But my Hair is Not my Own!

A common refrain from the head-shaving proponents among us sounds something like this:

“But my hair is not my own, it HAS to be shaved off!”

While there may be validity to part of this statement the conclusion is rash and ill-conceived.

Take a look around you.

No one’s making a dent in this disease by engaging in what is ultimately an unsustainable and potentially harmful practice…..a practice that drives this pathogen into deeper, darker, and more dangerous terrain. If Morgellons can alter DNA and effectively hijack your hair, what makes you think it will stop there? Long-time sufferers are well aware that this pathogen ultimately adapts to its’ circumstances, up to and including scalp shaving.

Faux hair, scalp lesions, and biofilm buildup can all be addressed without going bald in the process. So why does the bulk of information surrounding this subject encourage Morgellons victims to shave all their hair off? An almost cult-like fanaticism clouds social media discussions with over-zealous adherents taking personal offense when alternatives to scalp-shaving are suggested. Sadly, many give in to the peer pressure, go bald, and live to regret the decision.

My hair was behaving in stereotypical Medusian fashion, attempting to slither its’ way into my eyes and ears, keeping me up night after tortuous night, and generally making my life a living hell. A regimen of French green clay and essential oils has prevented Medusa from doing her worst, but I’m under no delusions. She will return in full, unbridled regalia if I let my guard down.

I experimented with shaving off portions of sideburns that behaved unnaturally, and that had transformed into something more resembling plastic fiber optic cable than strands of human hair. I discovered the stubble that grew back in its stead was far more attractive to this pathogen than my pre-existing hair — a phenomenon echoed by many disappointed by their head-shaving efforts. Morgellons appears to thrive both on and under skin that’s been compromised by shaving. I also discovered it’s entirely unnecessary to shave the hair in an effort to restore it to a more natural state or to treat the scalp itself.

Since publishing Medusa Revisited, I’ve moved out of a highly contaminated home environment into something more tolerable, and have found I can forgo my clay poultice step entirely, but that jar of French first aid is always at the ready when emergency strikes.

Nowadays, I spray my scalp with an elixir the Morgellons organism simply cannot tolerate:

I add 14 drops of NOW Essential Oil of Oregano and a drop or two of fractionated coconut oil to a 2oz spray bottle, shake, then top the bottle off with 70% rubbing alcohol. When I find the scent of oregano overwhelming I add a few drops of essential oil of cedarwood to balance out the nose. This potent mixture is thoroughly sprayed over entire scalp and sideburns. I apply this spray like I would hair dye by parting out sections of hair to expose the scalp – section by section – then vigorously massage into scalp to ensure follicle penetration.

But first, I slather up locks and scalp with Kirk’s Castile Bar Soap, rinse with hot water, then condition with a non-petroleum based hair-smoothing conditioner and comb through. When rinsed off with water as hot as one can stand, a smoothing conditioner will considerably inhibit the organism’s ability to cling to the hair cuticle, which is the outermost layer of the hair shaft. Clean and treated hair is then confined up and off the shoulders in a bun or hair clip.

I’ve observed health concerns of a far more serious nature echoed from the shaven than those who’ve taken proactive measures to maintain their head of hair. The bald are generally sicker than their haired counterparts, so why would I follow their lead? I’m not going to take advice from those who appear from both their own images and personal testaments to be far worse off than I…. and only getting sicker.

I’m going to keep my hair.

4 thoughts on “But my Hair is Not my Own!

  1. Agreed keep the hair. When I first became aware of how infected I was and the weirdness with all the hair on my body it exploded much worse. My hairs had little white/clear fibers growing out of the ends and many also had fibers coiled up around the hairs. Naturally I figured erroneously that removal of the hair would stop it in it’s tracks and allow me to cleanse myself. Boy was I wrong. Until I shaved my head and all my body hair the symptoms were confined to below my knees, below my elbows and on my scalp. After shaving I noticed within an hour of drying off I had painful itchy outbreaks of those all too familiar red spots all up my arms and along my shoulders, up my chest and back and all over my face. Then a day or two later the black specks and other strange objects along with stinging itching sensations started and I began to really freak out. It got so bad on my face I was forced to breathe through a straw to avoid inhaling morg particles and fibers constantly. At night I could not sleep with a straw in my mouth so I used medical tape to cover my lips and surrounding skin. I went to A&E thinking surely they would see how much junk was coming out of my skin only to be refused an examination by two doctors, told I was delusional and then coerced to take anti psychotics which I vehemently refused. Now I can’t even see my GP as I have delusions of parasitosis on my permanent record. This was a year ago. I’m still infected and there is no area uninfected on my body now. The only relief I get is to physically extract the morg junk from itchy stinging locations. At first I was bearing the pain and then removing the morg junk with a sticky roller as it emerged. I could feel hard lumps under the skin and the stinging sensations were getting more and more common. I started to feel strange static electricity sensations on the stinging sites. When one area started up it was like they all started up and my skin was humming with intense sensations constantly. It got so bad I could not even sleep. Then one day I got angry and literally started ripping chunks out of my flesh where the sensations were. The more I did it the more I noticed it was easing my pain and extracting the strange morg junk under the skin. Over the last few months I’ve been perfecting it so that I can extract the material while causing as little trauma as possible. It’s clear it regenerates after extraction but I think if I keep it up I may be able to pick it out quicker than it can regenerate. Some areas are problem areas that regenerate quicker like my wrists, scrotum, anus, scalp crown, inside sides of feet and upper shins. You should email me so we can talk more.

    Liked by 1 person

  2. I cut my hair much shorter, as it was simply thinning out and tangling quickly (you know how it gets). Keep the hair, unless you can’t maintain it, due to illness. This stuff will get anywhere, and it does. I’m so sad and sorry we are left to fight alone, without MDs. I can’t believe how unmodern modern medicine is. It’s (almost) scarier than the disease.

    Liked by 1 person

  3. I was presented with this article in a Morgellons group when asking whether or not I should shave my head. I am glad I read it before making the decision as I can not afford to make this problem any worse than it already is. Thank you to the author for presenting this case against shaving. I shall continue my own daily regimen while adding some great tips from the article. Most importantly oregano oil.

    Like

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