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Post by medic642 on Nov 4, 2013 17:30:10 GMT -5
Hello, I am new, I have Morgellons, with several colored fibers, many lesions on my face now and spreading, but they are all over my body. What is this you guys are talking about with pin worms, larve, and machines ? Please explain,,,,also where do you get that tree oil and stuff you guys are using, also is their any doctors in Sacramento, Ca. That believe in Morgellons? Any help or response is appreciated, i'm ashamed to show my face outside, and do you guys nurse your lesions daily too? I noticed that under alot of them it seems like the skin had turned to liquid. I also have Multiple Sclerosis Thanks
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marigold47
New Member
Am detoxing and changed diet, nothing yet is working. Ivermectin/Fenbendazole, hope it helps soon.
Posts: 2
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Post by marigold47 on Nov 9, 2013 23:49:01 GMT -5
Hello ! I am also new, it has gotten to the point where I am isolating now, it's moved from just on my chin to under my chin on my neck. Have trie to not obsess about this disease but it's difficult. Am tired of the layers of makeup (always afraid it will come off) it takes to go out in public AND the long sleeves I have to wear. Help ! Somebody please tell me there is a way to resolve the lesions. I know I will have this for the rest of my life but would like to at least resolve the lesions. Have done alot, am doing alot, no progress.
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Post by pmamama on Dec 6, 2013 14:16:11 GMT -5
Most of the natural soaps and oils mentioned are available at a health food market, but you can also find good deals online. There is so much different information about what works for certain people on websites, but I think it's best to do research on your symptoms and the remedies which could help YOU particularly. I'm new on here too. I spent the last year and a half in isolation, thinking that one day i would feel better, but I am getting worse each day. I am at the point where I just want help...I'm desperate for support and some guidance / information from others who are dealing with this. I am in so much pain. It feels like there is a fire inside my hands and feet, crushing my bones! I can't bear the pain any longer!!! I don't know if pain medications would even work because it is so intense. Does anyone else notice their bones seem to be disintegrating? I don't mean to scare anyone...I just want to see if there is anyone who knows what could be causing these bodily deformities. When I have seen Drs they always look astounded by what my bones look like..and also the strange bulls-eye rashes which will not heal. They look frightened, almost as if they KNOW what it is but do not want to be held accountable for treating it. I have NOT received proper medical treatment...I just keep getting sent to different drs who refer me to the next. I am seeing a Lyme Disease specialist soon. Does anyone have advice about undergoing antibiotic treatment for Lyme while it has progressed to the unmistakable symptoms of Morgs?
THANK YOU FOR ANY HELP AND ANSWERS YOU CAN PROVIDE! please help us newcomers out!!!
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Post by Admin on Dec 6, 2013 14:44:05 GMT -5
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