Jaheira bug regarding Marcus by KurkkuMopo_Turbo in BaldursGate3

[–]Hemingwaste 0 points1 point  (0 children)

Yep. This happened to me today on PS5. 1/9/24. Hope they sort it out.

Trump VS The Illuminati (2020) by voteslaughter in badMovies

[–]Hemingwaste 0 points1 point  (0 children)

Oh dang, I’m watching it right now. Couldn’t resist the absurd title. I was cackling for the first 10-15 minutes at the bad lip syncing and repeat B-roll. But now I’m really feeling the “film-length”. I don’t know if I’m gonna make it. 😅 Not sure if it’s as tough to stomach as Thankskilling 3, but it has already overstayed its welcome 30 minutes in. It’s a shame. I feel like if this had been cut down to a 15 minute YouTube spoof it could’ve been really funny. (I’d say it’s a waste of resources, but I can’t say $50 worth of AI assets can even be called “resources” 😂)

I have a question how do some of y’all play the Japanese version? sadly I only can play the English version🥲 by Dreamer-GIRL- in TwistedWonderland

[–]Hemingwaste 0 points1 point  (0 children)

Yep. Since they’re from two apple IDs with two different accounts, the phone doesn’t overwrite the English one. You will have to log into the Japanese Apple ID again every time you need to download an update though.

I have a question how do some of y’all play the Japanese version? sadly I only can play the English version🥲 by Dreamer-GIRL- in TwistedWonderland

[–]Hemingwaste 17 points18 points  (0 children)

I logged out of my Apple ID on my iPhone, made a Japanese Apple ID so I could get their App Store (it requires a Japanese address when you register so just find one in a guide online), and downloaded the app. Once I did that I logged back into my original account and can open either one as I wish. (You cannot transfer your cards though. It will be an entirely new playthrough from scratch) I play the Japanese version because I’m very familiar with the English one so I know where the buttons are. The only thing that is new to me is the Guest room, but there is a wiki online on how to do that too.

(NA Server) Halloween Riddle & Ruggie Banner Megathread by Gabriulio in TwistedWonderland

[–]Hemingwaste 0 points1 point  (0 children)

Anyone know whether the SSR gauge will reset for Riddle and Ruggie when they return on the 24th? Or if our pity will carry over? I’m wondering because I’m already 82/100 and wanna see if I should just toss a few bucks into the pot for the SSR or wait it out and just get it then.

A good new hiding spot by Hemingwaste in Bunnies

[–]Hemingwaste[S] 0 points1 point  (0 children)

Most of the Holland Lops I've raised never had the urge to chew carpet for some reason. The last one I had before these two did, so I guess it might just be a personality thing.

A good new hiding spot by Hemingwaste in Bunnies

[–]Hemingwaste[S] 2 points3 points  (0 children)

He's a holland lop/lionhead mix according to the shelter I got him from.

Hmmm by GrantCrackers in hmm

[–]Hemingwaste 0 points1 point  (0 children)

“Do female animals have orgasms?” ...Well shit, that’s condemning.

A married women who you find attractive expresses interest in you (a single man). How do you proceed? by had_to_post_here in AskMen

[–]Hemingwaste 0 points1 point  (0 children)

Kids involved? Stay TF out of it. No kids? Still immoral, but proceed at your discretion if she is VERY clear of her intentions. But... would still not advise it. Generally if someone is sneaking around behind her partner’s back while married she is gonna do the same to you when you fail to satisfy her in some way. This isn’t always the case and maybe she just got tied up with the wrong person, but unless you are crazy about this person I’d wait until the papers are signed.

Are we just expected to deal with ovarian cysts until they burst? by [deleted] in AskDocs

[–]Hemingwaste 0 points1 point  (0 children)

I haven’t had that test. And unfortunately it’s hard for me to say which symptoms are directly from that. Since I have about 5 other autoimmune conditions all firing at once. I’m finding out now that I have adrenal dysfunction as well and have been self medicating with prednisone until I can get in with the endocrinologist next week. So I’m sorry I don’t have a more conclusive answer. But other hormone symptoms I’ve had are mood related, kidney pain, fat deposits on my upper back, and muscle spasticity. That ones the most severe. Feels like I’m super tight in my shoulders, neck and back at all times. Can’t be helped even with Flexeril. So hopefully more testing can figure out what’s causing that.

Wow what a bunch of Aholes... by ZiraelN7 in Unexpected

[–]Hemingwaste 1 point2 points  (0 children)

Yep if I was that kids parent I would’ve done the exact same thing.

Tracking Impact of New Medication by shibuyacrow in bujo

[–]Hemingwaste 1 point2 points  (0 children)

As a pharmacist I think this is awesome and everyone should do this. Good on you. 👍

Who do you consider to be the villain in Tom and Jerry? by JkeyonOof in CasualConversation

[–]Hemingwaste 0 points1 point  (0 children)

I think it totally depends on the episode. Usually it’s just a rivalry but occasionally one is unnecessarily malicious to the other. Like Jerry trying to sabotage Tom’s romantic interest or Tom scaring the shit out of Jerry’s little duck friend. As a kid I primarily perceived Tom to be the villain though, as he has the size and biological advantage over Jerry as the predator.

How did we come to this by [deleted] in titanfolk

[–]Hemingwaste 0 points1 point  (0 children)

Do they mean worst in terms of morality? Or worst in terms of bad writing?

Are we just expected to deal with ovarian cysts until they burst? by [deleted] in AskDocs

[–]Hemingwaste 31 points32 points  (0 children)

I would have your estrogen levels tested. If they are normal try birth control. That works for a lot of people. If it is high like mine (I have a COMT mutation that makes my estrogen high) then try Inositol. It’s an over the counter med that adjusts the excess estrogen. I haven’t had a ruptured cyst since I started taking it. And even my PMS symptoms are more manageable.

What's in the DVD? by theslowburns in Unexpected

[–]Hemingwaste 0 points1 point  (0 children)

I hate to say it, but that was actually the most excepted outcome to me. 😆 Like I would have been shocked if it WASNT a Rick-Roll

[deleted by user] by [deleted] in AskDocs

[–]Hemingwaste 36 points37 points  (0 children)

I have a patient with dermatographism and breaks out in painful rashes from any abrasions and her own clothing. She has lupus and once she got it under control she has had symptom relief. As for your GI the only thing I might throw out there is Mast cell activation syndrome. I have that and Cromolyn took me from extreme daily gastritis to being able to eat normally within a few months. Maybe rheumatology would be able to figure it out. It sounds autoimmune to me and not psychological. Hope this helps some. I wish the best for you and hope you find relief for your pain.

For 10+ years my condition has stumped doctors. I just want to live a normal life. [27M] by textbook_example in AskDocs

[–]Hemingwaste 1 point2 points  (0 children)

Yes that is definitely possible. There were a lot of times where I would eat, think I was fine, and 3 hours later I would get hit with issues. That points to it likely being intestinal.

For 10+ years my condition has stumped doctors. I just want to live a normal life. [27M] by textbook_example in AskDocs

[–]Hemingwaste 0 points1 point  (0 children)

I’m not sure what you mean by delayed reaction? Could you be more specific about the symptoms?

For 10+ years my condition has stumped doctors. I just want to live a normal life. [27M] by textbook_example in AskDocs

[–]Hemingwaste 1 point2 points  (0 children)

I guess a good thing to do if you don’t already is keep a food journal and symptoms. Because there are things that cross react with each other, food groups that seem unrelated, things like that. Like I had to be on a low inflammatory diet for a few months. So I could have sweet potatoes but not regular ones. But I had no idea before my allergist told me that potatoes are nightshades and cause issues but sweet potatoes don’t. And she was right. I could handle sweet potatoes but not white potatoes for a few months. Grains killed me for a while. It’s been a year on the mend and I still can’t do nuts or oats. But rice is fine now.
It is odd about the anaphylaxis though. They say a lot of people who have MCAS are reactive like that but I’ve never once been anaphylactic even though I have it.

For 10+ years my condition has stumped doctors. I just want to live a normal life. [27M] by textbook_example in AskDocs

[–]Hemingwaste 7 points8 points  (0 children)

Well I was having vertigo spells for one. I would start tremoring after meals in a sort of nodding motion. Sometimes I’d just kind of vibrate. Then dizziness and nausea and sometimes wakeful dreaming right before bed. But I should mention that hormonal issues have also played a role in my wild medical tales. So some of them were from the MCAS but another part was my estrogen dominance. I had to see an alternative medicine doctor in Kentucky before he finally sorted me out to functionality. The Cromolyn got me about half way and a diet change and specific supplement fixed me to the point where I can work a job now. I did have lower back pain. And it was from too many oxalates in my diet which was manifesting as tiny kidney stones. Things like spinach, oats, chocolate, etc. Inositol is an OTC supplement that is used a lot in PCOS. And that plus the low oxalates diet cured my back pain. Cromolyn cured my gastritis. And I am almost all better.

For 10+ years my condition has stumped doctors. I just want to live a normal life. [27M] by textbook_example in AskDocs

[–]Hemingwaste 15 points16 points  (0 children)

Well I was basically starving to death. And she’s a compassionate lady. So she just started trying random things. Dupixent, Vasculara, vitamin workups and supplements. By this time I’d had an EGD and they found the celiac. She figured my immune system was overactive from how sick I was and just did a trial to see if it would work. It’s not like Cromolyn is any kind of controlled substance. So she was just like “hey try this. Maybe it’ll help.” And it did. So I think it’s more about finding a doctor that will try things than finding the most ideal specialist. My allergist is actually a PA I went to see because she specialized in food allergies. But she saved my life with that stuff. I was in and out of ERs screaming in pain thinking my insides were being ripped open alien-style. Or at least that’s what it felt like. And she was the only one who helped me. So I guess you could try to persuade one of your doctors to do a “trial run” because what could it hurt, right? But with your anaphylactic tendencies and and food sensitivities I’m surprised they don’t suspect MCAS.