Had a Heart Attack today at age ~30. Be safe guys.

Do you use an Ai with that dose?
I stopped using AI about 5 years ago and will never use them again
How are you getting this printout?
I do mine in Excel but this looks way cooler
Ah, that's from hospital mate!
Is primo one of the worst offenders when it comes to lipids?
I don't think so, but maybe I'm mistaken?

They did a 1968 study giving female breast cancer patients 1,200mg Primo / wk and that wasn't one of the acute sides mentioned
 

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I stopped using AI about 5 years ago and will never use them again

Ah, that's from hospital mate!

I don't think so, but maybe I'm mistaken?

They did a 1968 study giving female breast cancer patients 1,200mg Primo / wk and that wasn't one of the acute sides mentioned
What does your estrogen hover around when. You did 350 for that period
 
No sides with it getting up to 90?

No sides as far as I can tell -- I have gyno from when I was 17 and first started gear. (I kept upping Dbol dose until I was taking 100mg a day because I wasn't sure if it was "doing anything". </facepalm>)

So if my E2 gets too high, I can feel my nips burning + gyno growing, which I don't.

I have libido issues but it's been that way forever regardless of what I take. Pretty sure it's from years of drug addiction messing up my neurochemistry.

Also how was your HDL on the 19 bloofwork?
I wish I could tell you. I didn't check my lipids EVER when I was young, only started in the last few years =(
 
Well, it finally happened to me.

Near end of my workout today I start feeling chest tightness & pain, hard to breathe.
Go to emergency room, get told I'm having a heart attack (STEMi).

"A 99% subtotal blockage was found in the second obtuse marginal (OM2) branch of left circumflex (LCx) artery."

Likely from vulnerable plaque rupturing during the workout and the thrombosis that follows narrowing the artery.
Single-vessel disease, no other obstructive disease discovered during angiogram.

Code:
- Impression: Inferior ST elevation microinfarction with culprit lesion of second obtuse marginal 99 percent subtotal occlusion
- Successful imaging guided primary PCI of second obtuse marginal with 3 x 20 mm Synergy stent
- Normal LVEDP
- No aortic stenosis
- Recommendation
  - Start aspirin 81 mg daily for lifelong
  - Start Brilinta 90 mg twice a day for at least one year
  - Start high intensity statin therapy for goal of less than 55
  - Obtain echocardiogram
  - Cardiac rehabilitation referral

Summary of Echocardiogram w/ contrast performed afterwards:
Code:
- Mildly dilated left ventricle
- Moderate concentric LV hypertrophy
- Mildly reduced LV systolic function
- EF 45–50% (down from 55% post-op, plausible post-MI myocardial "stunning", expect recovery)
- Hypokinesis of inferoposterior wall
- Mild to moderately enlarged left atrium
- Mild to moderate mitral regurgitation
- Mild tricuspid regurgitation
- Mild pulmonic regurgitation

Stay safe, folks.
I am sorry for you but you didn't write anything about your lifestyle.

Maybe you run with high BP since a long time, maybe you eat tons of saturated fats.

Stay safe doesn't mean anything.
 
No sides as far as I can tell -- I have gyno from when I was 17 and first started gear. (I kept upping Dbol dose until I was taking 100mg a day because I wasn't sure if it was "doing anything". </facepalm>)
Were you then sure it "does something" when you had hit 100mg?

They did a 1968 study giving female breast cancer patients 1,200mg Primo / wk and that wasn't one of the acute sides mentioned
Those were the golden years for anabolics. They used them to treat anything. No matter what illness you had, doctors gave you a chance to get swole.

I wish that had never changed. Just imagine what kind of steroids we would have by now, had they poured GLP1-drug kind of money into researching them.
 
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Were you then sure it "does something" when you had hit 100mg?

Yeah, because I got gyno almost instantly LMAO

Went from no sides, not sure if it was fake sugar powder, to suddenly I wake up and my nips burning, hurting and itching

That's when I realized it was definitely dbol.

I wish that had never changed. Just imagine what kind of steroids we would have by now, had they poured GLP1-drug kind of money into researching them.

I didn't want to be sad this early in the morning.... =(
 
A genuine negative for calcification, but plaque, unless you've had sub 60 LDL your entire life, you have some degree of accumulation. During the Korean War the US started checking soldiers during autopsies, and for example, 85% of 22 year olds had established plaque, some even had arteriosclerosis!

Within a generation or two this disease will be extinct. You'll get a lifetime PCSK9 inhibitor, essentially a heart disease "vaccination" during childhood that'll neutralize PCSK9 for good and there won't be any accumulation of plaque.
Received my bloods back this week and have some relavant results attached. Running 250 Test, 150 Primo, 2.4 GH, 5 mg Tirz. A few interesting points including improvements from previous when running just 140 Test TRT. 40mg Atorvastatin year round.

I did find out this is too much Primo for this level of Test for me as my sensitive E2 came back at 16. Strangely no joint issues but stomach bloating that I believe I wrongly attributed to a virus but now believe it was the low E2
 

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Yeah, because I got gyno almost instantly LMAO
And there was me, when I was even a few years older, keeping my 2x5mg Dbol run to 5 weeks, because I was worried about my liver. When the general forum consensus was that 8 weeks are a safe length for such a cycle, obviously at higher doses than mine.

I didn't want to be sad this early in the morning.... =(
I haven't given up that there will not be an anabolic renaissance.
Just imagine cheap gene testing and AI designing afforable custom anabolics for every man.


PS: Thanks again for putting this all out there! There will be that one guy, that you will never know about, that you scared into being more more diligent with his health.
 
Received my bloods back this week and have some relavant results attached. Running 250 Test, 150 Primo, 2.4 GH, 5 mg Tirz. A few interesting points including improvements from previous when running just 140 Test TRT. 40mg Atorvastatin year round.

I did find out this is too much Primo for this level of Test for me as my sensitive E2 came back at 16. Strangely no joint issues but stomach bloating that I believe I wrongly attributed to a virus but now believe it was the low E2

Not bad man!

If you switch to Pitavastatin, you may see a 10+ point boost to HDL, a very clinically significant increase that would make plaque regression move at a good pace with your fairly low LDL. I saw an 11 point jump from 39 to 51 on 200mg Test. Unless you're on Atorvastatin due to kidney disease, Pita is superior.

 
Not bad man!

If you switch to Pitavastatin, you may see a 10+ point boost to HDL, a very clinically significant increase that would make plaque regression move at a good pace with your fairly low LDL. I saw an 11 point jump from 39 to 51 on 200mg Test. Unless you're on Atorvastatin due to kidney disease, Pita is superior.

I'm sure you've mentioned this in one of your many posts, but what HDL-promoting supps do you take personally (fish/krill oil, omega 3, dietary sources, niacinamide etc)?
 
Not bad man!

If you switch to Pitavastatin, you may see a 10+ point boost to HDL, a very clinically significant increase that would make plaque regression move at a good pace with your fairly low LDL. I saw an 11 point jump from 39 to 51 on 200mg Test. Unless you're on Atorvastatin due to kidney disease, Pita is superior.

your september cholesterol is my goal man.

im not on statins yet but with reta/cardio im on 45 hdl 60 ldl. trying to squeeze last bit of hdl up and ldl down before jumping on.
 
Not bad man!

If you switch to Pitavastatin, you may see a 10+ point boost to HDL, a very clinically significant increase that would make plaque regression move at a good pace with your fairly low LDL. I saw an 11 point jump from 39 to 51 on 200mg Test. Unless you're on Atorvastatin due to kidney disease, Pita is superior.

Thanks brother. I will give Pita a try as moving the needle on HDL has been really tough. BTW - I bought some Ezitimebe on your recommendation but after these bloods I'm wondering if I need it? Thoughts?
 
Thanks brother. I will give Pita a try as moving the needle on HDL has been really tough. BTW - I bought some Ezitimebe on your recommendation but after these bloods I'm wondering if I need it? Thoughts?

Ezetimibe is the most benign LDL reducing compound there is. Since it's "cost free", and there's a measurable benefit to getting LDL below 40 per the latest guidelines, I strongly recommend you use it. You're in or near plaque regression territory. Studies show lower LDL is the primary driver of regression. The sooner and faster regression takes place the "deeper" the cleaning of your arteries will be. The longer plaque remains the greater the amount that will harden and become unremovable,

The LDL drop from Ezetimebe isn't usually huge, but if you happen to be in the 15% of genetic "dietary cholesterol hyperabsorbers", it may be a very large reduction.
 
I'm sure you've mentioned this in one of your many posts, but what HDL-promoting supps do you take personally (fish/krill oil, omega 3, dietary sources, niacinamide etc)?


None. The latest ESC (Euro Society of Cardiology) lipid guidelines directly addressed this. The problem with HDL increases from supplements is that they don't increase production of APO-I. This is the protein that gives HDL its ability to remove cholesterol from arteries and transport it back to the liver. So what's happening is you're producing low or non-functional HDL. At best it's neutral, but giving a deceptive sense of being useful based on the HDL number, At worst, there's evidence non functional HDL becomes inflammatory.

Pitavastatin stimulates the production of APO-I, along with HDL. So Pitavastatin is producing functional HDL. In fact the boost to APO-I is likely improving the function of all your HDL.

The only other way to significantly increase APO-I is exercise.

After LDL, HDL function (efflux capacity), is the greatest factor determining how much regression of plaque is possible.

The reason for the "rush" is that once LDL is low enough that you're no longer depositing it in arteries, there's a limited window for regression before plaque stabilizes, which is good, but means it's no longer able to be removed. Removal is better than stabilization.

You can get it tested with Boston Heart Diagnostics HDL Map test if you're curious, $169.



 
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