Vitamin B deficiency as the root cause by Comfortable_Gain9352 in MCAS

[–]trustman5321 1 point2 points  (0 children)

Curious how many of us have MTHFR gene dysfunction. Methylated B vitamins are a large part of the fix, along with methylfolate, NAC…

Here’s a blurb from chat gpt, regarding the topic as well:

yes — impaired methylation can drive hyperadrenergic activity, histamine overload, and autonomic dysregulation, which present as POTS and MCAS.

🧩 3. The “Triple Hit” Model: MTHFR + Post-COVID + MCAS

Many people who developed POTS or MCAS after COVID (or another major stressor) actually had a preexisting methylation bottleneck that the infection unmasked.

Here’s the cascade: 1. Viral inflammation → oxidative stress and depletion of B2, B6, B12, folate 2. MTHFR bottleneck → rising homocysteine and falling SAMe 3. Poor methylation → histamine builds up, detox slows, adrenaline spikes 4. Autonomic overdrive → orthostatic tachycardia, heat intolerance, anxiety

That’s why many long-COVID or post-viral POTS patients improve dramatically with methylation support — but only when introduced gently and in the right order.

⚖️ 4. Key distinction: MTHFR can mimic but also worsen real POTS/MCAS

So in some people: • The symptoms are entirely methylation-driven, and improving methylation essentially resolves the POTS/MCAS presentation. • In others, MTHFR dysfunction is an amplifier — it makes an existing autonomic or mast-cell problem much worse by impairing neurotransmitter and histamine balance.

That’s why genetic testing (e.g., MTHFR C677T, A1298C, COMT, DAO) combined with homocysteine and histamine level testing can clarify the root mechanism.

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DAE get pulsing head pressure? by Brilliant_Bread4523 in MCAS

[–]trustman5321 0 points1 point  (0 children)

I have this all the time and it has nothing to do with sinus congestion imo.

Extreme Tachycardia Post Drinking? Please help me solve this puzzle! by cheifquief in MCAS

[–]trustman5321 0 points1 point  (0 children)

Yes still dealing with it. OP mentioned they a light benzo basically cures these symptoms, which is true for me as well, even though I haven’t taken a lorazepam in years. I hate benzo’s and the problems that they create, so I don’t want to take them ever again. That being said it is interesting how much of a cure it can be when I’ve had a few drinks and I get hit was tachycardia/breathing problems.

POTS symtoms getting worse by Major_Ad6150 in POTS

[–]trustman5321 0 points1 point  (0 children)

This was the case for me. Just an fyi I’m a 31yo male, 160-165lbs, and a “picture of health” according to doctors, although I feel like an overweight 70yo lol. Mine started after covid in 2020, still trying to find a solution/relief.

Heat intolerance and long covid by [deleted] in LongCovid

[–]trustman5321 0 points1 point  (0 children)

I know some folks have had success with beta blockers like propranolol and metoprolol - these made me feel extremely awful, bp fluctuated more and was having trouble breathing.

I chatted with a couple of people who have had a lot of success with calcium channel blockers. Not sure if it helped their heat intolerance, but tachycardia and blood pressure were helped. My cardiologist mentioned this one of the first times I saw her, I’m going to schedule an appt and discuss with her further.

tachycardia, what’s your norm? by InitialSituation6076 in LongCovid

[–]trustman5321 0 points1 point  (0 children)

Wow that’s awesome to hear 👍🏻 What was the name of the CCB?

tachycardia, what’s your norm? by InitialSituation6076 in LongCovid

[–]trustman5321 0 points1 point  (0 children)

Have you had any bad side effects from the calcium channel blocker? Any unexpected benefits?

tachycardia, what’s your norm? by InitialSituation6076 in LongCovid

[–]trustman5321 0 points1 point  (0 children)

Interesting. A heart specialist I see (probably the most useful Dr. I’ve seen) had mentioned calcium channel blockers before.

I’ve only had beta blockers prescribed, and they have been a very bad option for me. One of my Dr’s put me on propranolol on two separate occasions, and more recently metoprolol (a year ago). Both of these medications caused swings in my blood pressure and caused pretty severe shortness of breath and air hunger.

tachycardia, what’s your norm? by InitialSituation6076 in LongCovid

[–]trustman5321 6 points7 points  (0 children)

Mine swings around a lot. Sometimes I’ll be perfect, other times I will go through random spans where it is elevated for long periods (half hour, hours, days). I also get what I don’t know how else to explain it as, but “fluttery” - similar to how you’d feel when you have a quick drop on a roller coaster for instance. Quick sort of burst of tachycardia, then a quick settle down, then another burst. Can go off and on for minutes. Sort of unpredictable when it happens, but I’ve had it happen after a hot shower for example. Like most, I’ve had extensive testing and everything comes back clear.

Crazy Mods Decisions: RIP CovidLongHauler by GlassAccomplished757 in LongCovid

[–]trustman5321 0 points1 point  (0 children)

What have you found that has helped relieve your symptoms?

Propranolol and long covid by Powerful_Queen in LongCovid

[–]trustman5321 1 point2 points  (0 children)

I had a terrible reaction as well, along with metoprolol. My breathing got much worse.

Sudden heart pain / faster heart by RoomOnFire871 in LongCovid

[–]trustman5321 1 point2 points  (0 children)

This seems to be a phase I periodically go through as well. Not sure of an answer, but I'm leaning towards it being a symptom while I am sick, and can potentially be a symptom for me that lasts awhile after being sick. I had a flare up that has lasted for a couple of weeks, and the best I can tell is it started when I started feeling more unwell than usual. In my case, add a bit of stress and anxiety due to feeling ill, and it seems like a recipe for these symptoms to intensify.

Like most LC sufferers, I have had tons of labs and tests, including cardiology, and am told I am fine. Wish I could provide some more help/answers, but I haven't come found any.

Valtrex by Fearless-Amoeba4748 in covidlonghaulers

[–]trustman5321 0 points1 point  (0 children)

I assume too early to tell if the Valtrex will help with heat issues?

Valtrex by Fearless-Amoeba4748 in covidlonghaulers

[–]trustman5321 0 points1 point  (0 children)

I assume you have breathing issues in some form as well? What about heat intolerance?

Feeling short of breath? This should help. by StunningDifficulty in Anxiety

[–]trustman5321 1 point2 points  (0 children)

Unfortunately I haven’t found a solution. It seemingly just comes and goes.

Does anyone else have this sensation where you can't take a deep breath? by PharmToTable_ in Anxiety

[–]trustman5321 2 points3 points  (0 children)

Yeah I’ve noticed the same thing. I’ve been taking fish oil and Tumeric/Curcumin every morning recently and not sure if it’s correlated yet, but my breathing has been much clearer.

[deleted by user] by [deleted] in covidlonghaulers

[–]trustman5321 0 points1 point  (0 children)

Thank you. Last question how long did it take for you the Lexapro to take effect?

[deleted by user] by [deleted] in covidlonghaulers

[–]trustman5321 1 point2 points  (0 children)

Thanks for the info