In the beginning I noticed what looked Like a parasitic worm of some sort with a cartoon like look and personality. I was sure I was losing my mind, of course. Also, the symptoms that others tend to see which was that bluish-green fuzz in my wounds and scabs and a fiber like material that looks like hair sometimes. I had the creepy crawling sensation like something was crawling all over my skin and itching 😫 especially my back the symptoms started on my neck and Chin and then my back and chest eventually moved to my fingers, back of the hands, arms and then legs in the thigh area. No doctor gave much interest and would barely look at me. I was embarrassed so actually sticking to an appointment was not something I always followed through with. If it wasn’t for my life partner, I probably wouldn’t have shown up to any of them. She would be the 1st to say I developed some psychosis and depression. I would stay up for 2 days cleaning and washing my hands and then sleep anywhere from 3 hours to a day and a half. I spent much longer to get any task done than I used to including my 3 hour baths. I was afraid of things in and out of my home but in December I was at least 7 months into the disease symptoms. I noticed a shift in my symptoms where it seamed to be changing constantly and my environment had much more influence. My 1st example of this was I had found a stinkbug in my son’s room and then a few days later noticed my sores on my hands where the exact shape and up to the same size. In my research I found that there where also smaller bugs called carpet beetles that looked like the same shape on a smaller scale but was also linked with carpet beetle dermatitis. Basically there are a few unlucky people here and there who develope a skin reaction to the shedding skins of the bugs and the hairs on the “catapilar like” young. The only true problem was this was only my problem for maybe a few days out of the month. When I read about that syndrome I was 100% sure this was the diagnosis and the cause of my morgellons. However it quickly turned into another problem when my symptoms changed again. In fact every couple of days it was as if I had a completely new illness and just like that sometimes would disappear to never be seen again. Suddenly in December this Faraway coronavirus we hear about on the news is at our doorstep in fact my partner and I both developed pneumonia like symptoms somewhere around January. Once those symptoms were gone after a couple weeks my next set of symptoms promptly followed. Like most people with morgellons I have a theory. For one thing I do not believe that morgellons is a disease I am one who believes that it is more a set of symptoms making it a syndrome. and I believe that the people who have been suffering from morgellons syndrome for the past couple decades has been because of electromagneticm waves. That’s right it’s another crackpot theory from the morgellons department. 5G just so happen to have then started in China in 2019 followed by the rest of the world and the coronavirus is only one thing that the world seems to be suffering from since then. There has also been different rashes like mine and some that are more like frostbite also children have their owncown related symptom which they are saying is an anti inflammatory response. I think that the people who had morgellons before this we’re just more sensitive to the 4G and now that 5G has come out there are more of us following in their footsteps. If you have any information that could prove this wrong or maybe even prove it right feel free to leave your stories or comments let’s put our experiences together and hopefully solve our problem. I almost forgot one of the scariest symptoms that I have had is seizures they started as kind of a twitching or jerking mostly when I lay down to sleep but have developed into seizures where I lose consciousness or are unable to respond for short periods of time. I’m sure I’ll come up with more things to share and I hope you do too.