The CDC has verified it before. The last time in 2018. A few months later, they took down all their research and everything since 2008 and the verification. I stopped keeping track after that time because I was being targeted and harassed and threatened by the CDC and organizations/ppl they work with. I had put a lot of pressure on them and speaking out to the world. But once I was threatened, I took down most of my research and information. I still have some videos up, but nothing useful. I had to..I have a family and these people are run by the NWO. There are still papers out there though that prove that morgellons is real.
I have had this stove 2020 and my mother has had it since 2000. I don’t see were anyone has mentioned what the skin ultimately does to your clothing and bedding. I have been using a pore vacuum for quite sometime and this is so much more that surface deep. I would give anything to be rid of this horrible life scaring disease. I went to the doctor with much hesitation because of what my mother has been through. I took samples of the these creature along with me. After these two lady doctors rushed off to look at the “dissection” I had committed on myself. They returned and told me I should find a support group and diagnosis was I have high anxiety . 😢 I salute anybody who believes this is not on my our minds, and it did anything to have a miracle happen to make it go away. I have beat my brains out trying to figure this out and I have so many theories… just tired
It sucks, You're bang on. It smells weird too. Nuttyish. I guess. Makes others around me sneeze. Using oil to make them all pop out is the best I can do for mine. They keep coming back though. It is utterly crap. I am a sensible dude too - psychologically very taxing to keep it together and not freak out. Does yours respond real bad to the sun/uv? I get severe rashes
I have started to heal mine!! I think I have a solution!! They are now very few and far between. I believe I have done something to heal them. I used clove oil (be careful, this will tank your liver if not used topically and sparingly where you are worst effected) UVC 254mn (or just lots of time in the sun if possible). Look into studies around UVC treatment for fungal issues - very dangerous so make sure you know what you are doing - sunlight was easier for me but I got good effect from short exposures to a 254mn lamp - make sure it doesn't go in your eyes. Sea water or salt water baths - make sure to rinse off and moisturize after Probiotics (L. acidophilus, L. rhamnosus, Saccharomyces cerevisiae [a yeast that outcompetes the fungus that at least in part causes this disease], B. Subtilis. - I believe the fibres could be a form of yeast as starting the S. Cerevisiae to outcompete it made a huge difference for me Coenzyme Q - 150mg I have also taken lots of vitamin C (500mg 2xdaily), vit D (25ug) daily B- vits (especially b12 1000ug 2x daily), Zinc 25mg NAC 1200mg Magnesium (bioglan active magnesium at night its important not to take it the same time is iron or zinc)100mg NMN (Nicotinamide Mononucleotide) 1250mg, TMG (trimethylglycine) 1000mg I also cut out milk and sugar from my diet for a while which really helped (it also sucked so bad but I believe this starves the disease out). ****If I had to wager what had the most effect I would say lots of sun and the probiotics were most valuable - and the vit b12 and vit C. Sunlight helps especially too. Getting adequate sleep and at least 20mins of exercise was important too. ***** Guys please take my comment with a grain of salt as some of these supplements and "treatments" can be extremely dangerous and there is hardly any real scientific basis for many of them. However, I have reduced my symptoms through one or a combination of these things - it is hard to say exactly what though.
I believe things like COVID (long covid), Spirochete infections (lyme for one), Autoimmune, candida or tinea are involved. This is an insidious disease that takes advantage of what appears to be a mix of genetic vulnerability or certain comorbidities and nutritional deficiencies that affect immune function. My confused MDs were not of much help so I had to fight this myself and I have been winning so far. I just want to get this info out there incase it helps someone, but ***please please be careful, what helps me may be really bad for you, do your own research, take the risks seriously, understand that I do not know out of all of this what helped most and that some of this could be bad for me, do not blindly follow what I am doing/taking without lots of research and consultation with you healthcare professionals if possible***
***PPS. Avoid Clove oil if you have any issues with your liver or kidney function - opt for something like cinnamon oil instead, it also shows promise as a topical treatment. Clove oil is extremely toxic to pets so don't let them get near the fumes and don't pat them for several hours after you have used it. Also don't overdo the clove oil, a busted liver is no joke and its literally as nasty as a panadol overdose. It takes the liver a long time to fully recover from clove oil - go do your research. Also overly high levels of vitamins can be very dangerous, same with magnesium and zinc. Too much ascorbic acid [vit C] without food can burn your stomach, UV rays of course can cause cancer and burns, some of the supplements I am taking are experimental and could have long term effects that are dangerous. Get blood tests if possible and work with your healthcare providers to address nutritional issues***
I swear on my father's grave that: this morning i was so sick of the crawling sensation on my face, that i put some frontline cat and dog spray on a cotton pad, and lightly patted my face. there was an immediate super tingling, and a whole mess of white fibers came out of i guess pretty much every pore. i collected some, and will send it to whomever would like to analyse it. thank you. ps I was very relieved to see that these fibers were not worms, or any apparently living thing.
I have tried everything also Please don’t try wasp and hornet spray though. I felt like it hit my nervous system like it does a wasp or hornet. I thought I was gonna die. It was horrible. Flying insect spray helps with the itch but honestly, I’ve been spraying myself down and scrubbing myself with sulfur soap and bleach in the shower and when I get out the shower, the amount of fuzz coming out of my skin is almost non existent. Before When I would shower, I would itch worse after washing. I hated taking a shower because I would itch so bad when I got out but now if I make sure to cover my whole body, even my scalp with bleach, I dilute it with water in a spray bottle. The itchy sensation isn’t as bad. The bad thing about that is though it’s really drying on your skin. I found the Palmer cocoa butter lotion isn’t too irritating. I Feel this lies way more than skin deep though I can guarantee that because of what comes out from under my skin. That fuzzy scaly surface on the lesion is just a barrier they build up, like a shield.
I think it’s in the water , tiny microscopic nematodes they are colourless and so small you won’t see them my skin showed candida glabrata that was an unexpected finding of course no meds were given that will help now it’s becoming systemic. Have you noticed the air in home seems weird like it’s either full of mold spores or noseeum midges ? I think I have mold spores in the air as well as noseeums that have took over . In the video crawling by Lincoln park the girl on video clearly has morgs and something is in the water watch that song video maybe it’s black goo programmable matter ? The video seems very much to be hinting at Morgs as a form of black goo watch it your see
Years ago Dane Wigington brought this issue to light in his weekly broadcasts concerning the ongoing process of geoengineering and the substances used during Solar Radiation Mitigation. Microparticles of materials are being dumped by the thousands of tons upon the public. Ticks?! Really!? Look to the sky.
Thank you for the all the hard work you have put into this! It gives me some hope knowing that people like you believe us. This is a horrible isolating disease and all the doctors I have seen the past 4 years like to label me as CRAZY. It is exhausting. Thanks Again!
Thank you for our belief systems and interactions with a present genome, isolation is very true and it's my identity 20 years later, it feels like I was left behind the world.
You are not crazy I think we just need to fight it from the inside out with a stronger fungus. I’m trying mushroom complex right now. I think it a living fungus like mold and the fibers are like spores.
There are 2 weak links in the trajectory to truth here. 1. The people that work in the Oklahoma State University lab. 2. Genbank Do I really need to say universities are controlled by money. The same goes for genbank. I say these things because for years, universities are pushing opinions in the direction of spirochaeta which is obviously bogus to me. Morgellons look nothing like spirochetes and the logic presence of them would create a situation of uncontrolled keratin and collagen fiber production is simply outrageous. I would do PCR for cordyceps, aspergillus, bacillus subtilis or any other fungus or bacteria that lends itself to genetic modification and merging with technology. I'd also have a long hard look at the sequences at Genbank which might have been swapped with data to fit the spirochete narrative.
Yeah I agree. Spirochetes if present are more like co infection to whatever this ridiculousness is. I can’t even find any real “medically accepted” pictures and videos of what this stuff does to your environment. For me I’m fortunate not to have lesions but my scalp and hair are ridiculous. It’s easy to tell if someone who has MD by just standing in a beam of sunlight. It’s like pig pen off Charlie Brown. “Dust” just coming straight from my head. It’s all in my clothes and bedding which you can also see. It’s a complete nightmare. I took antibiotics antifungals anti parasitics for 3 years to no avail. It’s too expensive to keep going to a Lyme doctor outside medical insurance and my GP won’t even address it. I feel hopeless but I’m looking for a good holistic doctor that can help. I’d like to find someone with some proven results. It’s difficult to find though. 😢.
I have been beating my brains out for years trying to figure it out and I am dead set on it being a fungus like a living fungus. The fibers are like spores that multiply at an intense rate. I have so many different ideas of what it could be. I am not a doctor I didn’t even graduate from high school but I will go to my grave trying to figure this out. I just want my life back. It feeds off of blood though that is why the lesions are so painful. They would have me committed if they seen how I vacuumed this stuff out of my skin. It is very bloody and I am not self mutilating or dissecting myself. I don’t even have to really do anything but scraped my finger over a scab and it’ll start bleeding and then just suck out what’s underneath there? It’s painful, but it would blow some people away it’s probably a good thing there is not a spot to put pictures on here. But at the same time, I wish there was because everybody that thinks it’s just a skin thing could see these massive blood sucking leach like things, the doctors they need to go deeper to see what’s living under your skin. A little biopsy will never get to the bottom of this.
@@InsideSalesDiva In general, forget the doctors. There are exceptions but the majority are protocol following govt reporting fools. You could try anti-nano devices from tony pantalleresco and FM8 and see if those help.
I have this and I have also been diagnosed with borrelia burgdorferi, borrelia mayonii, bartonella, anaplasmosis, tick borne relapsing fever, and babesia. Thank you so much for your research!
Oh my....I haven't had my full diagnosis yet but I didn't know it could have multiple diagnosis. I have the symptoms of the morgellons and there was a whole bunch of time I can't eat meat .get sick.. but thanks for sharing that ... That helps me to know the right path to go for testing ..n I pray for ya..this is so horrible and people don't understand the torture and physical and mental pain we go through....❤ Thankyou angain..
@Daily Driver I've had 3 basic cdc Lyme tests from my regular doctor in the past that were all negative. I was able to get Carecredit and used that to get Vibrant test. Yes, it's extremely expensive, but I am so thankful that I have answers.
This is an insult to the Intramural Research Program at the NIH and the work done by Wilhelm Burgdorfer, Ph.D. along with countless colleagues that spurred more than 6,000 studies on clinical, epidemiological, and bacterial aspects of Lyme disease. These researchers had the fortitude and confidence to submit their work to prominent medical journals after careful review and scrutiny. Looking at this logically, are we to believe that through thousands of hours of research by highly trained scientist and medical personnel, all of these people failed to mention anything that resembles morgellons disease in the details of Lyme disease? I can tell you why there was no mention of anything resembling morgellons disease in the more than 6000 studies. Because it wasn't there. There is no correlation between morgellons disease and Lyme disease anymore then there is a correlation between morgellons and diabetes, or the countless ailments known at this time. Unfortunately, OSU has lost its way in the area of scientific research on this matter. In the 17-year history OSU's research of morgellons disease has led people no closer to real answers then when started. One must understand that each department at OSU has to submit a presentation such as this. There is nothing special about this one. In fact, I would conclude it is harmful to the morgellons community and those that suffer. The goal would be to submit scientific findings regarding morgellons disease to other prominent scientific establishments around the world so it can be scrutinized by scientific scholars. Something OSU has yet to do publicly. Some may mention, "What about articles submitted to PubMed/Dove Press/Google Scholars by LLMD's"? Simply put, Dove Press is a pay to play publication, and PubMed/Google Scholars are simply a search engine. They do not give validity to articles submitted. While morgellons has been proven to be much more than a dermatology issue back in 2010, there has been very little done to combat misinformation. Institutions such as Mayo Clinic and Wikipedia still reference morgellons as a skin disorder while OSU stands by and continues to allow this to now turn into disinformation. Let's all be a little smarter and expect a higher level of performance from our scientific community. While OSU has produced some great works in the past on other subjects, it has been a failure with regards to morgellons disease. We expect better.
Huh, so why has the CDC finally came out with the findings of Morgellons being a physical disease and not psychological. Yes,it's been a long time coming, but I believe they just did this in the last few months. Plus, if you do not suffer from this, shut the F up. This is a very serious disease and just because the disease itself may not be deadly, it does have a very high suicide rate in sufferers. It's because of people like you,that don't know what they are talking about, are making them feel less than dirt and taking any little hope away that pushes them to the point of murdering themselves. I'll pray for you, you pray for me 😊
Great information! I would love a link to the poster you showed on screen. I could not read the names of the organisms and you said them really quickly.
I appreciate your research and work. My background is in micro and nanotechnology... so from what I have experienced it is bio-nanotechnology (some of it self replicating). It is horrific and much of it looks not of this world. I dare say bioweapon!
I have got it, I don't think its a bioeapon. Maybe, I think its my body making it though. Cooking oil gets them out by the thousand. So i have been using that before showering
@@mindbox11 I worked for a big tech companybuilding nano and microchips from the bare silicone to after all of it's layers were on. I worked closely with engineers all along the way. Then, after not woking for a while I started breaking out in bizarre looking sores. Someof the things that came out of me were chips, quantom dots, claws, spiders, webbing, fibers, ants, glass like substance, sticks and much of it is so horrible I can't put words to what came out of me...a massive living nightmare.Whoever has this I truly feel for them.
It is encouraging to find the research you are doing. Thank you. I don't know if I have Morgellons as I don't get red and blue fibers, but I have a lot of the other symptoms. These happened soon after I encountered a lot of ticks. I do feel that my condition is also fungal related and I wonder if you have done any research into a fungal connection to Morgellons.
I wish so bad there was a cure. This disease is one of cruel and punishment. I am on year 6 of a breakout and my head is no longer mine. My hair (hairlike Im sure its not hair it just looks that way) Is constantly moving there are pools of hard biofilm that switches from liquid to solid constanly. My eyes can hardly see to read my nose has tunnels all through it. They fill up with the biofilm and then it hardens. There is a dark brownish substance on my head and when the biofilm starts it's moving gravity pulls it down over my face when it moves it leaves those brownish chunks stuck in the film impeded in the when the biofilm goes from liquids to solids. I'm at the end of my rope the brain fog makes so I cant do simple multitasking and it's taken me almost 15 minutes to type this. I need help I cant take it no more. anyone?? I will put a video up showing some of this. One last thing my hair glows bluish green dots and the clear hair has taken over I forget what they arre called cyan something. I could share some pics and vids that ive not seen online yet.
Dear friend, what you are narrating is something tremendous. I consider that even being in such a complex situation it is advisable to remain calm, and of course what you say is not an invention, several participants in chats mention similar things. I leave you a brotherly hug.
Me too also has been almost six years. Started for me in 2018 and I understand every word you said. I feel like I’m wasting my life away in the bathroom taking hours in the shower trying to feel clean again to no avail. Can’t talk about it or you are deemed crazy. We look like drug addicts to most people bc lesions on our body and a lot of ppl with morgs call them bugs. Honestly the most logical explanation I’ve heard is the way it’s been described by Harold Kautz-Vella. I recommend listening to his explanation about it. It atleast gave me answers to most of my questions about this disease. He has some very controversial topics that he researches Morgellons happens to be connected to those. It doesn’t coincide with mainstream science which is why I only heard of him recently. I pray we all get some relief I agree with you that this disease really takes away your will to live. The mental anguish it causes is worse than the physical pain and discomfort. It’s torture.
I am with you my friend. I have prayed for an answer to fight this. I heard Salt, Light and Iodine. So, light may be fighting the skin with UV/UB rays to kill topical things. Salt has helped me to break the biofilm. But there are also helpful all natural salts that are helpful when eaten. Celtic salt, etc. Iodine needs to be taken orally. Look up Saturated solution of Potassium Iodine. There are other natural things I'm doing for my skin now. I'm being the guinea pig until I get a scrub together for biofilm. I'm also working on a spray that kills this stuff naturally. When I'm done, I can help many ppl to clear the dermal issue. But it's a multi faceted disease. There are many steps we have to take to heal. Can't wait to see the punishment of the evil that created this atrocity. God says not to touch His anointed and do His prophets no harm! Psalm 91- only with your eyes shall you see how the wicked are punished. And my Jesus will Always protect and provide my needs. Looking forward to formulating cure for the biofilm and skin ailment. It will be from God and His creation. Not AI or Nanotech. Jesus is in control Be encouraged. Help is on the way!
I’m on this boat too! I completely understand everything you have stated. It started in 2018 for me. But I had suspicions bf that. I too have lost my life and identity to this crap. I isolate myself. It’s a constant struggle NO ONE understands. I don’t even try to explain it to ppl anymore. Why bother.
It does feel hopeless. Doctors will be dismissive, so I'm not sure what to tell you as far as that's concerned. It is systemic and makes the entire body sick, along with crawling, biting, stinging, and burning sensations. It does go into remission after 5 - 10 months (seems like forever) and then life will return to normal for a couple years. Listen to music, meditate, and try to make the pain transformative. When you're well, make the most of every minute.
So did I. And I mean everything! It invaded my home, my clothes Even my animals had to be put down they so infected! I couldn't keep😢 them and did not want to infect others if adopted. This was 15 yrs ago. I lived in a hotel for two years so that I could move to other rooms when my body parasites infected it. I've found ways to manage it now and I'm left completely traumatized. It has destroyed my life. 😊
I have the disease and it was during a time when I had a low immune system and had to fight a staphylococcus infection that ultimately caused an amputation. I have researched the disease and have found that it seems to be prevalent among women who are menopausal, low thyroid levels, and high cortisol levels. If I receive steroid injections and steroids by mouth during flare ups .. I have hardly any symptoms. I feel like it is a autoimmune condition that is attacking itself. My itching is controlled by weekly bleach baths, vitamin D , sunlight, and not sweating. Hope they find a cure soon because this is a horrible horrible disease and frustrating that they label it in our head
How do you cure MD? Using over syllabled medical terms only helps your grade in class but helps no one get well infact this plague has shown how medical industry controlls doctors so they dont cure but administer diagnosis for the come back.
I think there is something in the immune systems of people with Morgellons that does not fight it like everyone else. I think it is something that everybody has living on or around them but there is something our immune systems are lacking that won’t fight this frap off. I feel everyone I live with would have this as well, it’s just they have immunity to is. The little white fuzz is on everything. I can’t wear certain types of material because of what my body does to it. My body ruins my clothes. I just hate it… I have to use a sweater shaver on my socks after every wash. On majority of my clothes. The little fuzz balls that are created from my skin are horrible.
I'm with you on that. You have these Morgellons groups, but using them for questions is comical. There are too many shills. You can't get a straight answer. I believe everyone that has Morgellons has a negative blood type.
Great to know, now where can us sufferers go to get treatment and help! because all the doctors I’ve been too are lucky if they can tie their shoes by themselves without sending you a 1000 dollar bill..and have no idea what your talking about…my infection has started out as as UTI and now has spread into my intestines, hair, face etc…over the course of 15 years without much professional help
I have lots and lots of samples that I've been saving over the years that I've been fighting this stuff so if I can give it to anybody who will do something with it please make a comment
can someone share what do you do to fight this? Is have been a terrible 2 years. have been in doctors, dermatologists, event witchcraft! this is really lame and hate it. Im using coconut oil and lemon juice. That seems to help it to pop out the skin. It seems they hate lemon juice. Coconut oil also helps a lot. Im tired :( ...
Is it possible to access the full research paper? There so much more information on this topic than what's available online. For example, the first reported case was not in 2002, it was in 1989 in the state of Missouri.
Please provide the link to this publication along with the graphic presented. We are trying to collect as much peer reviewed research as possible to assist my poor 73 y.o. sister who is suffering terribly from MD.
Thanks Samantha. I have a lot of questions. One obvious one: if this is bacterial, what are the macroscopic materials which are embedded in wounds and under intact skin?
Omg thank you! I’m struggling so badly because of this! And I’ve been to several doctors, whom barely looked at my head, str8 to mental health. How can I be a study candidate or who can I see for help?
Difficulties of diagnosis that’s an understatement in all the nonsense about it being a mental condition is absurd put somebody’s skin under a black light with the black lens not the regular one the one they used to look for glow in the dark rocks, put somebody’s skin under that black light with time lapse photography and you can watch the fibers come out for me. They’re very small, bright blue, but when you turn off the black light, you can’t see them there’s no mistaking there’s no doubting it when you watch it actually come out of your skin for me, there’s also something that looks like a very small parasitic worm scabs at the surface of my skin and under 12 X a jewelers loop that I have I’ve seen things that look like a flying insect. I know it sounds fantastical but I think you’re fine using that black light very very very informative. I could use some help. Thank you I appreciate you.
I would like to see the link between mold in home and also who has pets. My dog was diagnosed with rare yeast from rabbits. We had lived in mold unknowingly.
I have a son who is 25 and went through he'll for 3 years. He was never diagnosed. I suspected limes, but no one believed me. He now has severe mental disorders. Can this be related? We are as a family not doing well because of this. I am looking for some help please. Thank you and Many Blessings
There's an excellent GMC parasitic twin it's about 55 bucks is for men specifically and there's one for women, you can also if you can get your doctor to prescribe you a parasitic cleanse that works as well... And topical ivermectin
She said all the fibers she's seen were keratin which means it's animal hair. She also says past research has given results 'from unknown to keratin', where are those studies? If it's unknown was it because they were using poor analysis?
I think it has to do with spirituality as far as being aware of it or not but yes you are right. Everyone is infected with this stuff. It appears to be building some type of network then goes into standby mode. It has many life cycles which makes sense considering it is a bioengineered set of silicon & aluminum based life forms.
Some clearer pictures would help my microscopic evidence. I cant fimd any evidence of the ones that come ffrom my chest evry morning. Treatment for scabies isnt wotking.
Nothing topical works, sir. I take a homeopathic called yeast guard, and Ashwaganda, and vitamin e. Benadryl and Sleepcalm at bedtime. Quit eating breads and sugars. I been fighting it for nearly 30 years. Also, drink only purified water. There's no cure, no doctors who care. I'm a disabled RN, so I searched for the answer for years. I got Lyme disease from a tick and all hell broke loose in my body. I put vitamin e on my skin and skin so soft oil from Avon. We have NO choice but to live with it. I quit focusing on it. Sending love and prayers. Take care. ❤
You can fight this easily. This is a problem of people bodies being too acidic, + air and water pollution with micro plastic everywhere. Solution is easy but many people will laugh and don't even try this and for them I can't do anything. 1. In the morning take one small spoon of baking soda, put in a glass, add half a lemon juice, it will react, top it off with a water and mix it good, drink, everything that is left in glass add more water and drink it, morning and evening, this will help in pulling your body back to a normal state which is more alkaline, less acidic state. If you can, add turmeric to the mix, it is as combine an elixir not only for this shit, but also returning our body state to alkaline instead of acidic removes the posibility of any type of cancer, as some people know, that cancer is nothing else then autoimmune disease ( your own body attack it self ) 2. Get zeolite powder. mix with water with 5 grams of zeolite in a glass of water, use every day once a day. Zeolite eliminates toxic stuff out of our bodies, repeat the step for zeolite for a month. With baking soda just after one month, reduce it to one spoon one glass of water every day.
Did this cure you? I recent also came to the conclusion about it being caused by acidity in one’s body. To eat clean and detox metals and we can heal ourselves. I’m going to try it. I know it is simple solution but it’s so hard for me to be disciplined enough to eat zero processed foods. Mostly Bc no energy means no money and eating a strict diet of all organic no processed foods expensive.
I have the disease and it was during a time when I had a low immune system and had to fight a staphylococcus infection that ultimately caused an amputation. I have researched the disease and have found that it seems to be prevalent among women who are menopausal, low thyroid levels, and high cortisol levels. If I receive steroid injections and steroids by mouth during flare ups .. I have hardly any symptoms. I feel like it is a autoimmune condition that is attacking itself. My itching is controlled by weekly bleach baths, vitamin D , sunlight, and not sweating. Hope they find a cure soon because this is a horrible horrible disease and frustrating that they label it in our head
Thank you! We need soooo much more research to allow medical validation of this horrific disease. Appreciate you greatly.
This youtube video may shed some light on your Morgellon's disease. ua-cam.com/video/DUdqyfBEjHg/v-deo.html
Yes, we need more research to prevent these patients from being shunned by the health field.
The CDC has verified it before. The last time in 2018. A few months later, they took down all their research and everything since 2008 and the verification. I stopped keeping track after that time because I was being targeted and harassed and threatened by the CDC and organizations/ppl they work with. I had put a lot of pressure on them and speaking out to the world. But once I was threatened, I took down most of my research and information. I still have some videos up, but nothing useful. I had to..I have a family and these people are run by the NWO. There are still papers out there though that prove that morgellons is real.
Please continue your research, so many people are suffering. With no hope.
I have had this stove 2020 and my mother has had it since 2000. I don’t see were anyone has mentioned what the skin ultimately does to your clothing and bedding. I have been using a pore vacuum for quite sometime and this is so much more that surface deep. I would give anything to be rid of this horrible life scaring disease. I went to the doctor with much hesitation because of what my mother has been through. I took samples of the these creature along with me. After these two lady doctors rushed off to look at the “dissection” I had committed on myself. They returned and told me I should find a support group and diagnosis was I have high anxiety . 😢 I salute anybody who believes this is not on my our minds, and it did anything to have a miracle happen to make it go away. I have beat my brains out trying to figure this out and I have so many theories… just tired
It sucks, You're bang on. It smells weird too. Nuttyish. I guess. Makes others around me sneeze. Using oil to make them all pop out is the best I can do for mine. They keep coming back though. It is utterly crap. I am a sensible dude too - psychologically very taxing to keep it together and not freak out. Does yours respond real bad to the sun/uv? I get severe rashes
I have started to heal mine!! I think I have a solution!! They are now very few and far between. I believe I have done something to heal them.
I used clove oil (be careful, this will tank your liver if not used topically and sparingly where you are worst effected)
UVC 254mn (or just lots of time in the sun if possible). Look into studies around UVC treatment for fungal issues - very dangerous so make sure you know what you are doing - sunlight was easier for me but I got good effect from short exposures to a 254mn lamp - make sure it doesn't go in your eyes.
Sea water or salt water baths - make sure to rinse off and moisturize after
Probiotics (L. acidophilus, L. rhamnosus, Saccharomyces cerevisiae [a yeast that outcompetes the fungus that at least in part causes this disease], B. Subtilis. - I believe the fibres could be a form of yeast as starting the S. Cerevisiae to outcompete it made a huge difference for me
Coenzyme Q - 150mg
I have also taken lots of vitamin C (500mg 2xdaily),
vit D (25ug) daily
B- vits (especially b12 1000ug 2x daily),
Zinc 25mg
NAC 1200mg
Magnesium (bioglan active magnesium at night its important not to take it the same time is iron or zinc)100mg
NMN (Nicotinamide Mononucleotide) 1250mg, TMG (trimethylglycine) 1000mg
I also cut out milk and sugar from my diet for a while which really helped (it also sucked so bad but I believe this starves the disease out).
****If I had to wager what had the most effect I would say lots of sun and the probiotics were most valuable - and the vit b12 and vit C. Sunlight helps especially too. Getting adequate sleep and at least 20mins of exercise was important too. *****
Guys please take my comment with a grain of salt as some of these supplements and "treatments" can be extremely dangerous and there is hardly any real scientific basis for many of them. However, I have reduced my symptoms through one or a combination of these things - it is hard to say exactly what though.
I believe things like COVID (long covid), Spirochete infections (lyme for one), Autoimmune, candida or tinea are involved.
This is an insidious disease that takes advantage of what appears to be a mix of genetic vulnerability or certain comorbidities and nutritional deficiencies that affect immune function. My confused MDs were not of much help so I had to fight this myself and I have been winning so far.
I just want to get this info out there incase it helps someone, but ***please please be careful, what helps me may be really bad for you, do your own research, take the risks seriously, understand that I do not know out of all of this what helped most and that some of this could be bad for me, do not blindly follow what I am doing/taking without lots of research and consultation with you healthcare professionals if possible***
***PPS. Avoid Clove oil if you have any issues with your liver or kidney function - opt for something like cinnamon oil instead, it also shows promise as a topical treatment. Clove oil is extremely toxic to pets so don't let them get near the fumes and don't pat them for several hours after you have used it. Also don't overdo the clove oil, a busted liver is no joke and its literally as nasty as a panadol overdose. It takes the liver a long time to fully recover from clove oil - go do your research.
Also overly high levels of vitamins can be very dangerous, same with magnesium and zinc. Too much ascorbic acid [vit C] without food can burn your stomach, UV rays of course can cause cancer and burns, some of the supplements I am taking are experimental and could have long term effects that are dangerous. Get blood tests if possible and work with your healthcare providers to address nutritional issues***
@@soundslike8454can you please let me know what’s helping you? 🙏
Wonderful research on this horrible disease. Thank for trying to find answers and treatments for those who suffer with this depressing disease.
I swear on my father's grave that: this morning i was so sick of the crawling sensation on my face, that i put some frontline cat and dog spray on a cotton pad, and lightly patted my face. there was an immediate super tingling, and a whole mess of white fibers came out of i guess pretty much every pore. i collected some, and will send it to whomever would like to analyse it. thank you. ps I was very relieved to see that these fibers were not worms, or any apparently living thing.
I have tried everything also
Please don’t try wasp and hornet spray though. I felt like it hit my nervous system like it does a wasp or hornet. I thought I was gonna die. It was horrible. Flying insect spray helps with the itch but honestly, I’ve been spraying myself down and scrubbing myself with sulfur soap and bleach in the shower and when I get out the shower, the amount of fuzz coming out of my skin is almost non existent. Before When I would shower, I would itch worse after washing.
I hated taking a shower because I would itch so bad when I got out but now if I make sure to cover my whole body, even my scalp with bleach, I dilute it with water in a spray bottle. The itchy sensation isn’t as bad. The bad thing about that is though it’s really drying on your skin. I found the Palmer cocoa butter lotion isn’t too irritating. I Feel this lies way more than skin deep though I can guarantee that because of what comes out from under my skin. That fuzzy scaly surface on the lesion is just a barrier they build up, like a shield.
I think it’s in the water , tiny microscopic nematodes they are colourless and so small you won’t see them my skin showed candida glabrata that was an unexpected finding of course no meds were given that will help now it’s becoming systemic. Have you noticed the air in home seems weird like it’s either full of mold spores or noseeum midges ? I think I have mold spores in the air as well as noseeums that have took over .
In the video crawling by Lincoln park the girl on video clearly has morgs and something is in the water watch that song video maybe it’s black goo programmable matter ? The video seems very much to be hinting at Morgs as a form of black goo watch it your see
I have done this too.
@@gina2190 Bio Engineered, Gmo food, dryer sheet fibers, plastic everthing...
Your all spot on. May God be with us
Years ago Dane Wigington brought this issue to light in his weekly broadcasts concerning the ongoing process of geoengineering and the substances used during Solar Radiation Mitigation. Microparticles of materials are being dumped by the thousands of tons upon the public. Ticks?! Really!? Look to the sky.
Thank you for continuing studying the silent disease. I just want to know what happening with my body.
I appreciate you 🙏🏼
This youtube video may shed some light on your Morgellon's disease. ua-cam.com/video/DUdqyfBEjHg/v-deo.html
Stay away from chem trails as much as possible
Thank you for the all the hard work you have put into this! It gives me some hope knowing that people like you believe us. This is a horrible isolating disease and all the doctors I have seen the past 4 years like to label me as CRAZY. It is exhausting. Thanks Again!
This youtube video may shed some light on your Morgellon's disease. ua-cam.com/video/DUdqyfBEjHg/v-deo.html
Thank you for our belief systems and interactions with a present genome, isolation is very true and it's my identity 20 years later, it feels like I was left behind the world.
You are not crazy I think we just need to fight it from the inside out with a stronger fungus. I’m trying mushroom complex right now. I think it a living fungus like mold and the fibers are like spores.
This has been a nightmare.I pray that this can be proven so we can get treatment.Thank you so much for your efforts.
This youtube video may shed some light on your Morgellon's disease. ua-cam.com/video/DUdqyfBEjHg/v-deo.html
There are 2 weak links in the trajectory to truth here.
1. The people that work in the Oklahoma State University lab.
2. Genbank
Do I really need to say universities are controlled by money. The same goes for genbank.
I say these things because for years, universities are pushing opinions in the direction of spirochaeta which is obviously bogus to me.
Morgellons look nothing like spirochetes and the logic presence of them would create a situation of uncontrolled keratin and collagen fiber production is simply outrageous.
I would do PCR for cordyceps, aspergillus, bacillus subtilis or any other fungus or bacteria that lends itself to genetic modification and merging with technology.
I'd also have a long hard look at the sequences at Genbank which might have been swapped with data to fit the spirochete narrative.
Having this disease is like being trapped in an episode of the X Files.
Thank you for this comment. There is absolutely no way en excess of keratin or collagen would create these insane side effects!
Yeah I agree. Spirochetes if present are more like co infection to whatever this ridiculousness is. I can’t even find any real “medically accepted” pictures and videos of what this stuff does to your environment. For me I’m fortunate not to have lesions but my scalp and hair are ridiculous. It’s easy to tell if someone who has MD by just standing in a beam of sunlight. It’s like pig pen off Charlie Brown. “Dust” just coming straight from my head. It’s all in my clothes and bedding which you can also see. It’s a complete nightmare. I took antibiotics antifungals anti parasitics for 3 years to no avail. It’s too expensive to keep going to a Lyme doctor outside medical insurance and my GP won’t even address it. I feel hopeless but I’m looking for a good holistic doctor that can help. I’d like to find someone with some proven results. It’s difficult to find though. 😢.
I have been beating my brains out for years trying to figure it out and I am dead set on it being a fungus like a living fungus. The fibers are like spores that multiply at an intense rate. I have so many different ideas of what it could be. I am not a doctor I didn’t even graduate from high school but I will go to my grave trying to figure this out. I just want my life back. It feeds off of blood though that is why the lesions are so painful. They would have me committed if they seen how I vacuumed this stuff out of my skin. It is very bloody and I am not self mutilating or dissecting myself. I don’t even have to really do anything but scraped my finger over a scab and it’ll start bleeding and then just suck out what’s underneath there? It’s painful, but it would blow some people away it’s probably a good thing there is not a spot to put pictures on here. But at the same time, I wish there was because everybody that thinks it’s just a skin thing could see these massive blood sucking leach like things, the doctors they need to go deeper to see what’s living under your skin. A little biopsy will never get to the bottom of this.
@@InsideSalesDiva In general, forget the doctors. There are exceptions but the majority are protocol following govt reporting fools.
You could try anti-nano devices from tony pantalleresco and FM8 and see if those help.
I have this and I have also been diagnosed with borrelia burgdorferi, borrelia mayonii, bartonella, anaplasmosis, tick borne relapsing fever, and babesia. Thank you so much for your research!
Oh my....I haven't had my full diagnosis yet but I didn't know it could have multiple diagnosis. I have the symptoms of the morgellons and there was a whole bunch of time I can't eat meat .get sick.. but thanks for sharing that ... That helps me to know the right path to go for testing ..n I pray for ya..this is so horrible and people don't understand the torture and physical and mental pain we go through....❤ Thankyou angain..
@Daily Driver My Lyme disease doctor used the Vibrant Lyme & co-infections test
@Daily Driver I've had 3 basic cdc Lyme tests from my regular doctor in the past that were all negative. I was able to get Carecredit and used that to get Vibrant test. Yes, it's extremely expensive, but I am so thankful that I have answers.
@@dailydriver6264 💗🙏💗
U look not sick at all
This is an insult to the Intramural Research Program at the NIH and the work done by Wilhelm Burgdorfer, Ph.D. along with countless colleagues that spurred more than 6,000 studies on clinical, epidemiological, and bacterial aspects of Lyme disease. These researchers had the fortitude and confidence to submit their work to prominent medical journals after careful review and scrutiny.
Looking at this logically, are we to believe that through thousands of hours of research by highly trained scientist and medical personnel, all of these people failed to mention anything that resembles morgellons disease in the details of Lyme disease?
I can tell you why there was no mention of anything resembling morgellons disease in the more than 6000 studies. Because it wasn't there. There is no correlation between morgellons disease and Lyme disease anymore then there is a correlation between morgellons and diabetes, or the countless ailments known at this time.
Unfortunately, OSU has lost its way in the area of scientific research on this matter. In the 17-year history OSU's research of morgellons disease has led people no closer to real answers then when started.
One must understand that each department at OSU has to submit a presentation such as this. There is nothing special about this one. In fact, I would conclude it is harmful to the morgellons community and those that suffer.
The goal would be to submit scientific findings regarding morgellons disease to other prominent scientific establishments around the world so it can be scrutinized by scientific scholars. Something OSU has yet to do publicly.
Some may mention, "What about articles submitted to PubMed/Dove Press/Google Scholars by LLMD's"?
Simply put, Dove Press is a pay to play publication, and PubMed/Google Scholars are simply a search engine. They do not give validity to articles submitted.
While morgellons has been proven to be much more than a dermatology issue back in 2010, there has been very little done to combat misinformation. Institutions such as Mayo Clinic and Wikipedia still reference morgellons as a skin disorder while OSU stands by and continues to allow this to now turn into disinformation.
Let's all be a little smarter and expect a higher level of performance from our scientific community. While OSU has produced some great works in the past on other subjects, it has been a failure with regards to morgellons disease.
We expect better.
Well said! You are right lymes has nothing to do with this
The ticks from lab 257 are what originally started to spread this. Get educated.
Huh, so why has the CDC finally came out with the findings of Morgellons being a physical disease and not psychological. Yes,it's been a long time coming, but I believe they just did this in the last few months.
Plus, if you do not suffer from this, shut the F up. This is a very serious disease and just because the disease itself may not be deadly, it does have a very high suicide rate in sufferers. It's because of people like you,that don't know what they are talking about, are making them feel less than dirt and taking any little hope away that pushes them to the point of murdering themselves. I'll pray for you, you pray for me 😊
Great information! I would love a link to the poster you showed on screen. I could not read the names of the organisms and you said them really quickly.
I appreciate your research and work. My background is in micro and nanotechnology... so from what I have experienced it is bio-nanotechnology (some of it self replicating). It is horrific and much of it looks not of this world. I dare say bioweapon!
Can you be more persistent with your background, since I have no clue of this hierarchy.
I have got it, I don't think its a bioeapon. Maybe, I think its my body making it though. Cooking oil gets them out by the thousand. So i have been using that before showering
They either come out better cuse of the lube or used to think it was no air supply - but this doesnt seem alive. Just annoying.
Agreed! I am an engineer and this stuff can’t be from this planet.
@@mindbox11 I worked for a big tech companybuilding nano and microchips from the bare silicone to after all of it's layers were on. I worked closely with engineers all along the way. Then, after not woking for a while I started breaking out in bizarre looking sores. Someof the things that came out of me were chips, quantom dots, claws, spiders, webbing, fibers, ants, glass like substance, sticks and much of it is so horrible I can't put words to what came out of me...a massive living nightmare.Whoever has this I truly feel for them.
it is changing being exposed to certain frequencies...
It is encouraging to find the research you are doing. Thank you. I don't know if I have Morgellons as I don't get red and blue fibers, but I have a lot of the other symptoms. These happened soon after I encountered a lot of ticks.
I do feel that my condition is also fungal related and I wonder if you have done any research into a fungal connection to Morgellons.
I wish so bad there was a cure. This disease is one of cruel and punishment. I am on year 6 of a breakout and my head is no longer mine. My hair (hairlike Im sure its not hair it just looks that way) Is constantly moving there are pools of hard biofilm that switches from liquid to solid constanly. My eyes can hardly see to read my nose has tunnels all through it. They fill up with the biofilm and then it hardens. There is a dark brownish substance on my head and when the biofilm starts it's moving gravity pulls it down over my face when it moves it leaves those brownish chunks stuck in the film impeded in the when the biofilm goes from liquids to solids. I'm at the end of my rope the brain fog makes so I cant do simple multitasking and it's taken me almost 15 minutes to type this. I need help I cant take it no more.
anyone?? I will put a video up showing some of this. One last thing my hair glows bluish green dots and the clear hair has taken over I forget what they arre called cyan something.
I could share some pics and vids that ive not seen online yet.
Dear friend, what you are narrating is something tremendous. I consider that even being in such a complex situation it is advisable to remain calm, and of course what you say is not an invention, several participants in chats mention similar things. I leave you a brotherly hug.
We need to talk in dealing with the same
Me too also has been almost six years. Started for me in 2018 and I understand every word you said. I feel like I’m wasting my life away in the bathroom taking hours in the shower trying to feel clean again to no avail. Can’t talk about it or you are deemed crazy. We look like drug addicts to most people bc lesions on our body and a lot of ppl with morgs call them bugs. Honestly the most logical explanation I’ve heard is the way it’s been described by Harold Kautz-Vella. I recommend listening to his explanation about it. It atleast gave me answers to most of my questions about this disease. He has some very controversial topics that he researches Morgellons happens to be connected to those. It doesn’t coincide with mainstream science which is why I only heard of him recently. I pray we all get some relief I agree with you that this disease really takes away your will to live. The mental anguish it causes is worse than the physical pain and discomfort. It’s torture.
I am with you my friend. I have prayed for an answer to fight this. I heard Salt, Light and Iodine. So, light may be fighting the skin with UV/UB rays to kill topical things. Salt has helped me to break the biofilm. But there are also helpful all natural salts that are helpful when eaten. Celtic salt, etc. Iodine needs to be taken orally. Look up Saturated solution of Potassium Iodine. There are other natural things I'm doing for my skin now. I'm being the guinea pig until I get a scrub together for biofilm. I'm also working on a spray that kills this stuff naturally. When I'm done, I can help many ppl to clear the dermal issue. But it's a multi faceted disease. There are many steps we have to take to heal. Can't wait to see the punishment of the evil that created this atrocity. God says not to touch His anointed and do His prophets no harm! Psalm 91- only with your eyes shall you see how the wicked are punished. And my Jesus will Always protect and provide my needs. Looking forward to formulating cure for the biofilm and skin ailment. It will be from God and His creation. Not AI or Nanotech.
Jesus is in control Be encouraged. Help is on the way!
I’m on this boat too! I completely understand everything you have stated. It started in 2018 for me. But I had suspicions bf that. I too have lost my life and identity to this crap. I isolate myself. It’s a constant struggle NO ONE understands. I don’t even try to explain it to ppl anymore. Why bother.
Co-infections are many, but is it not all treated by sski and antifungals?
It does feel hopeless. Doctors will be dismissive, so I'm not sure what to tell you as far as that's concerned. It is systemic and makes the entire body sick, along with crawling, biting, stinging, and burning sensations. It does go into remission after 5 - 10 months (seems like forever) and then life will return to normal for a couple years. Listen to music, meditate, and try to make the pain transformative. When you're well, make the most of every minute.
This is fabulous Samantha. Thank you so much for your diligence.
The CEHF is a fake and fraud organization
Thank you so very much for researching this it's such a horrible disease I've lost everything because of it
This youtube video may shed some light on your Morgellon's disease. ua-cam.com/video/DUdqyfBEjHg/v-deo.html
So did I. And I mean everything! It invaded my home, my clothes Even my animals had to be put down they so infected! I couldn't keep😢 them and did not want to infect others if adopted. This was 15 yrs ago. I lived in a hotel for two years so that I could move to other rooms when my body parasites infected it. I've found ways to manage it now and I'm left completely traumatized. It has destroyed my life.
😊
Me too...
It has nothing to do with a damn tick. Randy has been working on this for 20 years. And still doesn't know wth??
I have the disease and it was during a time when I had a low immune system and had to fight a staphylococcus infection that ultimately caused an amputation. I have researched the disease and have found that it seems to be prevalent among women who are menopausal, low thyroid levels, and high cortisol levels. If I receive steroid injections and steroids by mouth during flare ups .. I have hardly any symptoms. I feel like it is a autoimmune condition that is attacking itself. My itching is controlled by weekly bleach baths, vitamin D , sunlight, and not sweating. Hope they find a cure soon because this is a horrible horrible disease and frustrating that they label it in our head
How do you cure MD?
Using over syllabled medical terms only helps your grade in class but helps no one get well infact this plague has shown how medical industry controlls doctors so they dont cure but administer diagnosis for the come back.
Ok and so what is the cure or helps against morgellons?
This youtube video may shed some light on your Morgellon's disease. ua-cam.com/video/DUdqyfBEjHg/v-deo.html
I'm just curious if the Rh negative people are the only ones having this outbreak and everybody else's body is just accepting it
I think there is something in the immune systems of people with Morgellons that does not fight it like everyone else. I think it is something that everybody has living on or around them but there is something our immune systems are lacking that won’t fight this frap off. I feel everyone I live with would have this as well, it’s just they have immunity to is. The little white fuzz is on everything. I can’t wear certain types of material because of what my body does to it. My body ruins my clothes. I just hate it… I have to use a sweater shaver on my socks after every wash. On majority of my clothes. The little fuzz balls that are created from my skin are horrible.
I'm with you on that. You have these Morgellons groups, but using them for questions is comical. There are too many shills. You can't get a straight answer. I believe everyone that has Morgellons has a negative blood type.
May G-d bless you in this important work.
Thank you for your research. I pray you find a cure.
Finally, something scientific ! Thanks! Keep researching please
Finally?? They have been gaslighting the public with this same nonsense for over ten years.
Great to know, now where can us sufferers go to get treatment and help! because all the doctors I’ve been too are lucky if they can tie their shoes by themselves without sending you a 1000 dollar bill..and have no idea what your talking about…my infection has started out as as UTI and now has spread into my intestines, hair, face etc…over the course of 15 years without much professional help
How do we get intouch with someone from the morgellons research team @ Oklahoma university ?! Please help
I have lots and lots of samples that I've been saving over the years that I've been fighting this stuff so if I can give it to anybody who will do something with it please make a comment
can someone share what do you do to fight this? Is have been a terrible 2 years. have been in doctors, dermatologists, event witchcraft! this is really lame and hate it.
Im using coconut oil and lemon juice. That seems to help it to pop out the skin. It seems they hate lemon juice. Coconut oil also helps a lot.
Im tired :( ...
Thank you for researching this curse. How nice to not be written off.
Probably came from gain of function be lab?
It is a miasma.
They are from gmo, water, air.
Look up loosh energy.
Resistant to HEAT, multi-organism
Is it possible to access the full research paper?
There so much more information on this topic than what's available online. For example, the first reported case was not in 2002, it was in 1989 in the state of Missouri.
Please provide the link to this publication along with the graphic presented. We are trying to collect as much peer reviewed research as possible to assist my poor 73 y.o. sister who is suffering terribly from MD.
Thanks Samantha. I have a lot of questions. One obvious one: if this is bacterial, what are the macroscopic materials which are embedded in wounds and under intact skin?
Research has shown the filaments primarily keratin and made by our own bodies in response to the condition
Colonies of microorganisms at different stages of the life cycle.
Did I miss if it said anything about whether this is contagious?
Omg thank you! I’m struggling so badly because of this! And I’ve been to several doctors, whom barely looked at my head, str8 to mental health. How can I be a study candidate or who can I see for help?
This youtube video may shed some light on your Morgellon's disease. ua-cam.com/video/DUdqyfBEjHg/v-deo.html
Difficulties of diagnosis that’s an understatement in all the nonsense about it being a mental condition is absurd put somebody’s skin under a black light with the black lens not the regular one the one they used to look for glow in the dark rocks, put somebody’s skin under that black light with time lapse photography and you can watch the fibers come out for me. They’re very small, bright blue, but when you turn off the black light, you can’t see them there’s no mistaking there’s no doubting it when you watch it actually come out of your skin for me, there’s also something that looks like a very small parasitic worm scabs at the surface of my skin and under 12 X a jewelers loop that I have I’ve seen things that look like a flying insect. I know it sounds fantastical but I think you’re fine using that black light very very very informative. I could use some help. Thank you I appreciate you.
How do we kill it?
Agrobacterium GMO spread to humans
Gangstalking is at the root.
I aggre
I would like to see the link between mold in home and also who has pets. My dog was diagnosed with rare yeast from rabbits. We had lived in mold unknowingly.
I had blood gene test wich cover 17500 pathogen no special finding in Nov. 2023 in China.
I have a son who is 25 and went through he'll for 3 years. He was never diagnosed. I suspected limes, but no one believed me. He now has severe mental disorders. Can this be related? We are as a family not doing well because of this. I am looking for some help please. Thank you and Many Blessings
There's an excellent GMC parasitic twin it's about 55 bucks is for men specifically and there's one for women, you can also if you can get your doctor to prescribe you a parasitic cleanse that works as well... And topical ivermectin
The 5%
She said all the fibers she's seen were keratin which means it's animal hair. She also says past research has given results 'from unknown to keratin', where are those studies? If it's unknown was it because they were using poor analysis?
I pray for a cure. My nose is rotting and they assume its drugs along with the skin lesions. I'm sick of being looked at a a crazy drug addict.
Live bacterium and cooling design.
Had it for 15 years
does your hair move on its own?
gf has it and it gets triggered at various times 😢
cantagious. You have no feeling?
Do you feel it as well when she has a flare up my bf says he feels and sees the fibers.
DOES IT SPREAD VIA INTERCOURSE?!
Disgusting bro!
Everybody has Morgellons.
Do the red wine spit test.
I think it has to do with spirituality as far as being aware of it or not but yes you are right. Everyone is infected with this stuff. It appears to be building some type of network then goes into standby mode. It has many life cycles which makes sense considering it is a bioengineered set of silicon & aluminum based life forms.
Some clearer pictures would help my microscopic evidence. I cant fimd any evidence of the ones that come ffrom my chest evry morning. Treatment for scabies isnt wotking.
Nothing topical works, sir. I take a homeopathic called yeast guard, and Ashwaganda, and vitamin e. Benadryl and Sleepcalm at bedtime. Quit eating breads and sugars. I been fighting it for nearly 30 years. Also, drink only purified water. There's no cure, no doctors who care. I'm a disabled RN, so I searched for the answer for years. I got Lyme disease from a tick and all hell broke loose in my body. I put vitamin e on my skin and skin so soft oil from Avon. We have NO choice but to live with it. I quit focusing on it. Sending love and prayers. Take care. ❤
You can fight this easily. This is a problem of people bodies being too acidic, + air and water pollution with micro plastic everywhere.
Solution is easy but many people will laugh and don't even try this and for them I can't do anything.
1. In the morning take one small spoon of baking soda, put in a glass, add half a lemon juice, it will react, top it off with a water and mix it good, drink, everything that is left in glass add more water and drink it, morning and evening, this will help in pulling your body back to a normal state which is more alkaline, less acidic state. If you can, add turmeric to the mix, it is as combine an elixir not only for this shit, but also returning our body state to alkaline instead of acidic removes the posibility of any type of cancer, as some people know, that cancer is nothing else then autoimmune disease ( your own body attack it self )
2. Get zeolite powder. mix with water with 5 grams of zeolite in a glass of water, use every day once a day. Zeolite eliminates toxic stuff out of our bodies, repeat the step for zeolite for a month. With baking soda just after one month, reduce it to one spoon one glass of water every day.
Did this cure you? I recent also came to the conclusion about it being caused by acidity in one’s body. To eat clean and detox metals and we can heal ourselves. I’m going to try it. I know it is simple solution but it’s so hard for me to be disciplined enough to eat zero processed foods. Mostly Bc no energy means no money and eating a strict diet of all organic no processed foods expensive.
Stop spreading this nonsense. Acid kills bacteria and fungus, exactly what sufferers would benefit from.
it will help, but will not cure, and does not heal the holes in your skin if you have them (yet)
##SpeakoniT
Lyme’s Disease
Micro plastics
not just micro plastics.
I have the disease and it was during a time when I had a low immune system and had to fight a staphylococcus infection that ultimately caused an amputation. I have researched the disease and have found that it seems to be prevalent among women who are menopausal, low thyroid levels, and high cortisol levels. If I receive steroid injections and steroids by mouth during flare ups .. I have hardly any symptoms. I feel like it is a autoimmune condition that is attacking itself. My itching is controlled by weekly bleach baths, vitamin D , sunlight, and not sweating. Hope they find a cure soon because this is a horrible horrible disease and frustrating that they label it in our head