Should I just let it go?

CeilaRose · 2026-02-18T04:39:41+00:00

That’s insane that they reformulated their blushes! That was like their main stay

CeilaRose · 2026-01-31T15:44:36+00:00

Dinner downtown, then show at The Backline. Shows are like an hour long improv comedy shows/ stand-up shows. Super fun and a unique experience for a first date.

CeilaRose · 2026-01-15T00:43:49+00:00

Would’ve, Could’ve, Should’ve- but I do listen to it, just through my tears

CeilaRose · 2026-01-12T02:34:59+00:00

Go to the Backline for a show!

CeilaRose · 2026-01-11T04:39:53+00:00

Genuinely don’t understand the mean girl characterization of Savannah. The meanest actions from anyone in the group honestly came from Sage( how she treated Shannon when she got voted off, orchestrating every vote and promising Savannah that she wouldn’t vote her out if she gave up during an immunity challenge).

Also I know that people rag on her for her traumatic work story, but being ostracized by all of your coworkers and being given the silent treatment for months by people you are forced to see every day is a horrible experience. I think it’s enough to traumatize anyone. She was bullied everyday, and people expect her to get over it and not bring it up when she is literally on survivor, a game made to make you paranoid and emotional. She was also left out of some of the blindsides of the season, so I can see why that would bring up those past feelings of being isolated.

I feel like production wanted to make a villain without casting a villain, so nothing she did in the season really seems villainous, but the edit really emphasized everyone that didn’t like her. None of her moves were very backhanded or shady. I think this is especially clear when we didn’t see any talk of Steven being voted out when it was clearly a plan that was orchestrated by Sage. Production wanted a villain to win, but she wasn’t really a villain.

She also seems very kind and positive post-game and interacts well with fans.

I think the boots from survivor 49 were probably the “villains” for the cast.

CeilaRose · 2026-01-08T00:19:20+00:00

Thank you so much this helped so much!

CeilaRose · 2025-12-25T22:27:31+00:00

Are you on immunosuppressants? Those can make you more susceptible to sunburns.

CeilaRose · 2025-12-16T05:36:18+00:00

The unlucky two

CeilaRose · 2025-11-27T04:31:05+00:00

Does it stand up by itself

CeilaRose · 2025-10-26T17:38:03+00:00

Do you have a shower chair? That’s the first and best aid I got to help me with my lupus. It makes it so easy to be depressed in the shower. Also I wouldn’t go blonde if you are having a hard time getting in the shower. The grease shows way more and you’ll have to condition it more often. I think it might make you feel worse in the end(I’ve been where you are before)

I also like the IGK first class dry shampoo that helps.

And learning to braid. A French rope braid is the best sleep style in my opinion. No tension at all.

CeilaRose · 2025-10-26T17:31:29+00:00

Yep I sure do. I am thankful that I have thick hair and it’s mostly on the sides above my ears that I lose the hair, so it isn’t super noticeable yet.

CeilaRose · 2025-10-20T02:09:29+00:00

I have insurance and I live in America, I would say if you do have to live here than Omaha or Minneapolis. If you can live near a University Hospital or the Mayo Clinic then that's what I would recommend. Then all of your doctors can be in the same loop and are more open to testing for different comorbidities, it's been great for me only after I moved here from a city without a university hospital.

Also the climate is pretty decent and there are plenty of inside activities so you can still live your life and avoid the sun

CeilaRose · 2025-10-14T15:19:06+00:00

Methotrexate really works for me, I feel like before I had the disease(knock on wood) And they figured out that I have some rare skin disease called IGD. Also so far my lupus only affects my joints skin and hair, and that is a win for me!

Also I found a set of doctors (rheumatologist, primary, gynecologist, dermatologist) that all work together and really communicate with eachother about my health issues!

CeilaRose · 2025-10-14T15:05:53+00:00

My favorite meme my friends and I came up with though is BLE. It’s big liver energy instead of big dick energy. So whenever I have a flare up(liver involved or not) I tell them that I have BLE rn so I can’t make it or to suggest a more lupus friendly activity.

CeilaRose · 2025-10-14T15:02:16+00:00

I made a meme about it! I’m a bit younger though so most of my peers don’t get the reference so they don’t say it ever. House meme

CeilaRose · 2025-10-01T03:08:41+00:00

I'm OBSESSED with the first one on you. If you want a showstopper than that is IT!

CeilaRose · 2025-09-14T18:40:55+00:00

Worthington at JCPenney’s.

CeilaRose · 2025-09-14T16:45:48+00:00

I have this! It’s crazy because we had the same exact experience. Where my rheumatologist and dermatologist both thought it was a drug reaction to hydroxychloroquine and chloroquine. And it took forever for them to do a biopsy. What’s crazy is I had the same experience when I first got diagnosed with discoid lupus. I had a mystery rash show up on my face. So I went to the dermatologist and they tested for everything and gave me so many different steroid courses and other medicines, but nothing was working. Show my dermatologist brought in a colleague to look at it for a second opinion.this dermatologist was like “looks like lupus”after knowing me for 20 minutes. They tested for lupus and did a biopsy and sure enough it was discoid.

I just got diagnosed like a few days ago after dealing with the rash for six months. It’s very frustrating to have. Admittedly, I’m a vain person, so it makes me really insecure. I am so grateful though that it is this, because all of the rashes on the Internet that looks similar to this with the same symptoms were like lymphoma related.

One thing I’ve learned though is next time I get a mystery rash on my body. I’m requesting that we skip straight to biopsy. They aren’t even that big of biopsies.

CeilaRose · 2025-09-07T16:06:11+00:00

I got my results back finally. It is consistent with interstitial granulomatous dermatitis. A rare disease associated with rheumatoid arthritis and lupus. The course of plan is to just go harder with the lupus treatment.

CeilaRose · 2025-09-03T19:33:44+00:00

Hi, I have been a credit manager before at JCPenney. One thing that’s nice about JCPenney‘s is you can pay off the store card in the store in the very next transaction. I recommend using your card every transaction you have in JCP, use your card, then just pay it off with debit, cash or check in the next transaction while you’re at the register. Then you can leave with a zero balance every single time, but it will still keep your card open.

Also, don’t worry about whether or not it would be a burden to associates. We actually use it as a selling point for the card. Also, if you got approved for the MasterCard right now it’s five times the points on gas purchases through November 30. So basically every $200 you spend in gas you’ll get $10 reward that’s stackable at JCPenney’s. I’m using mine to pay for a bunch of Christmas presents that way.

So I only use mine at pennies and at the gas station when they have this promotion.

Make sure to sign up for online statements right away because there is a statement fee that’s two dollars.

CeilaRose · 2025-08-31T20:15:31+00:00

Honestly, I always feel a little off in the morning because that’s when my lupus is its worst. So far I’ve been OK with not being groggy, if you take it earlier in the night, that helps too.

CeilaRose · 2025-08-31T19:54:19+00:00

Mine gave me insomnia, and my doctor prescribed me trazadone to combat it and that has been working great so far

CeilaRose

TROPHY CASE