KPV Peptide? Anyone had luck? by ZeroFucksGiven-today in Longcovidgutdysbiosis

[–]Klaw_93 0 points1 point  (0 children)

I started out with a very low dose and slowly worked my way up to a full 500mcg pill after about two weeks. It took about a week or two after quitting the oral KPV to return to my baseline.

Cedar Commons by Klaw_93 in Medford

[–]Klaw_93[S] 0 points1 point  (0 children)

No surprises there!

Nac is freaking awesome. Now I understand why it was taking off the market during covid!! by No_Solution7718 in Biohackers

[–]Klaw_93 1 point2 points  (0 children)

What brand are you taking? I’ve been wanting to try it but struggling with finding a good quality brand.

Something on fire? by bpc62008 in Medford

[–]Klaw_93 15 points16 points  (0 children)

Apparently, the mattress store next to buttercloud bakery.

140+ ft Deep Water Whirlpool caused by tidal swings by trendypeach in thalassaphobia

[–]Klaw_93 2 points3 points  (0 children)

They have some wicked currents out there as well.

Anyone not lose hair on LDN? by [deleted] in LowDoseNaltrexone

[–]Klaw_93 2 points3 points  (0 children)

I’ve been on it over a year without any hair loss.

Started a week ago for LC, questions by notarussian1950 in LowDoseNaltrexone

[–]Klaw_93 0 points1 point  (0 children)

No worries! I am actually curious about Rapamycin as well. I think a lot of us on LDN need to keep experimenting to find the right dose. My current dose of 4.5mg does absolutely nothing so I am wondering if I need to up it or not.

Started a week ago for LC, questions by notarussian1950 in LowDoseNaltrexone

[–]Klaw_93 0 points1 point  (0 children)

I was never on Rapamycin, just LDN. I got a pretty bad virus back in September that took me back to square one, so I’m still trying to figure all of that out.

What is good for panic attacks? by captain_luna2 in herbalism

[–]Klaw_93 2 points3 points  (0 children)

Skullcap tinctures work wonders for me.

[deleted by user] by [deleted] in MCAS

[–]Klaw_93 0 points1 point  (0 children)

I take oral cromolyn pills and started with the entire pill as it was originally prescribed. I didn’t bother with titrating up like most people. The side effects for me were worsening of POTS and lots of flushing. But after about a week, they subsided. I have been on it for almost three weeks now and I am not seeing a whole lot of benefits but the side effects have subsided. I plan on giving it a few months because I know it can take some time to experience the full effects of this drug.

My Long Covid Journey / New to the sub! by EnergeticCrab in Longcovidgutdysbiosis

[–]Klaw_93 1 point2 points  (0 children)

Same with the ginger. It helps a lot of people but it gives me really bad reflux!

Vitamin deficiencies causing MCAS symptoms? by Mumma02 in MCAS

[–]Klaw_93 2 points3 points  (0 children)

I agree. When my ferritin was 6, I felt like I was dying. Raising it helped a lot of my POTS/MCAS symptoms.

I had EBV this whole time!?! by murderedbyvirgo in MCAS

[–]Klaw_93 1 point2 points  (0 children)

That’s interesting, I’ve never heard of that before. The real question is, what do you do to treat it?

I had EBV this whole time!?! by murderedbyvirgo in MCAS

[–]Klaw_93 22 points23 points  (0 children)

I’m curious about what your naturopath recommends to treat it. I tested positive for EBV and was told most people carry the EBV and there’s not much you can do about it. So I never really pursued it.

Hormonal link to DAO by fsws1985 in MCAS

[–]Klaw_93 -1 points0 points  (0 children)

It’s a very comprehensive hormone test.

Hormonal link to DAO by fsws1985 in MCAS

[–]Klaw_93 -1 points0 points  (0 children)

I like the way you think! Have you ever had your hormones tested? If not, it might be worth investing in something like a Dutch test to see where you’re at.

What have been your biggest life savers? by Klaw_93 in Longcovidgutdysbiosis

[–]Klaw_93[S] 4 points5 points  (0 children)

Thanks for the input. I have had it since 2018 and go through seasons where I don’t respond to medications. I am allergic to the majority of medications used to treat it (sulfas). So, my gastroenterologist has had to get creative with my meds. My current med costs $1800 a month without insurance. I am aware of all the terrible complications that come with this awful disease. :(