jmendoza251g
New member
Carder1ne has about a 24 hour half life so you can dose all at once if you want. If you feel like spreading them out that is fine too
Thanks Yates , does everyone take them at once or is anyone spreading them out?
Carder1ne has about a 24 hour half life so you can dose all at once if you want. If you feel like spreading them out that is fine too
I have always dosed carderine 1 time a day, first thing in the morning. I'm sure other people dose it differently but I see no reason to do soThanks Yates , does everyone take them at once or is anyone spreading them out?
I have always dosed carderine 1 time a day, first thing in the morning. I'm sure other people dose it differently but I see no reason to do so
I have always dosed carderine 1 time a day, first thing in the morning. I'm sure other people dose it differently but I see no reason to do so
I guess you could move some of your dose closer to your workout. It should still have the same effect no matter how you dose it though, as long as it is dosed at least once edIf doing IF I feel spacing out may be more beneficial? To avoid hypo sides? Or just move the bolus dose closer to workout..?
If doing IF I feel spacing out may be more beneficial? To avoid hypo sides? Or just move the bolus dose closer to workout..?
Can OL GW be taken for 12 weeks @ 21mg daily?
in the human trials they ran it a 2.5mg, 5mg & 10mg per day for 12 weeks.
To my knowledge there hasn't been any human trials on GW has there?
Yes there has. But we only ever hear about the fact is causes cancer in rodents. Not to mention almost every study I've seen with rodents they gave them huge doseages for their body weight etc.
Yeah that part I know. Just wasn't aware on the human study. I knew about the rodents and monkeys but not this one. I got some reading to do
There definitely have been human studies done on carderine. It almost seems like big pharma gave up on carderine because of the chances of it being abused as a performance drug. I could be way off though
This. As it increases endurance by up to 45% (what I've read) it could be a grey are for marathon runners or sprinter... Well any sport really.
They studies it in rats, mice Rhesus Monkeys & humans.
Only the rats got cancer.
Human Studies
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There are 2 theories as to why GW research was discontinued...
Theory 1: Had something to to with WADA and this being used by athletes for performance enhancement.
The more likely reason...
Theory 2: GW was being research to help with Cholesterol levels. It had such a profound effect on both
lowering bad cholesterol and raising good Cholesterol, GSK (the manufacturer), decided to stop research
because this was just too effective. It had a permanent effect on cholesterol levels. Drug companies are
looking to drugs that people need to take the rest of their lives. This would have cut into profit margins of
other cholesterol drugs that they already sell, and people take daily forever.
To give you an example on this kind of thinking. Nightline or 20/20 (one of those nighttime reporting shows)
had a special on a while back about people contracting infectious bacterias, likestaph and MRSA while
staying in Hospitals around the country.
One of the reasons why these have got so out of hand these bacterias have gotten so out of hand, is that
research into new antibiotics has almost stopped. Most companies have no new antibiotics being researched.
The reason...?
Profit..!
Pharma companies are putting more money, and more research into drugs that people can take long term.
Drugs for Blood Pressure, Drugs for Cholesterol, Pain Management, Diabetes, and other life long illnesses.
The program went on to say that there is no money in Antibiotics, because people only take them for 7-10
days, and then they are done with them. These are drugs that cure an illness, not treat it.
So, the reality is, rather then putting the money into the research of drugs that can cure illness, they would
rather treat illnesses instead, because longterm treatment is more profitable, then shortterm cures.
^^this makes way too much sense
I would stack them, you will get better effect from the gw while on anabolics imo. I like gw in pct just for the fact that it helps regulate my bp, something I have struggled with in some of my past pct'sI am currently using Legend (LGD) and have an unopened bottle of Cardar1ne. Would it be better to start stacking the two and continue the GW through PCT or start the GW at the beginning of PCT and continue it solo four weeks post PCT?
I am currently using Legend (LGD) and have an unopened bottle of Cardar1ne. Would it be better to start stacking the two and continue the GW through PCT or start the GW at the beginning of PCT and continue it solo four weeks post PCT?
Ill be stacking mine in the second half of my cycle and through pct till it runs out
Cant wait ill be starting cycle of osta and mk677 next month then adding cardarine at week 4
That will be a nice stack there man.
Got my stuff sorted out... Going to wait til October to run cardar1ne since I'm slowly reverse dieting; I don't want to take it with less than 100g daily carbs. I'll be at 125-150g in October and still climbing so I figure thT will be the perfect time to throw it in to this stack:
September: coming off clomid; add in letrone 1 cap, ghar1ne 10mg nightly
October: letrone 1 cap, ghar1ne 20mg, Cardar1ne building up to 14mg
November: probably drop the ai/have one on hand based off blood work, ghar1ne 30mg, cardar1ne 14-21mg based on effects
December: drop ghar1ne, cardar1ne 14-21mg
All will most likely include ep1c unleashed and cycle LJ 100 at 6 weeks on/2 weeks off. Seems to be an effective method for me based off my recent blood work!
Then in January I'd start all over again![]()
Sounds great man. Are you keeping a log on here somewhere?
UPDATE:
1) today (Fri., August 7th) was day 17 on Cardarine, day 10 @ 21 mg.
2) training time was unchanged, but I added weight to 3 movements, 1 stayed the same but I was able to add a rep to each set.
3) I'm recovering faster not only between sets, but after training. I feel fresher, less drained despite adding weight consistently while in a caloric deficit.
4) fat loss is very discernable at this point, yet I feel constantly pumped and full.
They studies it in rats, mice Rhesus Monkeys & humans.
Only the rats got cancer.
Human Studies
Invalid Link Removed
Invalid Link Removed
There are 2 theories as to why GW research was discontinued...
Theory 1: Had something to to with WADA and this being used by athletes for performance enhancement.
The more likely reason...
Theory 2: GW was being research to help with Cholesterol levels. It had such a profound effect on both
lowering bad cholesterol and raising good Cholesterol, GSK (the manufacturer), decided to stop research
because this was just too effective. It had a permanent effect on cholesterol levels. Drug companies are
looking to drugs that people need to take the rest of their lives. This would have cut into profit margins of
other cholesterol drugs that they already sell, and people take daily forever.
To give you an example on this kind of thinking. Nightline or 20/20 (one of those nighttime reporting shows)
had a special on a while back about people contracting infectious bacterias, likestaph and MRSA while
staying in Hospitals around the country.
One of the reasons why these have got so out of hand these bacterias have gotten so out of hand, is that
research into new antibiotics has almost stopped. Most companies have no new antibiotics being researched.
The reason...?
Profit..!
Pharma companies are putting more money, and more research into drugs that people can take long term.
Drugs for Blood Pressure, Drugs for Cholesterol, Pain Management, Diabetes, and other life long illnesses.
The program went on to say that there is no money in Antibiotics, because people only take them for 7-10
days, and then they are done with them. These are drugs that cure an illness, not treat it.
So, the reality is, rather then putting the money into the research of drugs that can cure illness, they would
rather treat illnesses instead, because longterm treatment is more profitable, then shortterm cures.
I just wanted to comment on the whole 'cancer' bit, which is what worries a lot of people who hear about Cardarine/GW-501516. All studies showing an incidence of cancer from GW-501516 included DMBA, which is a carcinogen in and of itself and accelerates cancer growth in studies. But usually there are signs of potential cancer development without DMBA, and in the studies everything was fine within reasonable dosage protocols.
In one study, which I am trying to track down again, it showed:
DMBA - X tested; 0 cancer
GW-501516 - X tested; 0 cancer
DMBA + GW - X tested; X cancer
It appears it was not GW-501516 alone that caused cancer, and the fear continued to get out of hand following the WADA letter. In fact, the company that produced GW-501516 continued their research with human clinical trials after the cancer/polyps study in mice, so clearly it didn't bother them, and no such side effects regarding cancer or polyps were reported with the humans.
Also, I want to touch on one of the potential concerns in the past which was that GW-501516 prevents cell apoptosis (programmed cell death, which is one of the ways that your body prevents cancer) which I believe was tied to COX-2 stimulation by GW-501516 (correct me if I'm wrong). This is why you'll see suggestions online in various forums recommending that you stack Cardarine/GW-501516 with a COX-2 inhibitor such as Tribulus Terrestris which was shown to have strong inhibitory activity on COX-2. As the study below shows:
"Evaluation of natural products on inhibition of inducible cyclooxygenase (COX-2) and nitric oxide synthase (iNOS) in cultured mouse macrophage cells."
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I personally would stack Tribulus Terrestris with Cardar1ne just to be safe, but I have zero concern using Cardar1ne in regards to its effects on my health and well-being.
Which tribulus product do you recommend?
I just wanted to comment on the whole 'cancer' bit, which is what worries a lot of people who hear about Cardarine/GW-501516. All studies showing an incidence of cancer from GW-501516 included DMBA, which is a carcinogen in and of itself and accelerates cancer growth in studies. But usually there are signs of potential cancer development without DMBA, and in the studies everything was fine within reasonable dosage protocols.
In one study, which I am trying to track down again, it showed:
DMBA - X tested; 0 cancer
GW-501516 - X tested; 0 cancer
DMBA + GW - X tested; X cancer
It appears it was not GW-501516 alone that caused cancer, and the fear continued to get out of hand following the WADA letter. In fact, the company that produced GW-501516 continued their research with human clinical trials after the cancer/polyps study in mice, so clearly it didn't bother them, and no such side effects regarding cancer or polyps were reported with the humans.
Also, I want to touch on one of the potential concerns in the past which was that GW-501516 prevents cell apoptosis (programmed cell death, which is one of the ways that your body prevents cancer) which I believe was tied to COX-2 stimulation by GW-501516 (correct me if I'm wrong). This is why you'll see suggestions online in various forums recommending that you stack Cardarine/GW-501516 with a COX-2 inhibitor such as Tribulus Terrestris which was shown to have strong inhibitory activity on COX-2. As the study below shows:
"Evaluation of natural products on inhibition of inducible cyclooxygenase (COX-2) and nitric oxide synthase (iNOS) in cultured mouse macrophage cells."
Invalid Link Removed
I personally would stack Tribulus Terrestris with Cardar1ne just to be safe, but I have zero concern using Cardar1ne in regards to its effects on my health and well-being.
Great explanation and write-up!
Very informative!!
Really, any Tribulus product should do the job, judging by the paper. I would go with the most economical purchase you can!
What about something like Rauwolfia Serpentina...since this is what i planned on using as a sub for traditional tribulus?