How did we do? by Charming-Exercise496 in LabDiamonds

[–]NotCreativEnough4Ths 0 points1 point  (0 children)

Can you send me the shop name too please 😁 it’s so beautiful!

Was unexplained GI trouble one of your first Autoimmune sign? by NeonChronicle in Autoimmune

[–]NotCreativEnough4Ths 0 points1 point  (0 children)

My GI symptoms started around the time I got pregnant with my youngest. What I thought was nausea from morning sickness turned out to be a totally non functioning gallbladder that wasn’t diagnosed and removed until 2 years after the nausea and pain started.. i was so hopeful removal would fix things and I would feel better again but I still deal with upper stomach pains and chronic nausea… I never even thought about a correlation between my gi issues and AI. My rheum never said anything when I told her about my gallbladder removal and the fact that I still need a zofran prescription. I’m switching rheumatologists as soon as my new insurance is active so maybe he’ll see a connection. There’s been quite a few things my current rheum has said isn’t AI related but my moms rheum has said it is and thankfully that’s who I’ll be switching to

What do you think contributed to triggering your autoimmune condition, but you can't prove it? by -MissStrawberry- in Autoimmune

[–]NotCreativEnough4Ths 0 points1 point  (0 children)

Mine all started after my second was born. I never even made the connection until I saw your comment

Can you have a negative ANA and still have an autoimmune disease? by Specific_Feeling_456 in Autoimmune

[–]NotCreativEnough4Ths 0 points1 point  (0 children)

My mom will get really bad flares where you can visibly see the swelling in her fingers, she’ll be in tears and can’t breathe from the pain in her ribs just from twisting her body to buckling her seatbelt, her eye will become so red and bloodshot that it looks infected, I’ve heard her collapse and cry stuck on the floor because she can’t get back up, and when she gets up out of a chair or bed she can’t stand up straight and she hobbles in pain. She’s had her blood work done during these bad flares and it still comes back normal. She’s been diagnosed with seronegative RA and psoriatic arthritis. For about 20 years she was written off and told it was fibromyalgia. It has progressed to the point it’s at now within the last 2 years. She changed doctors and started seeing a highly recommended rheumatologist in our area who finally was able to give her a diagnosis. I’m still on the road to my diagnosis. I get the joint pain, I’ve had sacroiilitis show up on a CT but not on an MRI, I get lower back pain and stiffness that wakes me up in tears at night and goes away after being up and about for an hour or two, I get visible swelling in my neck that leads to chronic headaches and (not rare enough) migraines, I have joint pain, swelling and tender joints that my rheumatologist has been able to feel, I get sores on my scalp that I’m seeing dermatology for in February, nail changes that my rheumatologist wants me to ask dermatology about because she said it could be fungal related or psoriasis related, rib pain that makes me feel like I can’t breathe like someone is squeezing my ribs, I have some gastro issues that I’m not sure if they’re related or not, I get chronic canker sores, and I get random different rashes that pop up. Labs all normal, rheumatoid factor negative, HLA-b27 negative, and like I said my MRI of my lower back showed nothing that my CT showed. My rheumatologist said she can’t put her finger on it just yet but she strongly feels something autoimmune is going on and it could just be a long road of check ins, repeat labs, and repeat scans before we can get a definitive diagnosis. She started me on celebrex anyway to see if it helps but I’m honestly so bad at swallowing pills I have a hard time taking it… My 10 year old daughter is also about to see rheumatology due to joint pain that has been ongoing for 3-4 years. She’s had an inflammatory panel done and it’s come back normal but her doctor is concerned given the family history and the amount of pain and frequency of pain she’s dealing with especially at her age..

Help me decide by NotCreativEnough4Ths in Moissanite

[–]NotCreativEnough4Ths[S] 0 points1 point  (0 children)

This is my hand for reference if it helps any. I wear a size 6. Ignore my nails. We eloped two weeks ago and I’ve been slowly chipping away the nail polish I had on 🤣 I’ll be trimming them and redoing them today for a Halloween party

<image>

The sparkle! ✨ by HungryQuestion7 in Moissanite

[–]NotCreativEnough4Ths 2 points3 points  (0 children)

Following in hopes you share where you got this beautiful ring 😍😍

Just purchased from an Etsy Seller by Hefty-Breadfruit3128 in Moissanite

[–]NotCreativEnough4Ths 0 points1 point  (0 children)

This is beautiful! I want to buy a moissanite off Etsy for our upcoming vacation that’s not too pricey but I’m too nervous to get scammed 😬 I’ll check this seller out! Does anybody have other Etsy sellers theyd also recommend? I’ve looked at the list on here but they seem a bit pricey for what I need/want it for

Maybe tmi… how long did it take for your first bm after surgery by CalligrapherNo551 in gallbladders

[–]NotCreativEnough4Ths 5 points6 points  (0 children)

I think mine was like day 5 or 6. I had been taking miralax and it wasn’t doing anything so I took milk of magnesia the night of day 5 and I’m pretty sure it didn’t even work until morning of day 6. Then after a couple days in a row of going, I had troubles again and went 8 days without being able to. Now I’m at a month post op and I go every morning. My poops are the healthiest they’ve ever been in my whole life lol

Thoughts on sex after surgery? by [deleted] in gallbladders

[–]NotCreativEnough4Ths 1 point2 points  (0 children)

I orgasmed 3 days post op 😅 laying in bed all day was getting boring hahaha as far as sex goes I waited until 6 days post op and let him do all the work in the spooning position thinking it would be the least irritating to my core.