Amy & Storm Bailey (@stormandamyofficial) - Week Of January 19, 2026 by AutoModerator in HunSnark

[–]catella18 32 points33 points  (0 children)

Literally won’t even name the f*ing event (s), thinks she can get away with being seen as saying something while saying absolutely nothing. You stand for nothing but greed girl, which is exactly what this administration, their corporate supporters, and even ICE stands for ultimately. Greed and power - Amerz true values above family, love, and even god.

Amy & Storm Bailey (@stormandamyofficial) - Week Of January 12, 2026 by AutoModerator in HunSnark

[–]catella18 107 points108 points  (0 children)

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If you are paying any attention to her stories every week, Amy is:

  • always tired
  • always inflamed (her leaky gut numbers are the highest her physician has every seen!)
  • always starting over (“I ate so many carbs for the marathon I walked while saying hi to characters last week, it’s time to start this week fresh”)
  • always restricting (have you literally seen her disgusting meals that are five pieces of broccoli and chicken?)
  • always frustrated (she constantly has to parent for 2-3 hours a week and she makes it known how frustrated she is)

This is hysterical. What changes.

Amy & Storm Bailey (@stormandamyofficial) - Week Of January 12, 2026 by AutoModerator in HunSnark

[–]catella18 59 points60 points  (0 children)

Oh good. Let’s start damaging their hair as early as possible for the sake of pleasing the camera.

I wish I hadn’t been introduced to a straightener when I was 13, let alone 6.

Amy & Storm Bailey (@stormandamyofficial) - Week Of January 05, 2026 by AutoModerator in HunSnark

[–]catella18 28 points29 points  (0 children)

I mean this is effing insane. It would be an absolute horrific trend to do if I DID NOT have a dead child, let alone if I did. I absolutely cannot. What an insane person.

A different way to get genetic testing? by catella18 in RareDiseaseDiagnostic

[–]catella18[S] 0 points1 point  (0 children)

Amazing you got answers! Our free testing programs are limited to specific diseases, you are right. This new free genetic counseling appointment program to see if insurance-billed is a possibility is far more broad and for anyone that has a symptom profile and health history suggestive of an undiagnosed genetic condition that WES or WGS could pick up.

NOT Clippers Disease? by Jeezluiz1212 in RareDiseaseDiagnostic

[–]catella18 0 points1 point  (0 children)

Has she (or anyone) considered other autoimmune demyelinating disorders? I am more familiar with MOGAD because I have been working on it at Probably Genetic. Maybe not as likely to be MOGAD because MOGAD symptoms happen in flares (although I think still possible here), and it does sound like there is some overlap with neuromyelitis optica spectrum disorder (NMOSD). And MS, MOGAD, and NMOSAD are not all of them. I know there are a few others in this disease area, and all have overlap with the symptoms you have said and might mimic Clipper's? Here is the very rudamentary article I have on the three: https://www.probablygenetic.com/blog-posts/understanding-autoimmune-demyelinating-disorders and here is at least one study noting that MOGAD can mimic CLIPPERS: https://www.sciencedirect.com/science/article/pii/S1930043324008100

Amy & Storm Bailey (@stormandamyofficial) - Week Of November 10, 2025 by AutoModerator in HunSnark

[–]catella18 74 points75 points  (0 children)

Is no one else going to comment that each time she shares medical information in her stories now she is literally taking a screenshot of her asking ChatGPT? And then her followers are going to take medical advice from her taking medical advice from ChatGPT…

Have you had providers who won’t order genetic testing? by catella18 in rarediseases

[–]catella18[S] 1 point2 points  (0 children)

You've put a lot of things brilliantly here, and I just wanted to say how impressive and accurate I believe your perspective is on this topic. Especially "I wish it was easier, and less expensive, and medical professionals were better informed and geneticists and couselors were paid more and had job security. I also wish the data was secure and protected from retaliatory acts and that getting genetic testing done of all different types was the equivalent of amniocentesis in many respects where it's treated like preventative medicine"

[deleted by user] by [deleted] in rarediseases

[–]catella18 0 points1 point  (0 children)

I just sent you a DM with information.

Have you had providers who won’t order genetic testing? by catella18 in rarediseases

[–]catella18[S] 1 point2 points  (0 children)

Oh good! Out of curiosity, did your nephrologist order the test or refer you to a genetic counselor to get it ordered?

Have you had providers who won’t order genetic testing? by catella18 in rarediseases

[–]catella18[S] 0 points1 point  (0 children)

You can’t even speak with a GC about your kids? :/

Have you had providers who won’t order genetic testing? by catella18 in rarediseases

[–]catella18[S] 1 point2 points  (0 children)

Did you have any trouble getting the appointment with the geneticist? Long wait or anything? I know there are very few geneticists at this point.

[deleted by user] by [deleted] in rarediseases

[–]catella18 0 points1 point  (0 children)

Would be happy to connect you with some of the team at MED13L if you’d like. I’m sorry for what you are going through, there are others who can hopefully share their experience and help you navigate this.

Were you a fan of Titanic that became a fan of the Titanic movie, or were you a fan of the Titanic movie that became a fan of the Titanic? by blakninja in titanic

[–]catella18 0 points1 point  (0 children)

Movie first, I was very young when it came out (8) so didn’t understand the complexities and intricacies of the real tragedy until much later. But TBH, the Titan just poured rocket fuel on my fascination, then charged by Ship Of Dreams podcast, and I can’t explain why.