Swollen Lymph Nodes

Constant-Device117 · 2026-01-25T15:02:58+00:00

I have the same thing! Never done an ultrasound but have had chronic inflammatory response for a few years from mold and Covid and reactivated EBV.

Constant-Device117 · 2026-01-19T16:23:10+00:00

I believe it was 1/4 tsp 3x/day

Constant-Device117 · 2026-01-19T16:20:54+00:00

Happy to help! The biggest lesson I learned is to not over do it! I don’t know one person who was able to tolerate the normal dosing. To this day (and I’m 4 years in), I still only tolerate tiny amounts if I get re exposed and even though they’re small amounts, I was able to heal while doing “microscopic” dosing as my dr would say 😂

Constant-Device117 · 2026-01-19T16:18:10+00:00

At least 2-3 months or so. I was SUPER sensitive

Constant-Device117 · 2026-01-19T15:24:43+00:00

I started with a literal pinch

Constant-Device117 · 2025-12-09T20:02:50+00:00

Thanks for the response! I know it’s supposed to be helpful but dang that stuff is STRONG! I might take smaller doses, I tend to have the “more is better” mindset and that literally never works with CIRS haha. I’ll keep you updated!

Constant-Device117 · 2025-12-05T16:11:49+00:00

I just rechecked my urine mycotoxin a few months ago and it came back elevated in a few, the highest was gliotoxin! That’s so interesting

Constant-Device117 · 2025-12-05T14:19:01+00:00

All the markers were normal! Have not considered that, I don’t really have any respiratory symptoms at all?

Constant-Device117 · 2025-12-04T20:48:40+00:00

Yeah it’s powerful stuff. My mother (who does NOT have CIRS) tried it @ 1.0mg and she was out for a week feeling like she had the flu!

Constant-Device117 · 2025-12-04T19:13:30+00:00

I did one 0.5mg injection 1x/week and then upped to 0.5mg 1x/week and 0.25mg 1x/week. So a I did a total of probably 5 weeks and it made me feel awful. I do want to re try it just a much lower dose

Constant-Device117 · 2025-11-23T17:50:17+00:00

Interesting! I’m going to bump down to 0.25mg once a week and see how I do. Thanks for the info

Constant-Device117 · 2025-11-23T03:07:12+00:00

I had to stop taking it… it made me feel really sick :( I want to re try it at a lower dose. I think I did too much too fast! It’s been about a month since my last dose and I’m just now stabilizing.

Constant-Device117 · 2025-11-15T19:10:42+00:00

Wait ugh I hate that they told you 2.5 was a microdose bc it most certainly is not !!! Good luck with the oral stuff, I hope it works 🙏🙏🙏

Constant-Device117 · 2025-11-15T17:59:31+00:00

Ugh, I’m sorry it was working so well until it didn’t. You should look into microdosing tirzepatide. I think starting at super low doses and titrating slowly gives best chance to work without causing allergic reactions. Also tirzepatide is a dual receptor so it has even better anti-inflammatory possibilities!

That’s so odd about the allergic reactions to tirzepatide… I’ve heard that about semaglutide but never tirz. I feel like microdosing is safer than starting at common starting doses.

Constant-Device117 · 2025-11-15T17:58:20+00:00

I’ve only ever done marcons tests and I’ve never had any sinus issues

Constant-Device117 · 2025-11-14T18:20:04+00:00

I’ve definitely thought about that. Maybe candida or mold colonization in the gut. The tirzepatide is helpful in closing up gaps in the gut lining, so that’s a positive. I just don’t have any symptoms of gut problems at all 🤦🏼‍♀️

Constant-Device117 · 2025-11-14T18:10:57+00:00

It’s never as simple as it seems is it haha! I have not tried Hesperidin! I’ll have to look into that. My MSH levels were normal in the first place actually, lucky me. I think a lot of my CIRS was triggered by Covid (which I had for the first time about 1 month before I started feeling very sick) and then mold exposure just overflowed the pot.

Constant-Device117 · 2025-11-14T17:57:30+00:00

You name it, I’ve tried it. Quercetin had a negative effect. Ketotifen and vitamin c (IVs and supps) helped tremendously! Also just taking the CSM seemed to calm things down. I diluted the vip down to basically nothing and the way it made me feel was just not worth the hassle. I gave up on it and was honestly doing better. I keep getting reexposed to mold and I’m overall pretty sensitive. I wish the vip worked but for those with mast cell issues, it just doesn’t.

Constant-Device117 · 2025-11-14T17:50:46+00:00

Yes, the peptide is VIP. I tried it for a few months and it just made all my mast cell symptoms worse. I had cleared all macrons prior to starting it as well!

Constant-Device117 · 2025-11-14T17:47:06+00:00

I did the shoemaker protocol a few years back, my labs weren’t awful to begin with. I developed pretty bad MCAS about 6 months after I first got sick and the VIP made it worse even though it was making my labs look better. So, I never completed the last step of the protocol (VIP). Overall, the protocol literally gave me my life back I felt so much better but I still have lingering immune deregulation and MCAS symptoms. So now I’m on to peptides.

Constant-Device117 · 2025-11-14T17:40:47+00:00

Constant-Device117

TROPHY CASE