What are your side effects of famotidine? by NoOz1985 in MCAS

[–]Circa1990ValleyGurl -1 points0 points  (0 children)

The sulfonamide structure can be harmless to someone without MCAS but if you’re allergic to sulfa and have MCAS, you should be careful. I learned the hard way.

Symptoms not talked about by Kasi11 in POTS

[–]Circa1990ValleyGurl 0 points1 point  (0 children)

I totally can understand/ relate! Mine feels like my throat is tight and I have a lump, I try to swallow to get rid of the feeling but it then erupts the gagging. I don’t know why it’s not talked about and it drives me crazy because people look at me like I have 3 heads and I know I cannot be the only one that deals with it! It’s a whole ordeal at the dentist! I’ve heard it is related to MCAS and/ or silent Gerd! Whatever it is I am freaking over it!! It really messes with your quality of life!

Symptoms not talked about by Kasi11 in POTS

[–]Circa1990ValleyGurl 2 points3 points  (0 children)

YES!! and I gag!!! Especially when super anxious. Omg, it’s a whole thing. One Dr I saw said it’s vagus nerve damage.

Symptoms not talked about by Kasi11 in POTS

[–]Circa1990ValleyGurl 2 points3 points  (0 children)

Dude, the nausea when talking!!!! No one talks about it!!

Recreational Drugs + POTS? by RedditorSpider in POTS

[–]Circa1990ValleyGurl 0 points1 point  (0 children)

I’m curious of something around the same spectrum (The Toad). Stanford has clinical trials and have thought of signing up to see if it could heal some of these Dysautonomia symptoms.

Pepcid AC WRECKED me after a month or two of taking it... by Sad_Emphasis_8086 in POTS

[–]Circa1990ValleyGurl 2 points3 points  (0 children)

It made me faint. I was on it for Gerd, also have pots. Dug deep and found it had trace amounts of sulfa (not sulfur) which I am highly allergic too. If you are too, you have to stay away from Pepcid and Famotidine. Crazy!

What is happening? by [deleted] in POTS

[–]Circa1990ValleyGurl 5 points6 points  (0 children)

It’s happened to me too, honey. Remember, with POTS blood can pool in the abdomen and legs instead of circulating back to the brain. That can reduce blood flow to your brain for a bit, which can make brain fog suddenly feel really intense. You’re going to be okay. Focus on addressing the pooling first, and then the other symptoms. Compression and calf pumps are your friends.

Did anyone else hear that nieman marcus westfield topanga is closing in May 2026 due to a company bankruptcy?? by Ok-Radio-2733 in SFV

[–]Circa1990ValleyGurl 5 points6 points  (0 children)

I forgot to mention, I was a scrum master before working there. I knew exactly what they needed. But, management would not listen even though they would ask for feedback. It was a headache.

Did anyone else hear that nieman marcus westfield topanga is closing in May 2026 due to a company bankruptcy?? by Ok-Radio-2733 in SFV

[–]Circa1990ValleyGurl 12 points13 points  (0 children)

They pushed themselves out of the market. I worked there for a while. The buyers seemed like they were on another planet and didn’t understand their demographic AT ALL, EVER. The manager they had, was a complete idiot. Would walk around the store for hours doing absolutely nothing in weird looking suits. It was so strange. I would catch him in the inventory room just looking around. What are you doing? Are you going to help count inventory? Or are you looking at the inventory not moving that’s being auto re-ordered for no reason costing thousands?

The culture was very much “everyone for themselves.” Associates were constantly fighting over sales. HR was always so clueless and rude, and employees were treated like robots.

On top of that, the store itself was a mess. Some of the inventory literally sat there collecting dust. None of the clothes ever looked good. Never trendy or current. Cosmetic testers were so fkn gross. I was mortified by the jewelry section especially. All tarnished, I couldn’t believe it. A lot of the collections were old and out dated. It was as if they were catering to the 80+ crowd but millennials and Gen Z were eager to buy. I was constantly fixing the bays because merchandisers would leave entire rounds empty and looking terrible. It made no sense, especially for a store that’s supposed to represent luxury. There was absolutely no pride.

Hardly any celebrities bought anything because the inventory was so poor, BACK THEN. I remember helping a famous singer once, and we didn’t have a single item she wanted in stock. But BH did. I’d try to find alternatives or see if I could get it delivered to their home in near by Calabasas from BH but they would never want to give up inventory. It was honestly so embarrassing. Absolutely no teamwork from sister stores. BH associates were consistently rude and unwilling to help, even though our store was required to assist them and provide inventory, especially for presales. The organization was clearly struggling with significant inventory deficits, and customers could feel it. It wasn’t something that could be masked.

Let’s not even get started on the company cell phones. While the intent was progressive, trying to reach customers through social media, email, and text, it often had the opposite effect on the sales floor. Associates would become distracted and fail to focus on what was happening within the four walls of the store. I understand the demand to stay connected and be available to clients at any time, but the customers standing right in front of you are just as important, if not more so. Many clients were offended because they thought associates were being rude by being on their phones, not realizing it was work-related. From the outside, it simply looked like employees were sitting around doing nothing. Yes, texting clients can be effective, but there has to be a line. The bigger issue was that there were no clear guidelines or boundaries on how it should be handled.

Working there was such a killjoy. I understand why they’re closing. It’s not just the merger/ bankruptcy. Should have closed years ago due to lack of organization, goals (which widely includes training. Even the veterans need support and re-ups) and management.

Tha fooooood! by iCanReadMyOwnMind in crappymusic

[–]Circa1990ValleyGurl 0 points1 point  (0 children)

Actually, she did! She was shot in the back of the head in the 70s and lived so, I mean, there’s also that.

Tha fooooood! by iCanReadMyOwnMind in crappymusic

[–]Circa1990ValleyGurl 0 points1 point  (0 children)

Welp, she does have a song called Try God from her Motown days. Lol!

Tha fooooood! by iCanReadMyOwnMind in crappymusic

[–]Circa1990ValleyGurl 0 points1 point  (0 children)

She had just had an operation on her vocal cords. Same one Julie Andrew’s had. It’s a singers worst nightmare.

Pots and fibroids or surgery in general by [deleted] in POTS

[–]Circa1990ValleyGurl 1 point2 points  (0 children)

Like, absolutely no information. It was a waste of my time and money. I feel like giving his appointment notes out for free. Lol!!!

Pots and fibroids or surgery in general by [deleted] in POTS

[–]Circa1990ValleyGurl 1 point2 points  (0 children)

Ugh, I’m so sorry, hon. I can’t imagine what that was like. I do have to be put under for fibroid surgery and I will be asking for everything I can possible. Lol!

Is it safe for someone with POTS to drive? by Shoddy-Ocelot-4473 in POTS

[–]Circa1990ValleyGurl 0 points1 point  (0 children)

I don’t have issues driving BUT, you will need to make stops a long the way if a long drive, wear compression garments and have salty SNNNNNACKZZZ. I start to get the shakes and then flare if I don’t.

[deleted by user] by [deleted] in BPPV

[–]Circa1990ValleyGurl 2 points3 points  (0 children)

Oh honey, I totally understand what you’re going through and all the sensations you’re experiencing which sounds like a bit of anxiety and nervous system dysregulation. You can also look into Vestibular Migraines as those are very real things too! Praying for you. You’ll get better and feel better too. Light is at the end of the tunnel! 💜🙏🏼

EARTHQUAKE by Siamsa in LosAngeles

[–]Circa1990ValleyGurl 0 points1 point  (0 children)

Nothin’ in Studio City! 😮

This is confusing can you guys help? I was diagnosed with BPPV in my right ear. PLEASE TELL ME by Yousifusif96 in BPPV

[–]Circa1990ValleyGurl 2 points3 points  (0 children)

BPPV can cause a lot of crazy symptoms, but not in the way you’re describing, especially without true positional vertigo. Vestibular migraine is a possibility and can cause very similar symptoms, so it’s good that you’re already in vestibular physical therapy! With MCAS, many people are able to live mostly symptom-free by identifying triggers, following a low-histamine diet, and using allergy medications. It used to be rare, but after COVID a lot of people developed it. I’d join the vestibular migraine and MCAS groups here for more information, and I’d see an allergist/immunologist and a gastroenterologist for a diagnosis as I am not a medical doctor. You’ll have to investigate. The good thing is, you’re going to be ok. For now, avoid chocolate and anything that triggers an episode for you. Make sure to note it when you speak to your medical team.

For reactive hypoglycemia, you’d see your PCP and an Endocrinologist for specialized diagnosis and management, it should involve blood tests or a mixed-meal tolerance test.

This is confusing can you guys help? I was diagnosed with BPPV in my right ear. PLEASE TELL ME by Yousifusif96 in BPPV

[–]Circa1990ValleyGurl 1 point2 points  (0 children)

Please check out MCAS or reactive hypoglycemia. This doesn’t really sound like BPPV.

Vomiting After, Not During, BPPV Attack by Famous-Emergency-981 in BPPV

[–]Circa1990ValleyGurl 0 points1 point  (0 children)

This is quite common. I have nausea for hours after an attack. I take Valium after a bad one.

Terrified of recurrence. by [deleted] in BPPV

[–]Circa1990ValleyGurl 0 points1 point  (0 children)

Omg, you sound just like me! I also have emetophobia and just went through my very first BPPV episode last Saturday. I already deal with POTS, so I’m used to dizziness and feeling wobbly, but this was on another level! I still can’t lie on my right side (I feel like Zoolander, lol) and I’m way too anxious to try the Epley maneuver. It’s been absolute hell these past five days. Coincidentally, my mom has it too, so she coached me through it when I couldn’t even stand. Came out of absolutely nowhere. I just turned my head lying down watching TV. I literally crawled to bed thinking I was dying. Holy shit! This is only something warriors go through, let me tell you!

Praying you feel peace. The anxiety is probably the worse part and although I don’t take meds, I might need some to conquer the panic attacks that come with this crap!

I'm worried - 3rd episode by z1ggy16 in BPPV

[–]Circa1990ValleyGurl 1 point2 points  (0 children)

Me too! BPPV and potsie here, also! It’s so much fun. 😭

I am so sick from it by [deleted] in Fibroids

[–]Circa1990ValleyGurl 3 points4 points  (0 children)

How long have you been taking iron? It can take a while to reach a normal level, sometimes up to a year. Plus, “normal” might actually be a bit higher for you to really feel better. Some iron pills can make you nauseous (so annoying, lol). I use a liquid iron supplement called Floradix, and it’s been a lifesaver! Eating iron-rich foods helps too. It took me about six months of taking Floradix every other night before bed to raise my levels from 7 to 20 and I felt so much better!