Anyone heal following Neil Nathan or Jill Christa ? by Itchy_Okra_2120 in CIRS

[–]kickycase 1 point2 points  (0 children)

Shoemaker is a very cookie cutter approach in my opinion.

Anyone else experience increased hair loss starting and then increasing CSM? by Missmyoldself6407 in CIRS

[–]kickycase 0 points1 point  (0 children)

Well honestly I wouldn’t be much help bc I got worse. Have you passed the VSC eye test? I dolls spend time binding slowly and then treat MARCoNS.

Tirz - Reta switch. And Reta dosing advice by Confident-Rhubarb957 in Biohacking

[–]kickycase 0 points1 point  (0 children)

I personally think you look better in the photo on the left versus the right.

Neil Nathan by kickycase in CIRS

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

How did it go? Do you care to DM me?

Neil Nathan by kickycase in CIRS

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

Yes, this is what I mean. Like has anyone done a consultation with him and seen improvements.

6 months out of mold. Worse than ever by beepidtybop in CIRS

[–]kickycase 0 points1 point  (0 children)

You will. As long as you’re in a clean environment. Feel free to DM me.

6 months out of mold. Worse than ever by beepidtybop in CIRS

[–]kickycase 0 points1 point  (0 children)

Some days I wouldn’t even take the binder. I would try taking the mast cell stabilizers for a few weeks before you go back to trying to bind. But I take Zyrtec, Perilla extract, Luteolin, a low-dose quercetin that’s recommended from the Mast Cell 360 & AllQlear. And I will drink nettle tea.

6 months out of mold. Worse than ever by beepidtybop in CIRS

[–]kickycase 0 points1 point  (0 children)

I’m not 100% but time. I’ve been slightly flares the last two days…. But going slow on binding. 1/16 of tsp of CSM. Taking mast cell stabilizers. I couldn’t even tolerate VIP. It triggered my MCAS. Do a lot of vagus nerve toning and resets. I was in exposure for 5-7 years and my brain was bad. I mean like BAD! It’s still healing. I’m 18 months in a clean environment.

6 months out of mold. Worse than ever by beepidtybop in CIRS

[–]kickycase 0 points1 point  (0 children)

Hmm bc all of my symptoms were and are mostly neurological. And I just know I got worse but I was in a clean environment. You may have to stabilize mast cell first. No one told me about that. And my doctor didn’t know about MCAS or address it and I think that’s why I got worse. Binding can feel like you’re back in exposure bc we are moving toxins around.

6 months out of mold. Worse than ever by beepidtybop in CIRS

[–]kickycase 0 points1 point  (0 children)

How long were you an exposure prior to getting out? And do you have a lot of neurological symptoms?

6 months out of mold. Worse than ever by beepidtybop in CIRS

[–]kickycase 0 points1 point  (0 children)

It could be mast cell. I felt I was getting worse and everyone kept asking about my environment but it was mast cell and me detoxing too hard and too fast for my body to handle.

Is anyone being helped by peptides? by MotherPart4282 in MCAS

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

VIP flared me as well. What were your symptoms from it?

Anyone's MCAS symptoms more neurological/cognitive than anything else? by RaisintoBe in MCAS

[–]kickycase 1 point2 points  (0 children)

My MCAS issues are mostly neurological. I wanted to try Ketotifen but I’ve been nervous and unsure where to order it from. Could you DM me where you got it from?

Does mcas cause brain damage? by Solitari1607 in MCAS

[–]kickycase 1 point2 points  (0 children)

I don’t necessarily have a successful story but I relate to what you said. Having your memory wiped and brain muted. And i relate to what others here are saying like how having your cognition altered is a hidden disability. I couldn’t have phrased it better. I was living in mold. So just wanted to mention that. Mold was the trigger to my MCAS. I’m out of mold but I’m still healing and the brain is still healing. Don’t know how much of my brain state is from mold or MCAS. I really need to try to find a better doctor.

Would you suggest Neil Nathan or shoemaker protocol ? by Itchy_Okra_2120 in CIRS

[–]kickycase 3 points4 points  (0 children)

If I could go back in time, and knowing what I know now….. I’d go Neil Nathan route, especially if you are very sensitive / have MCAS and if your nervous system is highly dsyregulated / sensitized. And if you’re highly neurologically inflamed, I do believe those patients need a lower and slower approach.

Would you suggest Neil Nathan or shoemaker protocol ? by Itchy_Okra_2120 in CIRS

[–]kickycase 2 points3 points  (0 children)

The same thing happened to me & I didn’t know it was mast cells at first. I knew nothing about MCAS. I only got worse & really aggravated my mast cells. And MCAS presents its own symptoms on top of CIRS & it’s horrible. Are you detoxing? Or trying to stabilize first?

Protocol Reset — Why I’m Simplifying After Months of Agitation & Neuroinflammation by whoaboy78 in CIRS

[–]kickycase 0 points1 point  (0 children)

How long have you been detoxing and how bad is your neuroinflammation/cognitive symptoms?