Does Parasitic Skin Disease - Morgellons - Even Exist? | NBC Left Field

[@Bob-zt7ok]

Anyone else find it scary that drs prescribe u anything jest to shut u up

[@smokedsalmon3907]

As sad as it is, it makes sense. If answers aren't clear, a lot of times it does start to look like mental issues. And the frustration of not getting treated can drive the patient to feel crazy. Eventually you are dealing partly with some mental issues, secondary to the first issue, and the patient still wants treatment, they want anything that will feel like it's helping. And then finally you get doctors prescribing just to prescribe to shut the patient up. Sick cycle.

[@two0nina]

Fuckin figures right!?

[@leotarollinson3519]

@@smokedsalmon3907 this is what is happening to me driving me crazy

[@vuelee5313]

@Shadow Boxer someone is doing this.... Not the government. Not cdc..... Black people are not slaves.... We all are... It's legal too... U get sick, u buy their products.. legal seee...

[@victorbeardman1610]

@Shadow Boxer I've suffered from this disease since I was a teenager, almost a child and more than 20 years later they still can't or won't tell me what kind of disease this is or they haven't even tried to help me just scammed me for money intentionally, these evil doctors and healthcare. I'm still suicidal because of this disease.

[@areneesouder]

They even denied that women had menstrual cramps, until not too long ago. I've had fibromyalgia and chronic fatigue syndrome for 36 years and I went through it over that, and still do with people, friends, family, whoever, still not getting just how terrible and serious my condition is and has been all this time. Ruined my plans for life. Btw, I'm 66 now, so I've been sick more years than I was healthy and energetic. Weird!

[@EmbalmerEmi]

I'm 28 and thankfully it wasn't hard to get my fibromyalgia diagnosis about 2 years ago,I got lucky and my psychiatrist was very understanding and vouched for me. There still isn't much treatment for fibromyalgia but at least it's on record.

[@michellegummeson4424]

I'm so sorry for your experience. I totally agree though, and I have the same diagnosis and stigma.

[@alizahalon]

"It's all in your head ". They used to say that about Chronic Fatigue Syndrome. They were wrong.

[@Intoxicanna]

I found a N.A.E.T. practitioner, and my fibromyalgia was actually layered food allergies that were taken care of one by one through NAET. No I don’t have that condition anymore…. There are doctors that do this technique. It is Nambudripod’s Allergy Elimination Technique.

[@SeamsToCultivateDignity]

​@@Intoxicanna i did the N.A.E.T. too! Y'all check into it. It can only help.

[@samanthageach3146]

I'm so sick of hearing stories of medical gaslighting. It has happened to me too. I almost ended my life due to horrific symptoms that my doctor would not help me with. I had to find solutions and ways to ease my suffering on my own which took longer than it should have because I was on my own. I have such a mistrust in doctors now. I have other reasons for that mistrust too. I will not be gaslit about what I KNOW I am going through any longer. Voices of those suffering from Morgellons and other difficult to diagnose conditions need to be heard. Our anger is justified. Doctors need to learn to not destroy the trust needed in the patient/doctor relationship. I want to scream whenever I think of the suffering my (former) doctor caused me. It is truly enraging. It breaks my heart to know that he is still in practice causing harm to other people. I have heard stories from several other patients of his and it's always the same kinds of horrible experiences.

[@rallythewords]

Gaslighting requires knowledge and intent. As 2020 revealed, Drs are clueless drones controlled by their $250,000 license and those who control such licensing. Most Drs are guilty of the Hippocratic oath if not outright criminal behavior.

[@roreetinkerbell6893]

How did you heal? 🙏

[@cyborggoat8392]

Yes! Testify, my friend!!

[@karenvasquez4546]

I hear you. I'm ditto"ed

[@joeyd.staats9546]

I guess just because you have a degree doesn't make you a dr. Most are narrow minded unable to think outside of the box

[@kathalanaoneg1456]

Listen to the patients for heaven's sake.

[@persephone2706]

Listen to the people who devote their lives to studying health, bodies, and psychological issues. There are professionals for a reason.

[@jjk2one]

@@persephone2706 In the 90's Fibromyalgia did not exist and was all in the person's head. Now it's a common diagnoses and lots of drugs are being prescribed by the professionals.

[@vuelee5313]

Update, if u know or feel you have this, look up my other comments on how to shower., Get rid of your bird nest, trees that have birds coming to your yards, stay away from farmers and animals. When hiking, don't. Excercise by cleaning your house like everyday using gloves. Use gloves at all time cleaning your dishes. Vacume ur couches, clean ur brooms, dustpans, vacumes with bleach wipes.... Here's the update..... ..... It's real and connected to everything. Everything is cross contaminated. so it's not in your mind. It's it's released by our government, or by aliens from outer space, it would be just like how these things are. Very very intelligent........ Being like an octopus they hide in the tinyst cracks and crannies of our bodies, (octopus change colors as well, becoming invisible to our eyes) causing a sting or ich from time to time.... When I was in highschool 20 plus years ago this topic came up. The conclusion was that if this thing is real then America and the world by 2020 should have this disease....... There's always hope, so shower correctly getting rid of 80 to 90 percent of this, clean your house, always use gloves doing dishes, clean your washers and dryers (yes dryers), and change your air filter every month.... Good luck.

[@beamersbeamer6514]

Stephanie Ann no listen to the patients. Just because doctors are not aware of this doesn’t mean it does not exist.

[@cindysnow802]

As if doctors never make a mistake! There is a saying " if it has hooves like a horse it's most likely a horse. But sometimes it's a zebra". " Doctors" used to believe lobotomies were a great idea and women were incapable of rational thought. So....you worship them I'll keep my mind open.

[@jaime4674]

Thank you for this Katie & Elise. And, thank you both for essentially helping all of those that suffer from being too sick, too weak, or too tired to fight the good fight. The world needs more like you both.

[@showcrazy2139]

Dr. Koo makes me wish that he had to spend a month or 2 with morgellons...I have it so bad that I have the "fake skin" that gets woven from the fibers. It's awful, and feeling like nobody believes you makes it even worse

[@jwol11741]

I pulled this out of my finger in 2005. At work we had a 50X stereo microscope. It was the weirdest thing I ever saw stuck in my skin. It had crystalized skin with black splotches. Red black and blue fibers. And an almost bark looking substance. 2 or 3 weeks later another one was on my wrist, same thing but bigger clump of crystalized skin with red and black splotches and only a couple fibers. I seen all this at 50X with perfect clarity. This happened to me about 3 or 4 more times. My friend actually pulled out the biggest one out of my elbow and when we looked at it in our inspection lab under the scope he freaked out and said I need to see a doctor. Then a couple days later he told me it is called morgellons and it doesnt exist. We both laughed. That was probably late 2007. Never had it again...its definitely real, I've seen the pictures and its EXACTLY what I remember. Hope I dont have a parasite, I feel fine but ....idk just really weird shit

[@daughteroftheking7617]

How did you treat

[@jwol11741]

@@daughteroftheking7617 I didn't treat it. I just pulled them out and it's been 13 years and never came back

[@jwol11741]

@@daughteroftheking7617 ..I never got it back

[@Jayden3649]

​​@jwol11741 yea it never came back because the it wasn't a parasite just fibers and debris it was real just not a parasite

[@carlo3976]

I did the same.

[@N0B0DY_SP3C14L]

What many don't realize is that the CDC study was basically a joke. It wasn't done by the CDC, it was done by Kaiser Permanente of Oakland, done mostly by interns with a tiny sample group, and the interns admitted to having most likely contaminated the results, so the study was deemed "inconclusive". That word does not mean they found nothing, it means they are unsure of the results. Less than $400,000 were allocated to the study, which in the microbiological studies world is less than a pittance. Nonetheless, so many of these 'respected' institutions like The Mayo Clinic cling to this faulty study to avoid lawsuits for malpractice after mistreating patients and outright lying to the public. It is truly a disgrace to the entire world of medicine.

[@magical8013]

My girlfriend actually has this disease and she's constantly taking pictures of things that she finds she finds. I cannot see it myself but I do believe that she does see these things, I just don't see it myself and she thinks I'm crazy. It's it's kind of weird because I can't explain being with somebody like this, they will do everything in their power to Convince you that they're not telling a lie, and I feel like an asshole because I can't see it.

[@dolceanstar]

It exists and I know from experience that if the only explanation the mind can find of the feeling of scampering tiny feet all over one's body is bugs. The mind will allow you to see bugs. It's actually a rather sane response, rather than not having a subject to focus on that one can so clearly feel. Although I thought I had Morgellons, it turned out to be a combination of an extremely poisonous plant in the garden and a house with rising damp. I do think Morgellons could also arise from ground contamination.

[@leacebee5892]

Its actually very kind that you're empthatetic towards her like this. Many do not have supportive partners. Trust me, as a MD sufferer, the things are very much real. Buy or borrow a cheap 100x microscope and there will be no mistaking the insanity that has invaded our bodies.

[@Truthseed313]

Wow

[@juliepeace418]

my gf has it and I can't see fibers either. I can see little black specs though when she scratches her palm. She is constantly itching and scratching at her body and has no history of mental illness. I'm at a loss of what to do. It consumes her and it is so sad.

[@kimberlydeeney5652]

@@juliepeace418 You're a very kind and empathetic person. In my case it was my mother who has this. It was twenty two years ago it started. At that time I was just starting to navigate the internet. We did it the old fashioned way. Get a good magnifying glass. I'd have to write a novel to tell you what we went through for three years, and that included one of the best Dermatologists up North who took the samples we brought in and tossed them in the trash. Nobody would make this up. Nobody wants to live like this. The only advice I can give is keep doing what you're doing and support her. The itching is horrific, and it goes in stages. The little black seed you see is the end stage. It loves the hands! In my mom's case. Take care of yourself as well though. I'd be awake with my mom 24/7 for days. Tried all kinds of concoctions. It started to get to where I was going to be the "crazy" one. We can't help if we're consumed as well. Sending you both healing vibes. One think that did help was Addoxa. Tetracycline it is. Not a cure but helped. Old fashioned black salve seemed to draw them out. Diet helped with the itching. Not full on macrobiotic, but close as I could get to it for her. 🕉

[@francesmagro5468]

Also for me I often felt a stinging sensation. What a horrible disease to go through & my heart breaks for all going through it.

[@mazzystar5342]

Frances Magro howd u rid of it

[@steel12city17cowgirl]

Wubba Wubba I don’t even think that the pictures look the same....at least mine don’t! And there are no fibers in these pictures and there are in Morgellons!!!!

[@Reptex_cs]

@@lesliepeters2952 I deleted my last comment here, the one that said "not even close". Im sorry, cause I think you're on to something. Not that it can explain Morgellons, I wouldnt know, but Candida looks more like something I might be struggling with. I have also had 2 cats die to strange diseases, the most recent one being just 5 years old. The previous one died to a black, mold-like wound that wouldnt heal on his leg.. Do you have any additional info on this? Websites describe it as nothing to really worry about from my understandig.

[@stevenhenderson9005]

CURE FOR MORGELLONS: Antipsychotic My mom got morgellons in 1998 and it is not a skin condition. It is an error in the bodies DNA coding incorrectly-added nucleotide. Antipsychotic will block dopamine D2/3 receptors and will stop the sensation of bugs crawling on you and will basically put the nucleotide back in place. The effects didn't take long for my mom and after a few months my mom no longer had to take the medication anymore.

[@stevenhenderson9005]

@@mazzystar5342 CURE FOR MORGELLONS: Antipsychotic My mom got morgellons in 1998 and it is not a skin condition. It is an error in the bodies DNA coding incorrectly-added nucleotide. Antipsychotic will block dopamine D2/3 receptors and will stop the sensation of bugs crawling on you and will basically put the nucleotide back in place. The effects didn't take long for my mom and after a few months my mom no longer had to take the medication anymore.

[@rbnluke]

The only difference between myself and the ladies in the video is that I am a man. I can't even begin to mention the similarities in our "delusion" . 14 doctors.....wanting to put me on antipsychotics. I know a woman who was locked up in a mental hospital by her family. One Dr basically told me the only chance of getting better is through diet. I cut out all sugar and gluten. I keep my diet alkaline. I eat loads of prebiotic foods and probiotic packed foods, mainly from fermented foods i make now (sauerkraut, kimchi) and goatmilk yogurt. No cow dairy from the US. No corn due to GMO and all corn including "non-gmo" corn is infected by gmo crops nearby. My cousin the farmer says that's been known for years by farmers. So with these changes, I am mending, less of any lesions. I still have fibers but the symptoms have greatly lessened. I shared this video with a friend who stuck by me and asked one thing, "sound like anybody you know?" . From fibers to microscope to crawling skin to delusional to borax to fixtures to supplements to $$$$$$ to many tears. Thank you thank you thank you. Peace and health to you ALL! respect

[@rbnluke]

Tincture not fixtures

[@rbnluke]

I forgot.....I had Lyme disease and now have chronic lyme

[@StayTunedNBC]

Thank you for sharing your personal experience with Morgellons.

[@___erika]

do you know what can cure eczema? my little niece has it bad, it makes me sad

[@___erika]

rbnluke that friend is a blessing, it's good to hear you had him/her through all of that..!

[@ConnieM.]

Omgosh. I'm suffering beyond belief from this and so is my poor sweet fur child kitty cat. Im so happy to be in the midst of others suffering from this. I'm sorry so many of us are suffering though. This disease will litetally make you feel like giving up at times because of the ABSOLUTELY HORRIBLE symptoms. It's AWFUL!!

[@irowebot]

Look into Spooky2. Their protocols for Morgellons & Lyme 100% work

[@irowebot]

Look into Spooky2's devices. The Central unit with plasma is definitely best, but even running their Remote protocols works. It's the only thing I've seen work with reproducible results.

[@irowebot]

KZbin keeps deleting my comments when I spell the name correctly 😑 Look into spooky two devices. The Central unit with plasma is definitely best, but even running their Remote protocols works. It's the only thing I've seen work with reproducible results.

[@ConnieM.]

@@irowebot Thank you. I will definitely look into those.

[@eyes2c..519]

Saturated solution sski it works treat it like sporotrichosis

[@terrioglesby8152]

It was a year in June since this began with me. I lost down to 94 lbs and ended up in a mental hospital. I'm still affected by these bugs. I found a place within me where I could mentally handle this. Me and my German Shepherd have this condition. I couldn't have gotten thru it this far if God wasn't helping me. God Bless and have mercy on all who are going thru this.

[@itsallabouturanus2997]

🌹🌹🌹

[@ophiolatreia93]

The bugs aren't real

[@davemwangi05]

@@ophiolatreia93 It looks like you're a bug and you ain't real.

[@rebels_finest7436]

@@ophiolatreia93 with a name like that, are you even real?

[@tiffanyclark299]

You should read the book “How to Get Your Life Back from Morgellons and Other Skin Parasites” by Richard Kuhns. He also has a conference call every Sunday for people to ask any questions. You can find the ones he has done in the past on KZbin.

[@boredhousewifelife]

I'm in years right now. I've been sick for so long. I'm in a huge amount of debt for all the different doctors and emergency room visits. I've never been given any real answers or help with trying to recover. I've had chronic hypokalemia and hypomagnesemia, and my heart will start beating extremely fast. My heart rate will go up to the 180bpm. I've been judged extremely harshly by some of the health care professionals. They take one look at me and immediately think I must be on drugs. I can't stand those "faces of meth" photos of drug users mugshots through the years of addiction. Even if these people were on drugs, I still think it's just wrong to make an example of anyone based of what you are seeing on the outside. It's hard to believe we have to even say things like that still after all these years. And addiction is a disease as well. Addicts need help and treatment for their illness, not to be shamed for what they looked like while on drugs. How awful that must feel, and I don't think it does anything to help their addiction or sway someone else away from trying drugs. And if that's the reason they use these tactics, they need to reevaluate how they are doing things. Things like this aren't effective, and it only causes more harm in the long run. Anyway, it's been impossible to get actual help with all the health issues I've been struggling with over the last few years. I've lost 60 pounds in the last year. At one point I really thought I was going to have to just check myself into a psychiatric hospital because I have to be losing my mind to have mental issues to the point of feeling this sick. Thankfully things like my potassium levels and high heart rate showed that something more was off instead of being all mental. I was sent to a cardiologist and nephrologist and neither could prove it being a heart or kidney problem. And now with Covid it's made the process even slower. Recently I started having worse symptoms. I have been using steroid cream and psoriasis gel. And when I put it on my skin and rub these little black specks that look and feel like a black grain of sand. Literally coming out of my skin. I googled it and info on morgellins came up. I can't believe I finally know what's wrong with me. I truly feel it's a miracle. Because the hardest part for me was not knowing what was going on with my body. So I constantly had fear that it was cancer or something that could kill me, and that has been the most debilitating part of it all. As much as it sucks to deal with this, it's better than a deadly disease or severe mental illness. I will find a way to manage this. And now my thoughts won't be constantly racing and I won't feel so much panic when I feel the pains and other body sensations that come and go throughout the day. I know I still have a long journey ahead of me, but I'm so grateful to finally have some answers. And once I get it under control and I start feeling better, I really want to find ways to raise awareness on this. Like they touched on in the video, I can definitely see how it could push someone to suicide. I'm lucky that I have a supportive husband and family. I don't have to work, my husband provides all that. The way some doctors have treated me was so incredibly hurtful. Hard to even put into words just how awful that made me feel. I can't imagine leaving and going home to no one, or not even having a home to come to either. My family still doesn't fully get what's going on, I try to stay patient and understand it's a hard thing to wrap your mind around. We have to really work to spread awareness and educate others so no one has to go through this living hell alone. When you're suffering so badly you just want some relief. When you reach out for help, only to be told it's all in your head, it's enough to break you. I want to do everything I can to make sure no one has to go through those kind if situations ever again. To anyone reading this, I believe you. You aren't crazy. You deserve help. You deserve support. Don't give up. Keep fighting. Hope is real. If you ever need someone to talk to please don't hesitate to message me. Much love and many prayers always 🙏🙏🙏

[@lgyver]

There's much info on this particular topic out there to discover. Best wishes on your journey.

[@lexantoniades4116]

Please message me I have got this and hospital has turned me away 5 times now

[@susansantoro6876]

@@lexantoniades4116 I’ve had Morgellons for two and a half years. I can no longer work. It has killed my memory me causes me pain and my stress level is off the charts. Doctors where I live want to treat me like a lab rat and a garbage pail in medication. I feel my skin crawling ans SEE it constantly every day. I have no quality of life left. I’m better than I was due to more cases coming forth but I pray for a cure. I miss ME.

[@jakejohnsonx]

Demons are real. They don’t want you to know.

[@maryjanney1361]

Am so grateful to you DR RORPOPOR HERBAL on KZbin, for curing my PCOS sickness within 14days, with your natural supplement......🤩🤩

[@davefagan2801]

Katie, I had a few tears after watching this short Documentary and everything you expressed is so very True!!! I started with itching on my head, it got so bad I ran to the Shower and black specks began to fall as the water washed over my head and body. By my side was my Hubby as he watched me freaking out with a terror I have never experienced! There is so much I want to share as I write a comment, but here I will stop my Friend. These past Four years have been a Journey into a nightmare that has left Dave and I Isolated from Friends and Family and Broke!! I must Add my Faith has been a blessing and having my wonderful Hubby by my side. I can not thank you enough for standing up for those of us who will never at this point, experience the Love, Dignity, and Normality in our world again! Well, my Friend that is until this Monster has the research, a possible Cure and put back in its Terror filled Box where it belongs. God Bless You and all of the Thousands out there that have found a way to live Alone Isolated, heartbroken in fear that life will NEVER be close to Normal again. Love You my friend!!! . Mary Fagan.

[@katieyussuf3335]

Love you Mary and Dave

[@leotarollinson3519]

i am dealing with this dont know what to do many may have this and dont know it

[@mattthompson1876]

Lay off the meth

[@ressurectionman]

mary and dave, i too have had personal experience with this. if you are still suffering and ready to heal yourselves, please contact me. its inexpensive and simple and totally harmless.

[@ressurectionman]

@@leotarollinson3519 please contact if you are ready to heal yourself. dont waste your money

[@zEropoint68]

did i hear that _dermatologist_ correctly that he's taking it upon himself to prescribe psych meds?

[@jakerodgerspyrotechnicfun8789]

Yes unfortunately alot of doctors actually do this all the time.

[@howtowithelizabeth7513]

zEropoint68 yep

[@christinemcmahon5370]

Yep. And eventually most will try it just for some Relief. Future world of zombies on meds. I recommend meditation.

[@zypherus6876]

Well to fair, morgellons aside, there actually is a mental illness that causes you to feel as though you have symptoms even though you don't. Such stimations may lead some people to believe that they have Morgellons when they don't. Those people, depending on the situation, may need psych meds. So before you bash all of those meds, remember some people actually need them

[@loft006]

Some psych meds are also anti-parasitic like ORAP

[@masterofwit339]

My very good friend has been battling this since April 2023. We just recently reconnected and I have been blown away by her experience specifically with morgellons but worse than that, her family _REFUSES_ to accept her suffering as a medical issue and has deemed her _MENTALLY ILL_ 🤬 I am committed to doing anything I possibly can to help her through this. Even if it’s only by educating myself and being her rock. Sending my heart out to every single human who is experiencing this unbelievably horrifying disease.

[@sharonjohnson4636]

You are a great friend! When I got morgellons disease 10 years ago, my lifelong best friend since high school informed me that we could no longer be friends after I told her what was happening to me. I was so shocked by this. We had been each other's rocks for decades through many difficult things. But since she worked as a therapist and she had become convinced that this was psychological in nature, she just abruptly ended our friendship. Don't know if she will ever know that kind of pain to not only be dealing with something so devastating, but then to also have a good friend abandon you forever due to it.

[@PrayingForTruth]

@@sharonjohnson4636 That's horrible--and her behavior proves that she wasn't such a great friend, if she'd end the friendship over her disbelief in Morgellons. I'm galled that she wouldn't at least say, "Show me the evidence that you've collected," or something that would indicate medically-scientific curiosity; instead, she demonstrated that the brainwashing of the medical industry holds sway with her. 😞 For what it's worth, I had one friend blurt out (in an online reply) to me, "Isn't Morgellons that psychological disease that makes people think that they have insects crawling on them?" (She didn't dump me as a friend after that remark, but I did leave that friendship over her lack of reciprocal communication over time.)

[@Michaella-l7e]

I hv found a cure that worked on me...Ozone sauna!! I was suffering for almost ten years and now I am finally well..!!forgot even the time I was so bad and desperate!!! Worth to check this option!!!!!

[@Michaella-l7e]

I have given my itching clothes to a microbiologist that had knowledge about Lyme and Morgellons disease and confirmed about seeing Morgellons fibers under the microscope.

[@Michaella-l7e]

Also, when a Morgellons patient has an Ozone sauna session, he leaves the sauna floor with fibers!! This is a great proof that we do not imagine all this. That those things came out of the body!! In my case that is what I had experienced.

[@rita6355]

Anyone get itchy after hearing about this?

[@devware5019]

I was with someone today I feel like I have it So weird

[@francesmagro5468]

This does exist. I've been through it. It was first diagnosed as a allergic response to an arthropod bite. Then I was told it was in my mind. This disease is very real. It took years for it to go away. Lysol spay and like brand would help greatly. You could actually hear the snapping sound when it is sprayed on your hands & hair. It is a disease that causes much stress when others do not believe you. So the disease may cause psychiatric problems but please remember, the disease came FIRST.

[@calexander6084]

Frances Magro Did you take any antibiotics for treatment?

[@marciabarlow4704]

Yes, Frances Magro, and thank you.

[@joyceshealy7191]

How u get rid of this...I'm begging...TORCHURED 3 years. I'm fixing to go soak in BLEACH!!

[@joyceshealy7191]

@@honeyrocks7691 help me please!

[@observer8477]

@@joyceshealy7191 it fixing us we cant fix it.i pretend its a delucion

[@Investigativebean]

The cdc also denied that Lyme disease was effectively an epidemic and not just endemic. Before COVID they denied that it could ever be chronic. This was despite knowing the pathology of syphilis, another spirochete cousin to Lyme, caused ongoing complications.

[@nickrogers8588]

That slow zoom into the Asian doctor really emphasized the feeling that he is a psychopath.

[@marthahutton9440]

Thank you

[@vuelee5313]

No offense taken. I'm close to the cure. I'm asian. Our cilivized nations have this. And this have been out since or most likely b4 the civil war. American civil war.

[@nickrogers8588]

@@vuelee5313 I didn't mean any offense. I was simply clarifying who I was talking about.

[@hihihihihello]

@@vuelee5313 is it something to do with the clothes people wear? wasnt cotton only widely available once america was widely populated (bit before the civil war)

[@benisrael5786]

I took note of that zoom in as well, but my thought was that is the most uncool zoom in I have ever seen

[@MichaelGrady]

Smart dust fungi?

[@bevy4290]

Yes.

[@saranjimable]

Thats one way to put them.

[@marthahutton9440]

Something

[@justmeisthatu9069]

Exactly making us antennas but the little metal fibers that they make are also controlled by LED lights that's why when you going to Walmart it feels like they come alive or when you get around any LED lights

[@lgyver]

Nano & NASA

[@WayTruthLife2100]

This is from CHEM TRAILS. It may be a spirochete, but the source of it is not from being bit by a tick. Many people "diagnosed" with lime disease have no recollection of a tick bite nor had any initial symptoms such as the bullseye ring rash in the location of the supposed bite. I think many people diagnosed with lime disease in the past decade or so have morgellons not associated with a tick bite.There is no "OFFICIAL" lime disease lab test as far as i know, rather they take an accumulation of symptoms from which to draw a conclusion for diagnosis. Its really sad this is mischaracterized as a mental illness when it is not and this nation has serious mental illness that is not being taken care of. The deep state actors don't want to label this because that would bring their other misdeeds and illegal activities to the surface. Plus, this is all part of the plan: POPULATION CONTROL, don't ya know.

[@grassroots8269]

you get my vote

[@noellesweeney8513]

Thank you for doing a story on this. Thanks for sharing Katie.

[@katieyussuf3335]

Noelle, thank you for sharing what you do, as well! 💗💗💗

[@giannaluva65]

@@katieyussuf3335 hi, was this you in the video? I’m a male, 28 yrs old. Started when I was 21. It affects me too. But I’ve had it on/off for years. It’s so confusing. It seems and feels like a parasite. What is it? It feels like parasites under the skin and traveling sometimes.. I had a weird bite this summer, circle bruise with a white kiddie and 2 red dots… but I’ve had this 5 years ago too. I take klonopin/benzos, the benzos STOP THE SYMPTOMS 85% IN THEIR TRACKS! So I’ve been off of it for a month, (because my fiance shot me with a gun, top through bottom wound in foot, I left the city for now, she’s in jail… wonderful then i ran out of my meds due to taking so much for my now PTSD… and great! I almost forgot I had this! Great timing!) and my symptoms came back full force! How are you doing today?

[@GloriaW888]

That's always a doctor's answer when they don't know the answer.

[@MeAarom]

Thank you for explaining and sharing. My so has it. I have been in health care 30 years. It's real. I support my son now researching to help him. Thank you for your honest video. I will keep learning and helping.

[@eyes2c..519]

Sporotrichosis treat it like tht it works saturated solution sski it works ❤

[@Mobst4]

​@@eyes2c..519can u please tell me if you found a cure? What is sski?

[@chrisnunez6863]

Have you tried washing your hair separate from ur face and body? Its on the scalp. The water hits your infected head and hair and runs off to your body. Notice how the face and shoulders and backside get it worse then the legs or front side..its because the runoff concentration. I started washing my hair separately from my body and face and it cleared up. I still have it in my scalp...trying to figure that one out....but it seems to be an algae. I also don't shave so my pores are less vulnerable and I use colder water to keep them smaller. And sweating is bad cuz it runs off and any sweat that touches ur skin will start to rash or look like ringworm. I hope this helps...it did for me. God bless and stay optimistic. One more thing I've been dealing with this 7 years now and its been a long lonely and difficult journey to be on. This is a real test of faith and strength and love. The faith that we will find the cure the strength to see it thru to help others and love from the people who are willing be supportive when they can simply just walk away with their normal lives and not hear are pains or see our tears from suffering. About the time when I started getting my lesions in my left arm that hurt so bad and had to shower cuz I though I had some itchy residue from a chemical i might have touched and right after the little balls of cottons pushed out, Is also when I had taken a dip in a vinyl above ground pool that went green. I remembered a talk About having to shock the water. ... Think if around the time u went swimming in a lake or pond or ocean ... And acquired it there. Algae can look like little cotton balls and there is translucent species. If u take a picture with ur camera and ur phone...(even a cheap one) and after u take look at it and zoom in on ur skin. U will see the abnormalities...that is not ur lens fukn up its the camera capturing with the human eye can't (and some cases won't see do to ignorance) it doesn't have to be a top off the line phone. Also my rags and towels all come dirty no matter what. I guess it has morphed into the next stage....lucky me.

[@johnnyjetson1713]

" I still have it in my scalp...trying to figure that one out....but it seems to be an algae. I also don't shave so my pores are less vulnerable and I use colder water to keep them smaller. And sweating is bad cuz it runs off and any sweat that touches ur skin will start to rash or look like ringworm." Chris, it's a fungus . Ringworm is a fungus too.a drug called Itraconazole that used for Candidiasis works well after a while The fungus attracts 'fungus gnats' which get into hair follicles, ley eggs and die - causing the area to become infected and HURT like hell. These eggs develop into larva which is what you can fee moving. 6% hydrogen peroxide kkills them on contact, but as not all are near the surface you will have to do this many times, and use a sponge/scourer to rub the crap off after the peroxide has been on a minute check my other posts about this that i've made in other videos comments good luck, TF it's beatable, you CAN Kill it, quick! The peroxide goes crazy on contact with the stuff but not with ANY thing else! And it destroys it! YES!

[@chrisnunez6863]

@@johnnyjetson1713 I tried something else becuz it was creating a biofilm. Everything I did was organic. I had to kill them and open up my follicles and it was a lot but I had help from best friend. The more u strip ur scalp of its oil the more its going to produce oils. So its like a catch 22. Cuz it's a fungus and bacteria. So I would kill one and aggregate the other. But I have been normal for a long time now. Water makes it worse u have to use a water soluble that can kill both. Like the Trojan horse style. I used limes a natural salicylic acid to remove the layers of gunk and its a great anti everything. and aloe vera a wonder plant Fresh. From the tree and yard. Let me know if u want know how to do this. Cuz every failed attempt without total eradication gives it a chance to build a tolerance to whatever a person is using. Please don't lose hope and give up. There is always a way. I know what ur going thru. And I am here to help anyone that I can. But I still use the honey and turmeric and ginger for my body once a week its only becuz its good for my skin and leaves it healthy even though its gone. Better then the chemicals. In soaps. Do u know if u have a vitamin k allergy? I do. My kids do and my siblings and mother did. We had a hypersensitivity to products with vitamin k in them and didn't know it was causing a lot of similar symptoms. Sorry for misspellings. I just woke up. But I need to respond back cuz I know the torture.

[@johnnyjetson1713]

@@chrisnunez6863 Bro, it's the 6% hydrogen peroxide that KILLS the bugs AND the biofilm On Contact! It will start to go kinda "soapy" when you rub it on the lesionsand other areas with fungus on them - they are usually itchy but go bezerkly itchy in a hot shower, SO THEN After having spent 30 or so seconds rubbing the peroxide/soap ON A SPONGE?SCOURE it on your lesions and sking - use the sponge to put the peroxide on your skin and then with just a wee bit of soap of the scourer, USE IT to SCRUB ALL that "white shit" OUT of the lesions, At the beginning of a treatment, I'll repeat this process maybe 2-3x a shower with at least one shower a day -- read my other posts here to see the routine That WORKS! Bottom line The Hydrogen Peroxide IMMEDIATELY On CContact DESTROYS this shit! The "soapy stuff" is dissolved biofilm! Then using the scourers to REMOVE AS MUCH AS POSSIBLE - using creams after etc Again, see my other posts for more detail BUT It was these 2 things alone that have helped me get rid of 97% of ALL my lesions, NEVER to return! You can do it too bro But IF you're Serious, get SERIOUS about what you eat, COZ YOU ARE WHAT YOU EAT LITERALLY! So don't "feed the fungus" OR attracts the gnats, which means LEARNING, TF for Google eh?! The library of the world at your fingertips And minds like mine who use it to Get Results - I was Never "delusional" BUT the doctors SURE WERE about their knowledge and abilities! You've found The Answer as to "how to STOP the HELL you're suffering" Get to it! 🤩 And if you can't find your answers with Googs, you can ask me here

[@melissahall6868]

@@johnnyjetson1713 what about in your hair? And what type of goods should you eat?

[@susanmartin9715]

I empathize… at first Lymes disease was not believed either. No insurance would recognize it. I had to search for a doctor … and then I had to pay the entire bill. Keep looking. I finally found a doctor that believed the lymes… and over time he helped me.

[@fernandosanchez521]

My wife is going thru this, and is a nightmare, doctors can't find anything even with all the test she had, i don't know what to do, can I have information about the doctor please 😢 is frustrating not to do something to help her.

[@melodylee4405]

Yes I have it, it came on the back of an actual scabies infestation, it's often vectors in from scabies, chiggers , mites of all types and ticks. And yes, it's WEIRD.

[@tmnashua]

I was hit with it in 2017 when everyone I knew was complaining of being bitten by fleas,most had no pets and saw them coming inside their home under the doors !! Predators after blood..Crazy..!!! nano bots from chemtrails?? Idk..

[@scazz007]

Who is watching this because of the fibres/worms in the face masks?

[@sheskawaii]

Took a pcr test from my job 2 weeks ago and got a parasite

[@russbrown3159]

my neighbor went delusional bout the same time i did...I rode in his pickup.

[@Andrea-xs4ny]

I landed here, wanting to know more about the disease that Joni Mitchell has. It's really other-worldly. What a shame patients are treated like they are. I hope that the medical community and the CDC come to realize that it's real. To all suffering from MD, I wish you health and hope.

[@peterburton3095]

The CDC know it's real. People are under the illusion that the CDC & the FDA are here to help us. Not so. They're apart of the satanic new world order who wants to depopulate the world.

[@dupisdisasterpiece1058]

@@peterburton3095 God and Satan are not real. What a load of deranged nonsense.

[@cheesyspace]

​​@@peterburton3095good depopulation of morons like you is good morgellons is mental disorder nothing more. Its hallucination.

[@suzyq5675]

​@@peterburton3095 No. They honestly do not know what it is.

[@candiceberg5232]

The CDC refuses to acknowledge this disease despite tgere bring over 20 studies linking it to specific bacterial infections

[@DavidDuffVague]

Test those fibers with gene testing and also identify their composition.

[@ginsuma1402]

They have tested them....totally foreign material...they have no clue what those fibers are. I believe it is a type of biological mycelium.

[@mayort6548]

@multisomebodyelse notme you're getting close

[@MaryLynnMcKenzie]

@@ginsuma1402 a fungus? we had a very wet spring here and there is a garage that is attached to the house that is rotten and soaked, a fungus makes sense. It hit us overnight. We sprayed for bird mites several times, then got a microscope and it is blue and red fibers that bite! WTF?

[@deutscheratze8930]

@@ginsuma1402 watch the german guy Harald kauz vella he is a pro

[@donwall9632]

I heard the fibres can not be burnt. Chemtrails

[@noraoros9974]

This is not a bacteria. It’s a transparent, stretchy, ( imagine coupons you get in the mail, those that don’t stick to your skin) organism, with behavior similar to warts. They travel along these ultra thin hairs that are constantly growing, some of which are barbed, which act like hooks to catch the ones that aren’t, they make the skin feel tingly. Than, there are ones that feel like splinters, those are different. They can’t survive outside, they surface as moles, or skin tags, when removed, have really long hairs attached. They will find there way to eyes, ears, nose, lips, gums, and throat.

[@mk8446]

Yup. I have them EVERYWHERE! My eyes will bother me so bad. I'm infected inside and out. It's nuts. We need to start suing doctors. They took an oath that they are supposed to help people and they aren't.

[@noraoros9974]

@@mk8446 I’m done with Dr’s. I’m looking for a scientist.

[@designlounge7466]

@@noraoros9974 did you ever figure out what this was? Or find some relief? I had this same exact thing you are describing for 10 years now. 20 lesions on my face alone at one point. Now I have three that have never healed and the oldest one is from 2016. Any new information would be greatly appreciated!

[@Brians-Easy-Low-Tech-Solutions]

Interesting that nobody can keep focus in the comments. People watch way way too much dumb tv (x-files) and even X-files wouldn't do episodes on stuff as daft as in the comments! CDC says there is no common cause, and all that means is that some people probably have a real disease and some others are crazy. If you have fibers "under unbroken skin", then you are likely to have the disease described by Middelveen, so for heaven's sake get your little phone microscope out, video it and put it on youtube! Especially if it is a squiggly fiber under unbroken skin, it will show that the thing is real because how could a person insert a twisted fiber under their skin? Even Penn and Teller couldn't do that. And, when you are taking the video, do a commentary to help people understand what they are looking at. And focus up and down to show that the fiber is under the skin and not on top. If you have fibers coming through show them too, but the proof that this thing is real is fibers growing under unbroken skin. Do as I suggest, and not only are you are doing real science but also being a real advocate for others with your condition. Another thing, many of you are suffering mentally and might not be able to do a coherent commentary, so, in that case, get a patient friend (without the disease) to do the microscope or magnifier work. Keep you commentary to the observable facts, don't talk about "chemtrails" (water vapor from burnt jet fuel condensing behind the jet) or other stupid crap.

[@TheKatarinaGiselle]

Funny, because the cdc finally admitted it IS real.

[@AltheHealer]

When?

[@elouise5593]

Yes, and associated with Lyme disease.

[@SonorousSilence]

Doctors had me thinking I was making up back pain until I needed surgery. 3 years of constant pain and surgery could've been avoided if they ordered an MRI early. My dentist said I needed a filling on a tooth I told him I didn't want to do at that time. He did it anyway. It got infected, and I lost my tooth to an infection he gave me. I hate being in a situation where I have to trust so-called doctors.

[@francesmagro5468]

My bout ended in 2007. Using rubbing alcohol on moist wipes & lysol spray even if not the brand also helped. I can remember spraying my hands & the loudest popping sounds could be heard, even on my hair. I prayed hard & God must have heard me.

[@NicoleReduls]

How can the specialist doctor say that these fibers are not parasitic when I can see them moving completly on their own in an invironment with absolutly no air current? And the way they move are extremly worm like.

[@glendajesus1071]

Marianne Middelveen did the Morgellons' community a disservice by suggesting the long hair-like fibers are probably just hair or other contaminates, and that we become too obsessed with our condition, thinking that everything is a Morgellons fiber! She needs to open her mind to the possibility of Morg fibers that don't match her narrow minded ideas about what they should all look like! Gravely unhappy with her particular views. But, the rest is terrific! Thanks for doing this! It means so much for all who suffer in silence!

[@no1sebfan]

my fibers were all microscopic or very very small ... my first thought was a hair when you see it that big. I agree with Marianne.

[@eyes2c..519]

Or she's pd off by the agenda by the ones who are creating the issue

[@crystalformobbin1409]

There is this weird hot sauce trick this guy who is a sufferer as well showed me you spread this hot sauce on ur hands like a paste anf watch them litterally start clumping up out of ur hands in gobs its gross

[@dtotheponcharo]

bleach too ive done it on my face shits crazy

[@andreavasquez63]

OMG I thought I was alone!!! I'm so tired of being told it's in my head that I'm crazy....I really wanted to die omg I'm not alone

[@happynancybear8709]

Oh boy. I started waking up in July with terribly itchy bites. Thought it was bed bugs. Threw out my bed n tons of clothes. Terminex said no bed bugs. I concluded scabies because I was expelling round specs in rows. But 4 doctors including dermatologist said no scabies. Started pulling on spots with tape n noticed small strings. Taking anti parasitic but still a few new wounds which seem to not heal n are making deep scars. I too, considered suicide. I live alone n touched no human to get scabies from. Biopsy said no as well. I was saving samples to show him but now I don't want to be thought crazy! Do people have round specs as well as fibers? The tape shows many strands, singular, but I rub off hard specs, dark and beige. Sores lasting forever. Any thoughts?

[@ressurectionman]

@@happynancybear8709 yes, bad shit but curable. got rid of mine, totally cured, no ongoing maintanance simple always works best. thyme, sage, marjoram,chamomile, rosemary,anise, star anise. a bit of each in pot 2 litres water, bring to boil with lid on. when coll seperate herbs and discard and can be used on effected aeeas. refrigerate you herbal tea, and drink 2 litres day, or as much as you can. do this till job is done, your body will tell you, but around 4 days to a week. naturally good food etc. . i want to hear your progress and pass the cure on please.

[@happynancybear8709]

@@ressurectionman thank you I will try it!

[@jaime4674]

@@ressurectionman Hi Anastasios. Thank u for sharing this info. on what cured you. So good to hear about ANYTHING that has killed this fungus, parasite, bug, worm, bacteria, virus, aspergillius/black mold, a mutated form of mold, or whatever it truly is...maybe all of these. I am going to try your remedy as soon as I am able to buy the herbs I don't already have. But will keep u posted. Do u have an email address or any other way to contact you, to keep u posted on my results? Thank u again!! JP

[@ressurectionman]

@@jaime4674 hi, jp, you can friend me on facebook.

[@frankurbano4015]

My girl has been plagued with this for probably over 7 yrs now. She suffered in silence and mostly had the problem really bad all over her scalp and thought she had ca6ght some kind of fungus from my gpa, who was prescribed a creme for his lesions- but dud by really do much help. She couldn't see them, but it got so bad she had ra ked her scalp raw , so bad that it hurt to shower! The doctor didn't want to "touch" that one. .would pass it along to a dermatologist, but no such appointment was made. She quickly got the hint. She tried biotin to help ei th growing hair back - it exasperated it!!She found by accident that eating raw garlic would make them "burst", if u will ( from the gooey sack they would protect themselves in) She could feel them moving in a clockwise motion and literally w ould follow them from one side of she scalp to the other but would hv to time its rotation movement in order to be able to dig it out! It strange stuff for sure..if sh e didn't drag it down the shaft quickly while pinching hard, they would go right back to the skin- almost as if it had teleported she would joke, lol.She feels that they hv an intelligence to the m and are ultimately connected to one another . She thought it was some kind of biotech being researched without her knowing. The black ones are blue black, can appear as a tadpole w 2 wispy tails, can slice like a razor, but are soft as a feather. There are yellow cotton balls that match ur hair colour, red ones and Brown ones too. She has had major pain in her sciatica when they deve lope on the backs of her legs..her joints hurt too. She now wears wigs and burns the ones she digs out.

[@lindabenstead6672]

What you said about cutting like razor, YES! Eactly!

[@freeloverboy8879]

It could be fungus due to hight carb diet. Tell her to try the no carb diet for a three weeks. And to take fluconazole

[@Uhohlisa]

Yeah you guys don’t sound crazy at all

[@Kjspun1021]

I went through 12 dermatologists telling me I was crazy. Horrible

[@Uhohlisa]

Because you are

[@sharonhiatt3859]

It comes from the aerosol spraying! There are multiple issues involved. NANOTECHNOLOGY!

[@MaryLynnMcKenzie]

I am staying with a friend and we both got them overnight??? Thought it was bird mites and sprayed, nothing stopped them. We got a microscope and they are blue and red fibers that bite. WTF?

[@sharonhiatt3859]

@@MaryLynnMcKenzieResearch Morgellons !

[@ElectreIsMore]

@@MaryLynnMcKenzie that bite ??? What do you mean

[@MrMarkRoads]

I had a tick bite when I was 12. I'm 56. It's been a very long hard painful road. I don't hold beliefs I just want it to end.

[@elouise5593]

Are you being treated for Lyme disease?

[@carriethompson84]

I was diagnosed with scabies so obviously I started paying very close attention to my skin, I did start picking because I thought that I can get rid of where the Mite was under the skin and then I started finding that I could literally push or squeeze out like a pimple, these little things that felt like half the size of a grain of rice or smaller but they felt like hard plastic coming out of the pores on my elbow and I'm still able to get some out but as far as the fibers, I haven't really seen anything like that but I keep getting these clear looking splinters around my wounds that he'll very slowly by the way so last night I finally did the Permethrin treatment correctly. The first time I did not do my scalp, the second time it wasn't strong enough, it was only 1% Permethrin so we never truly got rid of it the second time and the first time I didn't do it right so last night I did our scale, the body, got up and washed everything and they got a shower but I did find my first gray hair but after finding some of these weird symptoms I looked at more videos about Morgellons which I have watched in the past but I never thought I had it so I didn't really get into it into detail. I did believe that it was real but I just didn't think that I had it and they are saying that it is due to the candida overgrowth which I do have. My doctor has in not officially diagnosed me with it but he has seen the symptoms and now I've got thrush basically if I don't brush my teeth right on time or even before 24 hours, I get a white coating on my tongue, I had these little rashes all over my body last summer but this summer I've only got about three or four, my belly button is slap full of this horrible smelling what can only be described as a yeast that I pull out with a bobby pin but ever since I put the Permethrin in my belly button, it has helped since last week, it doesn't smell as bad and it's not getting as bad so I'm wondering now, where the mites hiding in and if so, why are they not inside the skin and so easy to pull out? I really don't know and I don't want to say that every single thing going on with me is linked to possible Morgellons but more than ever I believe that it is real and then I might even have it. Again I'm not seeing any fibers, I don't get lesions that form on their own except the wounds that I had that I inflicted on myself trying to get the mites out, they would then try to go back up under the wound because they make the skin hard over them and the scab gets hard already so it was the perfect environment for them so it would make the wound worse and hard to heal so I can't describe the silver hair that I have started to get in the past few months. I just pulled one out about 30 minutes ago and I thought I had my first gray hair because I'll be 34 years old this year and now I'm not so sure if it's really a gray hair or part of morgellons but I put it close to my phone, it didn't do any crazy wiggily stuff but whatever came out of my hair when I got out of the shower yesterday before doing the scabies treatment, the fibers are pulled out of my hairbrush, it's a fairly new hairbrush, they were very electro-magnetic and I did not even have my phone near me but they were just swaying back and forth all by themselves and I thought that was pretty crazy so I don't know what's going on. I'm thinking about making some videos and uploading it to my channel. I'm very stressed out right now and I have a lot going on in my personal life so I don't know if I'm trying to look for an escaped or if this is really happening, I know the plastic splinters I pulled out of my Bobby and my son's body and they kept coming back to. My doctor said that we can do a treatment but the treatment would consist of some type of medication where they have to take your blood every month than I have lost my Medicaid and I just got it back so I think I'm going to have to talk to him about doing something to cure this yeast overgrowth or I'm not going to get better because they think Morgellons isn't linked not to Lyme disease but to candida overgrowth, it's a fungus is what they think. I think it's from the government in the CDC created this s***

[@shantinaturechild6385]

It looks lime you "only" have scabies. Hard enough but l suggest to transition to a raw ripe fresh organic alkaline produce diet, get rid of mercury fillings of you have any and don't eat cooked, baked, fried starches, nuts and seeds unless sprouted into microgreens and no animal products or oils except maybe coconut oil. All the best.

[@pamelaroach319]

I've seen the swaying hairs.i have morgellons.

[@imafuckingrobot]

Girl you have excessive keratin production and systemic yeast/candida. Listen to your doctors and take a treatment for yeast.

[@carriethompson84]

@@imafuckingrobot that's the problem, that post was from a year ago and I don't have scabies anymore but I did, I was diagnosed with scabies for a fact. That was the worst it ever but my doctor at the time, he quit or retired. I don't know, someone from the office called and said that he was no longer there and I had 30 days to find a new doctor and that they would give me a 30-day prescription but after that they could not do anything else for me. However, he just kept saying that it look like ringworm but it's not ringworm. I have put different antifungals on it and it does not respond at all, I've done it for the full 2 weeks, I've tried doing it for a full month. Every single day. In the winter it will go almost completely away and then in the summer, it comes right back. At one point, he says that there was an option and some medication that I could take but it was very hard on your liver and I would have to do blood work every month so that just was not an option at the time because I was self-pay paying out-of-pocket. A lot of the issues have gone away but I do still get the red patches and it kind of looks like psoriasis but I really do think that is some type of candida and because it is summer. Most of the other issues have gone away, I think I was just severely stressed out at the time and I was looking for things just to forget what I was going through

[@odoricomorales.martinez9872]

Carrie thompson , lanpruebanpara ver si tienes morguellon , es sentir quebte caminan en la cara y si los atrspars parecen basuritas sin pies ni cabeza ,yanincrustadosben la piel se sacan con masaje , frotandose con las manos usando aceite para bebe , cuando empiezan a salir se sienten en lasmpalmas de las.manos , los puedes atrapar con sevilleta y ponerlos en una bolsa,ya cuando termines de sacar los que se pueden todavia , lenpones acido muriatico un chorito (poco)y cierras la bolsa solo asi se mueren,, no te lo pongas tu, el morguellon ( losnparasitos no tematan , lo que mata a la gente que losntiene es el estrés y lo wue se ponen para matarlos (toxicos) si te crecennen lanpiel tapandolos con cinta Masking mueren ,se da uno cuenta , porque dejan de crecer, se adwuiere la Reyna ?por contacto con personas infestadas y crece la Reyna en 6 años empieza a Reproducirse

[@UserUser-oy8ch]

y'all see that 2008 inside edition vid where a scientist said the strings are like nothing he's ever seen

[@catherine8579]

I have invisible illnesses that can't be seen on tests etc & my illnesses are only just now being taken seriously as real illnesses in the last approx15 years, so i can only imagine how much more frustrating it would be to have actually have something physically there to show symptoms & still not be believed.

[@oneoffbear1812]

She said the infrared sauna helps... I get weird break outs that look similar that clear up when I got to the tanning bed regularly

[@manuelflores9359]

It got so bad i was using gas and paint thinner.lighter fluid. I just wanted to go away

[@treylerparkmark]

this is so scary. i hae recently been dealing with this same problem. ive had rashes and skin problems since i was 15 and i have never really been sure what was wrong with me at 34. i honestly am not sure if what i have is exactly the same. i dont know that they are different colors. they seem to look very much like my hair. seemingly all of my hair now are these things. they definetly react in a way that is very clear to see. jesus it sounds crazy to even talk about this. its so easy to pass over. idk if it takes a long time for these things to reproduce enough to become visible. i havent actually seen anything but a rash i have had since 15. i had always blamed it on food intolerances. its definetly effecting my health in ways that are almost intolerable. its so disheartening to know that although this thing or things are effectively ruining my life i have little to no chance of ever recieving any help.

[@christinemcmahon5370]

Morgellons is just as typical as any other reason we go to the doctor. All they do is lift the hood, check the fluids, sell you some RX and send you on your way. My Mother lived with Morgellons for over 40 years and of course got no help only a stigma and lost respect from some of her own children. Someday they might tell us what they truely know.

[@MaryLynnMcKenzie]

why are they not helping? 40 years! How did she live with it. It is driving us crazy. We got it overnight and then thought it was bird mites and sprayed a million times and nothing killed them. Got a microscope and found these strands of blue and red. Now what????

[@christinemcmahon5370]

I do believe "they" are finally acknowledging something is going on. But I'm afraid they just don't know what to do. Sorry Mom never found relief. Personally I don't spend alot of time outside. I try to eat real non processed food and I drink a ton of water. I also am a frim believer in meditation. If you make it a habit it helps. Much love and I believe you!

[@christinemcmahon5370]

Another problem with my Mother was she was a seamstress. Always at the sewing machine. Always had a needle and thread in hand. Consequently she was sure this is why she had itchy burning "thread" fibers she could see. This disease had nothing to do with her sewing.

[@WelfareChrist]

I think there are patients who suffer from somatization or delusional parasitosis who get mixed in with people with actual morgellons and this sets the whole thing back. What’s most frustrating is that even if it is psychiatric (and I don’t think it is ONLY psychiatric) these people are still actually suffering and dismissing their experiences seems cruel either way.

[@WelfareChrist]

Having said this it did occur to me that these patients should at least be open to taking psych meds if for no other reason then to prove they don’t work. Pretty sure I’d do that if I were in this situation. Being overtly hostile to the very possibility it’s psychiatric reads to me as very suspicious.

[@sarahassan2067]

11 months deep in the same symptoms of morgellons. (Imagine this started with me in the lock down Febuary-2020, and turned my life into Hell! and I actually had a strong belief that this was some how a sort of Ecological imbalance that was linked to Covid-19, Especially that I heard once that some countries executed a large number of bats, so I thought may be some kind of a very nasty No-see-ums had their numbers increased drastically ! ..poor me! but it was still driving me crazy - as an Expression - the crawling feeling and biting in areas that were completely blocked by a pillow/wall/chair or even through a very heavy clothes and blankets!! I even sewed a plastic suit out of some plastic bags, one day when I was almost crying out of lack of sleep .. and it didn't help!). It's only 2 weeks ago when I stopped searching about a variety of potential insects that might cause me these symptoms, and started searching only about the feeling and that was when I first heard about Moregellons. Now, It's both so heart breaking to know the medical situation from this condition, like how doctors first assumptions for such a miserable and mystery health condition would be by so easily calling us nuts! So we can't add another word?! .. but I'm also so relieved to learn that I'm not alone in this World. God bless all the Sufferers from the bottom of my heart.

[@sheskawaii]

Hello. Try turpentine

[@sarahassan2067]

@@sheskawaii Hello. Do you mean to apply turpentine oil on my skin? the same type that has been used in oil painting? Can you tell me more about it? Thank you for trying to help!

[@Truthseed313]

@@sheskawaii seriously?

[@sheskawaii]

@@Truthseed313 yes that and take bath with borax. So mix diatomaceous earth in ur water. It gets rid of the.

[@freeloverboy8879]

Could be fungal infection from too much carbohydrates innthe food. Try a no carbohydrates diet anf fluconazole for a few weeks

[@offgridphyllismathison5798]

Hydrogen peroxide added to baths and drink apple cider with water and eat a ton a garlic this will help

[@vuelee5313]

HP is a great medical medicen.

[@janedoe878]

Doesn't it bleach the hair? Read someone else suggested it as well for scalp as well for body. See if I can find that comment again ..

[@ruthdean5410]

Yes it does change hair colour

[@selfawareness333]

Any time the doctors say it’s all in your head just know that it’s man made and the doctors are trained to say it’s all in your head. Also look into Ozone Therapy.

[@davemwangi05]

Yes they're brainwashed to repeat that mantra. It trickles down from the top echelons at CDC and FDA down the chain of commands to the clueless drug pushers aka doctors. The top echelons know the truth, the lower guys are tools/pawns absolutely clueless.

[@selfawareness333]

@@davemwangi05 exactly!

[@pablo6305]

I take them pills for radiation exposure. Iodone or something I ripped label off so my wife wouldnt think I have shit in my skin. I tell ya if it is in my head then why do doctors make you feel like there is nobody that can help me. You dont treat mentally unstable person the way Ive been treated. I know doctors know.. They try to get me to react. I was asked what's wrong with me by at least 20 people in 2 hour period. Then doctor comes in and acts like he doesnt k iw why im there. They delibritly want me to snap so they can straight jacket me up so they dont have to be reminded that they are letting people suffer.

[@rebels_finest7436]

Ozone therapy just heard about this but heard is one of the best healing methods around

[@pablo6305]

@@selfawareness333 i definitely will. Thanks pray your right.

[@chrishendricks1160]

I had this disease back when I was addicted to meth..I'm 3 years clean and the disease mysteriously went away 3 years ago..lol..just sayin..that's my experience anyway.

[@StringTips-gr2ig]

Wow, for what it's worth I'm praying for these people

[@nfbconnect]

It’s been 5 years since I got pneumonia which led to systematic inflammation that led to these lesions bursting on my face and then I developed full body CRPS and lost the ability to walk. It took me a year plus to learn to walk again. I just found out about Morgellons two days ago there is no doubt that these are the threads coming out of my face. The colors, the pop release, the groupings, the feeling of it all 24/7… I’m heartbroken to think I was naive and didn’t realize the dermatologists I went to just gave me medicines they knew wouldn’t work - just get me to go away. They gave me false hope and the meds have taken over my life. It was so cruel. I’ve been put on 30 pills a day and I’m no better. I went from my owning my own business to being homeless. The pain is something I wouldn’t wish on my worst enemy.

[@carlamolina695]

Stay strong buddy

[@missdesireindependance5194]

Look to doing a parasite cleanse.

[@Truthseed313]

I just found out today that I have it. Saw interviews with people talking about. Not sure how long I've had it. I can see that it's going to be a struggle.

[@CamilleThorntonMandarinLife]

Mine started the same way. Was diagnosed with Adult Allergic Asthma. A few years after that, an MRI showed lung lesions that were written off to pneumonia scarring. Conditions progressed and disseminated all over my body, mucous membranes, glands and joints. Have become debilitated. My primary care doc the only one who has hung in there with me to find answers. We are now looking and testing for Nocardia. Have new MRI scheduled next week. Nocardia typically starts in the lungs from inhaling contaminated, soil, sand, dirt, compost etc and will disseminate if left untreated. Also has the filamentous fibers, granules shedding etc.

[@kingofthemeahhscoolcatstha8488]

Those of us who don't see any other side but the one presented to us on a daily basis will only be aware of only one truth. It's only until you experience it for yourself that you realize that not only are you not crazy it's everyone else. Unfortunately for me I do not have insurance. I live in the mountains. And have no idea what to do? The clinic in the town nearest to me will not look at me because I owe The a bill. If anyone's willing to help me find a solution I would love to get my life back. I am not able to sleep or hold down a job because the fibers that are coming out of my fingers bother me to the point where I spend more than half my day trying to find ways to not look like I'm on drugs. My face is also suffering as well I get these lesions on my face that have more than one hair growing in that spot. Thanks for your bravery to the woman who posted this. And on a final note there are also men that suffer from you as well.

[@aquinnqueens2721]

As soon as I started watching this video i knew it had something to do with Lyme disease. Sadly Canada is going to take the approach as America in dealing with Lyme disease. This is not a good thing

[@MeagainIA2011]

I experienced something like this many years ago. It would start by a red, itchy rash, then overnight, there would be these whitish pale fibers that would catch on everything making the itchy rash worse. I pulled the fibers out of my skin, which weren't exactly excruciatingly painful, but felt like I was ripping a scab off a wound. Then it would clear up and go away. (these things would appear near my wrists, both sides). Then a week or so later it would reappear. If I ignored the fibers, they would become even bigger and stick up higher from my skin. I can't explain it how I determined that perhaps some on my clothing. And I began to pay attention to what I wore. And the one stretchy cotton tshirt like top I began to identify would irritate my skin at the wrists. Sewed at the ends of my shirt sleeves was smallish plastic gold appearing stuff. I stopped wearing the shirt and this fibrous rashes stopped appearing. About a month after tossing the shirt in the trash, there was a story on the national news saying clothing that were made in Malaysia were infested with a worm that would appear just as it did on me. American's were advised to stop wearing the clothing, return them if possible for a refund. I have never encountered this 'infestation' since. That was in 1983 at the age of 23y. Today I am 63y. And this infected clothing has appeared in America after that, oh, like 10ish years later also. And they too, came from Malaysia. So I'm convinced in this wormish tale. Wanna know what else I think? This appears and affects a smallish band of people, and the American Govt knows of it but tries to keep the lid on infestation because its a far more problem coming out of the orient, specifically with large mangrove trees where these parasitic worms live. Thus squelching the selling of clothing overseas to America.

[@Mrs.Robinsons]

Very Interesting! I bet illegals in USA dont help! They dont read your English/words of wisdom & dont care

[@e.boydbartlett5951]

I suffer from this disease and have no idea what to do about it. I empathize with all those similarly situated who like myself have no clue how treat this disfiguring painful illness

[@Isschade1]

could you lose ALL your hair over your entire body ?

[@melissahall6868]

Mine are always in my hair on my head, I have shaved my head twice and it's still there???

[@barbaradalzell2597]

I've had this for over ten yrs. I've been diagnosed with parasitic delusions! And that's it. I still suffer today!

[@nannieweeleeeee2417]

4 yrs for me,it's a living horror story

[@barbaradalzell2597]

@vince furchill It's not. I am BIPOLAR CYCLING 2 NOT schizophrenic. I know this because; (A) I have been to MANY psychologists, therapists, counselors. I have been seeing them since I was three years old it started because of a sexual abuse I suffered when I was a very young child. One of them would have at least considered the possibility. ESPECIALLY after my family Dr. Diagnosed me with "parasitic hallucinations". (B) I have been diagnosed as bipolar in some degree since I was about 12 years old. I have been diagnosed as cycling bipolar 2 since I was 19 (and have continued being diagnosed that way, treated, and medicated) and I'm in my mid-30s now. (C) I am also a therapist. I'm an addiction therapist for traumatized women. (D) I do not show signs or have a single symptom of schizophrenia unless you want to count Morgellons. (E) I have seen first hand what schizophrenia really is. My first husband and the father of my oldest child (who is now deceased because he committed suicide a few years ago), and an ex boyfriend that I was with for almost 6 yrs, both suffered from schizophrenia. So I am very well experienced in this area. I would like to say I was not offended and was not trying to be defensive in this situation and I know u were only trying to help me. The problem here though is i have heard this many times and have been tested for it. You cannot accurately diagnose someone you have never met let alone off of ONE THING YOU KNOW ABOUT THEM. When you do that to ppl like me it gets very aggravating. I dnt think you understand the stress and shame that is associated with suffering from Morgellons.

[@barbaradalzell2597]

@@nannieweeleeeee2417 Absolutely! Ppl try to give us "answers" based on assumptions because they don't believe. That only makes it that much worse and proves our point thoroughly that ppl who dont go through it dont understand and doubt us! Ppl (including DRS.) NEED TO LEARN TO LISTEN AND NOT ASSUME!

[@andreavasquez63]

Me too

[@TheCountfilth]

@vince furchill how did you find that out?

[@gracerobertson8772]

The CDC sorta sucks.

[@richardleetbluesharmonicac7192]

10 years of misery I’ve had seven plastic surgeries in Mexico because no doctor in the US would touch me. The spines break the skin and catch on fabric. You can’t ignore it.

[@Essays4College]

Have you ever had Lyme disease? What do you think caused it? When did you notice the symptoms first?

[@themysteryofbluebirdboulevard]

You're pronouncing it wrong

[@marciabarlow4704]

I went to a doctor and He diagnosed what I was experiencing as MORGELLONS! I did not self diagnose. But he did not suggest a treatment. More important that defining what it is, I want a TREATMENT!

[@MrMarkRoads]

@Chancellor Merkelisms tried it. Nope

[@ressurectionman]

marcia, if you are ready to heal yourself please contact, i too suffered, doctors totally useless

[@ressurectionman]

@@mariasawders4229 my heart goes out to both of you. i, too copped the same obstacles with doctors etc. maria, this cured me, and no reason why it will not work on others and simple and inexpensive. thyme, sage, marjoram, chamomile, rosemary, anise star enice,[and many other herbs with similar properties that dis infect, clean out the system.] anyways, place a bit of each in a pot of 2 litres of water, and bring to boil with lid on. when cold, seperate herbs and refrigerate the now tea. drink 2 litres per day or as much as you can. this should take around four to five days. if not totally gone by then, check out your envuronment, diet etc. some medications may block your path. most medications are made from petrochemical manufacturing waste products. be strong, thank morgellon and order him to leave

[@gnostaoticanarchangautand]

My guy try gallium metal. It might be the spicy cure.

[@ressurectionman]

@@mariasawders4229 hi maria, how are you managing things. what i can give and have been is hope and strength to you to heal. maria, im in my 60's, and no hidden agenda, other than help, when possible. my sympathies for your mum. avoid stress as it makes it worse, sounds corny, but think good positive thoughts, and make future plans without morgellon, and thank morgellon for his job is done, you have learned from him and its time for morgellon to go, he is now in the way of your progress. eat fresh food, lots of colour and lean meat well cooked , and the herbal tea. thyme is very powerful cleanser, so are all the others i listed, and many more in nature. if ok by you, ill see if your on facebook

[@gnosticjournals]

That Dr. is lying his a** off! Notice how nervous he is when he talks.

[@dvdburno]

kinda strange they give piperazine. its also used in dogs to get rid of parasites

[@tonygilbert6106]

Doctors don't want to look stupid

[@jasonbaldwin1915]

Where can you get tested for this? I'm 99% sure I have it... unexplained lesions.. and fibers that feel like your pulling Cobb webs.. over the lesion... any help would be appreciated

[@kodasierra9054]

Omg it looks kinda like lint!! But sticks like glue man! I'm going through this same thing and it's life altering!!!! Help!!!!! My baby girl has it now its in both our stools, black specks, has fungus characteristics to me, usually looks like pepper or salt, like to little dots side by side, depending how you look at it, (am I crazy? Ughhh) like fine mini strands of black hairs and the crazy is EVERYWHERE, clothes, skin, big lesions, sores all over, aching, severe fatigue... oh God I could go all day....

[@janeandre4119]

i have morgellons disease and i tried taking ivermectin 15mg...it work but very slow and sometimes painful inside. it will paralize the crawling inside. i drink it after meal. i hope the doctors will try ivermectin for patient.

[@TB-dm6vz]

allergic dermatitis and oral allergy syndrome feel comparable to morgellons, especially on days I eat things or use products I’m allergic to. I randomly feel the sensation of stings on random parts of my body which make me itchy all night.

[@beautysoulandspirit]

Sehr schön beschrieben. So habe ich es final auch gefühlt. Ich denke auch es ist eine Nebenwirkung von Microplastik und aufgenommenen Toxinen. Der Körper kann sich nicht dauerhaft davon befreien und entwickelt diese verzweifelten Mechanismen. Ich habe aufgehört verseuchte Dinge wie Fisch und minderwertige Lebensmittel zu essen. Es ist weg. Es hat auch eine energetische Komponente, aber das ist ein anderes Thema. Es gibt eine Vielzahl an Möglichkeiten dagegen zu arbeiten. Gute Besserung an alle die noch damit kämpfen. 💖

[@c.m.303]

​@@beautysoulandspirit Sounds like you recovered from this. I have to ask, what worked for you? And if it was just time.. how long did it take?

[@beautysoulandspirit]

@@c.m.303 I wrote u an answer but seems like deleted. U can contact me if you want to but cannot write in here.

[@staceysumner8242]

Not year round there are atleast 5 bugs that are doing this I literally have had this on and off outbreaks. My job has made me a realize it might never end for me. Fungus 3 kinds was caused by the Japanese beetles the day they hit my yard was the 2nd or 3rd round of them boogers lol literally boogers. I'm a 27 year dog Groomer and I just kept on wondering why I had a war going on and this us 4th year of it. The beetles are vicious 3 kinds maybe cause we're we live and the midges and no seeums are some bite n nuts and can drive you nuts its the over and over again cycle 4 years in a row same thing over and over. I was diabetic bad sugar levels and high blood pressure and fat as heck now none of this affects me can't explain really. And yes you saidabout only time before they get inside well let's say they did on me bumps in head I'm a picker couldn't stop and magnifier in mirror probably the first year looking at my head and up my nose. I could see them going from one hair follicle to another but only when I was getting ready for work needless to say I was late the whole entire first year going nuts and the bumps and sores well I picked one that was driving me crazy and it kept on til I finally broke it open and pulled it off and there it was a darn midge so I could right a book cause Jan and Feb midge and no seeums till they get run off by the other bugs cause them spring tails and beetles ground carpet Japanese they coming and they bite even harder then the midges sheesh what a life. Chlorahexadine 17 dollars tractor supply kills fungus cause anyone that has this will have to realize your dog's do also and the brown stuff is our next nightmare MITES ears dogs cats ear mites and oak mites and one I don't know what kind of mite maybe this year i can identify it. Think there is way more to this than anyone realizes. And these videos were they say the things just fall off is cracking me up. I can pull one out for anyone atleast 50 times a day. They are blood suckers and they are right on a vain all the time I can rid my body of all this with all my tricks but not my nose it's a never ending story literally. Doctors no clue they can't see it hmmmmmmmmmmm 😅😅🎉😂😂 I'm over being upset after 4 years 😊if I could figure out something for yhe nose that would work o man. I have tried it all unless there is sone thing I haven't thought of peace thanks for reading my book.

[@curtismosley7697]

Come from that blood rain they had years ago and people was breaking out behind it some pets died because of it CDC trying to cover it up

[@christinawatts593]

Blood rain?

[@curtismosley7697]

@@christinawatts593 you didn't see it on the knew???

[@catladyoftroyn.y.8713]

TIP. Use your house aloe vera plant. Apply aloe vera juice directly into lesions. Open aloe leaf up, place bit of open aloe vera leaf on top of lesion, and secure with band-aid. Leave on 12 hours. Reapply. It cured some hard healing lesions on my back within two days!!!

[@bruinfan2966]

I am as sane as it gets, and confirm that this condition is very real. My "morgellons" (who knows what it really is) finally went into a state of remission a few years back after about 4 years of absolute torment. At it's worst, I was producing the hideous red, blue and black fibers on a daily basis, with almost nonstop biting/burning sensations over my arms, hands, legs and face. I would also get frequent large (2-4") "J" shaped cuts/abrasions that would spontaneously appear on my arms and legs every week or so. I'd feel a burning sensation on my arm or leg and say to my wife, "hey, come here and watch this!" and the cut would slowly appear before our eyes. When you'd look closely you'd see that it was actually a succession of puncture like marks where the skin was broken. It was the freakiest thing ever. Mine started with a full body rash similar to scabies and then transitioned into the fiber, stinging and spontaneous lesion stage a few weeks after the initial rash abated. After getting brushed off by my Primary and a couple of derms, I took matters into my own hands and in my desperation tried almost everything under the sun, including things I'm too embarrassed to admit (you know what I'm talking about if you're in the Morgellons "community.") The symptoms slowly began to lessen maybe three years into the ordeal and things became much more livable. I suppose my immune system just got used to the presence of whatever this is and stopped responding so violently or maybe even eliminated it over time. Who knows? I am just so happy that I'm through with this (for now).

[@eyes2c..519]

Treat it like sporotrichosis sski saturated solution ❤

[@Mrs.Robinsons]

Many Thanks - USA here and medics dont believe me. I imagine the influx of illegals aren't going to help with diseases

[@Kairosabe]

Look the planes. They are sprying us

[@Uhohlisa]

lol

[@armoryourcastle]

I believe I have the answer to get rid of this!

[@leacebee5892]

... yes? What's your answer?

[@tonygilbert6106]

We will see our Justice one day soon ! I have suffered for 8 years

[@Lexi-x4c]

Thank you for your willingness in getting to know me

[@62flamenco]

It's a metal implantation in every species on the planet, humans, animals, avians, etc. The tiny fibers are metal based. They are not of this planet though. I don't know where they originated, but the prototype is a "creature" - I'll call it a creature, for lack of any other way to describe what came out of my skull. It was 6 inches in length. It consisted of pod like structures joined like popette beads. It's exterior "skin" was an aqua color. Inside each pod were thousands of black fibers. Each pod was connected by a brown branch like attachment. The "head" was a red jell like substance. Around its "neck" was a brown "necklace" and dangling from the "necklace" were two stunning golden disks the size of a dime, razor sharp. Embedded in each disk were white worms all bunched together. The red jell like substance had a black dot, sort of like an eye. This "creature" came out of my skull and landed in the sink in my bathroom. It didn't hurt because I had had major surgery and had my nerves cut in the area of the skull where this tiny hole appeared, with a small amount of blood. I am only writing the beginning of what has become a nightmare journey to deal with all of this. I freaked when I saw this "creature" in the sink and very stupidly threw "the find of the century" down the toilet by throwing a kleenex over it and throwing it into the toilet bowl and flushing it. Before I did that though, I called my husband in to see this strange creature and he witnessed it. The medical profession is idiotically unaware of this phenomenon and they dismiss people who are suffering. I am convinced this is NOT an illness and it is not contagious. If you want to test to see if you have the debris, put a handheld microscope on the sole of your foot and capture what you see on your computer screen. I can't say I have a cure for this, but I have found that Plumbum Metallicum, a homeopathic liquid or pill ingested will cause metal to be expelled from the body. It's a lengthy process, but will eventually cause the body to rid itself of these metal "creatures." Research Plumbum Metallicum and you'll see that it causes the body to expel metal. I can say alot more, but space does not permit it here.

[@melisentiapheiffer3034]

A German Proffessor on KZbin describes it the way you have explained it.

[@patriciadavis7444]

PRAY THE BLOOD OF JESUS CHRIST OVER THIS SITUATION AND BREAK ALL CURES THAT TRY AND TAKE OVER THE LIVES OF THOSE PEOPLE ...IN JESUS CHRIST MIGHTY NAME AMEN

[@thomasnolasco5790]

I have all this fibers coming out of me . I'm tired if this itchy things coming out of my pores

[@Worldsphuked]

There has to be a shortage of Crowe. Too many “doctors” have had to eat it & the rest will eventually. No doubt

[@yeetman4953]

?

[@ChildofGod2743]

I would like for them to eat the hard evidence that "doesn't exist". Especially Dr. KOO-KOO!

[@marypaino1327]

Stricker does not know what he is talking about. There is an identifiable entity that has different life stages, the fibers are only part of the whole picture of Morgellons. Drs at the Holman foundation refused to discuss this, so even they are guilty of denying what Morgellons is

[@kennashley3114]

if you had it,you wouldn't think it may not exist.

[@stevenhenderson9005]

CURE FOR MORGELLONS: Antipsychotic My mom got morgellons in 1998 and it is not a skin condition. It is an error in the bodies DNA coding incorrectly-added nucleotide. Antipsychotic will block dopamine D2/3 receptors and will stop the sensation of bugs crawling on you and will basically put the nucleotide back in place. The effects didn't take long for my mom and after a few months my mom no longer had to take the medication anymore.

[@anelissastanibol5417]

fibres seem to be part of stage #2 morgellons. what follows is the presence of unidentified parasites stage #3 and in stage #4 pseudo fungal infection half plant and half animal. stage #1 is bilateral rash. lymphocytic folliculitis or nodular prurigo, or a form of psoriasis. treatment needs holistic approach as this condition covers the lot

[@theresageiger584]

How please help

[@theresageiger584]

@@stanibol I'm sorry I don't understand what you are saying Can you get well or not

[@stanibol]

@@theresageiger584 some have reportedly reached remission. Katie Y is back at work. I am not. On the dole. Not enough funds to buy all the preparations. Fb Groups Detox dudes, mold avoiders, morgellons groups are divided on which protocol is best. Brave new world good luck everybody!

[@theresageiger584]

@@stanibol so you don't have to go to a clinic to get well

[@theresageiger584]

@@stanibol so what have you done

[@krispykawaii9516]

Reading the comments. It seems like the people suffering are not mentally okay.

[@Mrs.Robinsons]

A lot of foreign languages through google translate make it appear to be so as well.

[@ChildofGod2743]

Dr.Koo-Koo at FR.6:34 should self prescribe the 'antipsychotic medication' and be force-fed the hard evidence that 'doesn't exist'.

[@karengriffin9022]

Actually, I visualized that, but just for a second, while saying the words "well, using diagnoses and meds is just something that gets done". A perceptive individual, he asked me if if did try that and i said come with me. We walked outside and I pointed to the asphalt and the cars and visualized the grain silos next to the DSM III and started talking about the problems with Captain Crunch and the supply chain that supports it.

[@thetoad7367]

Same thing with crystal meth users. These morgellons must have some link with crystal meth users and morgellon sufferers. Wonder what the connection could be?

[@joyceshealy7191]

I don't EVEN KNOW WHAT CRYSTAL METH IS AND AM SUffering GREATLY. HOW DARE U TRY TO CONNECT THIS WITH SOME KIND O F DRUG ABUSE!!WTF?

[@tgrlilly]

Liam Wood you're an idiot.

[@homersimpson3136]

It's painful when people don't believe the truth, especially me being the second coming.

[@giannaluva65]

I try and tell everyone about you!

[@christopherhouchins417]

Either they (the doctors) are in on it and are covering it up or they are just plain foolish. As I understand it everyone has them to some degree.

[@muddthekingofnothing6249]

Rubbing coconut oil on my lesions helps me. This disease has tortured me for over 10 years God bless those of you who suffer. I hurt to.

[@joebonetto5406]

I have this stuff and its scarring my face real bad. I had 4 lesions on my left cheek that where scattered out and they combined to make one big lesion that stayed open for almost 2 years. I was put on humira for psoriatic arthritis and about 6 injections into it my wound finally closed. This wound had a fruit fly half burrowed into my wound at one point. So know its a big pink scar with fibers or hairs that hurt and won't come out because its stuck in hard sebum or something. I know I have hard white rice sized bumps all over my wound and they have fibers in them that are white and stringy. I also get those black fiber balls that have pink and blue in it also and if you look at 60x you can see that its a bunch of fibers tangled in a ball of bio film. This sux!!!!

[@allicianpeters3595]

PURPLE RAIN!!!!

[@yvetteriera3874]

Absolutely not maybe in some cases but not all! Many cases are people that have been Targeted Individuals with RF Directed Energy Weapons and Smart Dust intentionally. The reason why I don't know people get targeted for many reasons experimental purposes will because you spoke up to someone like a doctor politicians

[@maryjohnson4110]

it acts like a fungus. Antifungle {sp} stuff like athetes foot spray and coconut oil works on the skin. I tested neg for lyme.