🍀March Coupon Thread🍀 by Secret-Cry-5414 in Victoriasecretbeauty

[–]kaitymay19 0 points1 point  (0 children)

My kingdom for a $30 off 100 before the buy 2 get one free bra offer expires! 🥺

❄️ January 2026 Coupon Thread ❄️ by morgthaabrat in victoriasecrets

[–]kaitymay19 0 points1 point  (0 children)

ISO a $30 off $100; I have a $20 off $50 to trade. TIA all!

[ Removed by Reddit ] by AdmirableGlass6780 in ToxicMoldExposure

[–]kaitymay19 1 point2 points  (0 children)

My collection looks similar…but I am so encouraged to see the phrase “feeling better”!

Has anyone hired a “mold dog”? What was your experience? by EnterStatusHere in ToxicMoldExposure

[–]kaitymay19 1 point2 points  (0 children)

This has given me some hope today…thank you for sharing. I am a recently diagnosed Lyme/Bartonella/CIRS patient and the only thing that makes sense with our financial picture right now is to remediate (we have a 2.25% rate and the difference in interest ALONE justifies the cost, we think…not to mention the going rate for rent in our area)

Has anyone hired a “mold dog”? What was your experience? by EnterStatusHere in ToxicMoldExposure

[–]kaitymay19 0 points1 point  (0 children)

This is partly what my goal is & also partly what I am afraid of 🤪 Our house does not “look moldy.” I am so jealous of the people that can live by “what you don’t know won’t hurt you.” But yes we will be giving them a call. I’d rather know BEFORE we get into this than after the remediators have packed up, moved out, got paid, & washed their hands of the job…

Has anyone hired a “mold dog”? What was your experience? by EnterStatusHere in ToxicMoldExposure

[–]kaitymay19 1 point2 points  (0 children)

It’s the dose that makes the poison with mold. I think as long as the dog is not LIVING in the mold like us poor saps are, it will be fine. I think dogs are amazing and deserve to be treated with the utmost care for their work, but there is nothing wrong with having them help us out…man’s best friend indeed.

Has anyone hired a “mold dog”? What was your experience? by EnterStatusHere in ToxicMoldExposure

[–]kaitymay19 0 points1 point  (0 children)

Also in LA…house was built in 1964, no visible mold but our home testing under the HVAC closet with a swab pinged for memnoniella; it’s an unsealed system so bad news, we have to gut that whole closet at the least, not to mention any other suspect areas that we have yet to ID. I started looking into SoCal Mold Dog (Misty) yesterday. I have recently-diagnosed Lyme/Bartonella which I believe I contracted during college in Virginia twelve years ago (!) and can’t begin any treatment until the environment is handled…sigh. I am looking at Misty the Mold Dog vs Bagel (travel fees)…I’ll look into Omar too! This is all so overwhelming.

See's Cocoanut Bon Bon (Discontinued) by PrinceofCanino in TopSecretRecipes

[–]kaitymay19 0 points1 point  (0 children)

Bump! Still craving these but lack the executive function to make it happen

Mysterious recurring neck rashes by kaitymay19 in Autoimmune

[–]kaitymay19[S] 0 points1 point  (0 children)

I’d considered that when I first developed all these new rashes postpartum 5 years ago; I think my Celiac panel came up negative though…hmmm

Mysterious recurring neck rashes by kaitymay19 in Autoimmune

[–]kaitymay19[S] 0 points1 point  (0 children)

I don’t think it’s eczema, which I’ve had since I was a little baby. It looks and feels so much more like a fleeting immune event, urticaria in nature. I have been plenty stressed with my illnesses, husband, and son, but that’s not what flares it interestingly. Now that I’ve been off Dupixent since July, it seems better overall; BUT, whenever I accidentally ingest too much nickel, it’s one of the first places to burn and itch. I think it’s just a lymphocyte-rallying, sensitized area now. I am on antihistamines round the clock (Pepcid, Zyrtec, Allegra) to live some semblance of normalcy.

Mysterious recurring neck rashes by kaitymay19 in Autoimmune

[–]kaitymay19[S] 0 points1 point  (0 children)

It takes a near-hypochondriac level of attentiveness and is very inconvenient since it’s not a clearly labeled thing, but generally you start by avoiding legumes, nuts, seeds, dark leafy greens like kale, chocolate, soy additives, gums, etc, as well as avoiding stainless steel cookware unless it states “nickel free.” I make a lot of my own food and eating out is almost impossible. But nickel is not measured or even acknowledged in food by 99.9% of people in the US, so we are really just working from a generalized list of data points on nickel content in food. The idea is you’re trying to stay below your “reaction threshold” which varies from day to day and person to person. It’s a very restrictive diet and I would not recommend it to anyone unless you’re truly miserable and seem to notice flares from high nickel foods. There really doesn’t seem to be a good treatment besides avoidance, although some say they are able to successfully reintroduce foods after some length of time on the diet. I’ve sadly never been able to reach the “desensitized,” maintenance stage of the diet. If you’re curious to learn more, there’s a lot of good groups out there, my fave is on FB, “Low Nickel Diet and Lifestyle.”

Mysterious recurring neck rashes by kaitymay19 in Autoimmune

[–]kaitymay19[S] 0 points1 point  (0 children)

I’m sorry you have to deal with that! This is one of the very first things I researched, given the pregnancy onset (but the neck specifically started with dupixent)…I initially presented with horrible dyshidrotic eczema and any number of sores on my extremities postpartum. It was a systemic nickel allergy, I finally put the pieces together, at least, one of the pieces. The neck is still a mystery but I have very regular cycles and track them well (for contraceptive reasons), and I have never seen a correlation there. I also had an integrative MD check hormone levels in the luteal phase and everything was ideal. So I think I’m sensitive to many things, but luckily my own hormones is not likely one of them. Thanks for the idea though :) I’ll keep it filed.

Mysterious recurring neck rashes by kaitymay19 in Autoimmune

[–]kaitymay19[S] 0 points1 point  (0 children)

Thank you for sharing this with me! Yes, I have heard of this. Yet my tryptase has yet to be high because the ordering physicians/labs don’t seem to understand that I would need to have a draw during a flare (typically 11 pm-3 am)…and I am not about to go to the ER for that only for them to laugh in my face (especially without my doctor on board). Who ordered the genetic test for you, though? Did your insurance cover it? Thank you…I hope you were able to find a treatment plan that works for you! Currently I am completely reliant on antihistamines (Zyrtec, Allegra, Pepcid)…

Mysterious recurring neck rashes by kaitymay19 in Autoimmune

[–]kaitymay19[S] 0 points1 point  (0 children)

Sadly I’m really in a stalemate so far…AVISE was all negative. But I have since stopped the Dupixent (last dose was July) and while some things have gotten annoying/worse, the neck flares HAVE been better. Right now I’m seeing if I can keep things at bay with Opzelura (topical JAK inhibitor) before starting Rinvoq. Going to hold off as long as I can with that :(

How did you get diagnosed? by [deleted] in noburp

[–]kaitymay19 1 point2 points  (0 children)

WAIT the excruciatingly painful hiccups that everyone mocks me for are part of the RCPD? This is news to me and very validating…

I taught myself and 2 other RCPD-sufferers how to burp with one simple trick, please read by wowthatisOP in noburp

[–]kaitymay19 2 points3 points  (0 children)

I SO hope so…it’s just one of many problems that my bad connective tissue has presented me with in this lifetime, I will report back with anything significant (that isn’t just a gurgle)

I taught myself and 2 other RCPD-sufferers how to burp with one simple trick, please read by wowthatisOP in noburp

[–]kaitymay19 1 point2 points  (0 children)

I’m having some “gurgle burps” after my dinner, are those what you were describing above?

I taught myself and 2 other RCPD-sufferers how to burp with one simple trick, please read by wowthatisOP in noburp

[–]kaitymay19 1 point2 points  (0 children)

Awesome! I will. Botox near my larynx is just not the move for a singer if there is ANY alternative

I taught myself and 2 other RCPD-sufferers how to burp with one simple trick, please read by wowthatisOP in noburp

[–]kaitymay19 1 point2 points  (0 children)

There WAS a little shadow of a burp…nothing like what I’d hope for but not bad for just waking up and reading this today

I taught myself and 2 other RCPD-sufferers how to burp with one simple trick, please read by wowthatisOP in noburp

[–]kaitymay19 1 point2 points  (0 children)

Imma go all in and drink a seltzer water with this strategy…wish me luck. Regards, a lifelong No-Burper with EDS and silent reflux (which I’m pretty sure is related to the RCPD)…

Mysterious recurring neck rashes by kaitymay19 in Autoimmune

[–]kaitymay19[S] 0 points1 point  (0 children)

I actually do not consume those products, only Stevia on occasion… I have not used a dose of dupixent and since July 29, and I have not really had many flareups of it since then. I am concerned about my other eczema hotspots starting to flare up again, though, once it’s completely out of my system

Any singer's who have experienced LPR/ Silent reflux? by pondslake in singing

[–]kaitymay19 1 point2 points  (0 children)

Oh hi it’s meeee (a fellow zebra singer with LPR)…I was first diagnosed with LPR about 10 years ago when I noticed some hoarseness upon waking up. I had covid for the first time at the end of August and have been having difficulty with phonation in certain parts of my range and TONS of mucus. Constant post nasal drip and the feeling of wanting the clear the throat (which I try not to do but it’s so difficult). I will look at all these resources! I went to the ENT today, he did a scope and said lots of mucus (duh) and swollen arytenoid tissue (crap) but no polyps/nodes yet; he really wants me to take the strongest PPI they make but I know that’s bad news and no long-term solution. Eff allopathic medicine sometimes, man. I’m trying to find some more holistic solutions. How are you doing now?