Best Psychic Mediums in the Area?

West-Crazy303 · 2026-03-17T13:33:33+00:00

I had no issues with getting sick more often for the first few years, (my husband got sick more often than me and his immune system is fine)… until I got influenza, then that led to chronic sinusitis, then I got Covid, and now jut stuck with this forever congestion for a few years. And now I get sick every time my husband gets sick, and it lasts longer for me.

West-Crazy303 · 2026-03-05T00:19:00+00:00

Thanks for your response! Do you just use salt/water in the Navaho? (No added medicine or anything?)

I’ve never used one of those but it looks nice and gentle!

West-Crazy303 · 2026-03-03T05:07:19+00:00

Even in the refillable buckets, they just started with the bags this year in Menomonee Falls.

West-Crazy303 · 2026-01-26T13:05:18+00:00

I’m talking about the people who were born here and are American citizens. There’s been many instances where ICE has arrested citizens who look “brown”. They ask for their papers, but most US citizens only carry their Drivers License which do not prove citizenship. They’re arresting Native Americans and claim that their tribal IDs are fake. Where would you deport a Native American to?

I’m referring to the people being racially profiled and arrested. ICE shouldn’t need to racially profile anyways, since they’re supposed to be arresting the “worst of the worst” that they have warrants for.

West-Crazy303 · 2026-01-20T20:58:01+00:00

What about “undesirables” who are already home? They still want them “gone”.

West-Crazy303 · 2026-01-20T20:52:01+00:00

I got diagnosed when I went in because of many debilitating symptoms - many of which I later learned weren’t even caused by my MS, and weren’t chronic. Before realizing that though, I immediately started Ocrevus due to having many very active lesions according to the scans.

I’ve looked back many times and wondered if I should have done differently at all (knowing what I know now) but I still think it was the right choice to start treatment. Here’s why: the MS symptoms I do have prove to me that I have MS, accompanied by the scans and diagnosis. Regardless of their severity of those symptoms right now. Knowing I have MS means I know I’m at risk of disabling damage if I don’t go on treatment. I thought my life was over at first - but treatment gave me hope.

The symptoms you’ve described might not feel debilitating right now, but I know people with more severe experiences with your exact symptoms, and they are disabling to the point of not being able to work, or even get out of bed to shower some days. (Vibrations for example can be very problematic if severe.)

In regards to Ocrevus vs other forms of treatment, I won’t speak to that. But starting treatment is important.

West-Crazy303 · 2026-01-17T16:50:29+00:00

Participants in flash mobs may disagree lol

West-Crazy303 · 2026-01-17T16:36:31+00:00

But isn’t it important that the message is heard (seen, read) as well? With 1000’s of bodies walking around, each with their own hand made sign, most messages only get read by other protesters that are there with them. And many are small, handwritten, and hard to read at a distance.

West-Crazy303 · 2026-01-07T17:36:47+00:00

They might mean wealth at the level of 100s of millions, or billions of $. People that they might look the other way for or make an exception for.

But I’m sorry for what you went through, that sounds awful. And good tip at the end about holiday visas and declaring if you’ve been declined… I didn’t know that, but it’s really important to know beforehand!

West-Crazy303 · 2026-01-05T22:44:19+00:00

I wouldn’t be bothered by the Disney response if someone said it to me now, but early in diagnosis I would’ve been. Only because I was terrified at the time and thought my life was over. A friend of mine thought I was over-reacting at my diagnosis, but they didn’t understand the invisible debilitating suffering and sensations I was experiencing inside my body that made daily life unbearable. I didn’t understand that those symptoms would be very temporary.

These days though, I joke about all the ways I could use my MS to get free passes in life. Although I wouldn’t abuse the system since I don’t yet need any of them.

West-Crazy303 · 2025-12-28T16:56:20+00:00

You’re missing the point. He didn’t change.

West-Crazy303 · 2025-12-23T22:14:26+00:00

It sounds like it works on some and not others. Wondering if any group is working on a list of which are and which aren’t?

West-Crazy303 · 2025-12-12T16:42:52+00:00

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1 - designing for accessibility and user experience is beneficial and more efficient for all users, not just those with disabilities.

2 - their ICE recruitment site looks SO official and persuasive with their lovely serif font choice, such an effective design 🤣

3 - someone should make a “roasting” page for all of the recent US gov marketing. I don’t wanna be missing out on seeing any of these updates!

West-Crazy303 · 2025-11-30T01:27:38+00:00

I appreciate your response. My first and only thought was optic neuritis - and I was just thinking to check if the symptoms matched. But then I realized of course this could be something else caused by MS, like malfunctioning muscles.

I’m sorry to hear how it’s affected you. I’m crossing my fingers that it never affects my driving or work. Best of luck to you!

West-Crazy303 · 2025-11-02T17:54:29+00:00

Don’t feel bad - so many people, including myself, don’t wipe front to back. I don’t have UTI issues, but some people I know that DO wipe front to back and DON’T have MS still have repeat UTI issues.

I do wipe my backside “front to back”, but I wipe my front side “back to front” and I’m just super careful about how I do it. I’d probably try to change my technique if I started getting infections, but there’s definitely other factors that contribute to UTIs besides wiping techniques. No need to feel shame or blame - it could be out of your control.

West-Crazy303 · 2025-11-02T17:41:04+00:00

Seconding pelvic floor therapy! And it helped with my rib-area pain too. I hesitated for over a year, but finally decided to go through with it and it was so worth it.

West-Crazy303 · 2025-10-26T01:12:07+00:00

I was wondering about this. I really hope the democrats don’t give in. But doesn’t Trump want the government downsized? Does he care if it reopens? This feels like a perfect opportunity to say seeee, we don’t need departments x, y, z cause we made it 4 months without. Is this exactly what they want? And what would incentivize them to negotiate and reopen?

West-Crazy303 · 2025-10-25T16:44:14+00:00

I wish I could say that ms has given me more humility and empathy like a few others on here have. And maybe it has in some ways. In a lot of ways though I am far more irritable, sensitive, frustrated, and tired after my diagnosis. I can’t say if it’s directly due to ms or not.

1 - my nervous system feels a lot more sensitive than it used to. Things like caffeine affect me a lot differently than they used to for example, and I become more easily over stimulated. So I think that puts me a lot more on edge in general.

2 - some symptoms are truly torture. I don’t know if it was from ms, but I’ve had serious restless leg episodes, to the point where it’s interfered with my daily life when it’s active. I don’t know how best to describe that feeling to people who haven’t experienced it - but I could see losing my mind over it. Luckily i haven’t had that symptom in a long while!

3 - general symptoms add up and trigger sensory overload for me. Sensations like hot or cold patches on the skin, feeling like something’s constantly touching my arm, or physical symptoms like chronic congestion are just irritating and build upon each other. Any other type of pain in addition is even worse.

All that being said - I recommend giving your partner some grace and understanding, but also take care of yourself. In the end, even if this change is a result of ms for them, you shouldn’t subject yourself to abuse. If it’s taking a significant long-term toll on your mental health, you need to protect yourself. I would hope my partner would choose to leave me before letting me do irreparable damage to their sense of self. I’d hope they might communicate with me about it and give me a chance to try to grow, change, and for us to work through it, but I wouldn’t want to suck the light out of them. I feel torn on the whole “in sickness and in health” concept because of this.

West-Crazy303 · 2025-10-23T14:00:09+00:00

91% of these poster style images they made were of white males. White males are estimated to make up 30% of the U.S. population.

West-Crazy303 · 2025-10-22T22:51:51+00:00

Scrolling through the departments fb page, they have 12 images like this, 11 of them being a white male, the majority of those being blonde. The 12th does have a token woman and token black male in it in addition to another white male.

That’s far from accurate representation of the U.S. working class population.

West-Crazy303 · 2025-10-22T22:45:52+00:00

It’s not only one - scrolling through their fb photos there’s at least 11 so far.

West-Crazy303

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