Posts by Ethan Reed2

amberskipper3 said:Lately, I’ve been seeing more and more media reports and even some academic papers claiming that the whole "eight glasses a day" rule is complete nonsense.
Personally, I’ve never been able to force down that much water in a single day, so I just stick to drinking whenever I actually feel thirsty.
My skin looks great, my weight is fine, and I don't have any dryness issues...
What’s everyone else’s take on this?

I’m right there with you.🙏 I actually read somewhere that overdoing it can mess with your sodium balance. Unlike you, my skin stays pretty dry regardless of how much water I chug. Plus, most of what we eat is already about 70-80% water anyway.
👍Just drink when you're thirsty!
☕

I’m dealing with something pretty similar. It used to be a massive ordeal, but once I figured out what was actually going on, things settled down. ☕
For me, the issues always popped up in the folds—right under the waistband of my underwear and on my backside since I’m sitting at a desk all day. I tried everything you can think of to soothe it: zinc oxide, various ointments, even those old-school home remedies.
It flared up back when I was heading into labor, too. My OB-GYN finally cleared things up by explaining it wasn't an ulcer, just inflamed hair follicles caused by constant friction. He prescribed some Betrion ointment, and that did the trick. Now, whenever I feel one coming on, I just apply it and I'm good to go. 👍

wiredlynx33 said:Honestly, this thread should just be shut down immediately; instead of actually brightening my day, I find myself feeling completely drained by the sheer amount of negativity being spewed by certain individuals. For goodness' sake!
☕

You're right. 🙏
I was actually waiting for someone to chime in and share their actual experience—you know, like "I took LDN for this long and felt like this" or "this part worked, but that part sucked." It would be helpful to get some real feedback.
Honestly, I don't care who's on anyone else's payroll. I'm on this forum for actual, firsthand experiences... nothing more, nothing less.
All this bickering is just going nowhere.
👎

Angela Wright said:Not necessarily. You have these tiny pharmaceutical outfits that don't have massive capital to burn on endless clinical trials; usually, those are the exact players cooking up the most innovative "smart" compounds and combinations.
To actually prove something works beyond a shadow of a doubt and secure that "evidence-based" stamp of approval, you have to run trials on a massive scale—and science, not Big Pharma, is what dictates that process. In fact, Big Pharma would much rather see the opposite happen.
So, looking at the preliminary data, there is evidence this drug works for certain conditions and isn't toxic, but I wouldn't go labeling it a "miracle cure" just yet.

You've got a point, and I wouldn't label it a "miracle" either, but waiting for absolute proof that something works...🤷. Which drug are you referring to that you know for a fact works unequivocally? I live with MS, and I can't think of a single drug that fits that description. It’s a different story when you consider that giant pharmaceutical corporations can fund trials for THEIR own drugs for years and then potentially "massage" the results before going public... claiming their drugs are amazing and so on. Sometimes patients just don't have the luxury of waiting for the conclusion of endless studies that haven't been officially recognized yet. They just want to feel better... I don't see what's wrong with that.

Angela Wright said:I took a deep dive into what’s currently published onPubMed. For the most part, the data shows the drug isn't toxic, and there are some promising signs that it actually boosts quality of life for patients. However, there's a catch—every single study includes the same disclaimer: we still need much more rigorous testing and development before we can claim any definitive, concrete results.

That’s just how it works whenever something is actually effective and affordable. The priority is always pushing expensive drugs to line the pockets of doctors and big pharma.

urbanorca said:Angela Wright, look, I’ve gone through the studies myself, plus over a hundred patient testimonials. There are tons of positive results out there.

I’ve been reading about this on various forums for quite a while now, and people seem to have great experiences. Even those who went through surgery to "get rid of it" mention they stopped all their other treatments but stuck with LDN, and they feel significantly better.
Now, here's my question for you... how does one actually get a hold of it? How do you track down this medication?
Not long ago, I ordered some vitamin supplements online from the US, and when they hit customs, things got messy. If I hadn't been so persistent, they would've just sent them right back to the sender. And those were just vitamins—imagine the headache if we were talking about actual prescription drugs. It was the same story when I was using Enkorten... I had to basically smuggle it across the border. Same with Prokarin. So, the big question remains: how?🤷
You mentioned being surprised by the lack of interest... Honestly, I used to feel the same way, but I've grown used to it. 🤷 Most people are pretty indifferent; they just stick to whatever their doctor tells them without doing any research or looking into anything themselves.
There are others, of course—people willing to try anything just to feel better—but they're definitely in the minority.
Thanks, truly, for taking an interest and contributing to a group of people you aren't even connected to. Some of us actually appreciate it. 👍

MS CASE HISTORY

Gender: F

Age: 42

Year of diagnosis and MS type (RRMS, SPMS, PPMS): 1998, PPMS

Pre-procedure therapies: interferon, IVIG, Cortisone, Procarin, vitamins, minerals, acupuncture, Lioresal, Sirdalud, Normabel, etc.

MS symptoms before procedure:
-fatigue,
-left hand clenched shut,
-left arm bent at the elbow,
-spasms, spasms, spasms...
-complete loss of strength in hands and legs,
-unable to walk,

Number of relapses before procedure

EDSS before procedure: 7.5

PROCEDURE

Location and date: Germany, April 22, 2010

Imaging and findings: Contrast CT showed 80% blockage in the left jugular and 40% in the right.

Procedure type: Balloon angioplasty, no stent used.

Post-procedure therapy: none

Symptoms after procedure:
-fatigue disappeared,
-can straighten my arm,
-easier to open my hand,
-regained strength in my hands,
-able to stand for about 15 minutes with support,
-spasms have almost completely vanished.

Number of relapses after procedure

EDSS after procedure: 7

MS Medical History

Gender: F
Age: 42
Diagnosis & Type: Diagnosed in 1998, PPMS

Hi everyone,
I’m starting a new thread on a topic we all care about—one that usually sparks some pretty heated debates. Since more and more people have undergone the "liberation" procedure, I thought it would be helpful if those who actually went through it shared their firsthand experiences. To keep things organized, I’m asking anyone who hasn't had the procedure to please refrain from commenting or debating here; let's keep this space strictly for those who have actually completed the treatment. I’m also suggesting a specific template to follow so we can bypass subjective opinions and stick to the raw facts. This format is adapted from the This is MS forum, where people from all over the world share their stories. These accounts are incredibly interesting, whether you've already had the procedure, are
planning to do it, or are just one of the skeptics watching from the sidelines.
----------------------------------------------------------------------------------------------------------------------------------------------------
MS HISTORY

Gender M/F
Age
Years since diagnosis and MS type (RRMS, SPMS, PPMS)
Previous therapies prior to the procedure
MS symptoms before the procedure
Number of relapses before the procedure
EDSS before the procedure

THE PROCEDURE

Location and date
Type of scan and diagnosis
Type of procedure performed
Post-procedure therapy
Symptoms after the procedure
Number of relapses after the procedure
EDSS after the procedure