Living with Morgellons-Treatment Suggestions

[Natashacbk]

Ditto-He has demonstrated and empathy and caring that I have yet to see anywhere else. You are right on!

Originally Posted by pmr

There's not much we know about our disease, but there's one thing I am sure of. My friend Marc Neumann. He has worked tirelessly on our behalf. His products are great. The DSP skin dries on my skin quickly and the nasty stuff can just be rubbed off. Out come all kinds of critters. Or you can leave it on and let it dry the suckers out. Since I've used the mouthwash he makes I haven't had a toothache. And If you have mucky stuff sliming your hair, the body wash, besides helping get stuff off your skin, will clean your hair very well.

I find it very odd that he has DSP cream, and suddenly there was this new cream called ESP. I'm not saying--I'm just saying....copycat out to make money?

The reason I know about Marc is that I bought some products from him and emailed him. Then he called me all the way from Germany. There have been lots of calls, and I feel like he is a very good friend. When he knew I was totally broke he sent me products. Not only his own, but things to help my sick gastrointestinal track, and even suits to wear around the house to help keep me from being reinfected. I remember standing in the kitchen, tears running down my face at his kindness, when I opened the boxes. I'm not the only person he has helped out like this. Go to his site: Morgellons Research Organization. Go to his blog.

And to clarify--he went to the hospital with a serious lung problem. It had nothing to do with Morgellons. His site was hacked and he is just putting it back together. And unlike others profiting from the sufferers of Morgellons, he also has it. His skin symptoms are gone, but we all know that Morgellons is not just a skin disease.

Marc never said his products cure Morgellons--but in my estimation, they are great and really help.

[Natashacbk]

I haven't had any problems with my hair...yet. However, I am not going to wait for that to happen so this is how I have been taking care of my hair:
I wet my hair and spray Marc's body wash on my scalp, then I rub it in and let it sit for a minute or two. I then take a mixture of Dr. Bronner's peppermint soap, a few drops of grapefruit seed extract and add a little of my favorite tea tree shampoo and a splash of dsp body wash...I shake it up and then I wash my hair -let it sit while I wash the rest of me with the same stuff. Sometimes I'll use eucalyptus instead of peppermint but always organic. I also use a natural bristle body brush to scrub my skin. After all that, which is not that complicated - I rub organic coconut oil all over my skin and I condition my hair with an organic tea tree conditioner and rinse with rosemary (which makes my hair shiny and healthy) So far so good...it seems to be working fine...no hair loss or dry, brittle hair. Oh yeah, I also condition my hair with Coconut oil every now and again.

By the way, I use Jane eyredale powder on my face to cover up the Morgellon's it rates very, very low in toxicity on the cosmetic database. Which people should look at in regard to the types of products they might use - it is very useful. I was very surprised to find that some of Dr,Haushka products rated very high in toxicity.

Hope this helps

Originally Posted by wootty1987

I agree Marc called me and offered advice as soon as registering on his site.

Has anyone had good success clearing away the Biofilm on forehead with the cream or wash?

I have the slimey crap mucking my hair - i am losing lots of hair too - has anyone seen a halt to thier hair loss when using the wash on scalp etc?

[ChatCat]

Sorry made boo boo

[ChatCat]

Originally Posted by wootty1987

I agree Marc called me and offered advice as soon as registering on his site.

Has anyone had good success clearing away the Biofilm on forehead with the cream or wash?

I have the slimey crap mucking my hair - i am losing lots of hair too - has anyone seen a halt to thier hair loss when using the wash on scalp etc?

--------------------
This was the question that I was trying to respond to (sorry I had problems with posting correctly)
From Wotty:

"Hi All,

Just something that i am wondering.

How many of the people with M's have the 'Biofilm' problem with their faces & scalp?

It confuses me why some don't have it and some do."
-----------------------------------


Hi Wooty,

I haven't had outward goo but I have it internally in my ears, nose and digestive track.
I won't get into the gory details. The good news is that it is breaking up more and I am feeling better that I have since I got Morg.
The more faithful I am at using my FIR Sauna and Pad day and night, the better I do. Also, things have improved since I have been using vibration to help break things up faster.

It is so good to hear that others are doing better also. This brings us all hope for ourselves and for those who will benefit from our experience in the years to come.

[ScarlettK]

Did you ever get any feedback on this WOOTY?

I'm new to this site, but all this info has been exponentially helpful in dealing with this SciFi-esque disease...this was my first week w/biofilm EVERYWHERE (i'm hoping that means I'm healing because it's my first week trying various protocols for detox).

My scalp problem is pretty bad based on the posts I've read so far... i have LOTS of hair loss from yanking at the lesions & trying to comb thru dried biofilm, dents from scraping old lesions (like Barack mentioned), & when I comb through my hair after a shower/bath soak it's just yellow slime everywhere. My body feels slimy & disgusting if I don't scrub my skin like crazy, especially the back of my neck. And I came "face to face" with the Morg insect as well -> came out of my scalp this week & zinc seems to fend him off from areas I apply it to.

Really, the tiny "black specks" & "fibers" are what I find most debilitating, as I am constantly feeling the crawling & haven't mastered the art of what clothes/environments are going to reinfect me.

Pleas let me know your progress if you get a chance because our symptoms are very similar, based on your posts... thanks!

Originally Posted by wootty1987

Hi All,

Just something that i am wondering.

How many of the people with M's have the 'Biofilm' problem with their faces & scalp?

It confuses me why some don't have it and some do.

[lamb]

Nobody really knows what "it" is. It sucks.
Wash your clothes in Dr.Bonner's Peppermint Hemp Soap.
Wish I knew that when this all started.
Best Wishes.

[brainstorming]

Hello, I'm a new member. I've been aware of morgellons for a year but had symptoms before that. What works best for me so far is using Gwen Scott's red wine treatment in conjunction with Young Living Essential Oil oregano oil.
The oregano oil is very strong so I often cut it with olive oil when I rub it on. If I am feeling morgellons like exhaustion and itchy, I do the following:

swish organic red wine in mouth, spit out in white paper bowel after 1-3 minutes

pour 2-3 drops off oregano oil in the bowel immediately after spitting. It is amazing to watch the oregano kill all the microbes.

I make sure the oregano has killed everything before I pour it down the sink and repeat.

Each time I repeat this process I can feel my energy returning more and more.
I will often rub oregano oil on first my feet and scalp and literally feel whatever is making me itch migrate away from the oregano and towards the wine in my mouth. The morgellons seem to like the wine alot.

I have to use caution when rubbing the oregano on my skin. If I do too much, it feels like too many morgellons die to quickly within my system and I get bad symptoms.

After I have done the wine treatment anywhere from 5-50 times and I feel more clear, I will often put 1 drop of oregano oil in a liter bottle of spring water and sip it very slowly. I urge caution, though, because like the rubbing this can cause too much disruption in the morgellons too quickly and I sometimes feels like my blood vessels are getting clogged, causing heart pain.

I noticed twice when I rubbed alot of oregano oil on my feet, calves, thighs, and abdomen, I felt a crawling sensation in my legs part of the night as I tried to sleep.

If I eat out and ingest food with GMO's, I immediately feel morgellons tired and have to do the treatment. Let me emphasize, I get immediate relief from doing the wine/oregono treatment and getting some of these parasites out of my system.

I buy most of my food at Whole Foods. For a while, especially last summer and fall of 2009, I noticed I would feel very itchy around the carrots, tomatoes, lettuce, avocado, and asparagus I would buy. I started rinsing all fruits and vegetables in a pot with one drop oregano to about 2 gallons of water, then rinsing a lot to remove the oregano. The oregano seems to kill whatever was making me itchy.

I hope some of this helps. I am trying to buy diatamaceous earth, food grade, for morgellons but also for lice.

I also use 35% hydrogen peroxide from Guardian of Eden, highly diluted of course, but am not sure if that is a good brand.

I have red dots all over my skin that were a mystery for years. Now I understand they might be a symptom of morgellons. I am very grateful for this website and forum.

Julia

[sd72]

I too had the red dots, its usually a sign of alcoholism and its effect on the liver, but for us its not.I have been having good luck with Magnesium, I know for people with kidney problems its dangerous, but I have been taking about 1500% daily, while covering myself in epsom salts spray(magnesium sulfate).
Candida cannot survive in a magnesium dense environment and I think either this is candida or a simliar fungus it has an effect on. It has cut down my symptoms drastically. Most Morgies I have heard suffer from Lyme and a High Hyalauronic acid content, which magnesium keeps in check.

I think these deficiencies are brought on by lyme, which would make sense in families, it one person way back had it, as its carried by the blood, so mother to next generation. So once the body is robbed of the magnesium by the high hyalauronic acid content, it has a very acid body to grow the fungus, further perpetuating it. See how it works for you if you wish, just be careful with any with kidney issue, best of luck to all battling this.

[Digit]

I'm using Epsom salts too.
Been looking at Fungus. Fungus Gnats their larvae and Collembola feed on and are attracted to some fungus. How about this for a candidate for the head lesions and freaky hairs and head protrusions.
Tinea capitis and Tinea favosa
Our Collembola look nothing like what the Americans call 'springtails' they're tiny mites and larvae that live in the soil. I'm adding Citronella to the mix this week.
Checklist of the Collembola: Synanthropic Collembola, Springtails in Association with Man
Fig 3 reminds me of 'the lizard' if as they say..
"If there were forms burrowing in human tissue they should be highly specialised in form, such as having a narrow, elongated wormlike body with strongly reduced eyes, antennae, limbs and furcula and having highly modified mouth parts for biting through human skin and underlying tissue."
Bio film, I read that it needed Iron to reach a point where it reduced motility and settled in, so maybe watch your iron intake. Ask Xib?

[Janice]

pringtails
Richard Houseman
Division of Plant Sciences

Springtails are tiny insects belonging to the order Collembola. About 700 species of springtails occur in North America, and more than 6,000 worldwide (Figure 1). They are wingless and have limited vision. These and other primitive features have convinced some scientists to exclude springtails from the class Insecta, placing them instead in a separate, exclusive class called Collembola.