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Andyrdj said:
I know alcohol is the one that is the main problem with ACT - the most excessive mech boozer I've heard of so far(friend of my dad's) has something like 2 pints of beer in a session.
Lets hope he never has a gastro bleed!
 
well...

well...

... I didn't want to mention Gastro bleeds for fear of sounding as if I'm scaremongering. But I'll ask the ACT regulars here for their knowledge.

I do suffer from stomach troubles here and there (too much rich food and drink in my life, which is why my girlfriend wants me to try a week of vegetarian food).

This sort of internal bleeding stuff - under what circumstances is it likely to happen?

I assume for a non ACT patient there are sometimes internal bleeding events - how much is it aggravated by ACT?
 
The heck of it is, you just never know. If you have ulcers, there is a fairly strong chance of one bleeding and if your anticoagulated, that bleed could be dangerous. Ulcers are so unpredictable though. I had one for years and didn't know it.
 
Facing genuine concerns

Facing genuine concerns

How did you find out, Ross? And how were you treated?

Ok, so here we come to an interesting point.
- Given what Ross said, and..
- When Geebee said that she didn't compromise her life in any way...

I suspect it was facilitated by a generally healthy lifestyle on her behalf? That she possibly wasn't in the Ulcer risk group?

Perhaps ACT changes you the least if you already live a healthy life - although small changes to Vit K content in salad may be needed, or you adjust the ACT dose.

I often suffer from indigestion and have partied very hard in the past. I would speculate, therefore, that my ulcer risk is higher than the average population.

So ACT for me would mean

1. A more considerable curtailing of my "activities"

2. A higher risk of adverse bleeding incidents.

Am I right?
 
While I was in my coma from my aneurysm bursting, they scoped my stomach and found an ulcer with a blood clot on top of it. I had a high stress job, didn't eat well, partied alot more then I ever should have and it all equated into a major health breakdown.

I still drink on occasion, but I'm not downing the fifth of rum a day that I used to do and I eat a little better now. You might say, I learned my lesson well and I was not on Coumadin at that time. I was placed on Coumadin for what they thought was a blood clot in the apex of my heart before VR surgery. It turned out to be a cyst on the pericardial wall and not a clot.

If your drinking and partying all that hearty, the drinks are going to kill you before warfarin does, but yes, your most likely in a higher risk category. I wouldn't say that I've curtailed anything, I'm just not stupid anymore.
 
ta ross

ta ross

Would you mind if I asked you, and other ACT types alike, what you would feel safe drinking in a single evening?
 
I have never had an ulcer but I do suffer from GERD so my doctor feels I am at risk for an ulcer due to the acid. I just don't do too much to create danger. As I have said, I do drink a couple times a week but never more than 2 or 3 glasses of wine (or the equivalent in other liquor). I also take low dose aspirin.
I would think more than a bottle of wine (or the equivalent in other alcohol) would be too much for someone on ACT. I have, on rare occasions, drank that much over an evening without issues. I would not, however, do so on a regular basis but that is just me. Others might feel differently. I do not like to feel out of control and too much alcohol has that effect on me.
Like I said, I just don't worry too much about things that might happen. I refuse to live my life that way.
 
I've seen in the last couple of days since I came back to reading this board, what I missed out on by not staying and debating my valve choice, or in my case ,lack of choice. I only knew that I didn't want to deal with blood thinners. I watched what my dad went thru being on them after having lung cancer and being on them. I don't think there is a right or wrong choice and everyone is entitled to their opinion and choice. I have seen that this board is frequented more by mechanical valvers than tissue valvers. I appreciate all the information I've received. I guess I feel lucky I haven't had to deal with it everyday. I haven't experienced depression(more than normal) about having had someone digging around in my chest and changing out parts. I know, or expect to have to have another surgery somewhere down the road. I'll deal with it when it comes. For me, I'm glad I have the valve I have. I think that Andy is going to be happy with his choice. I didn't know until he told me that the TFX is the state of the art tissue valve.
 

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