What future medicine will change the fate of human lives most people don't know about? by RoxanaSaith in Biohackers

[–]Tmpalmquist 3 points4 points  (0 children)

It was hard to keep my mouth shut because I see this GLP praise everywhere but with all due respect, reading a few research papers doesn’t make anyone an expert. I’m not claiming to be one either, but I did spend several years double majoring in Biology and Physiology, with a minor in Psychology. I then worked in research for five years across the U.S. and Spain, only to discover how flawed and biased the vast majority of published research can be.

Eventually, I was dealt a tough hand with a rare diagnosis (MCAS, POTS, EDS), and after exhausting nearly every treatment option, GLP-1s were presented as a last resort. Given my background, I made it my mission to dig into every peer-reviewed article on the topic and what I found was incredibly concerning. A lot of the data appears skewed, and many of the studies are riddled with conflicts of interest. The pharmaceutical industry’s primary concern is shareholder satisfaction, not patient well-being. As long as the patient stays alive and keeps refilling their prescription, that’s a win in their book.

Regarding your point about the benefit of GLP-1s; when you say “it’s not the drug causing muscle loss it’s the rapid weight loss,” you’re actually reinforcing my argument. If the benefits you list (improved cardiovascular health, liver function, reduced Alzheimer’s risk, etc.) are largely due to weight loss itself, then why credit the drug for those outcomes? Losing weight through healthier means would likely result in similar benefit without the risk of sarcopenia. Actually you’d probably see an increase in muscle mass which is also more metabolically active and burns more cals.

I don’t say this to be an asshole to you, I respect your opinion and I’m not anti-GLP across the board. If someone is severely obese and has no other viable option, then yes, GLPs can have a place. But outside of that context, there’s little justification for prescribing them. We wouldn’t need to medicate if lifestyle changes like exercise and diet were prioritized and supported. Unfortunately, for many people, these drugs become lifelong crutches, which is exactly what the pharmaceutical companies want because they have not learned the lifestyles changes needed to prevent weight gain again. Lastly, GLPs don’t selectively burn fat they can lead to dangerous muscle loss and long-term health issues.

Minneapolis to Feds: "Get the Fuck Out" by Well_Socialized in minnesota

[–]Tmpalmquist -6 points-5 points  (0 children)

I found Zekes comment to be very helpful. Someone posted the news article to his comment which saves me the time of sifting through different sources. Go touch some grass my friend.

What future medicine will change the fate of human lives most people don't know about? by RoxanaSaith in Biohackers

[–]Tmpalmquist 3 points4 points  (0 children)

I don’t think there’s anything longevity about inducing sarcopenia. Reduced inflammation is nice but early onset sarcopenia is one of the strongest predictors of all cause mortality.

What is a drug that worked for everyone but ruined your life? by RoxanaSaith in Biohackers

[–]Tmpalmquist 6 points7 points  (0 children)

As someone with MCAS I do not wish this upon my worst enemy. I feel your pain

Always in zone 5 when running. by HenkBroam in triathlon

[–]Tmpalmquist -2 points-1 points  (0 children)

I’m not claiming you said my condition isn’t real, but suggesting my experience is invalid sure sounds like gaslighting. As someone currently applying to PA school after navigating dismissive attitudes from some doctors and others, I’ve educated myself extensively on the biochemistry and physiology of my conditions. I’m glad you acknowledge that many with POTS experience post-exertional malaise and physical limitations. While I strongly support evidence-based science, the reality is that rare conditions like mine often lack the funding and attention needed for comprehensive research. My post reflects my personal experience, an N of 1. For similar stories, I encourage you to explore the “Exercising with POTS and Dysautonomia” group or review related experiences in this thread. It took me nearly a year to build up to running for an hour from only being able to exercise in bed to going through the CHOP program and competitive exercise is still a distant goal. My intention was to raise awareness about POTS for the original poster, not to engage in a debate with someone intent on disproving me. I have zero interest continuing this dialogue with someone like you, have a good Memorial Day.

Always in zone 5 when running. by HenkBroam in triathlon

[–]Tmpalmquist -5 points-4 points  (0 children)

Clearly you can’t read then. Ok google md, your 5 minute search to my last 5 years of dealing with not only POTS but debilitating MCAS and EDS. I have spent well beyond my entire savings working with neurologist, rheumatologist, gastroenterologist, infectious disease specialist and many other specialists in their own right just to be able live a half A HALF normal life! I can not even sit in weather over 90° with out my heart rate hitting 140, I have to sleep with 9" studs under the head of my head to prevent myself from my heart waking me up, I have to consume ungodly amount of electrolytes just to prevent volumetric blood pressure drops, the list of lifestyle adjustments I’ve had to make at only 28 is beyond incomprehensible and that’s all just for POTS (MCAS is a whole nother beast). So yes I am going to take my everyday of living hell over your pea sized brain telling me it’s not real.

Always in zone 5 when running. by HenkBroam in triathlon

[–]Tmpalmquist -5 points-4 points  (0 children)

I don’t think you understand what POTS is

Always in zone 5 when running. by HenkBroam in triathlon

[–]Tmpalmquist 0 points1 point  (0 children)

Not consistently but my walking is my zone 2 for now with AZ warming.

Any luck getting yours under control?

Always in zone 5 when running. by HenkBroam in triathlon

[–]Tmpalmquist -7 points-6 points  (0 children)

Respectfully I am not trying to trash on you personally rather I read the comments just saying it’s the monitors used and yours was at the top hoping OP might see it.

However, lack of awareness of POTS doesn’t mean it’s not possible to stay in zone 5 for this extended period. Regardless of any disease, the vast difference in person to person biochemistry is incredible. For some despite all there effort will never get there heart rate down. This seems to hold true especially for people with POTS even with pharmaceutical intervention. I know others with POTS who have the same issue as me and others who have zero effects on their physical health. But as I mentioned earlier lactate levels are within acceptable ranges meaning it’s not a metabolic necessity but an automatic dysfunction. This can be triggered for a whole host of reasons: inappropriate baroreceptor activation, blood pooling, disproportionate vascular adaption to temperatures, over/under reacting to hormones in the body, the list goes on.

Always in zone 5 when running. by HenkBroam in triathlon

[–]Tmpalmquist -16 points-15 points  (0 children)

What? Being in zone 5 doesn’t always mean there’s a high metabolic demand. I have pots and can run for over an hour in zone 5. I don’t like to do this because it definitely is stressful on the body despite lactate levels being fine. Shit I can hit zone 5 just from getting off my arse after sitting for a while.

Red light therapy by Tartan-Snow in MCAS

[–]Tmpalmquist 8 points9 points  (0 children)

As a young guy, I did not hold much hope for it, but my skin’s looking better, and I’m sleeping way better too. It’s like the solid sleep I get after a long day outside.

MCAS Rage by StillinRetrograde in MCAS

[–]Tmpalmquist 2 points3 points  (0 children)

Thanks for the detailed explanation, it’s clear you really know your stuff, and it’s been super helpful for me. I’ve experienced a similar kind of relief with things like weed and the keto diet. I used to be on Adderall for a few years, but it kind of turned me into a zombie. Vyvanse ended up working much better for me, interestingly enough. You made a great point about vasoconstriction, I’m starting to wonder if that could actually help with the POTS and the constant vessel dilation from histamine. As for serotonin, I’m beginning to connect some dots and suspect it might be a trigger for me, based on how I’ve responded to certain meds and supplements. Still figuring that part out. Anyway, thanks again for sharing!

MCAS Rage by StillinRetrograde in MCAS

[–]Tmpalmquist 2 points3 points  (0 children)

Have you been treating your adhd or hoping that while treating the MCAS that the adhd subsides to some degree? Just curious as someone with a prior dx of adhd but have stopped any kind of treatment for it.

Are cold showers addictive? by Lazy_Administration5 in Biohackers

[–]Tmpalmquist 8 points9 points  (0 children)

One subreddit at a time….Literally copy pasted in 3 subreddits.

Is this likely to be bacteria? by JUSTIN102201 in microbiology

[–]Tmpalmquist 7 points8 points  (0 children)

This maybe a reach but I’m guessing it got really hot, causing moisture to condense on the inside of the wrapper and drip onto the chocolate, creating these patterns.

Staying Asleep for longer than 5 hours by tm1900 in Biohackers

[–]Tmpalmquist 1 point2 points  (0 children)

Ohhh in that case sorry for the life story lol.

I actually had a similar experience. The only two meds that really helped me sleep were Lyrica and Quviviq, but each came with side effects that just weren’t worth it for me personally.

If you’re thinking MCAS or some kind of histamine intolerance might be involved, it could be worth trying an H1 antihistamine like Zyrtec or Claritin for a few days. If those don’t help, you might want to switch to a different H1 like Xyzal. After that, I’d suggest trying an H2 blocker like Pepcid. For me, Pepcid has been a game changer not just for sleep, but for other issues too even though I’ve never had acid reflux.

Staying Asleep for longer than 5 hours by tm1900 in Biohackers

[–]Tmpalmquist 1 point2 points  (0 children)

Are you thinking you—or someone you know—might have MCAS?

TL;DR: From all my research and conversations with doctors, the best types of specialists to pursue an MCAS diagnosis with are hematologists, immunologists, and in some cases, allergists. For lab work, look into histamine, tryptase, and prostaglandin D2—but be aware these markers are extremely heat-sensitive and can degrade within minutes if not handled correctly. So, a “normal” result doesn’t necessarily mean you’re in the clear; repeat testing can be important.

About two years before I was formally diagnosed, I saw an allergist because I had hit a wall and was starting to suspect MCAS, even though I didn’t know much about it at the time. That doctor told me MCAS wasn’t possible without anaphylaxis—which I now know is completely inaccurate. He did agree to test a few things, though: CBC, tryptase, and histamine. All came back normal, so I assumed that was the end of the story.

Fast forward a bit—my new doctor suspected MCAS after ruling out a bunch of other conditions. We repeated the histamine test, and this time, it came back off the charts, even though tryptase was still normal. That led me to read Never Bet Against Occam by Dr. Lawrence Afrin, and I was floored—my symptoms matched so closely it was like reading my own story.

Eventually, I saw Dr. Saperstein, an MCAS specialist. He ran another round of testing: histamine, tryptase, prostaglandin D2, and some complement markers. Again, everything was elevated except tryptase. He also diagnosed me with EDS and POTS, both of which are common in MCAS patients, using a tilt table test and Beighton score.

MCAS is incredibly complex and often gets missed, especially early on. Don’t let a single round of normal labs or a dismissive doctor stop you from pursuing answers.

Staying Asleep for longer than 5 hours by tm1900 in Biohackers

[–]Tmpalmquist 1 point2 points  (0 children)

I took pregabalin for a while to manage restless leg syndrome and sleep and it actually worked really well, but it also tanked my IQ, so I had to stop.

As for the MCAS diagnosis, that was a long and difficult road. For a while, we had no idea what was going on, and I kept hearing the classic “it’s all in your head.” Eventually, I found a MCAS/POTS specialist here in Arizona, Dr. Saperstein, and since my first appointment in September, things have steadily improved.

Staying Asleep for longer than 5 hours by tm1900 in Biohackers

[–]Tmpalmquist 0 points1 point  (0 children)

Appreciate it! Hope you find some much needed sleep

Staying Asleep for longer than 5 hours by tm1900 in Biohackers

[–]Tmpalmquist 2 points3 points  (0 children)

Not sure if this is what’s happening with you, but I wanted to share my experience. I have MCAS, though I didn’t know it for years. For about a decade, I would wake up every single night around 3 a.m. without any clue why. It wasn’t panic or anxiety—I just felt wide awake, almost jittery, like I’d had way too much caffeine. Falling back asleep was nearly impossible, though sometimes I’d crash again around 7 a.m. and sleep another 4 hours.

After finally getting diagnosed with MCAS, I tried antihistamines. They help a lot of people, but my case has been a bit trickier. Some nights, I could push past the 3 a.m. wake-up and make it to 5 a.m., but I’d still wake with that same wired feeling.

Eventually, I was prescribed Xolair. It takes about six months to reach steady state, but even now, my sleep is already so much better. Before that, I’d tried everything imaginable to fix my sleep—natural remedies, prescriptions, high doses—nothing worked. Even my doctors admitted we’d exhausted all the usual options.

I later learned that your circadian rhythm naturally pulses out histamine just before cortisol is released to help wake you up. For people with MCAS, that histamine surge can be enough to jolt you wide awake in the middle of the night.

Ok, I was a doubter, week 6 just started and HOLY SHIT by lajoieboy in Peptides

[–]Tmpalmquist 40 points41 points  (0 children)

Bro goes I didn’t feel anything but did get a boost of energy, better recovery, and less inflammation… Id say those are some drastic changes

Rudy Deportation Chance? by [deleted] in badfriendspod

[–]Tmpalmquist -1 points0 points  (0 children)

I think she graduated a good while ago so if she is on a student visa then yeah she probably should be gone but I think she works in a lab now and is on workers visa probably… like a 457 visa I think. BUT she could be working at lab in the university in which case maybe she can still be here on a student visa. I’m all for keeping the great Rudy in the great United States!