smooth as it could have gone, it is tough but I was out of the hospital in 5 days back to work in 3 weeks. Everyone different though.

Take care and stay calm (easier said I know) you are doing the right things.

All the best

REPLY

Hi, my name is Teresa and I am actually from Australia. Whenever I need to know anything medical I always look up Mayo clinic.
Around 8 years ago I went to the doctor with chest pain, shortness of breath, after a few tests I was diagnosed with bicuspid valve with mild stenosis. I started seeing my cardiologist every 2 years and just before Christmas this year I went for my usual stress test etc and had an abnormal test so had a ct scan, I followed up with my cardiologist a week later and he told me that my aorta was much bigger and he was referring me to a surgeon. I was confused and felt that any question would sound dumb (I thought I should have known what a large aorta meant) that’s when I asked the question on google and the Mayo clinic gave me the answer, I had an aortic aneurysm. so the surgeon called and got me in within a week. This stressed me, he explained to me that I had a 47mm thoracic aortic aneurysm and that he would have to keep a close eye on me. So I am scheduled to have a follow up ct in November 2026. The growth of my aneurysm I was told is faster than normal as it went from 44mm to 47mm in 2 years.
I feel like I have not been well informed because the first time I heard someone tell me I had an aneurysm was just a couple of months ago and I didn’t and still don’t know what questions to ask or what to do with this shock information. I have been very stressed about it.

REPLY
Profile picture for caroline58 @caroline58

@davidneal
I have fibromuscular dysplasia in the cerebral artery and carotid arteries and some in the spine, we get aneurysms and dissections. I work as a nurse.
We should not lift weights at all and not run because it increases blood flow in the arteries, from the heart to the femoral arteries it is not a long way. So I do nothing like that, long walks are my exercise.

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@caroline58
Thanks very much for your reply. I will be talking to my GP and others about appropriate exercise, but the message certainly seems clear to reduce straining, weights, running, and anything else that spikes blood pressure. I am hoping that swimming (freestyle) will also be OK, as I live near the sea.

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Profile picture for davidneal @davidneal

Hi everyone,
My name is David and I am 70 years old and was diagnosed in mid 2024 with aneurysms in both my left and right Common Iliac Arteries. It seems that these sort of aneurysms are less common and most discussion is around aortic aneurysms (understandable, as that's the name of the group!). My left CIA aneurysm seems to be expanding quite rapidly which is concerning:

Right CIA Left CIA

mid 2024 16mm 17mm
Jan 2026. 17.3mm 23mm

My wife and I have looked at our lifestyle changes during the specific period when the most rapid growth occurred and feel that some of the exercises and other things I do may have been contributing factors:
- body pump classes (not heavy weights, only up to 12 kg total weights - especially squats, weighted hip raises, overhead weight moves)
- mat pilates - Russian twists with weight, planks, pushups etc
- some heavy gardening - removing tree stumps etc
- not controlling my breathing when doing the above, and sometimes probably unwittingly holding my breath during the lifting/straining move
- saunas
- we drink about 10 units of alcohol per week.

I will be making some changes/reductions in the above areas, but would also welcome any other thoughts on lifestyle changes and other measures (apart from surgery!) that may assist in slowing the growth rate of the aneurysms. Also is there anyone else on this chat with common iliac artery aneurysms. Thanks.

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@davidneal
I have fibromuscular dysplasia in the cerebral artery and carotid arteries and some in the spine, we get aneurysms and dissections. I work as a nurse.
We should not lift weights at all and not run because it increases blood flow in the arteries, from the heart to the femoral arteries it is not a long way. So I do nothing like that, long walks are my exercise.

REPLY

Hi everyone,
I am a retired science/health teacher, age 69, female, 5'11, 225#.

I was diagnosed with a 4.6cm ascending aortic aneurysm in 2016 and have been monitoring it yearly since then. (It is interesting how the measurement can vary by facility/equipment/radiologist. I have been measured as low as 4.3 and as high as 5.3.) I went to the Mayo Clinic in Rochester in October and met with a cardiologist in their Aortic Clinic. After all the tests, the latest measurement is 5.3 at the root and 4.2 ascending. My aortic valve has moderate regurgitation, most likely from the dilated aortic root pulling on it. This alone is probably not enough for surgery. But, I also have 8 points on the Ghent scale for Marfan Syndrome, even though I don't have a known genetic mutation for Marfan. There is a familial link as my brother had a similar aortic graft, then TAVR in TAVR, and pacemaker. All these things together make me a candidate for surgery at this time.

My surgery is scheduled for April at the Mayo Clinic. The plan is to replace the aortic valve with a tissue valve and a Dacron graft from the root up to the arch. I am comfortable with the idea of surgery, especially when the alternative might be a possible dissection. I know it is better to do this at age 69 rather than 5 or 10 years from now. I am somewhat concerned about the recovery: cardiopulmonary bypass dementia, sternotomy pain, movement in daily life with a sternotomy, recovery time, etc. (I'm one of those people who needs to be prepared for anything, and if it doesn't happen, great.)

My local cardiologists added Amlodipine and increased my Metoprolol prior to the upcoming surgery.
So, for the next 75 days, I will be learning as much as I can, losing weight, walking, and managing stress. The stress part is hard as I am also helping to care for my Mom (91) and Dad (96) who have health issues.

Five generations of my family have been Mayo patients. I know the expertise and care there are world-class.

Any information and advice are welcome. Thank you.

REPLY

Hi everyone,
My name is David and I am 70 years old and was diagnosed in mid 2024 with aneurysms in both my left and right Common Iliac Arteries. It seems that these sort of aneurysms are less common and most discussion is around aortic aneurysms (understandable, as that's the name of the group!). My left CIA aneurysm seems to be expanding quite rapidly which is concerning:

Right CIA Left CIA

mid 2024 16mm 17mm
Jan 2026. 17.3mm 23mm

My wife and I have looked at our lifestyle changes during the specific period when the most rapid growth occurred and feel that some of the exercises and other things I do may have been contributing factors:
- body pump classes (not heavy weights, only up to 12 kg total weights - especially squats, weighted hip raises, overhead weight moves)
- mat pilates - Russian twists with weight, planks, pushups etc
- some heavy gardening - removing tree stumps etc
- not controlling my breathing when doing the above, and sometimes probably unwittingly holding my breath during the lifting/straining move
- saunas
- we drink about 10 units of alcohol per week.

I will be making some changes/reductions in the above areas, but would also welcome any other thoughts on lifestyle changes and other measures (apart from surgery!) that may assist in slowing the growth rate of the aneurysms. Also is there anyone else on this chat with common iliac artery aneurysms. Thanks.

REPLY
Profile picture for sarastewart @sarastewart

Hi Steve,

First, you want to find out how many centimeters your aneurysm is. Short people can’t wait as long as tall people. Tall people can wait sometimes all the way to 6.0. From reading everyone’s input in this support group it seems like 5.5 is about the average time we have until we need to undergo surgical intervention. For ascending aortic aneurysms, you need to know where exactly the aneurysm is located - an MRI or CT scan will tell your surgical cardiologists the answer. From what I’ve read, if it’s too close to the aortic root, you may not be a candidate for surgery. We’re talking open heart surgery at this point as the only option; however, they just did what I think was the first endovascular surgery on an ascending aortic aneurysm over in California at Stanford. The medical community is becoming more and more creative so we have lots of hope. Just get as thin as possible to make it easier for the medical community to help you. Stop smoking and start an exercise program under your cardiologist watchful eye. Many of us have lived for years, knowing we have an aneurysm. This is not fun but reality. God is in control. Sara💐

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Hi Sara,
I was told my ascending aorta is at 4.1 cm.
I'm 5'10". Never a smoker, 180 lbs.

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Profile picture for Teddy Elizabeth W @teddyebee

Hi all, thanks for being here, I'm really glad I found this group as my anxiety is up again about my descending thoracic aortic aneurysm. I've been all alone with this since 2007 and basically forgot about it after 2012 when they stopped scanning me, until September 2024 when I requested a scan before I headed out alone on an extended RV journey. Now I'm moving to Florida and really want to be evaluated at the Mayo in Jacksonville. What do I do next? Also, can anyone relate to my "watchful waiting" journey?

More on my journey: I was originally diagnosed in 2007 with a 2.9 cm "non-penetrating aortic dilation with multiple outpouchings." In 2012, my then cardiologist said it was stable and no reason to scan me ever again, unless I became symptomatic, which I may have been a couple of times, but scans were negative and determined to be panic/anxiety (gee, I wonder why??). In 2013, I was also diagnosed with an undifferentiated connective tissue disorder, which my mom and her grandfather also had. I've never had any follow up on that diagnosis. Then in September 2024 before I headed out on an extended RV journey alone, I requested a scan, and my cardiologist of two years flipped out when she saw the results. She referred me to vascular surgery and surgeon says noooo, we don't do stent grafts for a 4.1 cm aorta with penetrating ulcer with pseudo aneurysmal components, come back in six months for another chest CT, which I did a couple weeks ago. Now the largest transverse diameter of my proximal descending thoracic aorta has grown from 4.1 cm to 4.2 cm, and the PAU has grown from 1.6 x 1.7 cm to 1.8 x 2.0 cm. I'm really hoping I can get some better coordinated care and more complete evaluation at the Mayo in Florida and also feel more confident about my plan of care, especially any exercise limitations. My current surgeon says no limitations on exercise or anything, but I just read something on the Univ. Michigan website that says there's anecdotal evidence that playing tennis (one of my favorite activities) can increase the risk of dissection! I'm just feeling very confused and alone so yeah, hoping someone here can relate and have any suggestions. Thanks!

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Hi Teddy;
You have already made a good move from the Doc who said noooo to the stent grafts. Except that 4.2 cm is not near the 5.5 cm that is generally accepted as the dia. at which to consider surgery. For example I have double aorta ascending aneurysms (4.2 & 4.5 cm) and at the accepted growth rate of 1/3rd cm per year, I have 3 years before I need to consider surgery. Now, I would trade my situation for yours any day for the following reason: Ascending aneurysms require OPEN HEART SURGERY with all of its attending problems, ie recovery etc. But Descending aneurysms can be repaired via minimally invasive incision in the groin where a tiny tube is inserted through blood vessels to reach the aneurysm where a stent is placed. Never gets too close to the heart itself. So, find a specialist to explain the procedure which should make your anxiety much more tolerable.
Mayo Clinic, Cleveland Clinic and others have been doing this procedure with much success,. So go out and enjoy your RV journey.

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