Muon's Case

[Muon]

2 posts back about brainstem:

Relationship Between Amyloid Precursor Protein in Seminal Plasma and Abnormal Penile Sympathetic Skin Response in Lifelong Premature Ejaculation

Decreased density of 5-HT neurons in the dorsal and median raphe nuclei also has been identified in APPswe/PS1DeltaE9 transgenic mice.27 Most cell bodies of 5-HT neurons are located in the brainstem at the level of the dorsal and median raphe nuclei and play an important role in ejaculation.4, 28 The decrease of these neurons might result in dysfunction of the 5-HT system. Moreover, higher Ab levels might be associated with decreased 5-HT.

[Muon]

Example of a recurrent pattern at the moment:

1) Subtle low grade stress is going on for a while--->
2) Subtle low grade burning sensation at various places on the body close to the skin, comes up and increases intensity gradually over time if stress is still present--->
3) Breathing rhythm gets gradually derailed
4) Getting cold and body doesn't adapt properly to the change in environmental temperature when switching different rooms with different Temperature
5) Glans penis feels sensitive in a weird way (increased sensitivity to friction, like clothing)
6) Other tissue can be affected by 1 as well (like throat gets dry)

Example of downward spiral:
3 can increase 1. 1 increases 2, the latter makes 3 worse.

This cycle can be broken once you neutralize stress. If the stress is present for a certain duration threshold then 3 keeps going on even if you decrease stress levels. Then you are stuck with ANS/breathing dysregulation symptoms which you will have to wait out before they reside.

My take: Stress--->Neuroinflammation of small sensory/autonomic nerve fibers.

https://www.mdpi.com/2075-4418/10/12/1022

[Muon]

Stress-->Th2 response (stress related to immunosuppression as in data I got from POIS induced measurement?)
https://www.sciencedirect.com/science/article/abs/pii/S0165247898000212
https://www.sciencedirect.com/science/article/abs/pii/S1043276099001885
https://onlinelibrary.wiley.com/doi/abs/10.1002/nur.1027
https://www.sciencedirect.com/science/article/pii/S1319016417301652

Through the above mechanisms, stress might influence the onset and/or course of infectious, autoimmune/inflammatory, allergic and neoplastic diseases.

These results initially indicated that stress may induce the skewing of the Th1/Th2 balance toward Th2-dominant immunity, which stimulates the occurrence of infectious diseases and allergic disorders.

Some infections might protect the host from Th2 responses. The host could react by increasing Th1 activity which counteracts the Th2 response from POIS. Some people reacted less to POIS during influenza.

A second orgasm makes symptoms worse because the first one already skewed it a bit towards Th2.

[Muon]

My mums autistic behaviours are increasing everyday and same with her high anxiety and low mood, she will not take any supplements now when I offer them to her. She keeps telling me she is fine and to leave her alone but she clearly isn't, its pretty frustrating. Her mum died of motor neurone disease and I worry about her developing something similar as her body clearly isn't functioning properly. Its likely she has many of the same gene mutations I do, if only she listened to me it probably would be cheaper to fix her health now rather than wait for a disease to develop down the line.

She helped her friend move out of a very moldy apartment the other day when she got back she had a butterfly rash on her face which I had never seen on her before which is quite concerning.

My mother gets these flares of butterfly rash on her face, mostly when stressed. You see this symptom in Lupus which is autoimmune. HOD's mother got Hashimoto's disease. Keep observing her behaviour, my brother got psychosis recently. I thought she liked the supplement? What was the name of the motor neuron disease?

[Iwillbeatthis]

My mother gets these flares of butterfly rash on her face, mostly when stressed. You see this symptom in Lupus which is autoimmune. HOD's mother got Hashimoto's disease. Keep observing her behaviour, my brother got psychosis recently. I thought she liked the supplement? What was the name of the motor neuron disease?

Yeah she improved massively on the EPA for the first week, then she went back to her normal behaviours I guess either because she was started taking a lower dose/less frequently or just environmental/diet factors overpowered the good effects from it. Now she's finished the bottle, I might buy her more but she would never buy any for herself as she has no self awareness to realise how much it improved her, and she spends no money on taking care of herself. I forgot to add she has been hyperactive her whole life she can't stop doing errands/tasks like she is wired sometimes.

I asked her the name of the motor neurone disease and she didn't know, but it was one that killed her mother.

I offered her to take liposomal glutathione today to see if it improved her behaviour but she refused to take any.

Yeah maybe the butterfly rash could have just been from the stress of helping her friend move rather than the mold. When moving a bit of furniture in my house with her, you could clearly see in her facial movements/expressions her body/nervous system couldn't handle the stress of carrying something heavy like a chest of draws. I am also aware that is a sign of lupus which is why it concerned me.

[BoneBroth]

I believe lupus is a food/stress/gut related issue. You should listen what Pharmacist Ben Fuchs has to say about it here.

[Iwillbeatthis]

I believe lupus is a food/stress/gut related issue. You should listen what Pharmacist Ben Fuchs has to say about it here.

Agreed I think most autoimmune conditions are due to this.

[Muon]

I believe lupus is a food/stress/gut related issue.

Stress as a trigger of autoimmune disease
This:"Unfortunately, not only does stress cause disease, but the disease itself also causes significant stress in the patients, creating a vicious cycle."

Stress proteins:
https://poiscenter.com/forums/index.php?topic=3725.0

[Muon]

Tried a bit of a green smoothie containing pineapple and spinach, pineapple gives me diarrhea, spinach does other things. Haven't touch those ingredients for years.

I had to run to the toilet in ~ 1 hour after ingestion and had solid brown stool (yesterday's food) covered in green diarrhea. It was tolerable after ingestion until it hit a particular spot in my intestines. I won't touch that stuff anymore. Still highly sensitive to those ingredients especially pineapple. IBS.

1 hour is also the timing that I start to feel bad after ingestion of foods like certain brands of chocolate (where other foods can start triggering local symptoms in oral cavitiy or stomach upon contact for example).

[Muon]

SEV/SE-mediated impairment of T-cell responses regarding my cytokine depression after O?

Seminal exosomes (SE) https://en.wikipedia.org/wiki/Exosome_(vesicle)
SE have already been implicated as immunosuppressive, inhibiting lymphoproliferative responses (2), the activity of phagocytic cells (11) and natural killer cell function (12). Thus, the immunosuppressive properties of seminal plasma appear to reside at least in large part within its exosome fraction.
https://poiscenter.com/forums/index.php?topic=2219.msg39466#msg39466

POIS cascade?:
https://en.wikipedia.org/wiki/Microvesicles#Inflammation
Microvesicles contain cytokines that can induce inflammation via numerous different pathways.[38] These cells will then release more microvesicles, which have an additive effect. This can call neutrophils and leukocytes to the area, resulting in the aggregation of cells.[3][42] However, microvesicles also seem to be involved in a normal physiological response to disease, as there are increased levels of microvesicles that result from pathology.

I don't think a doctor or anyone on this forum considered the involvement of seminal exosomes in POIS. 

[Muon]

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Long standing low grade (oral) mucosal activation accompanied with dryness.
Sometimes I can wake up with a well-developed layer of mucus in oral cavity. Thickness will be decreased withing a few minutes after waking up. Consuming food while layer is intact will give no contact sensitivity, friction or irritation. Consuming food while layer is diminished will induce symptoms. Not eating will still give a sense of low grade activation (has to do with wake and sleep state, as soon as I wake up subtle activation creeps in). Stress will induce or increase sense of activity in mucosal layer and makes me more reactive to food upon contact. Edit: Tongue is more reactive than rest of oral cavity at his moment.

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1)Intestinal B cell-activating factor: an indicator of non-IgE-mediated hypersensitivity reactions to food?
2)Food Intolerance of Unknown Origin: Caused by Mucosal Inflammation? A Pilot Study
Intestinal Epithelial Barrier Dysfunction in Food Hypersensitivity
Food intolerance and mucosal inflammation

Take a look at the first two papers: BAFF could be involved. Increased (local) IFN-g is being mentioned and could be induced by BAFF. These things play a role in delayed hypersensitivity (non-IgE). Food sensitivities were present before the onset of POIS. Low grade mucosal inflammation? And could this be translated to the male genital tract (MGT) as well? Does a mucosal inflammatory mechanism sensitize the MGT to components of semen?

1)Conclusion:
In conclusion, increased levels of BAFF in blood and gut lavage fluid suggest that BAFF might be a new mediating mechanism of hypersensitivity reactions to food. Significantly higher levels in non-atopic compared with atopic patients and no correlation between BAFF and IgE levels suggest that BAFF might be particularly involved in non-IgE-mediated reactions. Locally and/or systemically distributed BAFF affects Th1 and Th2 responses and might have an impact on both local (gastrointestinal) and systemic (extraintestinal) symptoms in patients with self-reported food hypersensitivity.

1)Increased IgG4:
The fact that the increase in BAFF was seen particularly in patients without indications of IgE-mediated atopic disease is interesting. BAFF is an important regulator of B-cell activation, proliferation, immunoglobulin CSR and immunoglobulin production.

1)"non-IgE-mediated or delayed-type hypersensitivity is much more difficult to diagnose26 and, maybe as a consequence, seldom recognized in clinical practice"

2)"Besides patients with FA, we could identify another patient subgroup with FH that was characterized by very low local IgE titers, low TNF-a, but increased proinflammatory IFN-g values. The significance and importance of the increased IFN-g values and a possible correlation with dysbiosis will be analyzed in a follow-up study"

Reduction of POIS symptoms by gluten-free diet in some POISers:
Wiki: In patients with celiac disease, serum BAFF levels are reduced after a gluten-free diet.[28] The same reduction could be present in the recently defined “Non Celiac Gluten sensitivity”

Type IV reactions can start 24h post trigger. Healthcare and research do not take this potential timing into account regarding measurements.

Healthcare doesn't investigate this. Absolutely worthless.

[Muon]

Immunophenotypical Characterization of a Brazilian POIS (Post-Orgasmic Illness Syndrome) Patient: Adding More Pieces to Puzzle
"The majority of these cells are expressing CD38+, which suggests that the activation in this patient is more likely to happen via the CD38 molecule and there is no clinical explanation to that finding"

https://en.wikipedia.org/wiki/CD38

"CD38 is most frequently found on plasma B cells"
Plasma cells produce IgG4. CD38 signaling involved? Cytokine receptors and CD40 are involved in Immunoglobulin class switching.

"CD38 can be a major regulator of NAD+ levels
These reaction products are essential for the regulation of intracellular Ca2+ (Decreased cytokine levels after O-->decreased [Ca2+]i?, CD38 activation on T-cells or indirect via changes in NAD+ metabolism?)
CD38 within the brain enables release of the affiliative neuropeptide oxytocin.
When nicotinic acid is present under acidic conditions, CD38 can hydrolyze nicotinamide adenine dinucleotide phosphate (NADP+) to NAADP.
Nicotinamide riboside (NR) and nicotinamide mononucleotide (NMN) are NAD+ precursors, but when NR or NMN are administered, CD38 can degrade these precursors before they can enter cells.
mice overexpressing CD38 exhibit reduced NAD+ and mitochondrial dysfuntion."

POIS-->CD38 signaling-->Depletion of NAD+-->fatigue (link to ME/CFS?). Niacin can interfere (how?).

It's present in semen:
Seminal CD38 is a pivotal regulator for fetomaternal tolerance

Redlabs-->CD38 serum levels https://redlabs.be/ordering-tests/request-forms/
CD38 docks to CD31 and CD16.

[Iwillbeatthis]

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3609577/ :

"In addition, we characterize two CD38 inhibitors: quercetin and apigenin"

[Muon]

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3609577/ :
"In addition, we characterize two CD38 inhibitors: quercetin and apigenin"

Very good find. Dumping this here:
Metabolism of cyclic ADP-ribose: Zinc is an endogenous modulator of the cyclase/NAD glycohydrolase ratio of a CD38-like enzyme from human seminal fluid

[Muon]

You have to try to rebalance your whole body.
If you work only the lumbar part, you will not have the expected result.
A bad posture requires a lot of energy from our body. I believe that the vagus nerve works hard to try to return the correct posture.
A wrong tension in our muscles ends up causing a stress on the body that activates defense systems that are related to inflammation. Try to do the work of improving posture throughout the body, I believe it will be of great value to achieve the target (cause of the problem).

Same here. Plus the "inflammation" can affect other tissue and the same process starts at the new local site. Already weak parts of the body seem to be more prone. Waldinger said something similar that POIS puts emphasis on scar tissue/weak parts (experiencing more intense symptoms at scar tissue compared to surrounding tissue). Not sure how he exactly formulated it but I bet these two behaviours are related (or the same). 

Edit:
Here it is. I can confirm this, got scar tissue myself from trauma/surgery.
Post orgasmic illness syndrome (POIS)
"An intriguing phenomenon of POIS is that during a POIS "attack", a latent illness and/or a previous scar of a trauma or surgery will become painful or sensitive again. As soon as POIS has disappeared the illness or scar sensitivity disappears as well. Probably this is also due to immunological processes that are activated during a period of active POIS."

Compression of the vagus nerve due to cervical instability in Ehlers-Danlos Syndrome

Vagus?: https://poiscenter.com/forums/index.php?topic=2545.msg39487#msg39487

Numb tongue, burning mouth, and other tongue pain from nerve impairment due to cervical instability

Also poor neck/body posture can induce anxiety in me (anxiety disappears when I adjust neck posture, seems like it's called mechanical anxiety), affects respiratory rate, decreases digestion, subtle increase in POTS-like symptoms.

Stress: https://youtu.be/r7pv_VY-hFQ?t=1692

POTS, Bell's Palsy: compression of nodose ganglion? Trigeminal neuralgia? https://youtu.be/r7pv_VY-hFQ?t=5462