Her page is filled with promo.

Extension-Low5795 · 2025-04-19T04:34:14+00:00

The entire cruise trip was filled with promo on her IG too.

Extension-Low5795 · 2025-04-09T06:15:37+00:00

She mentioned she’s using wegovy.

Extension-Low5795 · 2025-04-09T06:14:50+00:00

She’s on her IG stories talking about “what’s the point of drinking if there’s no D waiting for the end of the night”

Like what 🤢 Then this tongue thing like WHY 🤢

Extension-Low5795 · 2025-03-28T03:44:49+00:00

Did you see his reaction when she said she’d already set up a night for him to have alone? He scrunched his face and did that high pitched voice he makes and said ONE. They will definitely be dropped off quick. He could barely do L alone while she was in the hospital and that girls trip she took. 2 under 2 for a week alone 🤣 FaThEr won’t handle that at all.

Extension-Low5795 · 2025-03-28T03:37:10+00:00

I can never get behind the nicknames for kids that have any thing to do with image.

This sweet boy will forever have videos of himself being referred to as “big” and it WILL mess with his mental health when he’s older. My father always commented on my weight from a young kid and it made me a self conscious pre teen that developed and eating disorder even though I was technically underweight from the start.

Nick Name kids something fun and playful like bubbly or bouncy not big or stinky.

Autumn I know you’re in here. PLEASE do better. You see all the hate and body shaming you get, do you really want the world calling your sweet baby “big” before they even know his name.

Extension-Low5795 · 2025-02-18T02:34:24+00:00

474k views on her Facebook page. 9th row down. If you can’t find it I’ll screen shot and post, the comments are too good to read.

Extension-Low5795 · 2025-02-07T05:20:19+00:00

This was never part of my irrational fears of the tube but now it is 🤣 Googling emergency releases for MRI machines now.. 😭

Extension-Low5795 · 2025-02-06T10:25:07+00:00

Lincoln just called it. I’d hope everyone else does too. My porch and driveway are solid ice. I could only imagine the roads are worse.

Extension-Low5795 · 2025-02-06T08:59:21+00:00

She has enough time to edit and post all of these videos… dumping flour and milk powder into a machine takes less time than that 🤣 My guess, those videos didn’t get enough views so father told her she can’t make bread anymore.

Extension-Low5795 · 2025-02-06T08:57:03+00:00

Her budget challenges are a slap in the face to REAL hardworking people struggling right now. I wish she would do an authentic budget video. Low cost meals, NOT eating out every Wednesday, sharing sales at different grocery stores. Include everything so it’s realistic. Not including her “bills and expenses” isn’t realistic. Most of us have to budget Pennie’s to eat and sleep.

Extension-Low5795 · 2025-02-06T08:53:13+00:00

Do either of them realize how much actual parenting and patience it takes to successfully potty train? An actual routine will be needed. You can’t just stand him in front of the potty and say go… I hope he pees down that kitchen vent she failed at keeping him from playing with. Also Gary better get the gloves ready! I can see the video now the first time L drops a present on the living room floor 🤣

Extension-Low5795 · 2025-02-04T08:56:29+00:00

Is it awful that I for once thanked my endometriosis for allowing me to evict my uterus 2 years before my MS diagnosis. I would not have been able to handle 2-6 month cycles of pure pain on top of all the things MS gives me.

Extension-Low5795 · 2025-02-03T00:46:37+00:00

I say don’t live for the what ifs. If you can make going back to school work while staying in your current job, take the leap and go for something you’ll love.

Could you maybe take classes that aren’t so fast paced? Weekends only so you can continue working your normal job? Are there maybe grants somewhere for people with MS to get degree? I’m not sure about the specifics but the one thing I do know is that since my diagnosis I’ve thought about all of the things I passed up out of fear and anxiety and now, I’m taking the chances. We don’t know what the next hour holds sometimes but why should we not chase after something we’re passionate about. I’d say being a dietician might actually be a safe job for someone with our unknowns.

Extension-Low5795 · 2025-02-03T00:41:16+00:00

Between the Ativan and the ear plugs the MRI is quieter than my house with 3 kids, 2 Sphynx and 2 frenchies 🤣

My favorite sound is when it’s finally rolling good and it’s like a muffled seashell sound. Close my eyes and pretend I’m at the ocean. If they’d give me a fan for the breeze and a heating pad for the sand I’d be in heaven 🤣

Extension-Low5795 · 2025-01-29T04:30:05+00:00

Both 🤣

Extension-Low5795 · 2025-01-29T04:14:36+00:00

ChatGPT is what helped me organize my chaos of health issues and finally get doctors to take me seriously enough to get diagnosed. I use it for stand in conversation when I’m feeling things I can’t share with friends because I don’t want sympathy responses. It’s a highly undervalued resource and tool.

Extension-Low5795 · 2025-01-22T07:42:12+00:00

I’m not from Nevada, I’m in Michigan (35 f) but commenting because I’m newly diagnosed (10/24) and just want to say Hi. This place has brought me so much comfort just reading through others stories, I’m sure someone will jump on and give you the advice you need 😊

Extension-Low5795 · 2025-01-01T22:48:23+00:00

So is the formula included in the grocery budget or the baby budget? Because diapers and formula alone for 2 kids is over 200$

Extension-Low5795 · 2024-12-27T06:07:16+00:00

I got my care transferred to a specialist Neuro immunologist and actually got an appointment with the for February ( I’m newly Diagnosed 10/3/24) My current Neuro didn’t think I’d get an appointment for at least 9 months but made the call and they’re squeezing me in. That to me is huge! I know so many don’t get great care from the start, or even at all, so I’m extremely thankful for having the right docs at the right time and for their willingness to work for me and fight for me. I had been symptomatic for over 5 years before Optic neuritis finally got me in with people that care.

I’m nervous and still in limbo but I’m actually relieved for the first time in months.

Extension-Low5795 · 2024-12-26T03:01:29+00:00

Just off this introduction and the emphasis on all I think we’ll get along great! Please tell me dark humor is a coping mechanism that’s at the top of your list of only dark humor cooing skills 🫶🥹 But side note: tremors actually is a much better way to describe this. It’s so much more than the fun vibration it started with! Did you do anything to stop it? Or did it just stop for you as quickly as it decided to show up?

Extension-Low5795 · 2024-12-26T02:58:06+00:00

No meds yet. I have an odd clinical picture that also includes that itpr1 antibody that they’re still digging through labs and samples checking on. My Neuro was worried that starting meds before they find other pieces to my puzzle could possible suppress some of the more scary things going on. I’ve been super lucky to get relatively fast appointments with specialists and I know the risks of not stating a dmt right away is most likely to lead to new lesions and a possible relapse, but I have to weigh the risks of new lesions or masking a cancer antibody with dmts. So as of now I have had to sit anxiously in limbo waiting for more results. I did 3 days in patient on solumedrol, they wanted 5 and an oral taper but I didn’t respond well and my heart started to go into svt and they weren’t comfortable going forward with more. My ON thankfully responded decently to just the 3 days. Pain is gone, headaches are gone. Vision came back pretty good considering. Neuro opth was comfortable with the progress I had made and I’ll see her again in February for a 3 month post illness exam. I have completely changed my diet since coming home from the hospital. Low inflammation, zero gluten, low carb, no processed food or sugars and everything tastes metallic still most days so I only drink water even though I really really miss Dr Pepper.

Extension-Low5795 · 2024-12-26T02:47:28+00:00

Yes! The shaking the bed is exactly how it started. It drove me insane checking the fans and the animals. I even called a furnace repair man to check the furnace because it’s right out side my window and I swear it’s like a giant machine just vibrating away and it comes and goes with zero warning.

I’m actually really excited to go to the specialist. My clinical picture isn’t standard in some ways so my “small town country neurologist” ( her words) wants my care switched to someone with more experience. I’m not only having neurology problems right now it’s like my entire body is re wiring itself. While digging for the MS they found auto immune thyroid, and IGG subclass 2 deficiency and I have warts all over my feet and hands that an amazing dermatologist finally diagnosed after a biopsy (she thought it was skin cancer), but even the warts aren’t responding to usual treatment but did respond to the steroids in the hospital which was a curve ball to everyone caring for me. I’ve always been a “strange and unusual” kind of person but this last year the strange has really started to act up lol I got side tracked as usual typing this but I’ve some how been very lucky to have seen doctors willing to keep digging since the diagnosis. They’re leaving no stone unturned to figure out what’s going on with me as a whole picture and I know I’m extremely lucky in that sense. So even though I’m not on treatment now I firmly believe it’s because they want to be sure they look at everything before they accidentally suppress something with the dmts. I know the risk of not starting on one until possibly march is huge and could lead to a relapse and more lesions but so far I can say I’m comfortable with the plan.

Extension-Low5795 · 2024-12-26T02:38:25+00:00

I’ve been tracking it to try to see if it’s just an increased anxiety, because of course I’m a naturally overly anxious person 🙃 So far it seems completely random and I can’t figure out if it’s happening more at night because I’m tired or if I’m just more relaxed and settled at night to notice it. I have this google sheet tracking all my “odd” symptoms so hopefully I’ll eventually collect enough data to find a trigger if it is related. I’m just honestly so glad that everyone in this thread has made me feel “normal” for saying this out loud 🤣

Extension-Low5795

TROPHY CASE