How is the plastic removed?
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Old March 5th, 2010, 11:51 AM
Cleft_Asunder has no status.
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Default How is the plastic removed?

So yeah, I got what feels like tumors on my head and if I press my tongue around the inside of my mouth I have nodules there. I firmly believe that it's not tumors but plastic that is being stored there by the body. That's why it NEVER goes away or changes. They have been there for years, probably blocking my whole circulatory system, while the parasites do their thing around it. It's in between my bones and skin.

Dr. Staninger says she gets rid of it by using opaline, an oxygen product applied to the skin. Has anyone tried this and does it work? What is the protocol? Is it mixed in with water then applied?

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Patients have described a tightening feeling over the scalp (like wearing a bathing cap), which is a silicone layer between the skull and skin. This was discovered by Dr Kajoo taking scalp biopsies. Patients that have this cap, if imagined, like a crown, also have a silicone shape in the middle of their forehead (pineal gland area) ?dragon shaped?, and then behind it a black fiber tubed network in the shape of a circle (not all patients have this, those that do, the shapes are the same and are physically visible. Patients that had this, had a tube that travels to the back of the brain.

To break up this scalp silicone, they have used ozone, Opaline granules or other oxygen products (without halides), on the scalp, which works.

Once the silicone starts to break up, the body starts to recognise it and will want to push it out causing side effects - fever, nausea and may get ill. All patients have ammonia in their blood also methemoglobin reductase problems, which means they couldn’t break down the ammonia or make vitamins needed.

When patients have an ammonia reaction, their heads or ears turn red, because of lacking B1 and B3. If the whole body turns red or patchy red or pink, then its carbon monoxide in the blood (which is a by product of the network breaking up). Taking Vitamin C can neutralise the carbon monoxide.

Patients say they hear a snap, crackle and pop and at the same time they get cold, like feel cold air on the skin, once on O2 treatment. Hilde traced this to a double walled nano tube breaking up. The tube is made up of carbon in middle, silicone in between and carbon monoxide.
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Old March 5th, 2010, 01:09 PM
ChatCat is Recovered! Thank you Dr. Staninger
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Quote:
Originally Posted by Cleft_Asunder View Post
So yeah, I got what feels like tumors on my head and if I press my tongue around the inside of my mouth I have nodules there. I firmly believe that it's not tumors but plastic that is being stored there by the body. That's why it NEVER goes away or changes. They have been there for years, probably blocking my whole circulatory system, while the parasites do their thing around it. It's in between my bones and skin.

Dr. Staninger says she gets rid of it by using opaline, an oxygen product applied to the skin. Has anyone tried this and does it work? What is the protocol? Is it mixed in with water then applied?
Hey Cleft,

Great post. I am working with Dr. S to get rid of Morg and have it in my head. It mainly seems to be in my ears, eyes and nose, but I am sure it is in my brain also because it affects my balance also at times.

I am doing much better now after working with Dr. This will be my third month.
I believe the trick is to try to follow her protocol as closely as possible.
The FIR is the most important, however the body has to be able to expel this crud.
It will come out but it will take time. I think that consulting with Dr. S on the phone has helped me tremendously and I spend at least 1 hr. daily in the MPS sauna along with sleeping with the pad under my pillow every night.

IMO, opaline oxy caps, Willards water, Happy Tummy 1 and HT protein are the three most important supplements to use. Shortly after using the oxy caps I felt Morg breaking up all over my body. Even though it was broken up, it took time to leave.

One more thing that really helps (while your in the sauna) is to use oxygenated coconut or olive oil all over the body esp where you feel Morg is most concentrated. I use it in my nose, ears and anywhere that I feel Morg activity and you can see & feel it coming out.

Keep us udated on your progress.

Thanks, cc

PS. can you post the link for where you got this quote from Dr. S. please, TY

Last edited by ChatCat; March 5th, 2010 at 01:14 PM.
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Old March 5th, 2010, 01:47 PM
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I don't have 15 posts yet so I can't post a link so fill in the blank.

morgellons-disease-research.com/Morgellons-Message-Board/morgellons-treatment/3857-dr-hildegarde-staninger-environmental-toxicologist.html#post25775

I'm going to head over to vitamin shoppe to try a bottle of oxygen caps. I cannot afford the infrared devices now so I need an alternative. Btw, I notice when I go outside and get fresh air, my face turns almost normal. Therefore it is evident to me that oxygen is important.
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Old March 5th, 2010, 02:33 PM
tcmgpt13 is "status viatoris."
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Some have felt opaline helps while some others here have said it did not make that much difference to their symptoms. That's about the size of it with Morgellons. What works for one does not necessarily work for another to improve symptoms.
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Old March 11th, 2010, 02:20 AM
Baraka Obam is FEARLESS LEADER
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Default A friend of mine sits in a wheelchair

my buddy has been crippled by this I am sure, he does not show lesions, but he has many of the other situations, they diagnosed stroke, but then found a undetermined mass in or on the spine. i will bet it is like the one I saw on my cat scan. he lost, as I did, the use of his left arm, now the other one hurts
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