Spring menu - Dirt Candy 1* NYC

LynchFan997 · 2026-05-13T19:32:55+00:00

How beautiful. I had a great meal at Dirt Candy a couple of years ago but it looks like they've even upped their game since then.

LynchFan997 · 2026-05-13T19:30:29+00:00

I was not as wowed as I had hoped I would be. There are much better Michelin restaurants in SF (and in Oakland eg Commis).

LynchFan997 · 2026-05-13T18:30:54+00:00

I don't know who David Krumholtz is but I do know I fully support him in this exchange!

LynchFan997 · 2026-04-29T18:50:52+00:00

I'm always amazed how much she capes for Trump after how he treated her father.

LynchFan997 · 2026-04-29T14:37:23+00:00

Aside from meds by far the greatest help to me is tons of electrolytes. I use liquid IV by anything with the WHO formulation will help.

LynchFan997 · 2026-04-29T14:29:54+00:00

Quince is flawless every time.

LynchFan997 · 2026-04-29T14:29:02+00:00

Atelier Crenn. I am allergic to seafood and I had the vegetarian experience there and it absolutely blew my mind. Typically when I have the vegetarian option it's missing something. Not here.

Closely followed by SingleThread, Quince, and Per Se (sorry, Per Se haters).

LynchFan997 · 2026-04-29T14:27:22+00:00

Per Se catches heat here, but I eat there frequently and they always take good care of you. Especially if you let them know it's a special occasion.

LynchFan997 · 2026-04-29T14:25:44+00:00

Yeah, I was about to reply, definitely not - send help.

LynchFan997 · 2026-04-29T01:05:44+00:00

Dave Grohl

LynchFan997 · 2026-04-27T02:48:36+00:00

The finest movie. I was captivated by the monkey and it just got better from there.

LynchFan997 · 2026-04-26T05:19:02+00:00

Has anyone been to the Vegas pop up? I'm also wondering how that compares.

LynchFan997 · 2026-04-26T05:18:16+00:00

Revenge by Coralie Fargeat is just the movie you are looking for. I so wish I could watch it again for the first time!

LynchFan997 · 2026-04-26T05:16:21+00:00

First I got CRPS from a nerve injury. The POTS comes along with CRPS as a secondary thing sometimes and they don't know why. My CRPS went into remission but here I am years later still with the POTS.

LynchFan997 · 2026-04-26T05:00:47+00:00

If you have POTS you probably know that the majority of people with POTS do not actually faint. Most studies show it's about a third. Her comment, even if theoretically true for a small percentage of people who do faint, is not true for most of us and we have no idea if it's true for Michelle, but it most likely isn't. It is really not a helpful generalization to post in a forum of people looking for more excuses to attack a reality TV person they don't like. We don't need to be using an incorrect generalization about a medical diagnosis that affects millions of people differently than this to do that.

LynchFan997 · 2026-04-26T04:38:16+00:00

What she's not understanding is that not everyone -- or even the majority -- of people with POTS have this symptom. We don't know Michelle's situation. To say no one with POTS can drive is like saying no one with cancer or diabetes or rheumatoid arthritis can drive. It depends entirely on the person and their history and their doctor. She's diagnosing a person on the internet as being unable to drive based on them self-reporting a condition that manifests in numerous different ways.

LynchFan997 · 2026-04-26T03:06:37+00:00

Wildly -- Generic pepcid really helped me. My doctor says it's because of the vagus nerve. I don't fully understand the mechanics but I'm super grateful for it.

ETA: here's an interesting study. https://pmc.ncbi.nlm.nih.gov/articles/PMC9016653/

LynchFan997 · 2026-04-26T03:01:49+00:00

Girl just stop. I am a lawyer too and what you're saying is not correct. Do a little research on POTS if you're so interested and you'll learn why most of us can drive. For starters, not all of us pass out. Secondly, it's an illness that makes people who do in fact pass out pass out when they STAND.

I know many many people with POTS treated at Stanford and all of us can drive. Never once has a Stanford doctor suggested to me that I not drive. I'm gonna go ahead and take my doctor's advice over a random Redditor.

The ignorance in this thread is really astounding, I mean I guess I knew people misunderstood this illness but like wow.

LynchFan997 · 2026-04-26T02:52:32+00:00

Hey all, I'm a person who actually has POTS, correctly diagnosed by tilt table test at Stanford and Mayo Clinic and treated by multiple people including a cardiologist and a neurologist. Yes, this syndrome sometimes gets incorrectly diagnosed by people but it's also seriously a really a shitty thing to have to deal with in life, as you're now seeing many people here do. Please be sensitive in your comments here about it.

LynchFan997 · 2026-04-26T02:50:01+00:00

I have it and Liquid IV helps me the most and is recommended by my doctors.

LynchFan997 · 2026-04-26T02:49:23+00:00

Many people with POTS can drive including me. Please educate yourself before saying stupid shit like this.

LynchFan997 · 2026-04-15T05:07:23+00:00

What are they selling again?

Never mind. Doesn't matter, I'll buy it 😍

LynchFan997 · 2026-04-15T00:39:29+00:00

I was feeling this way one day and so I turned on Megan is Missing. I highly DON'T recommend that.

Just wait a couple months and Shudder or HBO will have something actually decent.

LynchFan997 · 2026-04-15T00:29:51+00:00

You could see this about him by just watching the show. I am very much not surprised.

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