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I would classify that as a win. Especially the loss of the hiccups.Ive noticed somethjng recently, Im on 20MG and I dont get the gastric slowing.
I get the appetite suppressant, as I can go all day without eating snd not notice.. but everything is moving through me.
Not like before.
Overeating hiccups have stopped.
15MG was hell, I was getting them daily, for hours at a time. Literally wanted to kill myself but someone kept me aroundI would classify that as a win. Especially the loss of the hiccups.
Have you trialled using digestive enzymes before meals? Actually helped a great deal for me on Reta. That is if the symptoms ever come back.15MG was hell, I was getting them daily, for hours at a time. Literally wanted to kill myself but someone kept me around
Ive noticed somethjng recently, Im on 20MG and I dont get the gastric slowing.
I get the appetite suppressant, as I can go all day without eating snd not notice.. but everything is moving through me.
Not like before.
Overeating hiccups have stopped.
Read up on how these drugs work. There is no tolerance per se.I've been on sema for 2 weeks now and have excellent appetite suppression at 0.25mg. I plan on staying at this dose until I feel appetite suppression decreasing. With a half-life of 1 week, my theoretical dosage would still increase with a weekly dose as written below:
Week 1: 0.25mg
Week 2: 0.125 + 0.25 = 0.375mg
Week 3: 0.25 + 0.1875 = 0.4375mg
Week 4: 0.25 + 0.21875 = 0.46875mg
At the end of week 1 I noticed a negligible increase in appetite suppression, but nothing that made it difficult to stay within my calorie deficit. Is it a bad idea to just wait until my theoretical blood level comes back down to ~0.125mg vs just dosing every week? I don't really see why I need higher blood levels if what I'm on already is working well. If I wait then I could dose as follows:
Target 0.125mg @ 0.25mg every ~10.5 days
I'm not doing this for cost purposes. I just want to minimize tolerance buildup. Curious if anyone else has spaced out longer than 1 week?
I always thought weight set point was bogus?Read up on how these drugs work. There is no tolerance per se.
These drugs will basically lower your "Weight" Set-Point. The higher the dose (up to a limit ofc), the lower the set-point. The appetite suppressing effects will become lower once you reach your new set point for the specific dosage you take. Once your weight reaches the set-point, you will literally not feel a damn thing from the drug (and that's good).
Stick with the official protocol and just pin once a week if you intend to reap the benefits of these drugs long term.
@Ghoul can you finally do a 101 sticky post with common questions and answers
It's certainly not bogus for these drugs.I always thought weight set point was bogus?
I don't believe in weight set point theory, so I will do some research. I know receptors can up and down regulate with prolonged exposure to agonists/antagonists, but I don't know about GLP1 receptors specifically.It's certainly not bogus for these drugs.
You can debate weight set point in general, but that's just how these drugs work. It's also a good analogy. We keep reading about people talking about tolerance when there simply is no tolerance.
You'll notice this as well when you use them for longer time.
On Reta for six weeks- zero fatigue- feel more energetic than normal. Lost 10% of my body weight so far.I've observed users complaining about fatigue with Tirz but when they add Reta it reverses and energises them.
Is anyone else experiencing this? Is there anything else to prevent the fatigue with Tirz?